| Other mutations in this stock |
Total: 3315 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110008P14Rik |
C |
A |
2: 32,381,764 (GRCm38) |
G3C |
possibly damaging |
Het |
| 1110032A03Rik |
C |
A |
9: 50,768,219 (GRCm38) |
|
probably benign |
Het |
| 1520401A03Rik |
G |
C |
17: 23,715,763 (GRCm38) |
A96G |
possibly damaging |
Het |
| 1600015I10Rik |
A |
C |
6: 48,932,468 (GRCm38) |
K549T |
probably benign |
Het |
| 1700001C19Rik |
T |
G |
17: 47,413,734 (GRCm38) |
N154T |
probably benign |
Het |
| 1700003E16Rik |
A |
C |
6: 83,161,115 (GRCm38) |
K74N |
probably damaging |
Het |
| 1700013G24Rik |
C |
A |
4: 137,454,992 (GRCm38) |
P153T |
probably damaging |
Het |
| 1700016C15Rik |
A |
T |
1: 177,741,017 (GRCm38) |
R27W |
possibly damaging |
Het |
| 1700017N19Rik |
T |
G |
10: 100,612,429 (GRCm38) |
M274R |
probably damaging |
Het |
| 1700019N19Rik |
T |
G |
19: 58,787,706 (GRCm38) |
K105T |
probably damaging |
Het |
| 1700030J22Rik |
G |
T |
8: 116,973,597 (GRCm38) |
T22K |
probably benign |
Het |
| 1700123K08Rik |
G |
T |
5: 138,563,553 (GRCm38) |
Q124K |
probably damaging |
Het |
| 1810046K07Rik |
G |
T |
9: 51,291,564 (GRCm38) |
P97T |
probably benign |
Het |
| 2310035C23Rik |
G |
T |
1: 105,719,615 (GRCm38) |
R734M |
probably benign |
Het |
| 2310050C09Rik |
T |
C |
3: 92,869,274 (GRCm38) |
Q34R |
probably benign |
Het |
| 2610021A01Rik |
G |
C |
7: 41,625,342 (GRCm38) |
L156F |
probably benign |
Het |
| 2610028H24Rik |
C |
A |
10: 76,452,863 (GRCm38) |
P85Q |
probably damaging |
Het |
| 2610042L04Rik |
A |
G |
14: 4,348,869 (GRCm38) |
E10G |
probably damaging |
Het |
| 2700081O15Rik |
C |
G |
19: 7,422,747 (GRCm38) |
P193A |
unknown |
Het |
| 2900011O08Rik |
C |
A |
16: 14,049,481 (GRCm38) |
R68S |
probably damaging |
Het |
| 3100002H09Rik |
T |
A |
4: 124,610,705 (GRCm38) |
D18V |
unknown |
Het |
| 3110018I06Rik |
C |
G |
12: 107,488,855 (GRCm38) |
R67G |
unknown |
Het |
| 3110082J24Rik |
G |
C |
5: 30,105,067 (GRCm38) |
A98G |
unknown |
Het |
| 4833420G17Rik |
C |
A |
13: 119,477,808 (GRCm38) |
T484K |
not run |
Het |
| 4833423E24Rik |
C |
T |
2: 85,518,462 (GRCm38) |
R102Q |
probably benign |
Het |
| 4921501E09Rik |
C |
A |
17: 33,065,657 (GRCm38) |
D724Y |
possibly damaging |
Het |
| 4921507P07Rik |
G |
T |
6: 50,574,021 (GRCm38) |
L483I |
possibly damaging |
Het |
| 4921511C20Rik |
A |
G |
X: 127,394,842 (GRCm38) |
K135E |
probably damaging |
Het |
| 4930415L06Rik |
A |
C |
X: 89,930,241 (GRCm38) |
N783K |
unknown |
Het |
| 4930447C04Rik |
G |
C |
12: 72,916,726 (GRCm38) |
F18L |
probably benign |
Het |
| 4930503B20Rik |
C |
T |
3: 146,650,956 (GRCm38) |
D66N |
probably damaging |
Het |
| 4930516K23Rik |
A |
T |
7: 104,059,288 (GRCm38) |
F105I |
probably damaging |
Het |
| 4930562C15Rik |
G |
A |
16: 4,866,248 (GRCm38) |
V236M |
possibly damaging |
Het |
| 4930595M18Rik |
C |
T |
X: 81,420,272 (GRCm38) |
G610R |
probably damaging |
Het |
| 4932415D10Rik |
A |
C |
10: 82,289,896 (GRCm38) |
L2427V |
possibly damaging |
Het |
| 4932415D10Rik |
G |
T |
10: 82,282,537 (GRCm38) |
L4880I |
unknown |
Het |
| 4932415D10Rik |
A |
G |
10: 82,293,228 (GRCm38) |
I1316T |
probably benign |
Het |
| 4933402D24Rik |
T |
A |
1: 63,756,335 (GRCm38) |
K90* |
probably null |
Het |
| 4933402J07Rik |
G |
T |
8: 87,568,574 (GRCm38) |
M113I |
probably benign |
Het |
| 4933403O08Rik |
C |
A |
X: 112,241,313 (GRCm38) |
R213S |
probably benign |
Het |
| 4933425L06Rik |
G |
A |
13: 105,111,144 (GRCm38) |
G324D |
probably damaging |
Het |
| 4933427D14Rik |
C |
T |
11: 72,159,000 (GRCm38) |
V852I |
probably benign |
Het |
| 4933427I04Rik |
T |
C |
4: 123,860,875 (GRCm38) |
L194P |
probably damaging |
Het |
| 5330417C22Rik |
C |
A |
3: 108,471,435 (GRCm38) |
W349L |
probably damaging |
Het |
| 5330417C22Rik |
C |
A |
3: 108,471,978 (GRCm38) |
G345C |
probably damaging |
Het |
| 5730559C18Rik |
C |
A |
1: 136,219,783 (GRCm38) |
R399L |
possibly damaging |
Het |
| 6430571L13Rik |
G |
T |
9: 107,342,527 (GRCm38) |
G60C |
probably damaging |
Het |
| 9430015G10Rik |
G |
C |
4: 156,122,011 (GRCm38) |
G76A |
probably benign |
Het |
| 9530053A07Rik |
G |
A |
7: 28,154,762 (GRCm38) |
G1717D |
probably benign |
Het |
| 9530053A07Rik |
G |
A |
7: 28,142,386 (GRCm38) |
S582N |
probably benign |
Het |
| A1cf |
A |
C |
19: 31,918,017 (GRCm38) |
I167L |
probably benign |
Het |
| A2ml1 |
A |
G |
6: 128,571,977 (GRCm38) |
F281L |
probably benign |
Het |
| A430005L14Rik |
CG |
C |
4: 153,960,665 (GRCm38) |
|
probably null |
Het |
| A730049H05Rik |
C |
A |
6: 92,828,066 (GRCm38) |
S69* |
probably null |
Het |
| A830018L16Rik |
C |
G |
1: 11,518,625 (GRCm38) |
Q89E |
probably damaging |
Het |
| AA986860 |
A |
C |
1: 130,742,991 (GRCm38) |
S317R |
probably benign |
Het |
| Aasdh |
C |
G |
5: 76,891,796 (GRCm38) |
|
probably null |
Het |
| Aass |
T |
C |
6: 23,078,857 (GRCm38) |
T719A |
probably damaging |
Het |
| Aatf |
C |
T |
11: 84,442,585 (GRCm38) |
A500T |
probably benign |
Het |
| Abca12 |
A |
C |
1: 71,284,070 (GRCm38) |
Y1618D |
probably damaging |
Het |
| Abca13 |
C |
A |
11: 9,335,182 (GRCm38) |
A3272E |
probably damaging |
Het |
| Abca13 |
G |
T |
11: 9,251,376 (GRCm38) |
G153C |
possibly damaging |
Het |
| Abca13 |
C |
A |
11: 9,267,461 (GRCm38) |
P301H |
probably damaging |
Het |
| Abca13 |
G |
T |
11: 9,294,342 (GRCm38) |
W2068C |
probably benign |
Het |
| Abca13 |
G |
T |
11: 9,335,181 (GRCm38) |
A3272S |
probably damaging |
Het |
| Abca14 |
G |
T |
7: 120,246,923 (GRCm38) |
G599V |
probably damaging |
Het |
| Abca15 |
G |
T |
7: 120,382,505 (GRCm38) |
G1061W |
probably damaging |
Het |
| Abca15 |
T |
G |
7: 120,346,026 (GRCm38) |
F442V |
probably benign |
Het |
| Abca2 |
G |
T |
2: 25,444,110 (GRCm38) |
V1800L |
probably benign |
Het |
| Abca4 |
G |
T |
3: 122,103,488 (GRCm38) |
W605C |
probably damaging |
Het |
| Abca4 |
C |
A |
3: 122,156,443 (GRCm38) |
S1805R |
probably damaging |
Het |
| Abca7 |
T |
C |
10: 80,006,559 (GRCm38) |
L1109P |
probably damaging |
Het |
| Abca7 |
C |
T |
10: 79,999,432 (GRCm38) |
R208* |
probably null |
Het |
| Abca8b |
G |
A |
11: 109,974,644 (GRCm38) |
T329I |
possibly damaging |
Het |
| Abca8b |
A |
T |
11: 109,961,908 (GRCm38) |
C761S |
possibly damaging |
Het |
| Abca9 |
G |
A |
11: 110,135,375 (GRCm38) |
A953V |
probably benign |
Het |
| Abcb10 |
C |
A |
8: 123,982,663 (GRCm38) |
G51C |
possibly damaging |
Het |
| Abcb11 |
C |
A |
2: 69,291,981 (GRCm38) |
G386V |
probably damaging |
Het |
| Abcb1b |
A |
G |
5: 8,827,441 (GRCm38) |
Y667C |
probably benign |
Het |
| Abcb4 |
C |
A |
5: 8,959,005 (GRCm38) |
R1221S |
probably damaging |
Het |
| Abcb5 |
C |
A |
12: 118,918,272 (GRCm38) |
G574V |
probably damaging |
Het |
| Abcb8 |
A |
T |
5: 24,400,995 (GRCm38) |
D226V |
probably damaging |
Het |
| Abcc10 |
C |
T |
17: 46,324,262 (GRCm38) |
A272T |
probably benign |
Het |
| Abcc10 |
G |
A |
17: 46,313,700 (GRCm38) |
H784Y |
probably damaging |
Het |
| Abcc12 |
T |
G |
8: 86,550,601 (GRCm38) |
K389T |
probably damaging |
Het |
| Abcc3 |
C |
G |
11: 94,361,275 (GRCm38) |
Q827H |
probably benign |
Het |
| Abcc6 |
C |
T |
7: 45,979,734 (GRCm38) |
D1363N |
probably damaging |
Het |
| Abcc6 |
A |
T |
7: 45,992,306 (GRCm38) |
|
probably null |
Het |
| Abcc8 |
T |
C |
7: 46,106,965 (GRCm38) |
S1439G |
possibly damaging |
Het |
| Abhd12b |
G |
A |
12: 70,163,451 (GRCm38) |
D134N |
probably damaging |
Het |
| Abhd13 |
A |
C |
8: 9,987,413 (GRCm38) |
K3N |
probably damaging |
Het |
| Abl1 |
A |
C |
2: 31,689,827 (GRCm38) |
K7N |
probably damaging |
Het |
| Ablim2 |
C |
T |
5: 35,848,858 (GRCm38) |
P409L |
possibly damaging |
Het |
| Abo |
C |
G |
2: 26,848,258 (GRCm38) |
V45L |
probably benign |
Het |
| Abtb2 |
G |
T |
2: 103,708,172 (GRCm38) |
E649* |
probably null |
Het |
| Acaca |
G |
C |
11: 84,260,720 (GRCm38) |
A815P |
probably damaging |
Het |
| Acacb |
G |
T |
5: 114,248,948 (GRCm38) |
R2386L |
probably benign |
Het |
| Acan |
A |
C |
7: 79,111,354 (GRCm38) |
H1938P |
probably benign |
Het |
| Acap3 |
C |
G |
4: 155,905,179 (GRCm38) |
N693K |
probably damaging |
Het |
| Acmsd |
G |
T |
1: 127,745,802 (GRCm38) |
V76F |
probably damaging |
Het |
| Actc1 |
C |
A |
2: 114,051,997 (GRCm38) |
C12F |
probably benign |
Het |
| Actl11 |
T |
G |
9: 107,931,700 (GRCm38) |
V1074G |
probably benign |
Het |
| Actl6a |
A |
C |
3: 32,726,543 (GRCm38) |
I411L |
probably benign |
Het |
| Actl9 |
C |
A |
17: 33,433,101 (GRCm38) |
P45Q |
possibly damaging |
Het |
| Actr10 |
C |
A |
12: 70,962,029 (GRCm38) |
A412E |
probably damaging |
Het |
| Actr1b |
T |
A |
1: 36,701,208 (GRCm38) |
H284L |
probably benign |
Het |
| Actrt2 |
G |
T |
4: 154,666,832 (GRCm38) |
N282K |
probably benign |
Het |
| Acvr1 |
C |
A |
2: 58,479,868 (GRCm38) |
G43V |
probably benign |
Het |
| Acy3 |
G |
T |
19: 3,987,107 (GRCm38) |
R13L |
probably damaging |
Het |
| Adam17 |
T |
G |
12: 21,361,737 (GRCm38) |
Q51P |
possibly damaging |
Het |
| Adam21 |
T |
G |
12: 81,559,743 (GRCm38) |
N415T |
probably damaging |
Het |
| Adam30 |
A |
G |
3: 98,162,360 (GRCm38) |
Y503C |
possibly damaging |
Het |
| Adam32 |
C |
A |
8: 24,948,750 (GRCm38) |
E16* |
probably null |
Het |
| Adam6a |
A |
G |
12: 113,545,321 (GRCm38) |
K438R |
possibly damaging |
Het |
| Adam7 |
A |
T |
14: 68,527,701 (GRCm38) |
S82R |
probably benign |
Het |
| Adamts10 |
C |
T |
17: 33,528,787 (GRCm38) |
R66W |
probably damaging |
Het |
| Adamts10 |
G |
T |
17: 33,528,788 (GRCm38) |
R66L |
probably damaging |
Het |
| Adamts12 |
G |
T |
15: 11,336,383 (GRCm38) |
C1518F |
not run |
Het |
| Adamts15 |
G |
C |
9: 30,910,700 (GRCm38) |
C480W |
probably damaging |
Het |
| Adamts16 |
C |
T |
13: 70,761,773 (GRCm38) |
R887K |
probably benign |
Het |
| Adamts18 |
A |
T |
8: 113,743,168 (GRCm38) |
I634N |
possibly damaging |
Het |
| Adamts2 |
G |
T |
11: 50,792,708 (GRCm38) |
R939L |
probably damaging |
Het |
| Adamts3 |
C |
T |
5: 89,775,351 (GRCm38) |
V199I |
not run |
Het |
| Adamts4 |
G |
A |
1: 171,258,783 (GRCm38) |
A715T |
probably benign |
Het |
| Adamts4 |
C |
G |
1: 171,258,784 (GRCm38) |
A715G |
probably benign |
Het |
| Adamtsl1 |
C |
T |
4: 86,342,177 (GRCm38) |
P883L |
probably damaging |
Het |
| Adamtsl1 |
T |
G |
4: 86,342,693 (GRCm38) |
M1055R |
probably benign |
Het |
| Adamtsl2 |
C |
A |
2: 27,081,720 (GRCm38) |
Q6K |
probably benign |
Het |
| Adcy1 |
G |
T |
11: 7,150,858 (GRCm38) |
R802S |
possibly damaging |
Het |
| Adcy1 |
G |
A |
11: 7,109,098 (GRCm38) |
D335N |
probably damaging |
Het |
| Adcy1 |
C |
A |
11: 7,149,536 (GRCm38) |
T672N |
probably damaging |
Het |
| Adcy1 |
G |
A |
11: 7,150,857 (GRCm38) |
R802K |
probably damaging |
Het |
| Adcy5 |
C |
G |
16: 35,290,185 (GRCm38) |
F907L |
probably benign |
Het |
| Adcy5 |
G |
T |
16: 35,156,321 (GRCm38) |
G75C |
unknown |
Het |
| Adcy5 |
G |
A |
16: 35,291,544 (GRCm38) |
V924M |
not run |
Het |
| Adcy8 |
T |
C |
15: 64,725,518 (GRCm38) |
T895A |
probably benign |
Het |
| Adcy9 |
G |
T |
16: 4,307,232 (GRCm38) |
P745Q |
probably damaging |
Het |
| Add2 |
G |
T |
6: 86,098,590 (GRCm38) |
K240N |
probably damaging |
Het |
| Adgb |
G |
T |
10: 10,378,742 (GRCm38) |
T1159N |
probably benign |
Het |
| Adgrb2 |
G |
T |
4: 130,017,563 (GRCm38) |
C1126F |
probably damaging |
Het |
| Adgrb3 |
C |
T |
1: 25,093,914 (GRCm38) |
D1364N |
probably benign |
Het |
| Adgre1 |
T |
G |
17: 57,361,729 (GRCm38) |
L30R |
possibly damaging |
Het |
| Adgrg4 |
G |
T |
X: 56,894,702 (GRCm38) |
V174L |
probably benign |
Het |
| Adgrg4 |
C |
A |
X: 56,914,259 (GRCm38) |
P601H |
probably benign |
Het |
| Adgrg5 |
G |
C |
8: 94,935,151 (GRCm38) |
W173C |
|
Het |
| Adgrv1 |
C |
A |
13: 81,559,634 (GRCm38) |
A1218S |
possibly damaging |
Het |
| Adh7 |
G |
A |
3: 138,223,731 (GRCm38) |
G87D |
probably benign |
Het |
| Adora2a |
C |
A |
10: 75,333,328 (GRCm38) |
Q209K |
probably benign |
Het |
| Adprhl1 |
C |
G |
8: 13,225,613 (GRCm38) |
A382P |
probably benign |
Het |
| Adprhl2 |
C |
G |
4: 126,321,661 (GRCm38) |
A4P |
unknown |
Het |
| Adprhl2 |
C |
G |
4: 126,321,567 (GRCm38) |
G35A |
probably damaging |
Het |
| Adra1a |
C |
A |
14: 66,727,628 (GRCm38) |
L356M |
probably benign |
Het |
| Adra2b |
C |
A |
2: 127,364,038 (GRCm38) |
D158E |
probably benign |
Het |
| Adra2c |
G |
C |
5: 35,280,904 (GRCm38) |
R340P |
probably damaging |
Het |
| Adss |
C |
A |
1: 177,776,493 (GRCm38) |
C182F |
probably damaging |
Het |
| Adss |
C |
A |
1: 177,796,498 (GRCm38) |
|
probably benign |
Het |
| Aff3 |
T |
A |
1: 38,329,872 (GRCm38) |
K347* |
probably null |
Het |
| Afg1l |
TGCGCGCG |
TGCGCG |
10: 42,478,353 (GRCm38) |
|
probably null |
Het |
| Afg3l2 |
C |
A |
18: 67,431,707 (GRCm38) |
L232F |
probably benign |
Het |
| Afmid |
G |
A |
11: 117,834,966 (GRCm38) |
D129N |
probably benign |
Het |
| Agap2 |
G |
C |
10: 127,080,225 (GRCm38) |
G202R |
unknown |
Het |
| Agbl1 |
T |
G |
7: 76,418,685 (GRCm38) |
L333R |
|
Het |
| Agbl4 |
G |
T |
4: 111,526,643 (GRCm38) |
G232W |
probably damaging |
Het |
| Agbl4 |
T |
A |
4: 110,660,839 (GRCm38) |
L109Q |
probably damaging |
Het |
| Ago4 |
C |
A |
4: 126,520,190 (GRCm38) |
|
probably null |
Het |
| Ahnak |
G |
T |
19: 9,008,856 (GRCm38) |
M2501I |
probably damaging |
Het |
| AI593442 |
C |
A |
9: 52,677,945 (GRCm38) |
G111C |
probably damaging |
Het |
| AI597479 |
A |
G |
1: 43,113,190 (GRCm38) |
H216R |
probably benign |
Het |
| Aipl1 |
G |
T |
11: 72,030,533 (GRCm38) |
P179T |
possibly damaging |
Het |
| Ak9 |
G |
C |
10: 41,348,251 (GRCm38) |
G524R |
|
Het |
| Ak9 |
G |
T |
10: 41,423,023 (GRCm38) |
W1573C |
unknown |
Het |
| Akap1 |
G |
T |
11: 88,837,167 (GRCm38) |
T663N |
probably benign |
Het |
| Akap13 |
G |
T |
7: 75,730,552 (GRCm38) |
R491L |
probably damaging |
Het |
| Akap14 |
G |
T |
X: 37,163,245 (GRCm38) |
P279H |
unknown |
Het |
| Akap4 |
G |
T |
X: 7,078,360 (GRCm38) |
E831* |
probably null |
Het |
| Akap6 |
C |
G |
12: 53,140,444 (GRCm38) |
T1547R |
possibly damaging |
Het |
| Akap8 |
C |
A |
17: 32,306,549 (GRCm38) |
V519L |
probably damaging |
Het |
| Akap9 |
G |
T |
5: 3,962,251 (GRCm38) |
G985W |
probably damaging |
Het |
| Akirin1 |
C |
T |
4: 123,750,067 (GRCm38) |
G33D |
probably damaging |
Het |
| Akr1cl |
C |
A |
1: 65,016,687 (GRCm38) |
G219C |
probably damaging |
Het |
| Alas1 |
G |
A |
9: 106,238,769 (GRCm38) |
R349C |
probably benign |
Het |
| Alas1 |
C |
A |
9: 106,243,367 (GRCm38) |
Q76H |
probably benign |
Het |
| Aldh1l1 |
GAA |
GA |
6: 90,557,284 (GRCm38) |
|
probably null |
Het |
| Aldh1l1 |
G |
T |
6: 90,583,173 (GRCm38) |
V601L |
probably benign |
Het |
| Aldh3a2 |
T |
G |
11: 61,264,283 (GRCm38) |
K145T |
probably benign |
Het |
| Aldoart1 |
C |
A |
4: 72,852,004 (GRCm38) |
R189L |
probably benign |
Het |
| Alg8 |
T |
G |
7: 97,383,761 (GRCm38) |
F285V |
probably benign |
Het |
| Alkbh8 |
G |
C |
9: 3,345,820 (GRCm38) |
G180A |
probably damaging |
Het |
| Alms1 |
C |
G |
6: 85,678,418 (GRCm38) |
N2846K |
probably benign |
Het |
| Alox12b |
G |
C |
11: 69,157,325 (GRCm38) |
V27L |
possibly damaging |
Het |
| Alox12b |
T |
A |
11: 69,157,323 (GRCm38) |
I26N |
possibly damaging |
Het |
| Aloxe3 |
C |
A |
11: 69,133,079 (GRCm38) |
L279M |
probably damaging |
Het |
| Alpi |
T |
C |
1: 87,099,072 (GRCm38) |
N428S |
probably benign |
Het |
| Alpk1 |
T |
A |
3: 127,673,438 (GRCm38) |
H1064L |
probably damaging |
Het |
| Alpk2 |
G |
C |
18: 65,305,611 (GRCm38) |
L904V |
probably damaging |
Het |
| Alpk3 |
G |
T |
7: 81,078,626 (GRCm38) |
L501F |
probably benign |
Het |
| Alpl |
G |
C |
4: 137,754,010 (GRCm38) |
S110R |
probably damaging |
Het |
| Alppl2 |
G |
A |
1: 87,087,666 (GRCm38) |
S391F |
probably damaging |
Het |
| Alppl2 |
G |
T |
1: 87,087,704 (GRCm38) |
H378Q |
probably damaging |
Het |
| Amer3 |
G |
T |
1: 34,589,013 (GRCm38) |
V778L |
probably benign |
Het |
| Ampd2 |
C |
A |
3: 108,080,064 (GRCm38) |
G151V |
probably damaging |
Het |
| Amz1 |
G |
T |
5: 140,744,073 (GRCm38) |
E121* |
probably null |
Het |
| Ang4 |
G |
T |
14: 51,764,148 (GRCm38) |
C114* |
probably null |
Het |
| Ank3 |
C |
T |
10: 69,951,010 (GRCm38) |
A968V |
possibly damaging |
Het |
| Ank3 |
T |
G |
10: 69,932,474 (GRCm38) |
L941R |
possibly damaging |
Het |
| Ank3 |
G |
C |
10: 69,991,215 (GRCm38) |
E1905Q |
|
Het |
| Ankar |
G |
T |
1: 72,689,961 (GRCm38) |
L342I |
possibly damaging |
Het |
| Ankib1 |
G |
A |
5: 3,692,763 (GRCm38) |
S1084L |
probably benign |
Het |
| Ankk1 |
T |
A |
9: 49,416,643 (GRCm38) |
Q412L |
probably benign |
Het |
| Ankk1 |
T |
G |
9: 49,421,911 (GRCm38) |
K91T |
probably damaging |
Het |
| Ankle2 |
G |
C |
5: 110,234,499 (GRCm38) |
E114Q |
possibly damaging |
Het |
| Ankmy1 |
C |
T |
1: 92,878,437 (GRCm38) |
G780E |
probably damaging |
Het |
| Ankmy2 |
T |
G |
12: 36,186,859 (GRCm38) |
M222R |
probably damaging |
Het |
| Ankrd11 |
C |
T |
8: 122,895,803 (GRCm38) |
V437M |
possibly damaging |
Het |
| Ankrd12 |
C |
A |
17: 65,970,338 (GRCm38) |
|
probably null |
Het |
| Ankrd36 |
T |
A |
11: 5,615,538 (GRCm38) |
F457L |
probably benign |
Het |
| Ankrd39 |
C |
G |
1: 36,542,005 (GRCm38) |
A88P |
probably damaging |
Het |
| Ankrd45 |
C |
T |
1: 161,163,283 (GRCm38) |
A202V |
possibly damaging |
Het |
| Ankrd49 |
C |
G |
9: 14,781,428 (GRCm38) |
A147P |
probably damaging |
Het |
| Ankrd6 |
C |
T |
4: 32,806,229 (GRCm38) |
E675K |
possibly damaging |
Het |
| Ankrd6 |
G |
C |
4: 32,824,486 (GRCm38) |
N142K |
probably damaging |
Het |
| Ankrd6 |
G |
T |
4: 32,806,326 (GRCm38) |
S642R |
probably benign |
Het |
| Anks3 |
T |
G |
16: 4,950,714 (GRCm38) |
Q255P |
probably benign |
Het |
| Ano2 |
G |
T |
6: 125,710,707 (GRCm38) |
Q58H |
probably benign |
Het |
| Ano2 |
T |
G |
6: 125,863,453 (GRCm38) |
Y362* |
probably null |
Het |
| Ano4 |
A |
T |
10: 89,112,945 (GRCm38) |
V101E |
probably benign |
Het |
| Ano5 |
T |
A |
7: 51,574,703 (GRCm38) |
V469E |
probably damaging |
Het |
| Ano6 |
C |
A |
15: 95,913,460 (GRCm38) |
P147Q |
probably damaging |
Het |
| Ano7 |
C |
A |
1: 93,394,465 (GRCm38) |
D398E |
probably benign |
Het |
| Anpep |
G |
C |
7: 79,827,639 (GRCm38) |
P727A |
possibly damaging |
Het |
| Anxa10 |
T |
G |
8: 62,063,070 (GRCm38) |
|
probably null |
Het |
| Aoc2 |
G |
T |
11: 101,326,420 (GRCm38) |
G443V |
probably benign |
Het |
| Aox4 |
G |
C |
1: 58,246,351 (GRCm38) |
E665Q |
possibly damaging |
Het |
| Ap1m2 |
G |
A |
9: 21,298,256 (GRCm38) |
R375* |
probably null |
Het |
| Ap1s1 |
G |
A |
5: 137,037,470 (GRCm38) |
T126I |
probably damaging |
Het |
| Apba1 |
C |
A |
19: 23,944,115 (GRCm38) |
S767R |
probably damaging |
Het |
| Apex2 |
C |
A |
X: 150,572,099 (GRCm38) |
G414V |
probably benign |
Het |
| Apoa4 |
C |
A |
9: 46,242,589 (GRCm38) |
R163S |
possibly damaging |
Het |
| Apob |
G |
T |
12: 8,004,978 (GRCm38) |
V1326L |
probably benign |
Het |
| Apob |
G |
C |
12: 7,998,011 (GRCm38) |
G997R |
probably damaging |
Het |
| Apobr |
A |
T |
7: 126,587,264 (GRCm38) |
E649V |
probably damaging |
Het |
| Apoh |
G |
T |
11: 108,343,459 (GRCm38) |
|
probably benign |
Het |
| Apol11b |
A |
C |
15: 77,638,007 (GRCm38) |
I30R |
probably benign |
Het |
| App |
A |
G |
16: 85,024,917 (GRCm38) |
L390P |
probably damaging |
Het |
| Aqr |
C |
G |
2: 114,109,991 (GRCm38) |
A1225P |
probably benign |
Het |
| Aqr |
C |
A |
2: 114,108,122 (GRCm38) |
R1283M |
probably damaging |
Het |
| Ar |
G |
T |
X: 98,151,009 (GRCm38) |
G410W |
probably damaging |
Het |
| Arfgef2 |
G |
A |
2: 166,894,712 (GRCm38) |
R1768Q |
probably damaging |
Het |
| Arfgef3 |
T |
A |
10: 18,591,437 (GRCm38) |
K2005M |
probably damaging |
Het |
| Arfgef3 |
T |
A |
10: 18,634,852 (GRCm38) |
H787L |
probably benign |
Het |
| Arfgef3 |
C |
A |
10: 18,608,358 (GRCm38) |
C1383F |
probably damaging |
Het |
| Arhgap1 |
C |
T |
2: 91,650,214 (GRCm38) |
A27V |
possibly damaging |
Het |
| Arhgap10 |
C |
A |
8: 77,277,175 (GRCm38) |
G667V |
probably benign |
Het |
| Arhgap10 |
T |
G |
8: 77,432,805 (GRCm38) |
S107R |
probably damaging |
Het |
| Arhgap11a |
C |
G |
2: 113,833,758 (GRCm38) |
A727P |
probably benign |
Het |
| Arhgap22 |
A |
T |
14: 33,362,522 (GRCm38) |
R253W |
probably damaging |
Het |
| Arhgap24 |
G |
A |
5: 102,880,807 (GRCm38) |
A283T |
probably benign |
Het |
| Arhgap24 |
G |
T |
5: 102,875,759 (GRCm38) |
V220F |
probably damaging |
Het |
| Arhgap25 |
G |
T |
6: 87,476,186 (GRCm38) |
L211M |
probably damaging |
Het |
| Arhgap31 |
G |
C |
16: 38,623,893 (GRCm38) |
Q201E |
possibly damaging |
Het |
| Arhgap33 |
C |
A |
7: 30,522,717 (GRCm38) |
R1263S |
probably benign |
Het |
| Arhgap40 |
C |
A |
2: 158,534,885 (GRCm38) |
P317T |
probably benign |
Het |
| Arhgap45 |
C |
G |
10: 80,029,052 (GRCm38) |
R950G |
probably damaging |
Het |
| Arhgap45 |
C |
A |
10: 80,025,536 (GRCm38) |
T511N |
probably damaging |
Het |
| Arhgap5 |
G |
A |
12: 52,518,463 (GRCm38) |
R739H |
possibly damaging |
Het |
| Arhgap9 |
C |
A |
10: 127,327,689 (GRCm38) |
T452N |
probably damaging |
Het |
| Arhgef11 |
C |
T |
3: 87,735,462 (GRCm38) |
P1434L |
not run |
Het |
| Arhgef12 |
T |
A |
9: 42,971,072 (GRCm38) |
Q1492L |
probably benign |
Het |
| Arhgef18 |
G |
T |
8: 3,453,224 (GRCm38) |
V877L |
probably damaging |
Het |
| Arhgef4 |
G |
T |
1: 34,804,926 (GRCm38) |
G1358C |
probably damaging |
Het |
| Arhgef4 |
G |
T |
1: 34,723,729 (GRCm38) |
D689Y |
unknown |
Het |
| Arid1a |
C |
A |
4: 133,720,550 (GRCm38) |
Q217H |
probably null |
Het |
| Arid4a |
A |
C |
12: 71,039,920 (GRCm38) |
K177N |
possibly damaging |
Het |
| Arid5a |
CGGG |
CGGGG |
1: 36,319,355 (GRCm38) |
|
probably null |
Het |
| Arl10 |
C |
G |
13: 54,580,724 (GRCm38) |
L188V |
probably benign |
Het |
| Arl14 |
C |
A |
3: 69,222,648 (GRCm38) |
P43T |
probably damaging |
Het |
| Arl4c |
T |
C |
1: 88,701,450 (GRCm38) |
Q72R |
possibly damaging |
Het |
| Arl6ip5 |
C |
A |
6: 97,229,555 (GRCm38) |
N65K |
probably benign |
Het |
| Armc2 |
C |
A |
10: 41,927,044 (GRCm38) |
Q544H |
probably damaging |
Het |
| Armc2 |
C |
G |
10: 41,963,656 (GRCm38) |
G438R |
probably damaging |
Het |
| Armc4 |
G |
C |
18: 7,129,487 (GRCm38) |
A897G |
probably damaging |
Het |
| Armc4 |
C |
A |
18: 7,216,973 (GRCm38) |
E680* |
probably null |
Het |
| Armcx4 |
C |
A |
X: 134,693,042 (GRCm38) |
A1233D |
not run |
Het |
| Armcx4 |
G |
A |
X: 134,694,091 (GRCm38) |
E1583K |
possibly damaging |
Het |
| Arnt2 |
G |
A |
7: 84,263,196 (GRCm38) |
P579S |
probably benign |
Het |
| Arpc3 |
C |
T |
5: 122,404,230 (GRCm38) |
P120L |
probably damaging |
Het |
| Arrdc5 |
C |
G |
17: 56,300,189 (GRCm38) |
A19P |
probably damaging |
Het |
| Arsi |
C |
A |
18: 60,916,780 (GRCm38) |
P245H |
probably damaging |
Het |
| Art2b |
T |
A |
7: 101,578,882 (GRCm38) |
Q283L |
not run |
Het |
| Arx |
G |
T |
X: 93,289,184 (GRCm38) |
A280S |
probably damaging |
Het |
| Asap3 |
TGGG |
TGG |
4: 136,240,201 (GRCm38) |
|
probably benign |
Het |
| Asap3 |
C |
A |
4: 136,241,503 (GRCm38) |
P753Q |
probably damaging |
Het |
| Asb15 |
G |
T |
6: 24,566,331 (GRCm38) |
D428Y |
probably damaging |
Het |
| Ascc1 |
G |
T |
10: 60,007,793 (GRCm38) |
R59L |
possibly damaging |
Het |
| Ascc2 |
G |
T |
11: 4,646,653 (GRCm38) |
R58L |
probably benign |
Het |
| Ascc2 |
G |
C |
11: 4,672,487 (GRCm38) |
G518R |
probably benign |
Het |
| Ash1l |
G |
A |
3: 89,043,217 (GRCm38) |
R2139Q |
probably damaging |
Het |
| Asic2 |
T |
G |
11: 81,967,670 (GRCm38) |
K172T |
probably benign |
Het |
| Asic2 |
A |
T |
11: 80,889,832 (GRCm38) |
L417Q |
possibly damaging |
Het |
| Aspg |
C |
G |
12: 112,113,081 (GRCm38) |
Q98E |
possibly damaging |
Het |
| Asphd1 |
A |
T |
7: 126,948,636 (GRCm38) |
L165Q |
probably damaging |
Het |
| Astl |
C |
T |
2: 127,356,545 (GRCm38) |
A360V |
probably benign |
Het |
| Asxl3 |
G |
T |
18: 22,522,220 (GRCm38) |
G1096C |
probably damaging |
Het |
| Atad5 |
A |
C |
11: 80,094,896 (GRCm38) |
S270R |
probably damaging |
Het |
| Ate1 |
C |
A |
7: 130,504,714 (GRCm38) |
D306Y |
probably benign |
Het |
| Atg7 |
G |
T |
6: 114,673,050 (GRCm38) |
V63F |
possibly damaging |
Het |
| Atg9a |
A |
T |
1: 75,186,559 (GRCm38) |
L299Q |
probably damaging |
Het |
| Atl1 |
C |
G |
12: 69,937,075 (GRCm38) |
L192V |
possibly damaging |
Het |
| Atl3 |
T |
G |
19: 7,510,037 (GRCm38) |
F106V |
probably damaging |
Het |
| Atp10a |
G |
T |
7: 58,788,447 (GRCm38) |
|
probably null |
Het |
| Atp12a |
G |
C |
14: 56,372,706 (GRCm38) |
G221A |
probably damaging |
Het |
| Atp13a2 |
A |
T |
4: 141,005,117 (GRCm38) |
S898C |
probably benign |
Het |
| Atp13a4 |
C |
A |
16: 29,422,587 (GRCm38) |
Q754H |
probably null |
Het |
| Atp1a2 |
A |
T |
1: 172,279,754 (GRCm38) |
I733N |
possibly damaging |
Het |
| Atp1a3 |
C |
A |
7: 24,998,688 (GRCm38) |
A198S |
probably benign |
Het |
| Atp1a4 |
C |
G |
1: 172,231,954 (GRCm38) |
R857P |
probably benign |
Het |
| Atp1b2 |
G |
T |
11: 69,601,315 (GRCm38) |
A269D |
possibly damaging |
Het |
| Atp2a3 |
C |
A |
11: 72,989,540 (GRCm38) |
H1016N |
probably benign |
Het |
| Atp2a3 |
G |
T |
11: 72,980,622 (GRCm38) |
G650C |
possibly damaging |
Het |
| Atp2b3 |
G |
A |
X: 73,535,424 (GRCm38) |
E343K |
possibly damaging |
Het |
| Atp6v0a4 |
G |
A |
6: 38,049,036 (GRCm38) |
S819F |
possibly damaging |
Het |
| Atp6v1e1 |
T |
C |
6: 120,804,119 (GRCm38) |
E97G |
probably benign |
Het |
| Atp6v1e1 |
T |
A |
6: 120,822,449 (GRCm38) |
|
probably benign |
Het |
| Atp6v1h |
G |
C |
1: 5,095,628 (GRCm38) |
R107P |
probably damaging |
Het |
| Atp7b |
G |
T |
8: 22,028,714 (GRCm38) |
P36H |
probably benign |
Het |
| Atp8b4 |
C |
A |
2: 126,414,429 (GRCm38) |
E203D |
possibly damaging |
Het |
| Atp8b5 |
A |
T |
4: 43,361,903 (GRCm38) |
R650W |
probably benign |
Het |
| Atp9b |
T |
A |
18: 80,765,865 (GRCm38) |
Q613L |
|
Het |
| Atpaf2 |
C |
A |
11: 60,416,775 (GRCm38) |
A46S |
probably benign |
Het |
| Atrn |
G |
T |
2: 130,946,193 (GRCm38) |
G305V |
probably benign |
Het |
| Atxn2 |
A |
T |
5: 121,777,990 (GRCm38) |
S420C |
probably damaging |
Het |
| Atxn7l1 |
G |
T |
12: 33,367,645 (GRCm38) |
A602S |
probably benign |
Het |
| Atxn7l1 |
G |
C |
12: 33,368,017 (GRCm38) |
A726P |
probably benign |
Het |
| Atxn7l2 |
A |
C |
3: 108,205,666 (GRCm38) |
S309A |
probably benign |
Het |
| AU022751 |
G |
T |
X: 6,082,314 (GRCm38) |
P216T |
unknown |
Het |
| AU022751 |
T |
G |
X: 6,082,321 (GRCm38) |
E213D |
unknown |
Het |
| Aup1 |
G |
T |
6: 83,056,633 (GRCm38) |
R306L |
probably benign |
Het |
| Aurkaip1 |
G |
T |
4: 155,832,763 (GRCm38) |
R156L |
probably damaging |
Het |
| Aurkc |
TGG |
TG |
7: 6,995,514 (GRCm38) |
|
probably null |
Het |
| Avl9 |
G |
C |
6: 56,736,764 (GRCm38) |
D336H |
probably damaging |
Het |
| Avpr1b |
C |
A |
1: 131,609,573 (GRCm38) |
S365Y |
probably damaging |
Het |
| Axdnd1 |
A |
T |
1: 156,349,063 (GRCm38) |
L714Q |
probably damaging |
Het |
| Azin2 |
C |
A |
4: 128,934,659 (GRCm38) |
D347Y |
possibly damaging |
Het |
| B3gnt5 |
A |
T |
16: 19,769,810 (GRCm38) |
R260* |
probably null |
Het |
| B3gnt6 |
C |
G |
7: 98,193,889 (GRCm38) |
R288P |
probably benign |
Het |
| Bag6 |
G |
T |
17: 35,139,310 (GRCm38) |
|
probably null |
Het |
| Bahcc1 |
G |
T |
11: 120,284,394 (GRCm38) |
V1765L |
probably benign |
Het |
| Bahcc1 |
G |
T |
11: 120,276,609 (GRCm38) |
G1279W |
possibly damaging |
Het |
| Bahd1 |
G |
A |
2: 118,922,403 (GRCm38) |
R717H |
probably damaging |
Het |
| Baiap3 |
C |
A |
17: 25,244,768 (GRCm38) |
R934S |
probably benign |
Het |
| Bbs10 |
G |
T |
10: 111,299,657 (GRCm38) |
L210F |
probably benign |
Het |
| Bbs10 |
G |
T |
10: 111,301,124 (GRCm38) |
R699S |
probably damaging |
Het |
| Bbs10 |
G |
C |
10: 111,298,908 (GRCm38) |
|
probably null |
Het |
| BC005561 |
T |
C |
5: 104,520,192 (GRCm38) |
V860A |
possibly damaging |
Het |
| BC024063 |
G |
T |
10: 82,109,050 (GRCm38) |
G168V |
probably damaging |
Het |
| BC080695 |
T |
C |
4: 143,572,252 (GRCm38) |
I255T |
probably benign |
Het |
| Bcan |
C |
A |
3: 87,990,750 (GRCm38) |
G635W |
probably damaging |
Het |
| Bcan |
C |
T |
3: 87,995,650 (GRCm38) |
D274N |
probably benign |
Het |
| Bcan |
T |
G |
3: 87,990,755 (GRCm38) |
N633T |
probably damaging |
Het |
| Bckdha |
T |
C |
7: 25,631,143 (GRCm38) |
S343G |
probably damaging |
Het |
| Bcl10 |
T |
G |
3: 145,930,513 (GRCm38) |
I55M |
probably damaging |
Het |
| Bcl11a |
G |
T |
11: 24,165,010 (GRCm38) |
K784N |
probably damaging |
Het |
| Bcl6 |
C |
G |
16: 23,969,958 (GRCm38) |
Q553H |
probably damaging |
Het |
| Bcorl1 |
T |
G |
X: 48,367,842 (GRCm38) |
L84R |
unknown |
Het |
| Bcorl1 |
GAAAA |
GAAA |
X: 48,375,090 (GRCm38) |
|
probably null |
Het |
| Bend6 |
C |
A |
1: 33,864,523 (GRCm38) |
Q173H |
probably null |
Het |
| Best3 |
T |
G |
10: 117,024,622 (GRCm38) |
L596V |
probably benign |
Het |
| Bmp4 |
A |
C |
14: 46,384,628 (GRCm38) |
V153G |
possibly damaging |
Het |
| Bmpr1b |
C |
A |
3: 141,842,954 (GRCm38) |
E438D |
probably benign |
Het |
| Bmpr2 |
G |
A |
1: 59,847,167 (GRCm38) |
R321Q |
not run |
Het |
| Bnc1 |
T |
G |
7: 81,974,542 (GRCm38) |
E312D |
probably damaging |
Het |
| Bok |
ACTCTCTCTCTCT |
ACTCTCTCTCTCTCT |
1: 93,694,045 (GRCm38) |
|
probably benign |
Het |
| Borcs5 |
A |
T |
6: 134,710,123 (GRCm38) |
Q147L |
probably benign |
Het |
| Borcs8 |
C |
G |
8: 70,141,971 (GRCm38) |
H49D |
probably damaging |
Het |
| Bpi |
G |
T |
2: 158,272,102 (GRCm38) |
G307W |
possibly damaging |
Het |
| Bpifa3 |
A |
T |
2: 154,130,471 (GRCm38) |
|
probably benign |
Het |
| Bpifb4 |
A |
C |
2: 153,942,832 (GRCm38) |
E153D |
probably benign |
Het |
| Bpifc |
C |
A |
10: 85,965,228 (GRCm38) |
A419S |
probably benign |
Het |
| Bptf |
C |
A |
11: 107,058,684 (GRCm38) |
G2270W |
probably damaging |
Het |
| Braf |
C |
A |
6: 39,643,182 (GRCm38) |
W487C |
probably damaging |
Het |
| Brap |
A |
G |
5: 121,675,377 (GRCm38) |
T298A |
possibly damaging |
Het |
| Brd2 |
C |
A |
17: 34,113,688 (GRCm38) |
G573W |
possibly damaging |
Het |
| Brd9 |
G |
C |
13: 73,944,751 (GRCm38) |
A287P |
probably damaging |
Het |
| Brdt |
G |
T |
5: 107,359,898 (GRCm38) |
S664I |
possibly damaging |
Het |
| Brinp1 |
C |
A |
4: 68,798,751 (GRCm38) |
E287* |
probably null |
Het |
| Brinp2 |
A |
T |
1: 158,247,171 (GRCm38) |
L460* |
probably null |
Het |
| Brinp2 |
C |
G |
1: 158,247,039 (GRCm38) |
G504A |
probably damaging |
Het |
| Brinp3 |
C |
T |
1: 146,902,076 (GRCm38) |
P754S |
probably damaging |
Het |
| Btg4 |
G |
A |
9: 51,119,175 (GRCm38) |
D192N |
probably benign |
Het |
| Btla |
G |
T |
16: 45,239,358 (GRCm38) |
V142L |
probably damaging |
Het |
| Bub1 |
C |
A |
2: 127,829,565 (GRCm38) |
W33L |
probably damaging |
Het |
| C130026I21Rik |
G |
T |
1: 85,113,523 (GRCm38) |
D71E |
probably damaging |
Het |
| C1qb |
C |
G |
4: 136,882,145 (GRCm38) |
G55R |
probably damaging |
Het |
| C1ql2 |
C |
G |
1: 120,341,624 (GRCm38) |
H169Q |
possibly damaging |
Het |
| C2cd4a |
C |
G |
9: 67,831,413 (GRCm38) |
G116A |
probably damaging |
Het |
| C2cd4c |
G |
A |
10: 79,612,465 (GRCm38) |
P283S |
possibly damaging |
Het |
| C4b |
A |
T |
17: 34,731,147 (GRCm38) |
L1383Q |
probably damaging |
Het |
| C530008M17Rik |
C |
A |
5: 76,857,246 (GRCm38) |
P485T |
unknown |
Het |
| C77080 |
G |
T |
4: 129,223,704 (GRCm38) |
S434Y |
probably damaging |
Het |
| C87977 |
A |
G |
4: 144,207,461 (GRCm38) |
F359L |
probably benign |
Het |
| C8a |
C |
A |
4: 104,862,686 (GRCm38) |
G76C |
probably damaging |
Het |
| Cabp7 |
T |
G |
11: 4,746,669 (GRCm38) |
N20T |
probably benign |
Het |
| Cacna1a |
G |
T |
8: 84,415,676 (GRCm38) |
R11L |
unknown |
Het |
| Cacna1b |
A |
T |
2: 24,626,884 (GRCm38) |
L54* |
probably null |
Het |
| Cacna1c |
T |
G |
6: 118,697,737 (GRCm38) |
K547T |
|
Het |
| Cacna1d |
C |
T |
14: 30,111,116 (GRCm38) |
A923T |
probably benign |
Het |
| Cacna1d |
A |
G |
14: 30,179,188 (GRCm38) |
F325S |
probably benign |
Het |
| Cacna1e |
T |
A |
1: 154,635,850 (GRCm38) |
T176S |
probably damaging |
Het |
| Cacna1g |
A |
T |
11: 94,438,111 (GRCm38) |
L1020M |
probably benign |
Het |
| Cacna1h |
G |
C |
17: 25,391,250 (GRCm38) |
P761A |
probably benign |
Het |
| Cacna1s |
G |
T |
1: 136,107,084 (GRCm38) |
E1322* |
probably null |
Het |
| Cacna2d2 |
G |
C |
9: 107,517,293 (GRCm38) |
A585P |
probably damaging |
Het |
| Cacna2d2 |
C |
A |
9: 107,526,102 (GRCm38) |
L921M |
probably benign |
Het |
| Cacna2d4 |
G |
T |
6: 119,312,450 (GRCm38) |
R815M |
probably benign |
Het |
| Cacnb1 |
C |
A |
11: 98,022,555 (GRCm38) |
|
probably benign |
Het |
| Cacnb4 |
C |
A |
2: 52,675,812 (GRCm38) |
|
probably null |
Het |
| Cacng5 |
G |
T |
11: 107,877,546 (GRCm38) |
P212T |
probably damaging |
Het |
| Cacng5 |
C |
G |
11: 107,884,346 (GRCm38) |
G66R |
probably null |
Het |
| Cadps2 |
A |
C |
6: 23,321,801 (GRCm38) |
L1031V |
probably benign |
Het |
| Calcoco2 |
C |
A |
11: 96,103,520 (GRCm38) |
W69L |
probably damaging |
Het |
| Calr |
C |
A |
8: 84,844,064 (GRCm38) |
|
probably null |
Het |
| Camk1g |
C |
A |
1: 193,362,100 (GRCm38) |
G2V |
probably damaging |
Het |
| Camk2b |
G |
C |
11: 5,977,940 (GRCm38) |
S447C |
possibly damaging |
Het |
| Camk2g |
C |
A |
14: 20,764,912 (GRCm38) |
W215C |
probably damaging |
Het |
| Camsap1 |
C |
T |
2: 25,936,639 (GRCm38) |
A1260T |
probably damaging |
Het |
| Camsap1 |
G |
C |
2: 25,940,881 (GRCm38) |
P461A |
probably benign |
Het |
| Camta1 |
G |
T |
4: 151,144,385 (GRCm38) |
H663Q |
probably benign |
Het |
| Cand1 |
A |
C |
10: 119,239,194 (GRCm38) |
I16S |
probably benign |
Het |
| Capg |
G |
T |
6: 72,555,476 (GRCm38) |
|
probably null |
Het |
| Capn1 |
C |
G |
19: 6,014,278 (GRCm38) |
V64L |
probably benign |
Het |
| Capn13 |
G |
T |
17: 73,341,110 (GRCm38) |
S298R |
probably benign |
Het |
| Capn6 |
C |
G |
X: 143,810,907 (GRCm38) |
G79R |
probably damaging |
Het |
| Car5b |
G |
T |
X: 164,000,310 (GRCm38) |
A90D |
probably benign |
Het |
| Car7 |
G |
T |
8: 104,548,959 (GRCm38) |
C180F |
possibly damaging |
Het |
| Card9 |
T |
A |
2: 26,357,796 (GRCm38) |
E181V |
probably damaging |
Het |
| Carnmt1 |
C |
G |
19: 18,679,213 (GRCm38) |
A170G |
possibly damaging |
Het |
| Carnmt1 |
G |
C |
19: 18,704,090 (GRCm38) |
C391S |
probably benign |
Het |
| Cartpt |
C |
A |
13: 99,899,983 (GRCm38) |
E86* |
probably null |
Het |
| Casc1 |
C |
A |
6: 145,205,293 (GRCm38) |
E18* |
probably null |
Het |
| Cask |
C |
T |
X: 13,533,489 (GRCm38) |
V785I |
probably benign |
Het |
| Caskin1 |
C |
A |
17: 24,505,038 (GRCm38) |
N933K |
probably damaging |
Het |
| Caskin2 |
A |
G |
11: 115,802,096 (GRCm38) |
L621P |
probably damaging |
Het |
| Caskin2 |
C |
A |
11: 115,803,620 (GRCm38) |
G385V |
probably benign |
Het |
| Caskin2 |
C |
G |
11: 115,802,103 (GRCm38) |
A619P |
probably damaging |
Het |
| Casq1 |
G |
T |
1: 172,215,914 (GRCm38) |
S191* |
probably null |
Het |
| Casz1 |
T |
C |
4: 148,944,359 (GRCm38) |
L1087P |
probably benign |
Het |
| Catip |
A |
C |
1: 74,367,789 (GRCm38) |
H240P |
probably damaging |
Het |
| Catsper2 |
C |
A |
2: 121,407,385 (GRCm38) |
W171C |
probably damaging |
Het |
| Cav2 |
G |
T |
6: 17,281,433 (GRCm38) |
V25F |
probably benign |
Het |
| Cavin2 |
G |
T |
1: 51,301,156 (GRCm38) |
G331C |
probably damaging |
Het |
| Cbfa2t3 |
G |
C |
8: 122,698,895 (GRCm38) |
|
probably benign |
Het |
| Cbx8 |
G |
A |
11: 119,039,119 (GRCm38) |
A216V |
possibly damaging |
Het |
| Ccdc113 |
G |
T |
8: 95,538,219 (GRCm38) |
R119L |
probably damaging |
Het |
| Ccdc121 |
C |
T |
1: 181,510,875 (GRCm38) |
E171K |
possibly damaging |
Het |
| Ccdc14 |
G |
T |
16: 34,706,498 (GRCm38) |
G306C |
probably damaging |
Het |
| Ccdc144b |
T |
C |
3: 36,018,888 (GRCm38) |
Q415R |
possibly damaging |
Het |
| Ccdc149 |
TTCTCTC |
TTCTC |
5: 52,420,813 (GRCm38) |
|
probably null |
Het |
| Ccdc151 |
C |
A |
9: 21,990,424 (GRCm38) |
V547F |
possibly damaging |
Het |
| Ccdc155 |
C |
G |
7: 45,184,254 (GRCm38) |
|
probably null |
Het |
| Ccdc158 |
T |
C |
5: 92,608,491 (GRCm38) |
M1086V |
probably damaging |
Het |
| Ccdc162 |
C |
T |
10: 41,553,131 (GRCm38) |
R645H |
probably benign |
Het |
| Ccdc162 |
C |
T |
10: 41,605,108 (GRCm38) |
D1318N |
possibly damaging |
Het |
| Ccdc162 |
G |
A |
10: 41,654,997 (GRCm38) |
T571I |
possibly damaging |
Het |
| Ccdc162 |
T |
G |
10: 41,690,092 (GRCm38) |
K85T |
probably benign |
Het |
| Ccdc171 |
G |
A |
4: 83,795,230 (GRCm38) |
A1169T |
probably damaging |
Het |
| Ccdc175 |
C |
A |
12: 72,112,308 (GRCm38) |
R619L |
possibly damaging |
Het |
| Ccdc180 |
A |
C |
4: 45,920,910 (GRCm38) |
K952T |
probably damaging |
Het |
| Ccdc180 |
A |
C |
4: 45,916,406 (GRCm38) |
K869T |
probably damaging |
Het |
| Ccdc187 |
G |
T |
2: 26,281,507 (GRCm38) |
Q320K |
probably benign |
Het |
| Ccdc28b |
C |
A |
4: 129,621,104 (GRCm38) |
G71C |
probably damaging |
Het |
| Ccdc33 |
G |
A |
9: 58,117,416 (GRCm38) |
P176S |
probably benign |
Het |
| Ccdc40 |
G |
A |
11: 119,252,008 (GRCm38) |
R864H |
probably damaging |
Het |
| Ccdc51 |
G |
C |
9: 109,092,226 (GRCm38) |
A394P |
probably damaging |
Het |
| Ccdc51 |
G |
T |
9: 109,092,148 (GRCm38) |
E368* |
probably null |
Het |
| Ccdc57 |
C |
G |
11: 120,860,488 (GRCm38) |
A919P |
possibly damaging |
Het |
| Ccdc57 |
C |
A |
11: 120,861,138 (GRCm38) |
Q872H |
probably null |
Het |
| Ccdc7a |
G |
T |
8: 129,026,663 (GRCm38) |
R196S |
probably benign |
Het |
| Ccdc80 |
G |
A |
16: 45,096,207 (GRCm38) |
S442N |
probably benign |
Het |
| Ccdc80 |
G |
T |
16: 45,095,786 (GRCm38) |
G302* |
probably null |
Het |
| Ccdc80 |
T |
C |
16: 45,116,344 (GRCm38) |
F711L |
probably damaging |
Het |
| Ccdc87 |
G |
A |
19: 4,841,923 (GRCm38) |
W814* |
probably null |
Het |
| Ccdc88b |
C |
A |
19: 6,849,740 (GRCm38) |
A1020S |
possibly damaging |
Het |
| Ccdc88c |
T |
C |
12: 100,945,770 (GRCm38) |
K602E |
possibly damaging |
Het |
| Ccdc94 |
T |
C |
17: 55,960,732 (GRCm38) |
F15S |
probably damaging |
Het |
| Ccdc96 |
C |
G |
5: 36,485,594 (GRCm38) |
R315G |
probably benign |
Het |
| Ccin |
A |
T |
4: 43,985,018 (GRCm38) |
Q475L |
probably damaging |
Het |
| Ccnb1ip1 |
C |
A |
14: 50,792,104 (GRCm38) |
R167L |
probably benign |
Het |
| Ccnb3 |
T |
C |
X: 7,009,375 (GRCm38) |
T322A |
possibly damaging |
Het |
| Ccr10 |
CG |
C |
11: 101,174,340 (GRCm38) |
|
probably null |
Het |
| Ccr10 |
C |
G |
11: 101,174,323 (GRCm38) |
G127A |
probably damaging |
Het |
| Ccr7 |
G |
T |
11: 99,144,980 (GRCm38) |
T372N |
probably damaging |
Het |
| Cct6b |
C |
A |
11: 82,764,065 (GRCm38) |
|
probably benign |
Het |
| Cct6b |
C |
T |
11: 82,723,939 (GRCm38) |
V408I |
probably damaging |
Het |
| Cd163l1 |
A |
T |
7: 140,224,857 (GRCm38) |
H591L |
probably benign |
Het |
| Cd164 |
G |
T |
10: 41,519,565 (GRCm38) |
A11S |
probably damaging |
Het |
| Cd177 |
G |
T |
7: 24,746,171 (GRCm38) |
Q616K |
probably benign |
Het |
| Cd180 |
C |
T |
13: 102,705,766 (GRCm38) |
P440L |
probably damaging |
Het |
| Cd200r1 |
A |
T |
16: 44,792,759 (GRCm38) |
I243F |
probably damaging |
Het |
| Cd209e |
C |
T |
8: 3,849,196 (GRCm38) |
G172E |
probably benign |
Het |
| Cd22 |
G |
T |
7: 30,869,530 (GRCm38) |
P693H |
probably damaging |
Het |
| Cd22 |
T |
G |
7: 30,867,963 (GRCm38) |
K732T |
probably benign |
Het |
| Cd3d |
A |
G |
9: 44,985,628 (GRCm38) |
D100G |
probably damaging |
Het |
| Cd59a |
C |
A |
2: 104,104,198 (GRCm38) |
Q4K |
probably benign |
Het |
| Cd69 |
G |
T |
6: 129,268,342 (GRCm38) |
C173* |
probably null |
Het |
| Cdc123 |
T |
G |
2: 5,804,985 (GRCm38) |
Q205P |
probably damaging |
Het |
| Cdc14b |
C |
G |
13: 64,274,669 (GRCm38) |
V28L |
possibly damaging |
Het |
| Cdc42bpa |
A |
G |
1: 180,065,093 (GRCm38) |
E274G |
probably damaging |
Het |
| Cdc42ep2 |
A |
G |
19: 5,918,492 (GRCm38) |
F62L |
probably benign |
Het |
| Cdc42ep5 |
A |
T |
7: 4,151,726 (GRCm38) |
L21H |
probably damaging |
Het |
| Cdh15 |
G |
C |
8: 122,864,259 (GRCm38) |
D416H |
probably damaging |
Het |
| Cdh16 |
G |
C |
8: 104,615,185 (GRCm38) |
P783A |
probably damaging |
Het |
| Cdh19 |
C |
G |
1: 110,932,214 (GRCm38) |
G179A |
probably damaging |
Het |
| Cdh19 |
T |
G |
1: 110,893,306 (GRCm38) |
Q567H |
probably benign |
Het |
| Cdh19 |
A |
T |
1: 110,895,387 (GRCm38) |
N522K |
probably damaging |
Het |
| Cdh22 |
G |
T |
2: 165,116,184 (GRCm38) |
P621H |
probably damaging |
Het |
| Cdh23 |
T |
A |
10: 60,310,770 (GRCm38) |
N2877Y |
probably damaging |
Het |
| Cdh23 |
T |
C |
10: 60,428,321 (GRCm38) |
N683D |
probably benign |
Het |
| Cdh7 |
G |
T |
1: 110,108,736 (GRCm38) |
G549C |
probably damaging |
Het |
| Cdh8 |
C |
A |
8: 99,190,205 (GRCm38) |
R426M |
probably null |
Het |
| Cdh8 |
G |
A |
8: 99,171,323 (GRCm38) |
P453S |
probably benign |
Het |
| Cdhr3 |
C |
A |
12: 33,080,324 (GRCm38) |
G171W |
probably benign |
Het |
| Cdhr3 |
G |
T |
12: 33,060,322 (GRCm38) |
P321H |
probably damaging |
Het |
| Cdk12 |
G |
T |
11: 98,203,941 (GRCm38) |
G192* |
probably null |
Het |
| Cdk14 |
G |
T |
5: 5,135,322 (GRCm38) |
Y212* |
probably null |
Het |
| Cdk5r2 |
C |
G |
1: 74,855,350 (GRCm38) |
P85A |
probably damaging |
Het |
| Cdk5rap2 |
C |
T |
4: 70,266,743 (GRCm38) |
G1157R |
probably damaging |
Het |
| Cdk6 |
T |
A |
5: 3,390,694 (GRCm38) |
C83S |
possibly damaging |
Het |
| Cdsn |
T |
G |
17: 35,555,825 (GRCm38) |
V417G |
possibly damaging |
Het |
| Cdsn |
T |
A |
17: 35,556,071 (GRCm38) |
L499Q |
probably damaging |
Het |
| Cdyl |
C |
T |
13: 35,815,966 (GRCm38) |
R77W |
probably damaging |
Het |
| Ceacam15 |
G |
T |
7: 16,675,583 (GRCm38) |
P9H |
possibly damaging |
Het |
| Cela2a |
G |
T |
4: 141,821,391 (GRCm38) |
P145T |
probably damaging |
Het |
| Celsr1 |
A |
C |
15: 85,963,100 (GRCm38) |
F1479V |
probably damaging |
Het |
| Celsr2 |
G |
T |
3: 108,412,341 (GRCm38) |
H1052N |
probably benign |
Het |
| Celsr2 |
C |
A |
3: 108,393,131 (GRCm38) |
R2871L |
probably benign |
Het |
| Cenpf |
G |
A |
1: 189,659,472 (GRCm38) |
T704I |
probably damaging |
Het |
| Cenpv |
A |
C |
11: 62,527,525 (GRCm38) |
F201V |
probably damaging |
Het |
| Cep112 |
G |
A |
11: 108,425,310 (GRCm38) |
G36D |
probably damaging |
Het |
| Cep152 |
C |
A |
2: 125,583,971 (GRCm38) |
G825C |
probably benign |
Het |
| Cep170b |
G |
T |
12: 112,741,012 (GRCm38) |
|
probably null |
Het |
| Cep192 |
A |
T |
18: 67,881,288 (GRCm38) |
K2451M |
probably damaging |
Het |
| Cep290 |
AGG |
AG |
10: 100,549,374 (GRCm38) |
|
probably benign |
Het |
| Cep295 |
G |
T |
9: 15,357,697 (GRCm38) |
P16Q |
probably damaging |
Het |
| Cep295nl |
T |
G |
11: 118,333,873 (GRCm38) |
Q48H |
probably damaging |
Het |
| Cep295nl |
T |
C |
11: 118,333,019 (GRCm38) |
E333G |
possibly damaging |
Het |
| Cep44 |
C |
G |
8: 56,544,128 (GRCm38) |
G125A |
possibly damaging |
Het |
| Cep97 |
C |
A |
16: 55,927,735 (GRCm38) |
G111C |
probably damaging |
Het |
| Cerkl |
C |
A |
2: 79,368,765 (GRCm38) |
Q160H |
probably benign |
Het |
| Cers1 |
C |
G |
8: 70,318,318 (GRCm38) |
P126R |
probably benign |
Het |
| Ces1a |
C |
A |
8: 93,036,085 (GRCm38) |
R186L |
probably benign |
Het |
| Ces1g |
G |
T |
8: 93,325,811 (GRCm38) |
H283Q |
probably benign |
Het |
| Ces2a |
C |
A |
8: 104,734,006 (GRCm38) |
|
probably benign |
Het |
| Ces2a |
A |
T |
8: 104,734,850 (GRCm38) |
E77V |
probably damaging |
Het |
| Ces3a |
A |
C |
8: 105,053,602 (GRCm38) |
K327T |
possibly damaging |
Het |
| Ces4a |
A |
G |
8: 105,131,977 (GRCm38) |
K9R |
probably benign |
Het |
| Cetn2 |
T |
G |
X: 72,914,889 (GRCm38) |
K127T |
probably damaging |
Het |
| Cfap100 |
G |
C |
6: 90,406,150 (GRCm38) |
A347G |
unknown |
Het |
| Cfap20 |
C |
T |
8: 95,434,525 (GRCm38) |
S16N |
possibly damaging |
Het |
| Cfap206 |
G |
C |
4: 34,719,661 (GRCm38) |
P251R |
possibly damaging |
Het |
| Cfap221 |
G |
T |
1: 119,995,141 (GRCm38) |
L24I |
probably benign |
Het |
| Cfap45 |
G |
T |
1: 172,545,284 (GRCm38) |
E515D |
probably benign |
Het |
| Cfap46 |
A |
C |
7: 139,639,548 (GRCm38) |
L1334V |
|
Het |
| Cfap65 |
G |
A |
1: 74,910,747 (GRCm38) |
R1200C |
probably damaging |
Het |
| Cfap74 |
C |
G |
4: 155,426,118 (GRCm38) |
R387G |
|
Het |
| Cflar |
C |
G |
1: 58,731,229 (GRCm38) |
C160W |
|
Het |
| Cflar |
G |
T |
1: 58,740,313 (GRCm38) |
|
probably null |
Het |
| Cgn |
A |
T |
3: 94,774,273 (GRCm38) |
V504E |
possibly damaging |
Het |
| Cgn |
T |
C |
3: 94,774,346 (GRCm38) |
R480G |
probably damaging |
Het |
| Cgn |
G |
T |
3: 94,776,178 (GRCm38) |
A389D |
probably benign |
Het |
| Chd1 |
G |
T |
17: 15,766,347 (GRCm38) |
V1482L |
probably damaging |
Het |
| Chd1 |
G |
T |
17: 15,768,733 (GRCm38) |
G1583C |
probably damaging |
Het |
| Chd4 |
G |
T |
6: 125,100,860 (GRCm38) |
R95L |
possibly damaging |
Het |
| Chd4 |
G |
T |
6: 125,101,598 (GRCm38) |
A228S |
probably benign |
Het |
| Chd5 |
G |
A |
4: 152,378,479 (GRCm38) |
R1363K |
probably damaging |
Het |
| Chd7 |
C |
G |
4: 8,844,313 (GRCm38) |
A1502G |
probably damaging |
Het |
| Cherp |
C |
T |
8: 72,470,953 (GRCm38) |
G101D |
|
Het |
| Chfr |
C |
G |
5: 110,144,895 (GRCm38) |
S176* |
probably null |
Het |
| Chil1 |
C |
G |
1: 134,189,230 (GRCm38) |
R319G |
probably damaging |
Het |
| Chil1 |
G |
T |
1: 134,182,779 (GRCm38) |
|
probably null |
Het |
| Chml |
C |
A |
1: 175,687,762 (GRCm38) |
G198C |
possibly damaging |
Het |
| Chmp3 |
G |
C |
6: 71,579,775 (GRCm38) |
A220P |
probably damaging |
Het |
| Chmp3 |
A |
C |
6: 71,560,964 (GRCm38) |
E58D |
probably benign |
Het |
| Chpf |
C |
G |
1: 75,475,458 (GRCm38) |
A613P |
probably benign |
Het |
| Chpf |
G |
C |
1: 75,475,470 (GRCm38) |
L609V |
probably damaging |
Het |
| Chrna2 |
C |
A |
14: 66,149,304 (GRCm38) |
L300M |
probably damaging |
Het |
| Chrna5 |
G |
T |
9: 55,004,482 (GRCm38) |
G189C |
probably damaging |
Het |
| Chrna7 |
A |
T |
7: 63,212,184 (GRCm38) |
L40Q |
probably damaging |
Het |
| Chst3 |
T |
A |
10: 60,185,676 (GRCm38) |
R450W |
possibly damaging |
Het |
| Chst4 |
A |
C |
8: 110,030,092 (GRCm38) |
F380V |
probably damaging |
Het |
| Chsy1 |
C |
G |
7: 66,172,226 (GRCm38) |
S736R |
probably damaging |
Het |
| Cic |
A |
C |
7: 25,271,019 (GRCm38) |
E58D |
possibly damaging |
Het |
| Cidea |
A |
G |
18: 67,358,853 (GRCm38) |
K61R |
probably null |
Het |
| Ciita |
C |
A |
16: 10,508,700 (GRCm38) |
P252T |
probably damaging |
Het |
| Cilp |
TGGG |
TGG |
9: 65,280,130 (GRCm38) |
|
probably null |
Het |
| Cipc |
G |
T |
12: 86,960,337 (GRCm38) |
G103C |
probably damaging |
Het |
| Cit |
G |
C |
5: 115,986,603 (GRCm38) |
G1526R |
probably damaging |
Het |
| Cited4 |
C |
A |
4: 120,666,814 (GRCm38) |
H4Q |
probably damaging |
Het |
| Ckap2 |
G |
A |
8: 22,169,794 (GRCm38) |
P557L |
probably damaging |
Het |
| Ckap2l |
C |
A |
2: 129,285,362 (GRCm38) |
D299Y |
probably damaging |
Het |
| Clca1 |
G |
T |
3: 145,013,921 (GRCm38) |
S429R |
probably damaging |
Het |
| Clcn1 |
T |
C |
6: 42,307,567 (GRCm38) |
V613A |
probably damaging |
Het |
| Cldn11 |
T |
A |
3: 31,150,306 (GRCm38) |
W53R |
probably damaging |
Het |
| Cldn18 |
T |
A |
9: 99,698,847 (GRCm38) |
K116M |
possibly damaging |
Het |
| Cldn23 |
A |
T |
8: 35,826,277 (GRCm38) |
L19Q |
probably damaging |
Het |
| Cldn34b1 |
T |
G |
X: 154,887,708 (GRCm38) |
K5T |
probably benign |
Het |
| Clec4d |
T |
G |
6: 123,274,686 (GRCm38) |
F176V |
probably benign |
Het |
| Clic1 |
G |
T |
17: 35,052,459 (GRCm38) |
G22W |
probably damaging |
Het |
| Clic6 |
G |
A |
16: 92,498,895 (GRCm38) |
D148N |
probably benign |
Het |
| Clip3 |
A |
C |
7: 30,298,838 (GRCm38) |
E236D |
probably benign |
Het |
| Clk1 |
C |
A |
1: 58,417,372 (GRCm38) |
R186L |
probably benign |
Het |
| Clstn3 |
C |
T |
6: 124,459,200 (GRCm38) |
V234M |
probably damaging |
Het |
| Cltc |
A |
G |
11: 86,702,632 (GRCm38) |
V1525A |
probably benign |
Het |
| Cmklr1 |
T |
A |
5: 113,613,891 (GRCm38) |
S350C |
probably damaging |
Het |
| Cmya5 |
C |
G |
13: 93,096,790 (GRCm38) |
D597H |
unknown |
Het |
| Cmya5 |
C |
G |
13: 93,063,579 (GRCm38) |
A3414P |
probably benign |
Het |
| Cnksr1 |
A |
T |
4: 134,232,135 (GRCm38) |
L396Q |
probably damaging |
Het |
| Cnksr3 |
C |
T |
10: 7,134,544 (GRCm38) |
R308Q |
probably damaging |
Het |
| Cnnm4 |
G |
T |
1: 36,505,751 (GRCm38) |
R697L |
possibly damaging |
Het |
| Cnot1 |
C |
G |
8: 95,748,277 (GRCm38) |
Q1103H |
possibly damaging |
Het |
| Cnot8 |
C |
G |
11: 58,113,090 (GRCm38) |
A117G |
probably benign |
Het |
| Cnppd1 |
C |
A |
1: 75,140,951 (GRCm38) |
G42V |
probably damaging |
Het |
| Cntn2 |
C |
A |
1: 132,527,788 (GRCm38) |
R237L |
probably damaging |
Het |
| Cntn3 |
T |
G |
6: 102,437,931 (GRCm38) |
|
probably null |
Het |
| Cntn4 |
T |
G |
6: 106,509,464 (GRCm38) |
N284K |
probably benign |
Het |
| Cntn4 |
T |
G |
6: 106,523,563 (GRCm38) |
F334V |
probably benign |
Het |
| Cntnap1 |
C |
A |
11: 101,182,898 (GRCm38) |
T625K |
probably damaging |
Het |
| Cntnap2 |
A |
C |
6: 47,271,148 (GRCm38) |
K1163Q |
probably benign |
Het |
| Cntnap3 |
T |
G |
13: 64,792,388 (GRCm38) |
N332H |
probably damaging |
Het |
| Cntnap3 |
AC |
A |
13: 64,740,872 (GRCm38) |
|
probably null |
Het |
| Cntnap4 |
A |
T |
8: 112,858,189 (GRCm38) |
K1086M |
possibly damaging |
Het |
| Cntnap5a |
T |
A |
1: 116,428,516 (GRCm38) |
V759E |
probably damaging |
Het |
| Cntnap5b |
C |
A |
1: 99,967,270 (GRCm38) |
T89K |
probably damaging |
Het |
| Cntnap5b |
C |
G |
1: 100,446,840 (GRCm38) |
Q734E |
probably benign |
Het |
| Cntnap5b |
C |
A |
1: 100,164,228 (GRCm38) |
S231R |
possibly damaging |
Het |
| Cobl |
C |
A |
11: 12,369,645 (GRCm38) |
E244D |
probably damaging |
Het |
| Cobl |
G |
T |
11: 12,253,433 (GRCm38) |
Q1090K |
probably benign |
Het |
| Cobl |
G |
A |
11: 12,375,827 (GRCm38) |
A223V |
probably damaging |
Het |
| Cog1 |
C |
A |
11: 113,651,982 (GRCm38) |
H151Q |
probably damaging |
Het |
| Coil |
C |
A |
11: 88,981,976 (GRCm38) |
P388T |
probably damaging |
Het |
| Col10a1 |
C |
A |
10: 34,395,178 (GRCm38) |
P382H |
probably damaging |
Het |
| Col11a2 |
G |
T |
17: 34,056,402 (GRCm38) |
G420C |
unknown |
Het |
| Col16a1 |
G |
C |
4: 130,072,878 (GRCm38) |
G882A |
unknown |
Het |
| Col17a1 |
CCCTGGTGGGCCTGG |
CCCTGG |
19: 47,649,429 (GRCm38) |
|
probably benign |
Het |
| Col18a1 |
C |
A |
10: 77,112,851 (GRCm38) |
A276S |
unknown |
Het |
| Col18a1 |
G |
C |
10: 77,055,709 (GRCm38) |
A1097G |
possibly damaging |
Het |
| Col1a2 |
A |
C |
6: 4,532,750 (GRCm38) |
T792P |
unknown |
Het |
| Col23a1 |
G |
T |
11: 51,549,708 (GRCm38) |
D142Y |
unknown |
Het |
| Col24a1 |
G |
A |
3: 145,342,498 (GRCm38) |
G619S |
probably damaging |
Het |
| Col25a1 |
AC |
A |
3: 130,182,795 (GRCm38) |
|
probably null |
Het |
| Col27a1 |
C |
G |
4: 63,225,788 (GRCm38) |
S571C |
probably damaging |
Het |
| Col5a1 |
G |
A |
2: 28,002,517 (GRCm38) |
R1014H |
unknown |
Het |
| Col5a2 |
C |
A |
1: 45,383,680 (GRCm38) |
G1126C |
probably damaging |
Het |
| Col5a2 |
C |
G |
1: 45,396,484 (GRCm38) |
G697A |
probably benign |
Het |
| Col5a2 |
C |
A |
1: 45,376,146 (GRCm38) |
V1478L |
possibly damaging |
Het |
| Col6a4 |
T |
C |
9: 106,000,797 (GRCm38) |
S1994G |
probably benign |
Het |
| Col6a4 |
G |
C |
9: 106,000,870 (GRCm38) |
C1969W |
probably damaging |
Het |
| Col6a6 |
G |
C |
9: 105,780,952 (GRCm38) |
A687G |
probably damaging |
Het |
| Col9a1 |
C |
A |
1: 24,214,588 (GRCm38) |
P464H |
probably damaging |
Het |
| Col9a2 |
C |
G |
4: 121,053,797 (GRCm38) |
A543G |
probably damaging |
Het |
| Colec11 |
C |
A |
12: 28,595,284 (GRCm38) |
Q129H |
probably damaging |
Het |
| Commd10 |
G |
T |
18: 46,990,566 (GRCm38) |
G163* |
probably null |
Het |
| Commd2 |
C |
A |
3: 57,646,857 (GRCm38) |
R141L |
probably damaging |
Het |
| Copb2 |
A |
C |
9: 98,586,146 (GRCm38) |
K737T |
probably benign |
Het |
| Coq3 |
C |
A |
4: 21,899,102 (GRCm38) |
P145H |
probably damaging |
Het |
| Coq4 |
G |
T |
2: 29,795,449 (GRCm38) |
Q158H |
probably null |
Het |
| Coq6 |
G |
C |
12: 84,370,963 (GRCm38) |
A226P |
possibly damaging |
Het |
| Coro6 |
ACCC |
ACC |
11: 77,467,865 (GRCm38) |
|
probably null |
Het |
| Cox6a1 |
C |
T |
5: 115,345,908 (GRCm38) |
G92S |
probably damaging |
Het |
| Cox6b2 |
C |
A |
7: 4,752,147 (GRCm38) |
V43L |
probably benign |
Het |
| Cpeb1 |
C |
A |
7: 81,359,728 (GRCm38) |
|
probably null |
Het |
| Cpeb2 |
G |
T |
5: 43,234,717 (GRCm38) |
G419C |
|
Het |
| Cpne1 |
C |
A |
2: 156,077,644 (GRCm38) |
D302Y |
probably damaging |
Het |
| Cpq |
A |
C |
15: 33,381,391 (GRCm38) |
D300A |
probably damaging |
Het |
| Cps1 |
G |
T |
1: 67,123,268 (GRCm38) |
G35V |
possibly damaging |
Het |
| Cps1 |
CTT |
CT |
1: 67,148,719 (GRCm38) |
|
probably null |
Het |
| Cpsf4 |
A |
T |
5: 145,167,415 (GRCm38) |
E20V |
possibly damaging |
Het |
| Cr2 |
G |
T |
1: 195,154,153 (GRCm38) |
Q901K |
probably benign |
Het |
| Crb1 |
CG |
C |
1: 139,237,086 (GRCm38) |
|
probably null |
Het |
| Crb2 |
C |
T |
2: 37,776,371 (GRCm38) |
P11S |
probably benign |
Het |
| Crebl2 |
G |
T |
6: 134,849,289 (GRCm38) |
E68* |
probably null |
Het |
| Crem |
T |
A |
18: 3,267,730 (GRCm38) |
E258V |
probably damaging |
Het |
| Crispld1 |
C |
A |
1: 17,728,613 (GRCm38) |
|
probably benign |
Het |
| Crispld1 |
G |
T |
1: 17,752,851 (GRCm38) |
A381S |
possibly damaging |
Het |
| Crtac1 |
T |
G |
19: 42,287,926 (GRCm38) |
E521A |
probably benign |
Het |
| Cry1 |
C |
A |
10: 85,144,197 (GRCm38) |
V416L |
probably benign |
Het |
| Crybg2 |
C |
A |
4: 134,082,660 (GRCm38) |
P1241H |
probably damaging |
Het |
| Cryz |
A |
T |
3: 154,621,769 (GRCm38) |
T277S |
probably benign |
Het |
| Csmd1 |
T |
A |
8: 16,037,198 (GRCm38) |
T1946S |
probably damaging |
Het |
| Csmd1 |
T |
C |
8: 15,998,814 (GRCm38) |
D2296G |
probably damaging |
Het |
| Cspg5 |
G |
T |
9: 110,251,050 (GRCm38) |
A429S |
probably damaging |
Het |
| Ctbp2 |
C |
A |
7: 133,015,290 (GRCm38) |
|
probably benign |
Het |
| Ctf2 |
T |
A |
7: 127,719,456 (GRCm38) |
I124F |
possibly damaging |
Het |
| Ctps |
G |
C |
4: 120,542,743 (GRCm38) |
D472E |
probably benign |
Het |
| Ctsf |
C |
A |
19: 4,856,306 (GRCm38) |
Q155K |
probably benign |
Het |
| Ctsj |
C |
T |
13: 61,004,115 (GRCm38) |
E43K |
probably damaging |
Het |
| Ctsq |
C |
A |
13: 61,037,123 (GRCm38) |
V250L |
probably benign |
Het |
| Cttnbp2 |
C |
A |
6: 18,408,709 (GRCm38) |
S971I |
probably benign |
Het |
| Cttnbp2 |
C |
A |
6: 18,408,725 (GRCm38) |
G966C |
possibly damaging |
Het |
| Cttnbp2 |
G |
T |
6: 18,420,836 (GRCm38) |
A892E |
possibly damaging |
Het |
| Cttnbp2 |
C |
A |
6: 18,501,960 (GRCm38) |
E60* |
probably null |
Het |
| Cubn |
T |
A |
2: 13,381,825 (GRCm38) |
E1543V |
probably damaging |
Het |
| Cul9 |
C |
A |
17: 46,520,576 (GRCm38) |
G1571* |
probably null |
Het |
| Cul9 |
C |
A |
17: 46,520,585 (GRCm38) |
G1568* |
probably null |
Het |
| Cutal |
G |
T |
2: 34,882,425 (GRCm38) |
R67I |
probably damaging |
Het |
| Cux2 |
C |
A |
5: 121,873,813 (GRCm38) |
G520* |
probably null |
Het |
| Cux2 |
G |
T |
5: 121,885,934 (GRCm38) |
T92K |
probably benign |
Het |
| Cxcr1 |
A |
T |
1: 74,192,392 (GRCm38) |
L157* |
probably null |
Het |
| Cyb561d2 |
G |
C |
9: 107,540,296 (GRCm38) |
C85W |
probably damaging |
Het |
| Cybb |
T |
C |
X: 9,438,240 (GRCm38) |
I564V |
probably damaging |
Het |
| Cybb |
G |
A |
X: 9,440,001 (GRCm38) |
H494Y |
probably damaging |
Het |
| Cyfip2 |
G |
A |
11: 46,222,615 (GRCm38) |
S968F |
not run |
Het |
| Cylc1 |
G |
A |
X: 111,123,146 (GRCm38) |
V399I |
unknown |
Het |
| Cyp11b1 |
T |
A |
15: 74,839,355 (GRCm38) |
K158I |
probably damaging |
Het |
| Cyp19a1 |
T |
A |
9: 54,176,599 (GRCm38) |
K169* |
probably null |
Het |
| Cyp1a1 |
C |
A |
9: 57,700,594 (GRCm38) |
S168R |
probably benign |
Het |
| Cyp26b1 |
T |
C |
6: 84,577,114 (GRCm38) |
S174G |
probably benign |
Het |
| Cyp2a4 |
G |
T |
7: 26,307,323 (GRCm38) |
G36* |
probably null |
Het |
| Cyp2a4 |
C |
T |
7: 26,310,841 (GRCm38) |
P264S |
probably damaging |
Het |
| Cyp2a5 |
G |
A |
7: 26,836,774 (GRCm38) |
R148H |
probably damaging |
Het |
| Cyp2a5 |
A |
C |
7: 26,835,497 (GRCm38) |
N45T |
probably damaging |
Het |
| Cyp2c29 |
G |
A |
19: 39,324,997 (GRCm38) |
M351I |
probably benign |
Het |
| Cyp2c54 |
G |
A |
19: 40,046,215 (GRCm38) |
P337L |
probably damaging |
Het |
| Cyp2c55 |
C |
T |
19: 39,035,513 (GRCm38) |
R344C |
probably benign |
Het |
| Cyp2j11 |
T |
G |
4: 96,307,303 (GRCm38) |
E385D |
probably damaging |
Het |
| Cyp2j11 |
G |
T |
4: 96,307,436 (GRCm38) |
S341Y |
probably damaging |
Het |
| Cyp2j5 |
G |
T |
4: 96,629,506 (GRCm38) |
P490T |
probably damaging |
Het |
| Cyp2j6 |
C |
A |
4: 96,536,068 (GRCm38) |
G151* |
probably null |
Het |
| Cyp39a1 |
A |
C |
17: 43,731,048 (GRCm38) |
E382A |
probably damaging |
Het |
| Cyp39a1 |
A |
C |
17: 43,725,577 (GRCm38) |
I333L |
probably benign |
Het |
| Cyp3a44 |
T |
C |
5: 145,791,664 (GRCm38) |
K250R |
probably benign |
Het |
| Cyp4a10 |
G |
T |
4: 115,518,326 (GRCm38) |
S2I |
probably damaging |
Het |
| Cyp4a12a |
G |
T |
4: 115,329,003 (GRCm38) |
|
probably null |
Het |
| Cyp4a14 |
G |
C |
4: 115,490,017 (GRCm38) |
A408G |
probably benign |
Het |
| Cyp4a30b |
G |
T |
4: 115,470,959 (GRCm38) |
R475L |
possibly damaging |
Het |
| Cypt14 |
T |
C |
X: 39,863,555 (GRCm38) |
K10R |
possibly damaging |
Het |
| Cypt15 |
A |
C |
X: 39,346,384 (GRCm38) |
K33T |
possibly damaging |
Het |
| Cypt2 |
G |
T |
X: 105,499,799 (GRCm38) |
R3L |
probably benign |
Het |
| Cyth2 |
C |
A |
7: 45,813,105 (GRCm38) |
R24L |
possibly damaging |
Het |
| Cytip |
C |
A |
2: 58,134,037 (GRCm38) |
S257I |
probably damaging |
Het |
| Cytl1 |
G |
T |
5: 37,735,695 (GRCm38) |
A50S |
probably benign |
Het |
| D430041D05Rik |
C |
A |
2: 104,256,856 (GRCm38) |
A592S |
probably benign |
Het |
| D430041D05Rik |
C |
A |
2: 104,154,935 (GRCm38) |
L1262F |
probably damaging |
Het |
| D5Ertd579e |
C |
G |
5: 36,615,762 (GRCm38) |
E430Q |
probably benign |
Het |
| D930020B18Rik |
C |
A |
10: 121,667,616 (GRCm38) |
A232D |
probably benign |
Het |
| Dab1 |
G |
C |
4: 104,728,078 (GRCm38) |
V472L |
probably benign |
Het |
| Dab2ip |
G |
T |
2: 35,708,868 (GRCm38) |
D191Y |
probably damaging |
Het |
| Dapk1 |
AC |
A |
13: 60,760,804 (GRCm38) |
|
probably null |
Het |
| Dars |
C |
A |
1: 128,372,207 (GRCm38) |
E347* |
probably null |
Het |
| Daw1 |
C |
A |
1: 83,183,300 (GRCm38) |
T121K |
probably damaging |
Het |
| Daw1 |
C |
G |
1: 83,180,391 (GRCm38) |
L54V |
probably damaging |
Het |
| Daw1 |
A |
C |
1: 83,209,255 (GRCm38) |
K262T |
probably damaging |
Het |
| Dbh |
T |
A |
2: 27,177,727 (GRCm38) |
L454Q |
probably damaging |
Het |
| Dcaf12l1 |
G |
A |
X: 44,789,897 (GRCm38) |
T8M |
probably benign |
Het |
| Dcaf8 |
G |
T |
1: 172,172,929 (GRCm38) |
R218L |
probably benign |
Het |
| Dcdc2c |
G |
T |
12: 28,524,707 (GRCm38) |
P139T |
probably benign |
Het |
| Dcxr |
GA |
G |
11: 120,727,208 (GRCm38) |
|
probably null |
Het |
| Ddhd2 |
C |
T |
8: 25,735,829 (GRCm38) |
M500I |
possibly damaging |
Het |
| Ddo |
C |
A |
10: 40,647,933 (GRCm38) |
H306Q |
probably damaging |
Het |
| Ddr2 |
G |
T |
1: 169,998,083 (GRCm38) |
T316N |
probably benign |
Het |
| Ddr2 |
T |
C |
1: 169,984,955 (GRCm38) |
Y656C |
probably damaging |
Het |
| Ddr2 |
T |
G |
1: 169,998,084 (GRCm38) |
T316P |
probably benign |
Het |
| Ddx51 |
G |
T |
5: 110,654,558 (GRCm38) |
E176* |
probably null |
Het |
| Deaf1 |
C |
T |
7: 141,301,474 (GRCm38) |
W573* |
probably null |
Het |
| Dedd2 |
C |
A |
7: 25,203,598 (GRCm38) |
R312L |
probably damaging |
Het |
| Def8 |
G |
T |
8: 123,459,966 (GRCm38) |
E428D |
possibly damaging |
Het |
| Defa21 |
T |
G |
8: 21,025,723 (GRCm38) |
F46V |
probably benign |
Het |
| Defa27 |
A |
G |
8: 21,315,598 (GRCm38) |
Q18R |
probably damaging |
Het |
| Defa27 |
C |
A |
8: 21,315,597 (GRCm38) |
Q18K |
probably damaging |
Het |
| Defb14 |
G |
T |
8: 19,195,120 (GRCm38) |
G38C |
probably damaging |
Het |
| Defb21 |
C |
A |
2: 152,573,833 (GRCm38) |
P22H |
unknown |
Het |
| Defb26 |
C |
T |
2: 152,508,301 (GRCm38) |
|
probably null |
Het |
| Dennd4b |
T |
G |
3: 90,279,495 (GRCm38) |
L1425R |
probably damaging |
Het |
| Depdc5 |
A |
T |
5: 32,943,282 (GRCm38) |
M846L |
possibly damaging |
Het |
| Dffb |
G |
T |
4: 153,972,843 (GRCm38) |
L126M |
probably damaging |
Het |
| Dgat2l6 |
C |
A |
X: 100,524,950 (GRCm38) |
Q10K |
probably benign |
Het |
| Dgcr14 |
C |
T |
16: 17,902,310 (GRCm38) |
G393S |
possibly damaging |
Het |
| Dgcr8 |
C |
T |
16: 18,278,318 (GRCm38) |
|
probably null |
Het |
| Dgkb |
C |
A |
12: 38,136,613 (GRCm38) |
L254M |
probably damaging |
Het |
| Dgkb |
A |
G |
12: 37,981,996 (GRCm38) |
Q19R |
possibly damaging |
Het |
| Dgkd |
A |
C |
1: 87,927,810 (GRCm38) |
S725R |
probably benign |
Het |
| Dgkg |
C |
A |
16: 22,588,398 (GRCm38) |
A146S |
probably benign |
Het |
| Dglucy |
A |
C |
12: 100,853,304 (GRCm38) |
K425T |
probably benign |
Het |
| Dhx30 |
C |
A |
9: 110,086,965 (GRCm38) |
G722C |
probably damaging |
Het |
| Dhx34 |
G |
A |
7: 16,218,644 (GRCm38) |
R19* |
probably null |
Het |
| Dhx57 |
T |
G |
17: 80,245,805 (GRCm38) |
K1231T |
probably damaging |
Het |
| Diaph3 |
C |
A |
14: 86,656,432 (GRCm38) |
C1136F |
probably benign |
Het |
| Dicer1 |
C |
G |
12: 104,731,020 (GRCm38) |
A93P |
probably null |
Het |
| Dip2a |
T |
G |
10: 76,280,820 (GRCm38) |
T890P |
probably damaging |
Het |
| Dip2a |
T |
A |
10: 76,266,323 (GRCm38) |
S1446C |
possibly damaging |
Het |
| Disp3 |
G |
T |
4: 148,250,957 (GRCm38) |
P908T |
probably damaging |
Het |
| Dlc1 |
C |
A |
8: 36,584,211 (GRCm38) |
G338C |
probably damaging |
Het |
| Dlec1 |
C |
A |
9: 119,138,786 (GRCm38) |
P1218T |
probably benign |
Het |
| Dlg4 |
G |
A |
11: 70,041,920 (GRCm38) |
G512E |
probably benign |
Het |
| Dlgap1 |
C |
T |
17: 70,815,209 (GRCm38) |
P878S |
probably damaging |
Het |
| Dll4 |
G |
T |
2: 119,326,052 (GRCm38) |
|
probably benign |
Het |
| Dmbt1 |
T |
G |
7: 131,088,812 (GRCm38) |
I925S |
unknown |
Het |
| Dmd |
A |
T |
X: 83,878,484 (GRCm38) |
L1453F |
possibly damaging |
Het |
| Dmd |
A |
G |
X: 83,627,286 (GRCm38) |
K225R |
probably damaging |
Het |
| Dmkn |
G |
T |
7: 30,776,497 (GRCm38) |
W25L |
possibly damaging |
Het |
| Dmrt1 |
C |
T |
19: 25,559,970 (GRCm38) |
T307I |
possibly damaging |
Het |
| Dmrt2 |
T |
C |
19: 25,678,000 (GRCm38) |
L321P |
probably damaging |
Het |
| Dmrtb1 |
T |
A |
4: 107,680,830 (GRCm38) |
D47V |
probably damaging |
Het |
| Dnaaf1 |
A |
C |
8: 119,575,441 (GRCm38) |
D27A |
possibly damaging |
Het |
| Dnaaf2 |
G |
C |
12: 69,197,850 (GRCm38) |
H146D |
probably damaging |
Het |
| Dnah10 |
G |
T |
5: 124,775,355 (GRCm38) |
A1883S |
probably benign |
Het |
| Dnah11 |
C |
T |
12: 117,931,177 (GRCm38) |
R3645H |
possibly damaging |
Het |
| Dnah11 |
A |
C |
12: 118,127,119 (GRCm38) |
I1030S |
probably benign |
Het |
| Dnah11 |
A |
T |
12: 118,130,799 (GRCm38) |
L845M |
probably damaging |
Het |
| Dnah14 |
G |
C |
1: 181,757,351 (GRCm38) |
E3216Q |
possibly damaging |
Het |
| Dnah17 |
G |
T |
11: 118,127,166 (GRCm38) |
L168M |
probably benign |
Het |
| Dnah2 |
G |
A |
11: 69,421,821 (GRCm38) |
A4306V |
possibly damaging |
Het |
| Dnah2 |
T |
G |
11: 69,516,481 (GRCm38) |
Y492S |
probably damaging |
Het |
| Dnah2 |
G |
A |
11: 69,498,667 (GRCm38) |
H800Y |
probably benign |
Het |
| Dnah2 |
G |
C |
11: 69,487,054 (GRCm38) |
N1317K |
possibly damaging |
Het |
| Dnah2 |
C |
G |
11: 69,516,523 (GRCm38) |
G478A |
probably damaging |
Het |
| Dnah2 |
G |
T |
11: 69,451,120 (GRCm38) |
Q2986K |
probably benign |
Het |
| Dnah3 |
A |
G |
7: 119,967,803 (GRCm38) |
V13A |
|
Het |
| Dnah6 |
T |
A |
6: 73,087,783 (GRCm38) |
E2605D |
possibly damaging |
Het |
| Dnah6 |
G |
T |
6: 73,133,559 (GRCm38) |
T1681K |
probably benign |
Het |
| Dnah7a |
A |
C |
1: 53,419,699 (GRCm38) |
L3760R |
probably damaging |
Het |
| Dnah7a |
T |
G |
1: 53,483,463 (GRCm38) |
K2872T |
probably damaging |
Het |
| Dnah7c |
T |
C |
1: 46,760,316 (GRCm38) |
F3379L |
possibly damaging |
Het |
| Dnah7c |
G |
C |
1: 46,639,665 (GRCm38) |
V1790L |
probably benign |
Het |
| Dnah7c |
G |
T |
1: 46,615,281 (GRCm38) |
G107V |
probably damaging |
Het |
| Dnah7c |
A |
T |
1: 46,646,992 (GRCm38) |
|
probably null |
Het |
| Dnah7c |
T |
A |
1: 46,467,302 (GRCm38) |
L180M |
probably benign |
Het |
| Dnah8 |
A |
G |
17: 30,648,540 (GRCm38) |
K322R |
probably benign |
Het |
| Dnah9 |
T |
A |
11: 66,037,474 (GRCm38) |
Q2123L |
probably damaging |
Het |
| Dnah9 |
C |
A |
11: 66,072,835 (GRCm38) |
G1764V |
probably damaging |
Het |
| Dnah9 |
G |
T |
11: 65,927,853 (GRCm38) |
L3220M |
probably damaging |
Het |
| Dnah9 |
T |
A |
11: 65,895,972 (GRCm38) |
I3612F |
probably damaging |
Het |
| Dnah9 |
A |
T |
11: 65,970,084 (GRCm38) |
L2820Q |
probably damaging |
Het |
| Dnaic1 |
G |
T |
4: 41,614,323 (GRCm38) |
R333L |
probably benign |
Het |
| Dnajb6 |
G |
A |
5: 29,752,445 (GRCm38) |
G75D |
possibly damaging |
Het |
| Dnajb8 |
A |
T |
6: 88,222,910 (GRCm38) |
M143L |
possibly damaging |
Het |
| Dnajc1 |
C |
T |
2: 18,293,987 (GRCm38) |
A259T |
possibly damaging |
Het |
| Dnajc11 |
G |
A |
4: 151,933,783 (GRCm38) |
D11N |
probably benign |
Het |
| Dnajc28 |
G |
A |
16: 91,617,033 (GRCm38) |
H108Y |
probably benign |
Het |
| Dner |
C |
A |
1: 84,383,980 (GRCm38) |
R636L |
possibly damaging |
Het |
| Dnhd1 |
A |
T |
7: 105,668,547 (GRCm38) |
K483M |
probably damaging |
Het |
| Dnhd1 |
G |
T |
7: 105,678,299 (GRCm38) |
K50N |
probably benign |
Het |
| Dnhd1 |
A |
T |
7: 105,703,036 (GRCm38) |
|
probably null |
Het |
| Dnhd1 |
GT |
GTT |
7: 105,703,580 (GRCm38) |
|
probably null |
Het |
| Dnmbp |
T |
A |
19: 43,889,367 (GRCm38) |
T422S |
probably benign |
Het |
| Dnmbp |
T |
A |
19: 43,866,688 (GRCm38) |
K265N |
probably damaging |
Het |
| Dnmt1 |
C |
A |
9: 20,926,554 (GRCm38) |
V381L |
probably benign |
Het |
| Dnmt1 |
T |
G |
9: 20,915,863 (GRCm38) |
K979T |
probably damaging |
Het |
| Dnmt3a |
G |
T |
12: 3,904,201 (GRCm38) |
W791L |
probably damaging |
Het |
| Doc2b |
A |
T |
11: 75,777,072 (GRCm38) |
L284Q |
probably benign |
Het |
| Dock10 |
A |
C |
1: 80,560,954 (GRCm38) |
L959V |
probably benign |
Het |
| Dock11 |
G |
T |
X: 35,984,848 (GRCm38) |
A699S |
possibly damaging |
Het |
| Dock2 |
A |
C |
11: 34,718,924 (GRCm38) |
F230V |
probably benign |
Het |
| Dock4 |
A |
T |
12: 40,631,614 (GRCm38) |
Y104F |
probably benign |
Het |
| Dock4 |
G |
C |
12: 40,631,616 (GRCm38) |
V105L |
probably benign |
Het |
| Dock7 |
C |
A |
4: 98,945,225 (GRCm38) |
G1945V |
unknown |
Het |
| Dock9 |
C |
A |
14: 121,651,782 (GRCm38) |
G308C |
probably benign |
Het |
| Dopey2 |
G |
T |
16: 93,803,546 (GRCm38) |
S2037I |
probably damaging |
Het |
| Dopey2 |
T |
A |
16: 93,769,581 (GRCm38) |
S1083R |
probably benign |
Het |
| Dopey2 |
G |
A |
16: 93,807,868 (GRCm38) |
G2132E |
possibly damaging |
Het |
| Dpagt1 |
G |
T |
9: 44,329,125 (GRCm38) |
V213L |
probably benign |
Het |
| Dpp10 |
C |
A |
1: 123,353,440 (GRCm38) |
E627* |
probably null |
Het |
| Dpp3 |
T |
G |
19: 4,922,341 (GRCm38) |
Q185P |
probably damaging |
Het |
| Dpp6 |
C |
A |
5: 27,398,998 (GRCm38) |
A142E |
probably damaging |
Het |
| Dpysl5 |
G |
T |
5: 30,778,120 (GRCm38) |
R189L |
probably benign |
Het |
| Drd2 |
G |
T |
9: 49,395,655 (GRCm38) |
E14* |
probably null |
Het |
| Dsc1 |
C |
A |
18: 20,114,538 (GRCm38) |
A7S |
probably benign |
Het |
| Dsc2 |
A |
T |
18: 20,035,299 (GRCm38) |
L701Q |
probably damaging |
Het |
| Dsg1c |
G |
T |
18: 20,283,573 (GRCm38) |
G844C |
probably damaging |
Het |
| Dsg2 |
C |
A |
18: 20,580,621 (GRCm38) |
F216L |
probably damaging |
Het |
| Dsp |
C |
G |
13: 38,197,190 (GRCm38) |
T2637R |
possibly damaging |
Het |
| Dst |
G |
T |
1: 34,188,467 (GRCm38) |
E1714* |
probably null |
Het |
| Dst |
A |
G |
1: 34,275,208 (GRCm38) |
K4397E |
probably damaging |
Het |
| Dst |
C |
G |
1: 34,165,143 (GRCm38) |
A806G |
probably benign |
Het |
| Dst |
G |
C |
1: 34,244,445 (GRCm38) |
E3330D |
probably benign |
Het |
| Dtx1 |
T |
C |
5: 120,683,295 (GRCm38) |
S396G |
probably benign |
Het |
| Dtx3l |
G |
C |
16: 35,933,183 (GRCm38) |
S351C |
probably damaging |
Het |
| Dtx3l |
C |
G |
16: 35,932,457 (GRCm38) |
C593S |
probably damaging |
Het |
| Dtx4 |
C |
G |
19: 12,491,909 (GRCm38) |
A285P |
probably benign |
Het |
| Duox1 |
G |
T |
2: 122,333,038 (GRCm38) |
G784W |
probably damaging |
Het |
| Duox2 |
T |
C |
2: 122,296,507 (GRCm38) |
T176A |
probably damaging |
Het |
| Dusp8 |
C |
G |
7: 142,090,077 (GRCm38) |
R33P |
probably damaging |
Het |
| Dusp8 |
C |
A |
7: 142,081,943 (GRCm38) |
G637W |
unknown |
Het |
| Dvl1 |
G |
T |
4: 155,855,611 (GRCm38) |
G400V |
probably benign |
Het |
| Dvl3 |
G |
C |
16: 20,530,881 (GRCm38) |
A535P |
probably damaging |
Het |
| Dydc2 |
C |
A |
14: 41,061,983 (GRCm38) |
R61L |
probably benign |
Het |
| Dync1i2 |
G |
T |
2: 71,247,884 (GRCm38) |
V306L |
probably benign |
Het |
| Dync2h1 |
G |
T |
9: 7,142,361 (GRCm38) |
P1195T |
probably damaging |
Het |
| Dync2h1 |
ACCC |
ACC |
9: 7,168,730 (GRCm38) |
|
probably null |
Het |
| Dyrk1a |
A |
T |
16: 94,691,762 (GRCm38) |
H618L |
probably benign |
Het |
| Dyrk4 |
T |
G |
6: 126,892,128 (GRCm38) |
K240N |
probably damaging |
Het |
| Dysf |
T |
A |
6: 84,072,685 (GRCm38) |
L372H |
probably damaging |
Het |
| Dzip1l |
G |
T |
9: 99,641,761 (GRCm38) |
G205V |
possibly damaging |
Het |
| E030025P04Rik |
C |
A |
11: 109,143,971 (GRCm38) |
Q30H |
unknown |
Het |
| E130114P18Rik |
G |
T |
4: 97,569,200 (GRCm38) |
P151Q |
unknown |
Het |
| E130308A19Rik |
G |
T |
4: 59,720,313 (GRCm38) |
C615F |
probably damaging |
Het |
| E230025N22Rik |
T |
A |
18: 36,695,824 (GRCm38) |
|
probably benign |
Het |
| E2f6 |
A |
C |
12: 16,820,273 (GRCm38) |
K142T |
possibly damaging |
Het |
| E4f1 |
G |
A |
17: 24,446,145 (GRCm38) |
S355L |
probably benign |
Het |
| Ears2 |
C |
G |
7: 122,055,710 (GRCm38) |
A112P |
possibly damaging |
Het |
| Ears2 |
C |
G |
7: 122,044,581 (GRCm38) |
G385R |
probably damaging |
Het |
| Ebna1bp2 |
A |
C |
4: 118,621,146 (GRCm38) |
K44T |
probably damaging |
Het |
| Ece1 |
T |
G |
4: 137,921,027 (GRCm38) |
F32V |
probably benign |
Het |
| Ecm1 |
T |
C |
3: 95,734,876 (GRCm38) |
I466V |
probably benign |
Het |
| Edil3 |
G |
C |
13: 88,944,870 (GRCm38) |
G40R |
probably benign |
Het |
| Eef2 |
G |
T |
10: 81,181,158 (GRCm38) |
|
probably null |
Het |
| Efcab3 |
C |
A |
11: 105,100,046 (GRCm38) |
A93D |
probably damaging |
Het |
| Efcab3 |
T |
G |
11: 105,108,772 (GRCm38) |
Y162* |
probably null |
Het |
| Efcab5 |
C |
G |
11: 77,132,139 (GRCm38) |
D583H |
probably damaging |
Het |
| Efcc1 |
G |
T |
6: 87,732,796 (GRCm38) |
E257D |
probably benign |
Het |
| Efs |
C |
A |
14: 54,920,336 (GRCm38) |
V173L |
probably benign |
Het |
| Egf |
C |
A |
3: 129,697,717 (GRCm38) |
|
probably null |
Het |
| Ehbp1 |
G |
C |
11: 22,095,590 (GRCm38) |
P720A |
probably benign |
Het |
| Ehbp1l1 |
T |
A |
19: 5,717,889 (GRCm38) |
M1129L |
probably benign |
Het |
| Ehd3 |
C |
A |
17: 73,805,285 (GRCm38) |
P15T |
probably benign |
Het |
| Ehf |
C |
A |
2: 103,279,518 (GRCm38) |
G115C |
probably null |
Het |
| Eif2a |
G |
T |
3: 58,548,884 (GRCm38) |
V435L |
probably benign |
Het |
| Eif2d |
A |
T |
1: 131,164,465 (GRCm38) |
K324N |
probably damaging |
Het |
| Eif2d |
C |
G |
1: 131,164,502 (GRCm38) |
P337A |
probably damaging |
Het |
| Eif3i |
C |
A |
4: 129,600,575 (GRCm38) |
|
probably benign |
Het |
| Eif4e2 |
G |
A |
1: 87,225,939 (GRCm38) |
M155I |
probably benign |
Het |
| Eif4g1 |
G |
T |
16: 20,673,408 (GRCm38) |
|
probably benign |
Het |
| Eipr1 |
G |
T |
12: 28,859,287 (GRCm38) |
Q184H |
probably benign |
Het |
| Ell |
A |
C |
8: 70,578,927 (GRCm38) |
S92R |
probably damaging |
Het |
| Ell2 |
A |
C |
13: 75,756,452 (GRCm38) |
K220T |
probably damaging |
Het |
| Ell2 |
A |
T |
13: 75,770,689 (GRCm38) |
N605Y |
probably damaging |
Het |
| Elmod1 |
T |
G |
9: 53,946,860 (GRCm38) |
K2T |
probably benign |
Het |
| Elmsan1 |
T |
A |
12: 84,173,499 (GRCm38) |
Q227L |
probably damaging |
Het |
| Elmsan1 |
G |
T |
12: 84,173,501 (GRCm38) |
H226Q |
probably damaging |
Het |
| Elovl5 |
G |
C |
9: 77,976,755 (GRCm38) |
R111P |
possibly damaging |
Het |
| Eme1 |
A |
C |
11: 94,650,696 (GRCm38) |
I100S |
possibly damaging |
Het |
| Eml4 |
G |
C |
17: 83,445,965 (GRCm38) |
R355T |
probably damaging |
Het |
| Enam |
C |
A |
5: 88,492,971 (GRCm38) |
P164H |
probably damaging |
Het |
| Eng |
G |
T |
2: 32,673,424 (GRCm38) |
G331C |
probably null |
Het |
| Eng |
G |
C |
2: 32,681,452 (GRCm38) |
R618P |
probably damaging |
Het |
| Eng |
C |
G |
2: 32,671,422 (GRCm38) |
I148M |
possibly damaging |
Het |
| Enpp3 |
T |
G |
10: 24,787,793 (GRCm38) |
T557P |
probably benign |
Het |
| Entpd1 |
G |
T |
19: 40,738,964 (GRCm38) |
A519S |
probably benign |
Het |
| Entpd7 |
G |
C |
19: 43,725,358 (GRCm38) |
L385F |
probably benign |
Het |
| Ep400 |
A |
C |
5: 110,756,635 (GRCm38) |
L33V |
unknown |
Het |
| Epas1 |
C |
T |
17: 86,827,946 (GRCm38) |
S669L |
possibly damaging |
Het |
| Epb41l2 |
G |
T |
10: 25,441,720 (GRCm38) |
G45V |
probably benign |
Het |
| Epb41l2 |
A |
T |
10: 25,499,902 (GRCm38) |
R80* |
probably null |
Het |
| Epc2 |
G |
T |
2: 49,535,300 (GRCm38) |
G396C |
probably damaging |
Het |
| Epha10 |
T |
C |
4: 124,883,942 (GRCm38) |
W50R |
probably damaging |
Het |
| Epha10 |
G |
C |
4: 124,885,775 (GRCm38) |
G138A |
probably damaging |
Het |
| Epha3 |
G |
T |
16: 63,585,012 (GRCm38) |
P695Q |
probably damaging |
Het |
| Epha4 |
T |
C |
1: 77,373,733 (GRCm38) |
*987W |
probably null |
Het |
| Epha4 |
T |
G |
1: 77,383,011 (GRCm38) |
K735T |
probably damaging |
Het |
| Epha5 |
C |
T |
5: 84,071,120 (GRCm38) |
D765N |
possibly damaging |
Het |
| Epha8 |
C |
A |
4: 136,938,696 (GRCm38) |
R383L |
probably benign |
Het |
| Ephb1 |
G |
A |
9: 102,223,398 (GRCm38) |
P38L |
probably damaging |
Het |
| Ephb3 |
G |
T |
16: 21,218,036 (GRCm38) |
G337V |
possibly damaging |
Het |
| Ephx3 |
T |
G |
17: 32,185,237 (GRCm38) |
N343T |
probably damaging |
Het |
| Epop |
C |
A |
11: 97,628,410 (GRCm38) |
R291L |
probably damaging |
Het |
| Eral1 |
T |
G |
11: 78,075,620 (GRCm38) |
K244T |
probably damaging |
Het |
| Erap1 |
T |
A |
13: 74,657,638 (GRCm38) |
L166H |
probably damaging |
Het |
| Erbb4 |
G |
T |
1: 68,328,259 (GRCm38) |
S433* |
probably null |
Het |
| Erbb4 |
CA |
CAA |
1: 68,298,402 (GRCm38) |
|
probably null |
Het |
| Ercc2 |
A |
C |
7: 19,385,668 (GRCm38) |
S136R |
probably benign |
Het |
| Ercc6 |
A |
T |
14: 32,526,487 (GRCm38) |
S332C |
probably benign |
Het |
| Ereg |
G |
T |
5: 91,090,120 (GRCm38) |
G155V |
possibly damaging |
Het |
| Erg |
T |
G |
16: 95,409,750 (GRCm38) |
Q81P |
possibly damaging |
Het |
| Erg |
T |
G |
16: 95,361,317 (GRCm38) |
Q317P |
probably damaging |
Het |
| Erh |
C |
A |
12: 80,642,804 (GRCm38) |
L15F |
probably benign |
Het |
| Erich2 |
C |
A |
2: 70,509,114 (GRCm38) |
D4E |
possibly damaging |
Het |
| Erich3 |
G |
T |
3: 154,762,430 (GRCm38) |
V840L |
|
Het |
| Erich3 |
T |
G |
3: 154,698,701 (GRCm38) |
I65S |
|
Het |
| Ero1l |
G |
A |
14: 45,299,890 (GRCm38) |
P193L |
probably damaging |
Het |
| Esp18 |
C |
T |
17: 39,408,166 (GRCm38) |
L19F |
probably damaging |
Het |
| Esrp1 |
A |
T |
4: 11,385,765 (GRCm38) |
L34Q |
possibly damaging |
Het |
| Esrp1 |
C |
T |
4: 11,384,396 (GRCm38) |
G96R |
probably damaging |
Het |
| Etv4 |
C |
T |
11: 101,770,590 (GRCm38) |
V412M |
probably damaging |
Het |
| Exoc3l |
G |
T |
8: 105,290,794 (GRCm38) |
S546Y |
possibly damaging |
Het |
| Exoc3l2 |
C |
A |
7: 19,480,061 (GRCm38) |
L471M |
probably null |
Het |
| Exoc3l4 |
G |
T |
12: 111,423,720 (GRCm38) |
W243L |
probably damaging |
Het |
| Exoc8 |
C |
T |
8: 124,896,666 (GRCm38) |
V321I |
possibly damaging |
Het |
| Eya1 |
G |
T |
1: 14,302,868 (GRCm38) |
P9Q |
probably damaging |
Het |
| Eya1 |
G |
C |
1: 14,252,430 (GRCm38) |
A270G |
probably benign |
Het |
| F5 |
C |
G |
1: 164,184,516 (GRCm38) |
F434L |
probably damaging |
Het |
| F830045P16Rik |
G |
T |
2: 129,536,530 (GRCm38) |
|
probably benign |
Het |
| Fabp1 |
A |
T |
6: 71,199,955 (GRCm38) |
Q10L |
possibly damaging |
Het |
| Fads1 |
T |
A |
19: 10,193,704 (GRCm38) |
L299M |
probably damaging |
Het |
| Fads3 |
A |
T |
19: 10,041,807 (GRCm38) |
I26F |
probably benign |
Het |
| Faf1 |
A |
G |
4: 109,840,356 (GRCm38) |
D293G |
probably damaging |
Het |
| Fam109a |
G |
C |
5: 121,852,907 (GRCm38) |
A111P |
probably damaging |
Het |
| Fam124a |
T |
C |
14: 62,606,408 (GRCm38) |
M455T |
probably benign |
Het |
| Fam124b |
A |
C |
1: 80,213,403 (GRCm38) |
F88V |
possibly damaging |
Het |
| Fam149a |
C |
A |
8: 45,342,458 (GRCm38) |
R672L |
possibly damaging |
Het |
| Fam160a1 |
G |
T |
3: 85,673,201 (GRCm38) |
L566I |
probably benign |
Het |
| Fam160b2 |
G |
T |
14: 70,586,204 (GRCm38) |
S575R |
not run |
Het |
| Fam161b |
G |
T |
12: 84,356,053 (GRCm38) |
Q268K |
probably benign |
Het |
| Fam166b |
A |
G |
4: 43,427,172 (GRCm38) |
S87P |
|
Het |
| Fam166b |
G |
T |
4: 43,427,171 (GRCm38) |
S87Y |
|
Het |
| Fam170a |
C |
A |
18: 50,281,584 (GRCm38) |
A99D |
possibly damaging |
Het |
| Fam170b |
A |
C |
14: 32,835,804 (GRCm38) |
N199H |
probably damaging |
Het |
| Fam171a2 |
C |
G |
11: 102,447,446 (GRCm38) |
A24P |
unknown |
Het |
| Fam196a |
G |
T |
7: 134,918,706 (GRCm38) |
L32I |
probably damaging |
Het |
| Fam208a |
T |
G |
14: 27,477,148 (GRCm38) |
L1341R |
probably damaging |
Het |
| Fam208a |
G |
A |
14: 27,429,208 (GRCm38) |
G47D |
probably damaging |
Het |
| Fam208b |
C |
A |
13: 3,576,636 (GRCm38) |
V1105L |
probably benign |
Het |
| Fam208b |
C |
A |
13: 3,588,429 (GRCm38) |
R434M |
probably damaging |
Het |
| Fam213b |
A |
C |
4: 154,898,989 (GRCm38) |
L6R |
probably damaging |
Het |
| Fam240a |
T |
G |
9: 110,916,509 (GRCm38) |
K29T |
probably damaging |
Het |
| Fam3b |
C |
A |
16: 97,481,844 (GRCm38) |
R77L |
probably damaging |
Het |
| Fam46b |
G |
T |
4: 133,486,682 (GRCm38) |
R288L |
probably damaging |
Het |
| Fam47e |
G |
T |
5: 92,579,668 (GRCm38) |
R145L |
possibly damaging |
Het |
| Fam71a |
C |
T |
1: 191,163,745 (GRCm38) |
V234I |
probably benign |
Het |
| Fam83g |
C |
A |
11: 61,707,470 (GRCm38) |
P728T |
probably benign |
Het |
| Fance |
T |
G |
17: 28,318,064 (GRCm38) |
L14R |
probably damaging |
Het |
| Fancm |
A |
C |
12: 65,094,926 (GRCm38) |
E440D |
probably benign |
Het |
| Fap |
C |
A |
2: 62,528,774 (GRCm38) |
S428I |
possibly damaging |
Het |
| Farp2 |
G |
C |
1: 93,580,461 (GRCm38) |
G627A |
probably benign |
Het |
| Farp2 |
G |
T |
1: 93,580,467 (GRCm38) |
G629V |
probably benign |
Het |
| Farp2 |
T |
C |
1: 93,580,136 (GRCm38) |
F519L |
probably benign |
Het |
| Fat1 |
A |
C |
8: 45,023,596 (GRCm38) |
H1893P |
possibly damaging |
Het |
| Fat1 |
G |
A |
8: 44,950,598 (GRCm38) |
D129N |
probably benign |
Het |
| Fat1 |
G |
T |
8: 45,036,838 (GRCm38) |
D3596Y |
probably damaging |
Het |
| Fat2 |
T |
G |
11: 55,310,121 (GRCm38) |
H709P |
probably damaging |
Het |
| Fat2 |
T |
G |
11: 55,303,700 (GRCm38) |
K1171T |
probably damaging |
Het |
| Fat2 |
G |
T |
11: 55,284,991 (GRCm38) |
A1632E |
probably damaging |
Het |
| Fat2 |
A |
G |
11: 55,282,795 (GRCm38) |
L2364P |
probably damaging |
Het |
| Fat3 |
T |
G |
9: 16,375,617 (GRCm38) |
H870P |
probably benign |
Het |
| Fat3 |
G |
T |
9: 16,375,429 (GRCm38) |
P933T |
probably damaging |
Het |
| Fat3 |
G |
T |
9: 15,947,526 (GRCm38) |
P3798Q |
probably damaging |
Het |
| Fat4 |
G |
T |
3: 38,983,359 (GRCm38) |
G3720V |
probably benign |
Het |
| Fat4 |
C |
G |
3: 38,983,815 (GRCm38) |
P3872R |
probably damaging |
Het |
| Fblim1 |
C |
T |
4: 141,595,371 (GRCm38) |
A34T |
possibly damaging |
Het |
| Fbn1 |
C |
T |
2: 125,387,350 (GRCm38) |
G504S |
possibly damaging |
Het |
| Fbxl16 |
G |
C |
17: 25,817,011 (GRCm38) |
G194A |
possibly damaging |
Het |
| Fbxl18 |
T |
G |
5: 142,886,424 (GRCm38) |
K352T |
possibly damaging |
Het |
| Fbxl19 |
CT |
C |
7: 127,761,275 (GRCm38) |
|
probably null |
Het |
| Fbxl21 |
C |
A |
13: 56,527,003 (GRCm38) |
L56I |
probably benign |
Het |
| Fbxl22 |
G |
T |
9: 66,511,888 (GRCm38) |
R156S |
probably benign |
Het |
| Fbxl4 |
T |
C |
4: 22,427,280 (GRCm38) |
L507P |
probably damaging |
Het |
| Fbxo17 |
G |
C |
7: 28,732,777 (GRCm38) |
G93A |
unknown |
Het |
| Fbxo24 |
T |
G |
5: 137,621,403 (GRCm38) |
K187T |
probably damaging |
Het |
| Fbxo28 |
T |
A |
1: 182,317,870 (GRCm38) |
I218F |
probably damaging |
Het |
| Fbxo30 |
A |
T |
10: 11,295,320 (GRCm38) |
E714V |
probably damaging |
Het |
| Fbxo32 |
C |
A |
15: 58,205,242 (GRCm38) |
D115Y |
probably damaging |
Het |
| Fbxo40 |
T |
A |
16: 36,969,599 (GRCm38) |
D383V |
probably damaging |
Het |
| Fbxo42 |
T |
G |
4: 141,180,534 (GRCm38) |
|
probably null |
Het |
| Fbxw19 |
T |
C |
9: 109,481,582 (GRCm38) |
K424R |
probably benign |
Het |
| Fbxw21 |
T |
C |
9: 109,145,537 (GRCm38) |
H305R |
probably benign |
Het |
| Fbxw25 |
C |
A |
9: 109,651,738 (GRCm38) |
W291C |
|
Het |
| Fdx1l |
C |
A |
9: 21,073,492 (GRCm38) |
M5I |
probably benign |
Het |
| Fer1l5 |
C |
A |
1: 36,390,563 (GRCm38) |
Y465* |
probably null |
Het |
| Fermt1 |
C |
G |
2: 132,906,756 (GRCm38) |
G649A |
probably damaging |
Het |
| Fermt1 |
G |
T |
2: 132,936,018 (GRCm38) |
P177Q |
probably benign |
Het |
| Fermt1 |
G |
T |
2: 132,941,943 (GRCm38) |
Q49K |
probably benign |
Het |
| Ffar3 |
A |
T |
7: 30,855,193 (GRCm38) |
F234Y |
probably damaging |
Het |
| Fgd3 |
C |
A |
13: 49,281,826 (GRCm38) |
D319Y |
probably damaging |
Het |
| Fgd5 |
A |
C |
6: 91,988,889 (GRCm38) |
K701T |
probably damaging |
Het |
| Fgr |
C |
A |
4: 133,000,170 (GRCm38) |
H461N |
probably benign |
Het |
| Fibcd1 |
G |
A |
2: 31,838,539 (GRCm38) |
T102I |
probably benign |
Het |
| Flg |
A |
C |
3: 93,279,962 (GRCm38) |
R240S |
probably benign |
Het |
| Flii |
C |
A |
11: 60,722,313 (GRCm38) |
G221C |
possibly damaging |
Het |
| Flnb |
T |
G |
14: 7,942,066 (GRCm38) |
I2348S |
probably benign |
Het |
| Flot1 |
A |
C |
17: 35,825,823 (GRCm38) |
K219T |
probably damaging |
Het |
| Flrt2 |
G |
T |
12: 95,778,912 (GRCm38) |
W8L |
possibly damaging |
Het |
| Flrt2 |
G |
T |
12: 95,779,559 (GRCm38) |
G224C |
probably damaging |
Het |
| Flywch1 |
A |
C |
17: 23,761,009 (GRCm38) |
W264G |
probably benign |
Het |
| Fmn2 |
G |
T |
1: 174,608,394 (GRCm38) |
V644L |
unknown |
Het |
| Fmo2 |
G |
T |
1: 162,887,598 (GRCm38) |
Q152K |
probably benign |
Het |
| Fmo2 |
C |
A |
1: 162,898,274 (GRCm38) |
G11V |
probably damaging |
Het |
| Fmo6 |
G |
C |
1: 162,926,132 (GRCm38) |
S147* |
probably null |
Het |
| Fmod |
T |
G |
1: 134,040,919 (GRCm38) |
Y232* |
probably null |
Het |
| Fn1 |
C |
G |
1: 71,597,411 (GRCm38) |
G2194A |
probably benign |
Het |
| Fndc1 |
T |
G |
17: 7,804,877 (GRCm38) |
K82T |
possibly damaging |
Het |
| Fndc1 |
C |
A |
17: 7,773,593 (GRCm38) |
G424* |
probably null |
Het |
| Fndc3a |
C |
A |
14: 72,567,373 (GRCm38) |
K489N |
probably damaging |
Het |
| Fndc3c1 |
G |
T |
X: 106,434,329 (GRCm38) |
P767T |
not run |
Het |
| Foxd1 |
G |
C |
13: 98,355,938 (GRCm38) |
G440A |
unknown |
Het |
| Foxd3 |
C |
A |
4: 99,657,066 (GRCm38) |
P148T |
probably damaging |
Het |
| Foxf1 |
G |
T |
8: 121,084,529 (GRCm38) |
R44L |
probably damaging |
Het |
| Foxi1 |
G |
T |
11: 34,207,488 (GRCm38) |
P179H |
probably damaging |
Het |
| Foxi3 |
G |
A |
6: 70,956,798 (GRCm38) |
A90T |
probably benign |
Het |
| Foxj2 |
G |
T |
6: 122,833,711 (GRCm38) |
A217S |
probably benign |
Het |
| Foxj2 |
A |
T |
6: 122,832,936 (GRCm38) |
|
probably null |
Het |
| Foxo3 |
T |
TG |
10: 42,275,265 (GRCm38) |
|
probably null |
Het |
| Fpgs |
C |
T |
2: 32,692,660 (GRCm38) |
R67H |
probably benign |
Het |
| Fpr3 |
C |
A |
17: 17,970,993 (GRCm38) |
H175Q |
possibly damaging |
Het |
| Fpr-rs7 |
C |
A |
17: 20,113,393 (GRCm38) |
W278C |
probably benign |
Het |
| Fras1 |
T |
C |
5: 96,758,142 (GRCm38) |
L3135P |
probably benign |
Het |
| Frem1 |
C |
A |
4: 82,999,983 (GRCm38) |
G574V |
probably damaging |
Het |
| Frem3 |
T |
C |
8: 80,615,431 (GRCm38) |
L1451P |
probably benign |
Het |
| Frem3 |
C |
A |
8: 80,611,503 (GRCm38) |
R142S |
probably damaging |
Het |
| Frg1 |
T |
A |
8: 41,399,638 (GRCm38) |
R186* |
probably null |
Het |
| Frmd4a |
A |
G |
2: 4,498,021 (GRCm38) |
D107G |
probably damaging |
Het |
| Frmpd3 |
G |
T |
X: 140,433,010 (GRCm38) |
E1575* |
probably null |
Het |
| Fryl |
T |
C |
5: 73,072,837 (GRCm38) |
D1659G |
probably benign |
Het |
| Fscb |
T |
G |
12: 64,472,930 (GRCm38) |
E587D |
unknown |
Het |
| Fsd2 |
T |
C |
7: 81,553,192 (GRCm38) |
E213G |
probably damaging |
Het |
| Fshr |
C |
G |
17: 89,046,667 (GRCm38) |
A88P |
probably benign |
Het |
| Fsip1 |
G |
T |
2: 118,136,483 (GRCm38) |
L454I |
possibly damaging |
Het |
| Fsip2 |
G |
T |
2: 82,989,665 (GRCm38) |
M5247I |
probably benign |
Het |
| Fstl3 |
G |
C |
10: 79,781,198 (GRCm38) |
V192L |
probably benign |
Het |
| Fstl5 |
A |
T |
3: 76,707,982 (GRCm38) |
K783N |
probably damaging |
Het |
| Fubp1 |
G |
A |
3: 152,222,087 (GRCm38) |
G391D |
probably damaging |
Het |
| Fxn |
C |
G |
19: 24,262,042 (GRCm38) |
R162P |
probably damaging |
Het |
| Fyb2 |
G |
C |
4: 104,913,660 (GRCm38) |
Q57H |
probably damaging |
Het |
| Gabpb2 |
G |
T |
3: 95,190,693 (GRCm38) |
T223N |
probably benign |
Het |
| Gabra3 |
C |
T |
X: 72,445,353 (GRCm38) |
S322N |
probably damaging |
Het |
| Gabra4 |
G |
T |
5: 71,623,895 (GRCm38) |
A391D |
probably benign |
Het |
| Gabrp |
T |
C |
11: 33,552,673 (GRCm38) |
E397G |
probably benign |
Het |
| Gabrr3 |
C |
A |
16: 59,407,482 (GRCm38) |
S34* |
probably null |
Het |
| Gadd45a |
C |
A |
6: 67,036,736 (GRCm38) |
G109V |
probably benign |
Het |
| Gal3st2b |
T |
G |
1: 93,938,685 (GRCm38) |
L36R |
probably damaging |
Het |
| Galm |
C |
G |
17: 80,183,233 (GRCm38) |
T273S |
possibly damaging |
Het |
| Galnt9 |
CG |
C |
5: 110,596,146 (GRCm38) |
|
probably null |
Het |
| Galntl5 |
C |
A |
5: 25,203,189 (GRCm38) |
P220T |
probably damaging |
Het |
| Galntl6 |
A |
C |
8: 57,857,558 (GRCm38) |
Y370D |
probably damaging |
Het |
| Garem1 |
T |
G |
18: 21,129,792 (GRCm38) |
K655T |
probably damaging |
Het |
| Garem1 |
G |
A |
18: 21,148,325 (GRCm38) |
H325Y |
probably damaging |
Het |
| Gatad2a |
T |
A |
8: 69,936,038 (GRCm38) |
|
probably null |
Het |
| Gba |
A |
T |
3: 89,204,005 (GRCm38) |
K26* |
probably null |
Het |
| Gbp3 |
G |
A |
3: 142,561,863 (GRCm38) |
V34M |
probably damaging |
Het |
| Gck |
C |
A |
11: 5,906,526 (GRCm38) |
M210I |
probably damaging |
Het |
| Gckr |
G |
T |
5: 31,300,831 (GRCm38) |
R172I |
probably damaging |
Het |
| Gdap1l1 |
G |
T |
2: 163,447,670 (GRCm38) |
R185L |
probably damaging |
Het |
| Gdf10 |
C |
T |
14: 33,932,532 (GRCm38) |
T332M |
possibly damaging |
Het |
| Gdf15 |
T |
C |
8: 70,629,890 (GRCm38) |
S189G |
probably benign |
Het |
| Gdf7 |
G |
T |
12: 8,298,578 (GRCm38) |
P240T |
unknown |
Het |
| Gdf7 |
C |
T |
12: 8,298,409 (GRCm38) |
R304H |
unknown |
Het |
| Gdf9 |
C |
A |
11: 53,437,525 (GRCm38) |
T436K |
probably damaging |
Het |
| Gemin4 |
G |
T |
11: 76,217,579 (GRCm38) |
|
probably benign |
Het |
| Gga3 |
T |
G |
11: 115,587,603 (GRCm38) |
Q454H |
probably benign |
Het |
| Ggt5 |
A |
G |
10: 75,602,618 (GRCm38) |
|
probably null |
Het |
| Ggt7 |
T |
A |
2: 155,491,078 (GRCm38) |
R622W |
probably damaging |
Het |
| Ggt7 |
T |
A |
2: 155,499,063 (GRCm38) |
N394I |
probably damaging |
Het |
| Gh |
G |
C |
11: 106,301,184 (GRCm38) |
R67G |
probably damaging |
Het |
| Ghdc |
A |
G |
11: 100,769,417 (GRCm38) |
L168P |
probably benign |
Het |
| Ghr |
A |
G |
15: 3,347,485 (GRCm38) |
Y85H |
probably benign |
Het |
| Gimap1 |
A |
C |
6: 48,743,249 (GRCm38) |
K265T |
probably damaging |
Het |
| Gimap1 |
T |
G |
6: 48,743,356 (GRCm38) |
*301E |
probably null |
Het |
| Gimap7 |
C |
A |
6: 48,724,153 (GRCm38) |
D224E |
probably benign |
Het |
| Gins3 |
G |
T |
8: 95,633,520 (GRCm38) |
|
probably benign |
Het |
| Gjc1 |
C |
A |
11: 102,800,008 (GRCm38) |
G390W |
unknown |
Het |
| Glcci1 |
A |
T |
6: 8,582,674 (GRCm38) |
Q345L |
possibly damaging |
Het |
| Glipr1 |
G |
T |
10: 111,988,837 (GRCm38) |
P155T |
probably benign |
Het |
| Glis3 |
G |
C |
19: 28,283,768 (GRCm38) |
P791R |
possibly damaging |
Het |
| Glra3 |
G |
T |
8: 56,062,500 (GRCm38) |
M203I |
probably benign |
Het |
| Gls |
C |
G |
1: 52,214,488 (GRCm38) |
D274H |
probably damaging |
Het |
| Gm10300 |
C |
G |
4: 132,074,809 (GRCm38) |
P38R |
unknown |
Het |
| Gm10324 |
A |
G |
13: 66,122,394 (GRCm38) |
K458R |
probably damaging |
Het |
| Gm10324 |
T |
A |
13: 66,122,673 (GRCm38) |
F551Y |
probably benign |
Het |
| Gm10324 |
G |
A |
13: 66,122,469 (GRCm38) |
R483K |
probably benign |
Het |
| Gm10340 |
A |
G |
14: 3,134,911 (GRCm38) |
R60G |
possibly damaging |
Het |
| Gm10803 |
G |
C |
2: 93,564,136 (GRCm38) |
Q84H |
unknown |
Het |
| Gm11565 |
C |
T |
11: 99,914,851 (GRCm38) |
S23F |
possibly damaging |
Het |
| Gm11567 |
C |
A |
11: 99,879,625 (GRCm38) |
Q130K |
unknown |
Het |
| Gm11567 |
G |
A |
11: 99,879,332 (GRCm38) |
S32N |
unknown |
Het |
| Gm11567 |
C |
A |
11: 99,879,421 (GRCm38) |
Q62K |
unknown |
Het |
| Gm11639 |
G |
C |
11: 105,001,967 (GRCm38) |
G4247R |
probably benign |
Het |
| Gm11983 |
T |
G |
11: 6,836,861 (GRCm38) |
K89Q |
unknown |
Het |
| Gm11983 |
T |
C |
11: 6,837,047 (GRCm38) |
K27E |
unknown |
Het |
| Gm12185 |
T |
G |
11: 48,908,086 (GRCm38) |
I527L |
probably benign |
Het |
| Gm12888 |
G |
T |
4: 121,324,808 (GRCm38) |
P29H |
probably damaging |
Het |
| Gm13089 |
G |
C |
4: 143,696,945 (GRCm38) |
H425D |
probably benign |
Het |
| Gm13103 |
A |
G |
4: 143,853,110 (GRCm38) |
S422G |
probably benign |
Het |
| Gm13178 |
C |
A |
4: 144,703,325 (GRCm38) |
G365W |
probably damaging |
Het |
| Gm13212 |
G |
C |
4: 145,622,968 (GRCm38) |
S325T |
possibly damaging |
Het |
| Gm15130 |
A |
G |
2: 111,144,587 (GRCm38) |
|
probably null |
Het |
| Gm16503 |
A |
C |
4: 147,541,156 (GRCm38) |
T36P |
unknown |
Het |
| Gm17019 |
C |
T |
5: 15,032,997 (GRCm38) |
|
probably benign |
Het |
| Gm17124 |
A |
G |
14: 42,597,223 (GRCm38) |
|
probably null |
Het |
| Gm19410 |
G |
T |
8: 35,792,611 (GRCm38) |
W800L |
possibly damaging |
Het |
| Gm21083 |
T |
G |
5: 15,577,458 (GRCm38) |
V41G |
probably benign |
Het |
| Gm21149 |
G |
C |
5: 15,476,412 (GRCm38) |
R18G |
not run |
Het |
| Gm21149 |
G |
T |
5: 15,472,148 (GRCm38) |
A236D |
probably damaging |
Het |
| Gm21190 |
A |
C |
5: 15,524,974 (GRCm38) |
D215E |
not run |
Het |
| Gm21190 |
G |
T |
5: 15,526,580 (GRCm38) |
T136N |
probably benign |
Het |
| Gm21190 |
G |
A |
5: 15,524,894 (GRCm38) |
P242L |
probably benign |
Het |
| Gm21680 |
C |
T |
5: 25,971,419 (GRCm38) |
S60N |
probably benign |
Het |
| Gm21886 |
G |
C |
18: 80,089,387 (GRCm38) |
Y185* |
probably null |
Het |
| Gm21886 |
G |
T |
18: 80,089,923 (GRCm38) |
L14M |
probably damaging |
Het |
| Gm28729 |
C |
T |
9: 96,492,088 (GRCm38) |
R401H |
unknown |
Het |
| Gm29609 |
A |
T |
5: 31,154,242 (GRCm38) |
W852R |
probably benign |
Het |
| Gm29797 |
G |
C |
2: 181,659,095 (GRCm38) |
A128P |
probably damaging |
Het |
| Gm30302 |
T |
C |
13: 49,786,462 (GRCm38) |
R591G |
possibly damaging |
Het |
| Gm30302 |
A |
C |
13: 49,787,848 (GRCm38) |
L39V |
probably damaging |
Het |
| Gm30302 |
T |
C |
13: 49,785,384 (GRCm38) |
D950G |
possibly damaging |
Het |
| Gm3238 |
G |
T |
10: 77,771,024 (GRCm38) |
P101Q |
unknown |
Het |
| Gm32742 |
G |
A |
9: 51,159,165 (GRCm38) |
Q76* |
probably null |
Het |
| Gm3285 |
G |
A |
10: 77,862,434 (GRCm38) |
C139Y |
unknown |
Het |
| Gm3543 |
T |
G |
14: 41,981,007 (GRCm38) |
N60T |
probably damaging |
Het |
| Gm364 |
T |
A |
X: 57,417,721 (GRCm38) |
N140K |
probably benign |
Het |
| Gm364 |
T |
C |
X: 57,463,184 (GRCm38) |
F487L |
probably benign |
Het |
| Gm3776 |
T |
A |
9: 78,258,763 (GRCm38) |
C18S |
probably benign |
Het |
| Gm4450 |
G |
T |
3: 98,456,455 (GRCm38) |
Q25K |
probably benign |
Het |
| Gm45618 |
T |
C |
7: 142,120,218 (GRCm38) |
K171R |
unknown |
Het |
| Gm45861 |
G |
A |
8: 27,584,869 (GRCm38) |
G1416S |
unknown |
Het |
| Gm4737 |
T |
C |
16: 46,154,229 (GRCm38) |
M262V |
probably benign |
Het |
| Gm4779 |
G |
T |
X: 101,792,186 (GRCm38) |
P504H |
unknown |
Het |
| Gm4788 |
G |
C |
1: 139,733,448 (GRCm38) |
C554W |
probably damaging |
Het |
| Gm4788 |
G |
T |
1: 139,698,256 (GRCm38) |
R827S |
probably benign |
Het |
| Gm47985 |
T |
C |
1: 151,183,141 (GRCm38) |
S178P |
possibly damaging |
Het |
| Gm4858 |
G |
T |
3: 93,074,055 (GRCm38) |
G53W |
probably damaging |
Het |
| Gm49336 |
C |
A |
14: 60,239,502 (GRCm38) |
C240F |
probably null |
Het |
| Gm5111 |
C |
A |
6: 48,590,309 (GRCm38) |
L153M |
unknown |
Het |
| Gm5538 |
C |
A |
3: 59,747,194 (GRCm38) |
Q150K |
probably benign |
Het |
| Gm5592 |
G |
A |
7: 41,286,319 (GRCm38) |
E82K |
possibly damaging |
Het |
| Gm5592 |
C |
A |
7: 41,288,681 (GRCm38) |
D462E |
probably benign |
Het |
| Gm5592 |
C |
G |
7: 41,286,317 (GRCm38) |
T81R |
probably damaging |
Het |
| Gm5862 |
TGGG |
TGG |
5: 26,018,487 (GRCm38) |
|
probably null |
Het |
| Gm5936 |
T |
G |
X: 74,842,035 (GRCm38) |
V347G |
probably benign |
Het |
| Gm6377 |
T |
G |
X: 109,198,293 (GRCm38) |
L160R |
probably damaging |
Het |
| Gm6588 |
T |
C |
5: 112,449,875 (GRCm38) |
V96A |
probably benign |
Het |
| Gm6614 |
A |
G |
6: 141,990,348 (GRCm38) |
F357S |
probably benign |
Het |
| Gm6871 |
C |
A |
7: 41,546,413 (GRCm38) |
G300V |
probably damaging |
Het |
| Gm7138 |
C |
G |
10: 77,776,853 (GRCm38) |
C31S |
unknown |
Het |
| Gm7145 |
A |
C |
1: 117,986,351 (GRCm38) |
K321T |
probably benign |
Het |
| Gm7298 |
G |
T |
6: 121,764,875 (GRCm38) |
D419Y |
possibly damaging |
Het |
| Gm7298 |
A |
C |
6: 121,764,870 (GRCm38) |
E417A |
probably benign |
Het |
| Gm732 |
A |
C |
X: 107,945,825 (GRCm38) |
I494S |
possibly damaging |
Het |
| Gm7534 |
C |
G |
4: 134,200,338 (GRCm38) |
R368P |
possibly damaging |
Het |
| Gm7534 |
A |
G |
4: 134,202,677 (GRCm38) |
S106P |
probably benign |
Het |
| Gm7579 |
G |
T |
7: 142,211,941 (GRCm38) |
G28V |
unknown |
Het |
| Gm8369 |
G |
C |
19: 11,511,624 (GRCm38) |
A92P |
probably damaging |
Het |
| Gm853 |
T |
A |
4: 130,221,704 (GRCm38) |
H17L |
probably benign |
Het |
| Gm8693 |
T |
C |
7: 22,691,842 (GRCm38) |
K159R |
probably benign |
Het |
| Gm884 |
C |
T |
11: 103,613,681 (GRCm38) |
G2487D |
probably benign |
Het |
| Gm8879 |
C |
G |
5: 11,130,351 (GRCm38) |
N75K |
probably benign |
Het |
| Gm8994 |
G |
C |
6: 136,329,023 (GRCm38) |
A161P |
possibly damaging |
Het |
| Gm9112 |
G |
A |
X: 102,707,027 (GRCm38) |
T72M |
probably benign |
Het |
| Gm9513 |
A |
C |
9: 36,476,511 (GRCm38) |
N31T |
probably damaging |
Het |
| Gm9573 |
G |
T |
17: 35,621,245 (GRCm38) |
S683Y |
unknown |
Het |
| Gm960 |
G |
T |
19: 4,625,903 (GRCm38) |
R734S |
unknown |
Het |
| Gm973 |
T |
G |
1: 59,524,602 (GRCm38) |
|
probably benign |
Het |
| Gm9758 |
C |
G |
5: 14,913,539 (GRCm38) |
V92L |
probably benign |
Het |
| Gm9805 |
A |
G |
17: 22,689,871 (GRCm38) |
Y34C |
probably benign |
Het |
| Gm9887 |
C |
A |
12: 69,371,941 (GRCm38) |
W173L |
not run |
Het |
| Gm9964 |
T |
C |
11: 79,296,400 (GRCm38) |
R74G |
unknown |
Het |
| Gm9992 |
C |
A |
17: 7,376,530 (GRCm38) |
G127W |
probably damaging |
Het |
| Gmip |
C |
T |
8: 69,816,292 (GRCm38) |
R496W |
probably damaging |
Het |
| Gmpr2 |
T |
G |
14: 55,672,743 (GRCm38) |
L10R |
probably benign |
Het |
| Gna12 |
T |
A |
5: 140,760,553 (GRCm38) |
Q379L |
probably damaging |
Het |
| Gna12 |
C |
A |
5: 140,762,607 (GRCm38) |
D185Y |
probably damaging |
Het |
| Gnas |
C |
A |
2: 174,298,606 (GRCm38) |
P249T |
unknown |
Het |
| Gnptab |
G |
T |
10: 88,431,368 (GRCm38) |
E440D |
probably damaging |
Het |
| Gpa33 |
C |
A |
1: 166,164,671 (GRCm38) |
C261* |
probably null |
Het |
| Gpat2 |
C |
A |
2: 127,430,882 (GRCm38) |
F171L |
probably benign |
Het |
| Gpat2 |
G |
C |
2: 127,433,808 (GRCm38) |
G502A |
probably damaging |
Het |
| Gpat4 |
C |
G |
8: 23,179,798 (GRCm38) |
S313T |
probably benign |
Het |
| Gpatch1 |
C |
A |
7: 35,310,485 (GRCm38) |
G55C |
probably damaging |
Het |
| Gpc5 |
T |
A |
14: 115,369,964 (GRCm38) |
L326Q |
probably damaging |
Het |
| Gpd1l |
C |
A |
9: 114,904,780 (GRCm38) |
G283W |
probably damaging |
Het |
| Gpnmb |
C |
A |
6: 49,051,832 (GRCm38) |
A428D |
possibly damaging |
Het |
| Gpr101 |
T |
G |
X: 57,501,274 (GRCm38) |
H172P |
probably benign |
Het |
| Gpr158 |
G |
T |
2: 21,810,690 (GRCm38) |
|
probably null |
Het |
| Gpr179 |
G |
C |
11: 97,336,648 (GRCm38) |
S1560R |
probably benign |
Het |
| Gpr26 |
C |
G |
7: 131,967,225 (GRCm38) |
L100V |
probably damaging |
Het |
| Gpr26 |
C |
A |
7: 131,967,048 (GRCm38) |
P41T |
probably damaging |
Het |
| Gpr39 |
G |
T |
1: 125,872,843 (GRCm38) |
G444W |
probably damaging |
Het |
| Gprasp2 |
G |
T |
X: 135,842,893 (GRCm38) |
G334W |
probably damaging |
Het |
| Gprin1 |
C |
A |
13: 54,740,397 (GRCm38) |
Q21H |
probably benign |
Het |
| Gpsm1 |
G |
T |
2: 26,327,345 (GRCm38) |
Q408H |
possibly damaging |
Het |
| Grb10 |
C |
A |
11: 11,944,845 (GRCm38) |
A359S |
possibly damaging |
Het |
| Grb7 |
G |
T |
11: 98,453,971 (GRCm38) |
|
probably null |
Het |
| Grb7 |
G |
C |
11: 98,454,484 (GRCm38) |
G456R |
probably damaging |
Het |
| Greb1 |
C |
A |
12: 16,696,756 (GRCm38) |
C1171F |
probably benign |
Het |
| Greb1l |
G |
C |
18: 10,515,305 (GRCm38) |
G699A |
probably damaging |
Het |
| Gria3 |
C |
A |
X: 41,478,647 (GRCm38) |
A113D |
probably benign |
Het |
| Grid2 |
A |
G |
6: 64,663,228 (GRCm38) |
Q810R |
probably benign |
Het |
| Grid2 |
G |
A |
6: 63,908,879 (GRCm38) |
M86I |
possibly damaging |
Het |
| Grik5 |
T |
A |
7: 25,013,804 (GRCm38) |
D793V |
probably damaging |
Het |
| Grin1 |
GCTCTC |
GCTC |
2: 25,297,907 (GRCm38) |
|
probably null |
Het |
| Grin3a |
A |
G |
4: 49,770,622 (GRCm38) |
S717P |
probably damaging |
Het |
| Grip1 |
C |
A |
10: 119,819,483 (GRCm38) |
|
probably benign |
Het |
| Grip2 |
G |
C |
6: 91,763,510 (GRCm38) |
P1023A |
possibly damaging |
Het |
| Grk2 |
C |
G |
19: 4,287,645 (GRCm38) |
M568I |
probably benign |
Het |
| Grk3 |
C |
A |
5: 112,957,314 (GRCm38) |
|
probably null |
Het |
| Grm5 |
G |
T |
7: 87,602,715 (GRCm38) |
G58W |
probably damaging |
Het |
| Grm6 |
C |
A |
11: 50,859,537 (GRCm38) |
P509H |
probably benign |
Het |
| Grm7 |
A |
G |
6: 111,358,149 (GRCm38) |
E507G |
probably benign |
Het |
| Grm7 |
G |
T |
6: 111,358,490 (GRCm38) |
V621F |
probably damaging |
Het |
| Grm8 |
G |
C |
6: 28,126,027 (GRCm38) |
S33R |
probably benign |
Het |
| Grpr |
A |
G |
X: 163,515,034 (GRCm38) |
L338P |
probably damaging |
Het |
| Grtp1 |
T |
G |
8: 13,200,199 (GRCm38) |
I17L |
probably benign |
Het |
| Gsdma |
C |
A |
11: 98,669,759 (GRCm38) |
P179H |
probably damaging |
Het |
| Gsk3b |
A |
T |
16: 38,208,070 (GRCm38) |
K297* |
probably null |
Het |
| Gspt2 |
GC |
G |
X: 94,637,468 (GRCm38) |
|
probably null |
Het |
| Gtf2h3 |
G |
T |
5: 124,579,175 (GRCm38) |
|
probably benign |
Het |
| Gtf2i |
C |
A |
5: 134,263,645 (GRCm38) |
G415V |
probably null |
Het |
| Gtf2ird1 |
T |
G |
5: 134,409,312 (GRCm38) |
|
probably null |
Het |
| Gtf3a |
G |
A |
5: 146,951,204 (GRCm38) |
C105Y |
probably damaging |
Het |
| Gtf3c1 |
T |
A |
7: 125,703,964 (GRCm38) |
I100F |
probably damaging |
Het |
| Gtse1 |
A |
G |
15: 85,868,746 (GRCm38) |
K354R |
possibly damaging |
Het |
| Guca1a |
T |
C |
17: 47,400,410 (GRCm38) |
I4V |
probably benign |
Het |
| Gucy1a2 |
A |
C |
9: 3,635,156 (GRCm38) |
K400T |
probably damaging |
Het |
| Gulp1 |
C |
A |
1: 44,788,479 (GRCm38) |
D260E |
probably damaging |
Het |
| Gxylt2 |
T |
G |
6: 100,783,191 (GRCm38) |
L229R |
probably damaging |
Het |
| Gykl1 |
A |
G |
18: 52,694,547 (GRCm38) |
K276E |
probably damaging |
Het |
| H2-Eb2 |
A |
C |
17: 34,334,309 (GRCm38) |
E156D |
possibly damaging |
Het |
| H2-M11 |
A |
C |
17: 36,548,770 (GRCm38) |
R218S |
possibly damaging |
Het |
| H2-Q2 |
A |
C |
17: 35,345,675 (GRCm38) |
Q351P |
probably damaging |
Het |
| H2-T3 |
A |
T |
17: 36,186,582 (GRCm38) |
L382M |
possibly damaging |
Het |
| H2-T3 |
C |
G |
17: 36,186,580 (GRCm38) |
L382F |
possibly damaging |
Het |
| Habp2 |
T |
C |
19: 56,317,760 (GRCm38) |
V426A |
probably damaging |
Het |
| Hacd1 |
C |
A |
2: 14,035,795 (GRCm38) |
M216I |
probably damaging |
Het |
| Hacd2 |
G |
T |
16: 35,106,325 (GRCm38) |
Q231H |
probably damaging |
Het |
| Hace1 |
A |
T |
10: 45,686,662 (GRCm38) |
N758Y |
probably damaging |
Het |
| Hal |
G |
A |
10: 93,489,893 (GRCm38) |
M89I |
probably benign |
Het |
| Hbb-bt |
A |
G |
7: 103,813,892 (GRCm38) |
|
probably benign |
Het |
| Hc |
T |
A |
2: 35,006,273 (GRCm38) |
|
probably null |
Het |
| Hcar1 |
T |
A |
5: 123,879,741 (GRCm38) |
|
probably benign |
Het |
| Hcfc2 |
G |
C |
10: 82,699,172 (GRCm38) |
R10T |
probably damaging |
Het |
| Hcls1 |
G |
T |
16: 36,961,492 (GRCm38) |
R321M |
possibly damaging |
Het |
| Hcn4 |
G |
T |
9: 58,858,148 (GRCm38) |
G638C |
unknown |
Het |
| Hdac1 |
T |
A |
4: 129,542,616 (GRCm38) |
Q5L |
probably benign |
Het |
| Hdac9 |
G |
T |
12: 34,373,987 (GRCm38) |
T536K |
probably benign |
Het |
| Hdgfl2 |
G |
T |
17: 56,079,825 (GRCm38) |
R24L |
possibly damaging |
Het |
| Hdgfl2 |
G |
T |
17: 56,097,016 (GRCm38) |
A281S |
probably null |
Het |
| Heatr1 |
T |
G |
13: 12,399,008 (GRCm38) |
N155K |
possibly damaging |
Het |
| Hecw1 |
G |
A |
13: 14,300,333 (GRCm38) |
A540V |
possibly damaging |
Het |
| Hells |
G |
T |
19: 38,965,407 (GRCm38) |
R765S |
possibly damaging |
Het |
| Helq |
C |
A |
5: 100,766,766 (GRCm38) |
L953F |
possibly damaging |
Het |
| Helz2 |
G |
C |
2: 181,237,564 (GRCm38) |
P754A |
probably benign |
Het |
| Heph |
G |
C |
X: 96,554,922 (GRCm38) |
E919Q |
probably damaging |
Het |
| Herc1 |
A |
C |
9: 66,434,576 (GRCm38) |
E1882D |
probably benign |
Het |
| Herc2 |
G |
T |
7: 56,132,498 (GRCm38) |
G1311V |
probably damaging |
Het |
| Herc2 |
G |
A |
7: 56,097,533 (GRCm38) |
V473I |
possibly damaging |
Het |
| Herc2 |
G |
A |
7: 56,131,292 (GRCm38) |
G1235D |
probably benign |
Het |
| Herc3 |
G |
T |
6: 58,843,858 (GRCm38) |
E76* |
probably null |
Het |
| Herc4 |
T |
G |
10: 63,307,749 (GRCm38) |
I686S |
probably benign |
Het |
| Herc6 |
G |
T |
6: 57,600,031 (GRCm38) |
G243V |
probably damaging |
Het |
| Herpud2 |
C |
G |
9: 25,130,622 (GRCm38) |
V85L |
not run |
Het |
| Hexdc |
C |
A |
11: 121,215,237 (GRCm38) |
P117T |
probably damaging |
Het |
| Hip1r |
A |
G |
5: 123,997,010 (GRCm38) |
Q403R |
probably damaging |
Het |
| Hist1h1b |
T |
C |
13: 21,780,094 (GRCm38) |
K154R |
unknown |
Het |
| Hist1h4i |
C |
A |
13: 22,041,214 (GRCm38) |
R37L |
probably damaging |
Het |
| Hist2h2ab |
G |
T |
3: 96,220,051 (GRCm38) |
A46S |
probably benign |
Het |
| Hivep3 |
C |
T |
4: 120,133,782 (GRCm38) |
R2160W |
probably damaging |
Het |
| Hlcs |
A |
C |
16: 94,262,659 (GRCm38) |
L367R |
probably damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,655,921 (GRCm38) |
V3199A |
possibly damaging |
Het |
| Hmcn1 |
G |
T |
1: 150,586,445 (GRCm38) |
Q5161K |
probably null |
Het |
| Hmcn1 |
A |
G |
1: 150,663,917 (GRCm38) |
V2941A |
probably benign |
Het |
| Hmcn2 |
G |
T |
2: 31,429,091 (GRCm38) |
R3934S |
probably damaging |
Het |
| Hmcn2 |
G |
C |
2: 31,344,029 (GRCm38) |
D269H |
possibly damaging |
Het |
| Hmcn2 |
C |
A |
2: 31,425,416 (GRCm38) |
L3726M |
probably damaging |
Het |
| Hmga2 |
G |
C |
10: 120,370,671 (GRCm38) |
P113A |
unknown |
Het |
| Hmgcs2 |
G |
A |
3: 98,290,945 (GRCm38) |
G55S |
probably damaging |
Het |
| Hmx2 |
A |
T |
7: 131,554,467 (GRCm38) |
E54V |
probably damaging |
Het |
| Hnf1a |
CA |
C |
5: 114,950,124 (GRCm38) |
|
probably null |
Het |
| Hnrnpa2b1 |
G |
T |
6: 51,467,243 (GRCm38) |
T20N |
probably damaging |
Het |
| Hnrnpf |
G |
A |
6: 117,923,784 (GRCm38) |
G10S |
probably benign |
Het |
| Hnrnph2 |
G |
T |
X: 134,605,133 (GRCm38) |
E76* |
probably null |
Het |
| Hnrnpu |
T |
G |
1: 178,332,215 (GRCm38) |
N434H |
unknown |
Het |
| Hnrnpul1 |
C |
A |
7: 25,724,664 (GRCm38) |
S721I |
probably benign |
Het |
| Hnrnpul1 |
G |
C |
7: 25,724,698 (GRCm38) |
P710A |
unknown |
Het |
| Hoxb1 |
C |
A |
11: 96,367,051 (GRCm38) |
P269Q |
probably benign |
Het |
| Hoxd9 |
G |
C |
2: 74,698,128 (GRCm38) |
A25P |
probably damaging |
Het |
| Hp1bp3 |
C |
T |
4: 138,221,673 (GRCm38) |
L16F |
not run |
Het |
| Hpd |
C |
A |
5: 123,181,475 (GRCm38) |
G49V |
probably damaging |
Het |
| Hps1 |
C |
A |
19: 42,766,686 (GRCm38) |
R272S |
probably null |
Het |
| Hsd17b13 |
G |
T |
5: 103,968,705 (GRCm38) |
P184T |
probably benign |
Het |
| Hsd17b3 |
C |
T |
13: 64,063,138 (GRCm38) |
G182S |
possibly damaging |
Het |
| Hsd3b1 |
T |
G |
3: 98,852,886 (GRCm38) |
Q263P |
probably damaging |
Het |
| Hsd3b2 |
C |
T |
3: 98,712,222 (GRCm38) |
E136K |
probably benign |
Het |
| Hsd3b3 |
A |
G |
3: 98,743,960 (GRCm38) |
V58A |
probably benign |
Het |
| Hsdl2 |
A |
T |
4: 59,617,706 (GRCm38) |
K478* |
probably null |
Het |
| Hspa1l |
G |
C |
17: 34,978,492 (GRCm38) |
K502N |
possibly damaging |
Het |
| Htr1f |
G |
T |
16: 64,926,077 (GRCm38) |
S284* |
probably null |
Het |
| Htr1f |
G |
T |
16: 64,926,874 (GRCm38) |
N18K |
probably benign |
Het |
| Htr7 |
G |
T |
19: 35,969,423 (GRCm38) |
T397N |
probably damaging |
Het |
| Htra2 |
C |
A |
6: 83,054,383 (GRCm38) |
R15L |
probably benign |
Het |
| Hunk |
C |
A |
16: 90,472,573 (GRCm38) |
P335H |
probably damaging |
Het |
| Huwe1 |
C |
A |
X: 151,856,575 (GRCm38) |
H356N |
probably damaging |
Het |
| Huwe1 |
A |
C |
X: 151,928,381 (GRCm38) |
K3958T |
unknown |
Het |
| Hyal4 |
G |
A |
6: 24,756,628 (GRCm38) |
V282M |
probably damaging |
Het |
| Hydin |
T |
G |
8: 110,541,600 (GRCm38) |
F2904V |
possibly damaging |
Het |
| Hyou1 |
G |
T |
9: 44,387,742 (GRCm38) |
E621* |
probably null |
Het |
| Ice1 |
C |
A |
13: 70,605,201 (GRCm38) |
C922F |
probably damaging |
Het |
| Ide |
C |
T |
19: 37,315,491 (GRCm38) |
V238M |
|
Het |
| Idh3b |
T |
A |
2: 130,281,542 (GRCm38) |
|
probably null |
Het |
| Ifi204 |
C |
A |
1: 173,751,628 (GRCm38) |
K550N |
probably null |
Het |
| Ifi206 |
T |
G |
1: 173,482,048 (GRCm38) |
K127N |
|
Het |
| Ifi27l2b |
C |
A |
12: 103,457,033 (GRCm38) |
G7C |
unknown |
Het |
| Ifi44 |
A |
G |
3: 151,732,453 (GRCm38) |
L399P |
probably damaging |
Het |
| Ifih1 |
T |
G |
2: 62,617,469 (GRCm38) |
Q297P |
probably benign |
Het |
| Ifitm1 |
C |
A |
7: 140,969,517 (GRCm38) |
T71K |
probably benign |
Het |
| Ifna5 |
C |
T |
4: 88,835,999 (GRCm38) |
H159Y |
probably damaging |
Het |
| Ifnab |
T |
G |
4: 88,690,718 (GRCm38) |
E170D |
probably damaging |
Het |
| Ift122 |
A |
C |
6: 115,915,994 (GRCm38) |
D854A |
probably damaging |
Het |
| Ift172 |
C |
A |
5: 31,276,924 (GRCm38) |
W490L |
probably damaging |
Het |
| Igfbp4 |
C |
G |
11: 99,051,515 (GRCm38) |
P234R |
probably damaging |
Het |
| Igfn1 |
G |
T |
1: 135,972,000 (GRCm38) |
H524Q |
probably damaging |
Het |
| Ighv1-12 |
C |
A |
12: 114,616,013 (GRCm38) |
G63V |
possibly damaging |
Het |
| Ighv14-4 |
C |
A |
12: 114,176,667 (GRCm38) |
C41F |
probably damaging |
Het |
| Ighv14-4 |
C |
G |
12: 114,176,672 (GRCm38) |
L39F |
probably damaging |
Het |
| Ighv1-52 |
C |
A |
12: 115,145,777 (GRCm38) |
V21F |
probably damaging |
Het |
| Ighv1-63 |
C |
T |
12: 115,495,645 (GRCm38) |
A111T |
possibly damaging |
Het |
| Ighv1-69 |
A |
C |
12: 115,623,253 (GRCm38) |
S87A |
probably benign |
Het |
| Ighv1-9 |
T |
G |
12: 114,583,834 (GRCm38) |
E29A |
probably benign |
Het |
| Igkv1-35 |
C |
T |
6: 70,011,034 (GRCm38) |
G93R |
possibly damaging |
Het |
| Igkv1-99 |
T |
A |
6: 68,542,262 (GRCm38) |
S68T |
|
Het |
| Igkv3-12 |
A |
T |
6: 70,518,611 (GRCm38) |
I41F |
probably benign |
Het |
| Igkv4-74 |
T |
C |
6: 69,185,345 (GRCm38) |
Q6R |
possibly damaging |
Het |
| Igkv6-32 |
T |
A |
6: 70,074,586 (GRCm38) |
|
probably benign |
Het |
| Igsf21 |
A |
T |
4: 140,067,215 (GRCm38) |
C116S |
probably damaging |
Het |
| Igsf5 |
C |
G |
16: 96,391,023 (GRCm38) |
S274C |
probably damaging |
Het |
| Igsf8 |
G |
T |
1: 172,318,354 (GRCm38) |
A406S |
probably damaging |
Het |
| Igsf9 |
G |
C |
1: 172,492,149 (GRCm38) |
G337A |
probably damaging |
Het |
| Igsf9 |
G |
T |
1: 172,495,226 (GRCm38) |
A586S |
probably benign |
Het |
| Igsf9b |
A |
G |
9: 27,317,353 (GRCm38) |
|
probably null |
Het |
| Ihh |
T |
G |
1: 74,946,094 (GRCm38) |
S411R |
probably damaging |
Het |
| Ik |
G |
T |
18: 36,753,515 (GRCm38) |
D347Y |
possibly damaging |
Het |
| Ikbkap |
T |
A |
4: 56,790,146 (GRCm38) |
T315S |
probably benign |
Het |
| Ikzf1 |
G |
T |
11: 11,758,194 (GRCm38) |
|
probably null |
Het |
| Ikzf3 |
T |
G |
11: 98,467,181 (GRCm38) |
E443D |
probably benign |
Het |
| Ikzf4 |
G |
A |
10: 128,634,230 (GRCm38) |
P527S |
possibly damaging |
Het |
| Il10ra |
A |
C |
9: 45,266,632 (GRCm38) |
S67A |
possibly damaging |
Het |
| Il16 |
C |
G |
7: 83,652,827 (GRCm38) |
S727T |
probably benign |
Het |
| Il17rc |
G |
T |
6: 113,476,795 (GRCm38) |
|
probably null |
Het |
| Il1rap |
G |
T |
16: 26,722,399 (GRCm38) |
R463S |
probably damaging |
Het |
| Il27ra |
C |
A |
8: 84,040,990 (GRCm38) |
W101C |
probably damaging |
Het |
| Il2ra |
C |
A |
2: 11,681,931 (GRCm38) |
A191D |
probably damaging |
Het |
| Il6st |
A |
G |
13: 112,493,618 (GRCm38) |
K333E |
probably benign |
Het |
| Impg1 |
C |
G |
9: 80,378,467 (GRCm38) |
R418S |
probably benign |
Het |
| Incenp |
C |
A |
19: 9,877,687 (GRCm38) |
W620L |
unknown |
Het |
| Inhbb |
C |
A |
1: 119,417,798 (GRCm38) |
V254L |
probably benign |
Het |
| Inpp4b |
C |
G |
8: 82,069,001 (GRCm38) |
A818G |
possibly damaging |
Het |
| Inpp5b |
CA |
C |
4: 124,797,840 (GRCm38) |
|
probably null |
Het |
| Inpp5d |
T |
G |
1: 87,703,131 (GRCm38) |
L671W |
probably damaging |
Het |
| Inpp5d |
T |
G |
1: 87,669,709 (GRCm38) |
F201V |
probably benign |
Het |
| Inpp5j |
G |
T |
11: 3,502,484 (GRCm38) |
Y255* |
probably null |
Het |
| Insc |
C |
T |
7: 114,811,639 (GRCm38) |
Q244* |
probably null |
Het |
| Insm1 |
C |
T |
2: 146,223,556 (GRCm38) |
Q431* |
probably null |
Het |
| Ints12 |
A |
C |
3: 133,102,464 (GRCm38) |
D201A |
probably damaging |
Het |
| Ints6l |
G |
A |
X: 56,497,935 (GRCm38) |
M527I |
probably damaging |
Het |
| Ints9 |
G |
A |
14: 65,037,454 (GRCm38) |
V620I |
probably benign |
Het |
| Ipo13 |
C |
A |
4: 117,904,630 (GRCm38) |
E458* |
probably null |
Het |
| Ipp |
G |
T |
4: 116,537,885 (GRCm38) |
G539V |
probably null |
Het |
| Iqca |
A |
T |
1: 90,045,725 (GRCm38) |
V775E |
probably benign |
Het |
| Iqcf3 |
G |
T |
9: 106,560,988 (GRCm38) |
P12Q |
unknown |
Het |
| Iqck |
C |
A |
7: 118,941,654 (GRCm38) |
R259S |
probably benign |
Het |
| Iqgap1 |
C |
A |
7: 80,768,309 (GRCm38) |
K104N |
probably benign |
Het |
| Iqgap2 |
A |
G |
13: 95,731,443 (GRCm38) |
I219T |
possibly damaging |
Het |
| Irgq |
G |
T |
7: 24,531,801 (GRCm38) |
G139V |
probably damaging |
Het |
| Irs2 |
T |
G |
8: 11,006,185 (GRCm38) |
D749A |
probably damaging |
Het |
| Irx6 |
C |
A |
8: 92,678,371 (GRCm38) |
P289H |
possibly damaging |
Het |
| Isl2 |
C |
A |
9: 55,542,215 (GRCm38) |
C58* |
probably null |
Het |
| Ism1 |
A |
C |
2: 139,731,874 (GRCm38) |
N48T |
probably benign |
Het |
| Itga7 |
A |
C |
10: 128,953,827 (GRCm38) |
K1012T |
probably benign |
Het |
| Itga8 |
C |
A |
2: 12,262,136 (GRCm38) |
A163S |
probably benign |
Het |
| Itga8 |
C |
A |
2: 12,301,832 (GRCm38) |
|
probably benign |
Het |
| Itga8 |
A |
C |
2: 12,247,518 (GRCm38) |
F294V |
probably damaging |
Het |
| Itga9 |
A |
C |
9: 118,843,530 (GRCm38) |
D790A |
probably benign |
Het |
| Itga9 |
G |
A |
9: 118,887,839 (GRCm38) |
V990M |
probably damaging |
Het |
| Itgad |
T |
A |
7: 128,190,087 (GRCm38) |
N574K |
probably damaging |
Het |
| Itgax |
G |
C |
7: 128,144,872 (GRCm38) |
R909T |
probably benign |
Het |
| Itgb2 |
A |
T |
10: 77,557,962 (GRCm38) |
Q412L |
probably benign |
Het |
| Itgb3 |
G |
T |
11: 104,643,623 (GRCm38) |
K435N |
possibly damaging |
Het |
| Itgb4 |
G |
A |
11: 116,006,520 (GRCm38) |
G1536R |
probably damaging |
Het |
| Itgb6 |
G |
C |
2: 60,611,468 (GRCm38) |
S666C |
possibly damaging |
Het |
| Itgbl1 |
G |
T |
14: 123,954,672 (GRCm38) |
G373C |
probably damaging |
Het |
| Itih4 |
GAA |
G |
14: 30,899,462 (GRCm38) |
|
probably null |
Het |
| Itm2c |
G |
A |
1: 85,906,527 (GRCm38) |
V188M |
possibly damaging |
Het |
| Itpka |
G |
C |
2: 119,742,800 (GRCm38) |
S141T |
probably damaging |
Het |
| Itpkc |
C |
A |
7: 27,227,638 (GRCm38) |
D284Y |
probably benign |
Het |
| Itpr1 |
T |
A |
6: 108,499,149 (GRCm38) |
W2275R |
probably damaging |
Het |
| Ivd |
G |
T |
2: 118,876,344 (GRCm38) |
K272N |
possibly damaging |
Het |
| Ivns1abp |
A |
G |
1: 151,351,033 (GRCm38) |
E12G |
probably damaging |
Het |
| Jak1 |
C |
A |
4: 101,163,681 (GRCm38) |
G654V |
probably damaging |
Het |
| Jak1 |
C |
T |
4: 101,163,722 (GRCm38) |
M640I |
probably benign |
Het |
| Jak2 |
G |
A |
19: 29,271,398 (GRCm38) |
E92K |
possibly damaging |
Het |
| Jak3 |
C |
G |
8: 71,680,683 (GRCm38) |
A340G |
possibly damaging |
Het |
| Jakmip3 |
G |
T |
7: 139,020,133 (GRCm38) |
R254L |
probably benign |
Het |
| Jmjd1c |
T |
C |
10: 67,238,174 (GRCm38) |
L1896P |
probably benign |
Het |
| Jph1 |
C |
T |
1: 17,097,352 (GRCm38) |
E85K |
possibly damaging |
Het |
| Jph4 |
G |
A |
14: 55,113,648 (GRCm38) |
R304C |
probably benign |
Het |
| Jun |
T |
A |
4: 95,051,378 (GRCm38) |
|
probably benign |
Het |
| Kank4 |
TGGAGGGGGGAGGG |
TGG |
4: 98,778,294 (GRCm38) |
|
probably null |
Het |
| Kat6a |
C |
G |
8: 22,910,154 (GRCm38) |
C310W |
probably damaging |
Het |
| Katna1 |
G |
T |
10: 7,759,785 (GRCm38) |
S328I |
probably damaging |
Het |
| Katnal2 |
T |
C |
18: 77,012,057 (GRCm38) |
K127R |
probably benign |
Het |
| Kbtbd2 |
T |
G |
6: 56,780,309 (GRCm38) |
E147D |
probably damaging |
Het |
| Kcna3 |
A |
T |
3: 107,037,266 (GRCm38) |
N282Y |
probably damaging |
Het |
| Kcna5 |
T |
A |
6: 126,533,716 (GRCm38) |
K483M |
probably damaging |
Het |
| Kcnb1 |
G |
T |
2: 167,188,402 (GRCm38) |
D74E |
probably damaging |
Het |
| Kcne2 |
C |
T |
16: 92,296,591 (GRCm38) |
A2V |
probably benign |
Het |
| Kcnh1 |
C |
A |
1: 192,418,737 (GRCm38) |
R573S |
probably damaging |
Het |
| Kcnh8 |
C |
A |
17: 52,894,061 (GRCm38) |
L508I |
probably damaging |
Het |
| Kcnj2 |
G |
T |
11: 111,072,135 (GRCm38) |
V118L |
probably benign |
Het |
| Kcnk18 |
G |
T |
19: 59,234,959 (GRCm38) |
A179S |
probably benign |
Het |
| Kcnq4 |
A |
C |
4: 120,698,497 (GRCm38) |
|
probably null |
Het |
| Kcns1 |
G |
A |
2: 164,168,633 (GRCm38) |
H69Y |
probably benign |
Het |
| Kcnt1 |
G |
C |
2: 25,906,796 (GRCm38) |
R809P |
probably benign |
Het |
| Kcnt2 |
G |
C |
1: 140,376,361 (GRCm38) |
W156C |
probably damaging |
Het |
| Kcnv2 |
G |
T |
19: 27,323,438 (GRCm38) |
A230S |
probably benign |
Het |
| Kcp |
T |
A |
6: 29,485,012 (GRCm38) |
E1247V |
probably benign |
Het |
| Kctd1 |
C |
T |
18: 15,063,125 (GRCm38) |
S147N |
unknown |
Het |
| Kctd12 |
C |
G |
14: 102,981,918 (GRCm38) |
G175R |
not run |
Het |
| Kctd19 |
A |
C |
8: 105,385,136 (GRCm38) |
F842V |
probably damaging |
Het |
| Kdm3b |
G |
T |
18: 34,809,069 (GRCm38) |
E738* |
probably null |
Het |
| Kdm4a |
T |
A |
4: 118,177,502 (GRCm38) |
S11C |
probably benign |
Het |
| Kdm4a |
C |
T |
4: 118,153,190 (GRCm38) |
E619K |
probably benign |
Het |
| Kdm5b |
G |
A |
1: 134,625,035 (GRCm38) |
D1250N |
probably damaging |
Het |
| Kel |
G |
T |
6: 41,687,572 (GRCm38) |
P644T |
probably damaging |
Het |
| Khdc1c |
G |
T |
1: 21,369,563 (GRCm38) |
E113* |
probably null |
Het |
| Khdrbs2 |
G |
T |
1: 32,333,662 (GRCm38) |
W139L |
unknown |
Het |
| Khdrbs3 |
T |
C |
15: 69,017,467 (GRCm38) |
L155P |
probably damaging |
Het |
| Kif12 |
GGGGC |
GGGGCCTCCACCCGGCGGGC |
4: 63,171,423 (GRCm38) |
|
probably benign |
Het |
| Kif12 |
T |
G |
4: 63,171,997 (GRCm38) |
E3D |
possibly damaging |
Het |
| Kif13b |
C |
G |
14: 64,803,344 (GRCm38) |
P1627R |
probably benign |
Het |
| Kif14 |
A |
T |
1: 136,496,653 (GRCm38) |
Q1002L |
probably damaging |
Het |
| Kif14 |
G |
T |
1: 136,500,016 (GRCm38) |
|
probably null |
Het |
| Kif18a |
G |
A |
2: 109,318,053 (GRCm38) |
G631R |
possibly damaging |
Het |
| Kif19a |
A |
T |
11: 114,786,590 (GRCm38) |
E600V |
probably damaging |
Het |
| Kif19a |
C |
A |
11: 114,789,829 (GRCm38) |
A925E |
probably benign |
Het |
| Kif1a |
G |
A |
1: 93,055,697 (GRCm38) |
P693S |
probably benign |
Het |
| Kif1a |
G |
C |
1: 93,021,316 (GRCm38) |
L1495V |
probably damaging |
Het |
| Kif1a |
G |
A |
1: 93,022,491 (GRCm38) |
R1405W |
probably damaging |
|
Incidental Mutation