Other mutations in this stock |
Total: 1505 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012A03Rik |
T |
C |
6: 32,058,492 (GRCm38) |
W36R |
probably damaging |
Het |
1700016H13Rik |
G |
A |
5: 103,649,568 (GRCm38) |
P25L |
probably damaging |
Het |
1700017N19Rik |
A |
T |
10: 100,605,639 (GRCm38) |
K170M |
probably damaging |
Het |
1700020A23Rik |
C |
T |
2: 130,405,852 (GRCm38) |
P77L |
probably damaging |
Het |
1700020L24Rik |
A |
G |
11: 83,440,506 (GRCm38) |
Q81R |
probably damaging |
Het |
2210408I21Rik |
A |
C |
13: 77,174,891 (GRCm38) |
D13A |
probably damaging |
Het |
2310003L06Rik |
G |
T |
5: 87,972,306 (GRCm38) |
Q307H |
probably damaging |
Het |
2410141K09Rik |
C |
T |
13: 66,431,741 (GRCm38) |
G228S |
probably benign |
Het |
2410141K09Rik |
A |
C |
13: 66,431,186 (GRCm38) |
C413G |
probably damaging |
Het |
2510039O18Rik |
G |
A |
4: 147,944,745 (GRCm38) |
E391K |
probably benign |
Het |
4833423E24Rik |
C |
A |
2: 85,502,077 (GRCm38) |
S201I |
probably benign |
Het |
4833423E24Rik |
T |
G |
2: 85,484,181 (GRCm38) |
K476T |
probably damaging |
Het |
4930415L06Rik |
T |
G |
X: 89,930,236 (GRCm38) |
D785A |
unknown |
Het |
4930415L06Rik |
C |
A |
X: 89,930,237 (GRCm38) |
D785Y |
unknown |
Het |
4930447C04Rik |
G |
C |
12: 72,939,395 (GRCm38) |
|
probably benign |
Het |
4931440F15Rik |
C |
G |
11: 29,825,007 (GRCm38) |
G150A |
probably damaging |
Het |
4932438A13Rik |
A |
C |
3: 36,987,567 (GRCm38) |
E2698A |
probably damaging |
Het |
4932438H23Rik |
T |
A |
16: 91,055,813 (GRCm38) |
H145L |
probably benign |
Het |
4933405L10Rik |
G |
A |
8: 105,709,763 (GRCm38) |
G197E |
probably damaging |
Het |
5430419D17Rik |
T |
C |
7: 131,246,633 (GRCm38) |
C839R |
probably damaging |
Het |
9130011E15Rik |
T |
C |
19: 45,818,905 (GRCm38) |
E684G |
probably damaging |
Het |
9430007A20Rik |
C |
A |
4: 144,528,669 (GRCm38) |
L220M |
probably damaging |
Het |
A4gnt |
C |
T |
9: 99,613,841 (GRCm38) |
S110L |
probably damaging |
Het |
A530099J19Rik |
C |
T |
13: 19,729,209 (GRCm38) |
|
noncoding transcript |
Het |
Aasdh |
T |
C |
5: 76,901,157 (GRCm38) |
|
probably null |
Het |
Abca13 |
A |
C |
11: 9,294,687 (GRCm38) |
Q2183H |
probably damaging |
Het |
Abca14 |
T |
A |
7: 120,216,135 (GRCm38) |
I202N |
probably benign |
Het |
Abca17 |
C |
G |
17: 24,346,219 (GRCm38) |
A80P |
probably damaging |
Het |
Abca17 |
G |
T |
17: 24,279,107 (GRCm38) |
P1419T |
probably benign |
Het |
Abca17 |
T |
A |
17: 24,279,079 (GRCm38) |
K1428M |
probably damaging |
Het |
Abca8b |
A |
T |
11: 109,976,482 (GRCm38) |
M250K |
probably benign |
Het |
Abcc1 |
C |
A |
16: 14,410,809 (GRCm38) |
H307N |
probably benign |
Het |
Abcc12 |
G |
A |
8: 86,560,279 (GRCm38) |
|
probably null |
Het |
Abcc8 |
A |
G |
7: 46,138,065 (GRCm38) |
F571L |
probably benign |
Het |
Abhd8 |
G |
A |
8: 71,461,801 (GRCm38) |
P61L |
probably benign |
Het |
Acan |
G |
T |
7: 79,088,200 (GRCm38) |
E218* |
probably null |
Het |
Acan |
G |
C |
7: 79,100,110 (GRCm38) |
S1543T |
probably benign |
Het |
Acan |
A |
C |
7: 79,111,354 (GRCm38) |
H1938P |
probably benign |
Het |
Accsl |
A |
C |
2: 93,865,948 (GRCm38) |
F106V |
probably benign |
Het |
Acnat1 |
T |
G |
4: 49,447,588 (GRCm38) |
K313T |
probably damaging |
Het |
Acot8 |
T |
C |
2: 164,799,813 (GRCm38) |
Q133R |
probably damaging |
Het |
Acox3 |
A |
T |
5: 35,588,222 (GRCm38) |
K18M |
probably damaging |
Het |
Acoxl |
A |
C |
2: 127,872,195 (GRCm38) |
D137A |
probably damaging |
Het |
Acsm5 |
A |
T |
7: 119,537,211 (GRCm38) |
K335M |
probably damaging |
Het |
Actn4 |
A |
C |
7: 28,894,578 (GRCm38) |
F855V |
probably damaging |
Het |
Acvr2a |
T |
C |
2: 48,870,373 (GRCm38) |
V47A |
probably benign |
Het |
Ada |
C |
G |
2: 163,728,116 (GRCm38) |
|
probably null |
Het |
Adam21 |
G |
A |
12: 81,560,686 (GRCm38) |
H101Y |
probably damaging |
Het |
Adam26a |
T |
A |
8: 43,569,698 (GRCm38) |
N252Y |
probably damaging |
Het |
Adam26b |
T |
C |
8: 43,520,597 (GRCm38) |
E456G |
probably damaging |
Het |
Adam3 |
C |
A |
8: 24,681,431 (GRCm38) |
|
probably benign |
Het |
Adamts14 |
A |
G |
10: 61,218,445 (GRCm38) |
F603L |
probably damaging |
Het |
Adamts18 |
T |
C |
8: 113,775,440 (GRCm38) |
K263R |
possibly damaging |
Het |
Adamts3 |
G |
A |
5: 89,684,449 (GRCm38) |
R932C |
probably damaging |
Het |
Adamtsl3 |
T |
G |
7: 82,499,714 (GRCm38) |
F319V |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,540,325 (GRCm38) |
S586P |
probably damaging |
Het |
Adcy1 |
G |
C |
11: 7,150,019 (GRCm38) |
A710P |
probably benign |
Het |
Adcy4 |
G |
A |
14: 55,780,956 (GRCm38) |
A178V |
probably benign |
Het |
Add1 |
T |
A |
5: 34,613,400 (GRCm38) |
L285* |
probably null |
Het |
Add2 |
G |
C |
6: 86,085,965 (GRCm38) |
R35P |
probably damaging |
Het |
Adgrb3 |
C |
T |
1: 25,131,271 (GRCm38) |
R982H |
probably damaging |
Het |
Adgrf3 |
T |
G |
5: 30,199,120 (GRCm38) |
K378T |
possibly damaging |
Het |
Adgrl3 |
C |
A |
5: 81,329,882 (GRCm38) |
H61N |
probably benign |
Het |
Adgrl3 |
A |
T |
5: 81,512,158 (GRCm38) |
D258V |
probably damaging |
Het |
Adgrl4 |
C |
A |
3: 151,500,175 (GRCm38) |
P175T |
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,476,672 (GRCm38) |
P3726L |
probably damaging |
Het |
Adra1a |
T |
G |
14: 66,727,496 (GRCm38) |
F312V |
probably damaging |
Het |
Aebp1 |
C |
T |
11: 5,871,460 (GRCm38) |
R620* |
probably null |
Het |
Afdn |
G |
A |
17: 13,883,780 (GRCm38) |
S1126N |
probably damaging |
Het |
Afg3l1 |
A |
C |
8: 123,488,242 (GRCm38) |
E216D |
possibly damaging |
Het |
Afp |
G |
C |
5: 90,505,015 (GRCm38) |
G448A |
possibly damaging |
Het |
Agap2 |
G |
T |
10: 127,088,242 (GRCm38) |
S775I |
unknown |
Het |
Agbl1 |
T |
G |
7: 76,419,904 (GRCm38) |
F143V |
probably benign |
Het |
Ahnak |
A |
T |
19: 9,016,082 (GRCm38) |
N4910I |
probably damaging |
Het |
AI413582 |
G |
A |
17: 27,564,241 (GRCm38) |
R51C |
possibly damaging |
Het |
AI464131 |
A |
C |
4: 41,497,557 (GRCm38) |
L691R |
probably benign |
Het |
Ak1 |
A |
T |
2: 32,630,271 (GRCm38) |
K27M |
probably damaging |
Het |
Aldh1b1 |
C |
T |
4: 45,802,540 (GRCm38) |
A26V |
probably benign |
Het |
Aldh1b1 |
G |
C |
4: 45,802,539 (GRCm38) |
A26P |
probably benign |
Het |
Alk |
C |
G |
17: 72,205,807 (GRCm38) |
G386R |
probably damaging |
Het |
Amn |
C |
T |
12: 111,275,683 (GRCm38) |
A368V |
probably benign |
Het |
Amotl2 |
TCC |
TC |
9: 102,723,698 (GRCm38) |
|
probably null |
Het |
Ampd3 |
T |
G |
7: 110,777,825 (GRCm38) |
L8V |
probably damaging |
Het |
Anapc2 |
G |
T |
2: 25,273,368 (GRCm38) |
G206* |
probably null |
Het |
Angel2 |
G |
A |
1: 190,937,554 (GRCm38) |
D144N |
probably damaging |
Het |
Angptl3 |
A |
G |
4: 99,034,520 (GRCm38) |
N266S |
probably benign |
Het |
Ank2 |
A |
G |
3: 127,029,509 (GRCm38) |
V397A |
possibly damaging |
Het |
Ankib1 |
T |
A |
5: 3,713,136 (GRCm38) |
E531V |
probably damaging |
Het |
Ankib1 |
C |
A |
5: 3,713,137 (GRCm38) |
E531* |
probably null |
Het |
Ankrd16 |
CCTCCGGTACTT |
C |
2: 11,779,818 (GRCm38) |
|
probably null |
Het |
Ankrd24 |
G |
A |
10: 81,638,656 (GRCm38) |
G74D |
probably damaging |
Het |
Ankrd44 |
A |
C |
1: 54,658,982 (GRCm38) |
L606R |
probably damaging |
Het |
Ankrd50 |
T |
G |
3: 38,457,165 (GRCm38) |
K351T |
probably damaging |
Het |
Anks4b |
G |
A |
7: 120,182,519 (GRCm38) |
D258N |
probably benign |
Het |
Anln |
T |
C |
9: 22,362,801 (GRCm38) |
E580G |
probably benign |
Het |
Ano3 |
G |
A |
2: 110,745,847 (GRCm38) |
L454F |
probably damaging |
Het |
Antxrl |
A |
T |
14: 34,067,971 (GRCm38) |
N340I |
probably damaging |
Het |
Anxa10 |
C |
T |
8: 62,092,506 (GRCm38) |
G64D |
probably damaging |
Het |
Aox1 |
G |
A |
1: 58,081,542 (GRCm38) |
V865M |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,719,237 (GRCm38) |
Y418C |
possibly damaging |
Het |
Ap5b1 |
A |
C |
19: 5,570,424 (GRCm38) |
K624T |
possibly damaging |
Het |
Apbb1 |
C |
T |
7: 105,559,136 (GRCm38) |
C654Y |
probably damaging |
Het |
Apbb2 |
T |
G |
5: 66,302,696 (GRCm38) |
K710T |
probably damaging |
Het |
Apc |
C |
T |
18: 34,313,167 (GRCm38) |
Q1021* |
probably null |
Het |
Apcdd1 |
T |
G |
18: 62,937,183 (GRCm38) |
F174V |
probably benign |
Het |
Apob |
A |
G |
12: 8,012,936 (GRCm38) |
N193S |
possibly damaging |
Het |
Apob |
A |
T |
12: 8,005,945 (GRCm38) |
K1476* |
probably null |
Het |
Apob |
C |
A |
12: 8,005,074 (GRCm38) |
L1358I |
possibly damaging |
Het |
Apobr |
G |
A |
7: 126,585,031 (GRCm38) |
R7H |
probably benign |
Het |
Apol11b |
A |
C |
15: 77,638,007 (GRCm38) |
I30R |
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,893,595 (GRCm38) |
T1727S |
possibly damaging |
Het |
Arfip2 |
G |
C |
7: 105,637,242 (GRCm38) |
L188V |
probably damaging |
Het |
Arhgap11a |
A |
G |
2: 113,842,894 (GRCm38) |
C115R |
probably damaging |
Het |
Arhgap18 |
A |
T |
10: 26,850,004 (GRCm38) |
|
probably null |
Het |
Arhgap26 |
G |
C |
18: 39,357,671 (GRCm38) |
|
probably benign |
Het |
Arhgap28 |
G |
A |
17: 67,861,277 (GRCm38) |
A465V |
possibly damaging |
Het |
Arhgdib |
C |
A |
6: 136,933,618 (GRCm38) |
K48N |
probably damaging |
Het |
Arhgef10 |
C |
G |
8: 14,964,191 (GRCm38) |
A364G |
probably benign |
Het |
Arhgef10l |
G |
C |
4: 140,581,735 (GRCm38) |
L17V |
possibly damaging |
Het |
Arhgef18 |
C |
T |
8: 3,439,628 (GRCm38) |
S320F |
probably damaging |
Het |
Arhgef28 |
G |
A |
13: 97,945,691 (GRCm38) |
R1203W |
probably damaging |
Het |
Arl5b |
G |
A |
2: 15,075,021 (GRCm38) |
M134I |
probably benign |
Het |
Armc1 |
C |
A |
3: 19,149,507 (GRCm38) |
S85I |
probably damaging |
Het |
Armc12 |
A |
G |
17: 28,532,059 (GRCm38) |
E83G |
probably benign |
Het |
Armc4 |
G |
A |
18: 7,266,919 (GRCm38) |
S394L |
probably benign |
Het |
Armh1 |
C |
T |
4: 117,213,795 (GRCm38) |
D378N |
probably benign |
Het |
Arsj |
G |
T |
3: 126,439,132 (GRCm38) |
R509M |
possibly damaging |
Het |
Arvcf |
G |
A |
16: 18,402,641 (GRCm38) |
R602H |
probably damaging |
Het |
Asb14 |
A |
G |
14: 26,903,348 (GRCm38) |
K220R |
probably benign |
Het |
Ascc2 |
C |
G |
11: 4,646,656 (GRCm38) |
A59G |
probably benign |
Het |
Asf1b |
G |
C |
8: 83,969,152 (GRCm38) |
A141P |
possibly damaging |
Het |
Ash1l |
C |
A |
3: 88,982,709 (GRCm38) |
L632I |
probably benign |
Het |
Asph |
T |
A |
4: 9,630,715 (GRCm38) |
N211I |
possibly damaging |
Het |
Astn1 |
G |
A |
1: 158,597,206 (GRCm38) |
R646H |
possibly damaging |
Het |
Astn1 |
C |
A |
1: 158,472,497 (GRCm38) |
P136T |
possibly damaging |
Het |
Astn1 |
C |
A |
1: 158,684,096 (GRCm38) |
Y1169* |
probably null |
Het |
Asxl3 |
A |
C |
18: 22,516,772 (GRCm38) |
K606T |
probably benign |
Het |
Atf7 |
C |
G |
15: 102,547,182 (GRCm38) |
G249A |
probably benign |
Het |
Atg14 |
C |
G |
14: 47,568,292 (GRCm38) |
A39P |
probably damaging |
Het |
Atg7 |
T |
A |
6: 114,695,686 (GRCm38) |
F205I |
probably benign |
Het |
Atm |
T |
G |
9: 53,531,687 (GRCm38) |
K92T |
probably damaging |
Het |
Atp11b |
G |
T |
3: 35,812,213 (GRCm38) |
G387V |
probably damaging |
Het |
Atp12a |
G |
A |
14: 56,386,141 (GRCm38) |
V879I |
probably benign |
Het |
Atp13a5 |
T |
G |
16: 29,282,062 (GRCm38) |
K681N |
probably benign |
Het |
Atp2b2 |
A |
C |
6: 113,842,306 (GRCm38) |
F9V |
probably damaging |
Het |
Atp6v1h |
A |
C |
1: 5,098,048 (GRCm38) |
K147T |
probably damaging |
Het |
Atp8a2 |
T |
G |
14: 60,027,970 (GRCm38) |
S306R |
probably benign |
Het |
Atp8b2 |
T |
C |
3: 89,954,568 (GRCm38) |
K226R |
probably damaging |
Het |
Atr |
A |
G |
9: 95,885,320 (GRCm38) |
|
probably null |
Het |
Atrn |
G |
A |
2: 130,973,399 (GRCm38) |
S745N |
probably benign |
Het |
Auts2 |
T |
G |
5: 131,476,554 (GRCm38) |
|
probably benign |
Het |
Avpr1a |
G |
C |
10: 122,449,577 (GRCm38) |
S258T |
probably benign |
Het |
AW551984 |
C |
A |
9: 39,590,603 (GRCm38) |
E736* |
probably null |
Het |
B3galt6 |
C |
A |
4: 155,991,934 (GRCm38) |
R228L |
probably benign |
Het |
B3gnt3 |
G |
A |
8: 71,693,765 (GRCm38) |
S40F |
possibly damaging |
Het |
B3gnt8 |
C |
T |
7: 25,628,150 (GRCm38) |
R2C |
probably damaging |
Het |
Barx2 |
G |
A |
9: 31,846,866 (GRCm38) |
P259S |
possibly damaging |
Het |
Baz2b |
T |
A |
2: 59,960,015 (GRCm38) |
E618V |
probably damaging |
Het |
BC016579 |
C |
T |
16: 45,653,948 (GRCm38) |
D32N |
probably benign |
Het |
BC051665 |
T |
G |
13: 60,784,643 (GRCm38) |
E76A |
probably benign |
Het |
Bcl9 |
G |
T |
3: 97,210,641 (GRCm38) |
Q246K |
possibly damaging |
Het |
Best3 |
C |
T |
10: 117,024,170 (GRCm38) |
S445L |
probably benign |
Het |
Bfar |
C |
T |
16: 13,697,460 (GRCm38) |
P304L |
probably damaging |
Het |
Birc6 |
A |
C |
17: 74,611,542 (GRCm38) |
E1932D |
probably damaging |
Het |
Bod1l |
C |
G |
5: 41,808,764 (GRCm38) |
V2653L |
possibly damaging |
Het |
Bod1l |
C |
T |
5: 41,821,146 (GRCm38) |
E942K |
probably damaging |
Het |
Bptf |
A |
C |
11: 107,074,582 (GRCm38) |
V1147G |
probably benign |
Het |
Braf |
A |
G |
6: 39,662,026 (GRCm38) |
C264R |
probably damaging |
Het |
Brca2 |
A |
T |
5: 150,542,763 (GRCm38) |
K1997N |
probably damaging |
Het |
Brf2 |
T |
G |
8: 27,123,991 (GRCm38) |
E389A |
probably damaging |
Het |
Brinp2 |
G |
A |
1: 158,246,989 (GRCm38) |
R521* |
probably null |
Het |
Brsk1 |
C |
T |
7: 4,707,372 (GRCm38) |
T460M |
possibly damaging |
Het |
Brwd3 |
A |
T |
X: 108,774,860 (GRCm38) |
V732E |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,986,618 (GRCm38) |
V863D |
probably damaging |
Het |
Btbd11 |
C |
T |
10: 85,387,857 (GRCm38) |
H177Y |
probably benign |
Het |
C1rl |
C |
A |
6: 124,508,742 (GRCm38) |
D357E |
probably benign |
Het |
C77080 |
C |
T |
4: 129,222,298 (GRCm38) |
A903T |
probably damaging |
Het |
Cacna1b |
T |
A |
2: 24,661,844 (GRCm38) |
K1096M |
probably damaging |
Het |
Cacna1b |
T |
A |
2: 24,733,945 (GRCm38) |
S208C |
probably damaging |
Het |
Cacna1f |
C |
G |
X: 7,610,251 (GRCm38) |
L144V |
probably damaging |
Het |
Cacna2d1 |
A |
C |
5: 16,194,763 (GRCm38) |
E121D |
probably benign |
Het |
Cacna2d3 |
G |
T |
14: 29,064,308 (GRCm38) |
A574D |
probably damaging |
Het |
Cadps |
C |
A |
14: 12,467,113 (GRCm38) |
D935Y |
probably damaging |
Het |
Camk2a |
T |
G |
18: 60,943,150 (GRCm38) |
|
probably benign |
Het |
Capn15 |
C |
T |
17: 25,963,347 (GRCm38) |
E530K |
probably damaging |
Het |
Carmil1 |
G |
A |
13: 24,044,182 (GRCm38) |
Q600* |
probably null |
Het |
Carmil3 |
C |
T |
14: 55,501,568 (GRCm38) |
T893M |
probably damaging |
Het |
Casp12 |
C |
T |
9: 5,354,582 (GRCm38) |
A317V |
possibly damaging |
Het |
Casp9 |
T |
G |
4: 141,805,461 (GRCm38) |
L223V |
probably benign |
Het |
Casz1 |
T |
C |
4: 148,944,359 (GRCm38) |
L1087P |
probably benign |
Het |
Catsper3 |
T |
G |
13: 55,808,104 (GRCm38) |
F328V |
probably damaging |
Het |
Cavin1 |
T |
C |
11: 100,958,658 (GRCm38) |
D382G |
probably damaging |
Het |
Ccdc116 |
C |
A |
16: 17,147,171 (GRCm38) |
|
probably benign |
Het |
Ccdc130 |
G |
A |
8: 84,258,909 (GRCm38) |
R244* |
probably null |
Het |
Ccdc14 |
G |
A |
16: 34,690,804 (GRCm38) |
M1I |
probably null |
Het |
Ccdc141 |
T |
G |
2: 77,128,272 (GRCm38) |
E161D |
probably benign |
Het |
Ccdc175 |
G |
T |
12: 72,128,379 (GRCm38) |
H507N |
probably benign |
Het |
Ccdc24 |
C |
T |
4: 117,871,063 (GRCm38) |
|
probably null |
Het |
Ccdc83 |
T |
C |
7: 90,244,046 (GRCm38) |
K168E |
probably damaging |
Het |
Ccdc87 |
A |
G |
19: 4,840,722 (GRCm38) |
K414R |
probably benign |
Het |
Ccr1l1 |
T |
G |
9: 123,977,850 (GRCm38) |
I187L |
probably benign |
Het |
Cd209a |
G |
T |
8: 3,747,017 (GRCm38) |
S80Y |
probably damaging |
Het |
Cd2ap |
G |
A |
17: 42,807,993 (GRCm38) |
T518I |
probably benign |
Het |
Cd300lb |
A |
C |
11: 114,926,034 (GRCm38) |
L61V |
probably damaging |
Het |
Cd36 |
T |
A |
5: 17,795,575 (GRCm38) |
|
probably null |
Het |
Cd40 |
A |
T |
2: 165,063,040 (GRCm38) |
K92M |
probably damaging |
Het |
Cd48 |
A |
T |
1: 171,695,727 (GRCm38) |
D46V |
possibly damaging |
Het |
Cd55 |
T |
G |
1: 130,452,479 (GRCm38) |
D254A |
probably benign |
Het |
Cd59b |
G |
C |
2: 104,081,003 (GRCm38) |
S23T |
possibly damaging |
Het |
Cd8a |
T |
C |
6: 71,373,686 (GRCm38) |
L45P |
possibly damaging |
Het |
Cd93 |
T |
A |
2: 148,442,364 (GRCm38) |
D354V |
probably benign |
Het |
Cd99l2 |
C |
T |
X: 71,441,146 (GRCm38) |
|
probably null |
Het |
Cd99l2 |
G |
T |
X: 71,441,088 (GRCm38) |
P63Q |
probably damaging |
Het |
Cdan1 |
T |
C |
2: 120,730,336 (GRCm38) |
S251G |
probably damaging |
Het |
Cdca2 |
G |
C |
14: 67,700,298 (GRCm38) |
T302S |
probably benign |
Het |
Cdca7l |
A |
G |
12: 117,872,411 (GRCm38) |
M206V |
possibly damaging |
Het |
Cdh22 |
T |
C |
2: 165,112,430 (GRCm38) |
S724G |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,413,644 (GRCm38) |
T832A |
probably benign |
Het |
Cdh7 |
C |
G |
1: 110,085,123 (GRCm38) |
I395M |
probably benign |
Het |
Cdh8 |
G |
T |
8: 99,279,502 (GRCm38) |
S151Y |
probably damaging |
Het |
Cdk11b |
G |
T |
4: 155,641,564 (GRCm38) |
|
probably benign |
Het |
Cdkal1 |
G |
C |
13: 29,777,236 (GRCm38) |
H117D |
probably damaging |
Het |
Cdr1 |
T |
G |
X: 61,184,104 (GRCm38) |
E485D |
possibly damaging |
Het |
Celf4 |
G |
C |
18: 25,496,249 (GRCm38) |
P406A |
probably benign |
Het |
Celf5 |
C |
T |
10: 81,466,949 (GRCm38) |
A301T |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,414,117 (GRCm38) |
S460C |
probably damaging |
Het |
Cenpf |
A |
C |
1: 189,652,931 (GRCm38) |
L2384R |
probably damaging |
Het |
Cenpp |
T |
C |
13: 49,647,658 (GRCm38) |
|
probably null |
Het |
Ces1a |
T |
G |
8: 93,025,607 (GRCm38) |
K374T |
probably benign |
Het |
Ces1b |
T |
C |
8: 93,064,966 (GRCm38) |
E335G |
probably damaging |
Het |
Ces1d |
T |
C |
8: 93,175,108 (GRCm38) |
K411R |
probably benign |
Het |
Ces1e |
T |
C |
8: 93,210,418 (GRCm38) |
T342A |
probably benign |
Het |
Ces2e |
A |
C |
8: 104,931,347 (GRCm38) |
K359T |
probably benign |
Het |
Ces2e |
A |
G |
8: 104,932,398 (GRCm38) |
|
probably null |
Het |
Cfap44 |
G |
T |
16: 44,401,466 (GRCm38) |
R14I |
probably damaging |
Het |
Cfap46 |
C |
T |
7: 139,635,064 (GRCm38) |
G1582R |
probably damaging |
Het |
Cfap57 |
C |
T |
4: 118,581,882 (GRCm38) |
D816N |
probably benign |
Het |
Cfap61 |
C |
T |
2: 146,129,227 (GRCm38) |
P919L |
probably benign |
Het |
Cfh |
A |
G |
1: 140,108,904 (GRCm38) |
L636P |
probably benign |
Het |
Cfh |
G |
A |
1: 140,147,718 (GRCm38) |
P243S |
possibly damaging |
Het |
Chd6 |
T |
C |
2: 160,966,488 (GRCm38) |
D1602G |
probably damaging |
Het |
Chil1 |
A |
G |
1: 134,189,500 (GRCm38) |
K345R |
probably benign |
Het |
Chrd |
T |
C |
16: 20,741,255 (GRCm38) |
F891L |
probably damaging |
Het |
Cilp |
TGGG |
TGG |
9: 65,280,130 (GRCm38) |
|
probably null |
Het |
Cilp2 |
C |
G |
8: 69,885,410 (GRCm38) |
K190N |
possibly damaging |
Het |
Cit |
A |
T |
5: 115,985,533 (GRCm38) |
S1421C |
possibly damaging |
Het |
Clca3a1 |
T |
G |
3: 144,746,953 (GRCm38) |
S590R |
probably damaging |
Het |
Clcn1 |
C |
A |
6: 42,300,360 (GRCm38) |
L462I |
probably benign |
Het |
Clcn1 |
A |
C |
6: 42,307,256 (GRCm38) |
K514T |
probably damaging |
Het |
Cldn4 |
G |
A |
5: 134,946,598 (GRCm38) |
L50F |
probably damaging |
Het |
Clec4g |
A |
C |
8: 3,707,796 (GRCm38) |
|
probably benign |
Het |
Clec4g |
T |
G |
8: 3,716,548 (GRCm38) |
N251T |
probably damaging |
Het |
Clu |
A |
C |
14: 65,976,913 (GRCm38) |
E278D |
probably benign |
Het |
Cmya5 |
C |
G |
13: 93,063,579 (GRCm38) |
A3414P |
probably benign |
Het |
CN725425 |
T |
G |
15: 91,245,762 (GRCm38) |
F276C |
possibly damaging |
Het |
Cnksr2 |
T |
G |
X: 157,853,220 (GRCm38) |
N854T |
probably benign |
Het |
Cnot7 |
ATTTATTTTTTA |
ATTTA |
8: 40,500,739 (GRCm38) |
|
probably benign |
Het |
Cnst |
G |
C |
1: 179,579,565 (GRCm38) |
G59A |
probably damaging |
Het |
Cntn3 |
A |
G |
6: 102,420,294 (GRCm38) |
L106P |
possibly damaging |
Het |
Cntnap4 |
C |
G |
8: 112,815,520 (GRCm38) |
P762A |
probably damaging |
Het |
Cntnap5a |
G |
A |
1: 116,060,251 (GRCm38) |
A171T |
probably benign |
Het |
Col17a1 |
A |
G |
19: 47,652,178 (GRCm38) |
S994P |
possibly damaging |
Het |
Col19a1 |
A |
C |
1: 24,279,940 (GRCm38) |
I1023S |
probably damaging |
Het |
Col4a1 |
T |
G |
8: 11,246,859 (GRCm38) |
|
probably benign |
Het |
Col4a4 |
A |
C |
1: 82,453,196 (GRCm38) |
L1662V |
unknown |
Het |
Col6a1 |
C |
G |
10: 76,709,559 (GRCm38) |
*1026Y |
probably null |
Het |
Col6a5 |
A |
C |
9: 105,926,067 (GRCm38) |
I1233S |
unknown |
Het |
Col7a1 |
C |
T |
9: 108,978,500 (GRCm38) |
|
silent |
Het |
Colec12 |
A |
G |
18: 9,848,727 (GRCm38) |
T302A |
probably benign |
Het |
Commd4 |
T |
C |
9: 57,156,256 (GRCm38) |
S73G |
probably benign |
Het |
Coro1c |
A |
G |
5: 113,850,649 (GRCm38) |
|
probably null |
Het |
Cpd |
C |
A |
11: 76,801,746 (GRCm38) |
C755F |
probably damaging |
Het |
Cpsf6 |
T |
C |
10: 117,356,041 (GRCm38) |
D518G |
unknown |
Het |
Creb3l4 |
C |
T |
3: 90,237,751 (GRCm38) |
V365M |
possibly damaging |
Het |
Crhr2 |
A |
G |
6: 55,103,216 (GRCm38) |
V126A |
possibly damaging |
Het |
Crim1 |
G |
T |
17: 78,367,835 (GRCm38) |
K824N |
probably benign |
Het |
Crispld1 |
A |
G |
1: 17,764,076 (GRCm38) |
T489A |
probably benign |
Het |
Crybg1 |
C |
T |
10: 43,997,311 (GRCm38) |
R1267H |
probably benign |
Het |
Cryzl2 |
G |
T |
1: 157,465,789 (GRCm38) |
L153F |
probably benign |
Het |
Csgalnact1 |
T |
C |
8: 68,401,330 (GRCm38) |
K273R |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,346,617 (GRCm38) |
D433G |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 16,200,058 (GRCm38) |
Q969K |
probably damaging |
Het |
Csmd1 |
T |
G |
8: 16,189,978 (GRCm38) |
K1140T |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 16,092,258 (GRCm38) |
D1544N |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 15,921,875 (GRCm38) |
T2985N |
possibly damaging |
Het |
Csmd3 |
G |
A |
15: 47,847,281 (GRCm38) |
P1637S |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 47,636,393 (GRCm38) |
L3027F |
probably damaging |
Het |
Csn2 |
T |
G |
5: 87,696,009 (GRCm38) |
|
probably benign |
Het |
Cspg4 |
C |
A |
9: 56,886,036 (GRCm38) |
L352M |
probably damaging |
Het |
Cspp1 |
C |
G |
1: 10,083,546 (GRCm38) |
D393E |
possibly damaging |
Het |
Ctcfl |
G |
A |
2: 173,118,344 (GRCm38) |
H149Y |
probably benign |
Het |
Ctnna3 |
C |
T |
10: 63,581,978 (GRCm38) |
S165F |
probably benign |
Het |
Ctnnd2 |
A |
C |
15: 30,966,813 (GRCm38) |
N970T |
probably benign |
Het |
Ctr9 |
T |
C |
7: 111,030,224 (GRCm38) |
L19P |
probably damaging |
Het |
Ctsd |
C |
T |
7: 142,376,597 (GRCm38) |
G403S |
probably damaging |
Het |
Cubn |
G |
A |
2: 13,294,229 (GRCm38) |
S3211L |
probably benign |
Het |
Cul3 |
A |
G |
1: 80,290,091 (GRCm38) |
V177A |
probably benign |
Het |
Cxcl16 |
C |
T |
11: 70,455,978 (GRCm38) |
G113E |
probably damaging |
Het |
Cyfip1 |
A |
C |
7: 55,875,052 (GRCm38) |
K144T |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 27,035,420 (GRCm38) |
K422R |
possibly damaging |
Het |
Cyp2a5 |
G |
T |
7: 26,841,107 (GRCm38) |
D69Y |
probably damaging |
Het |
Cyp2b23 |
C |
G |
7: 26,681,411 (GRCm38) |
A130P |
probably benign |
Het |
Cyp2c50 |
C |
T |
19: 40,097,955 (GRCm38) |
A321V |
possibly damaging |
Homo |
Cyp2c68 |
C |
T |
19: 39,739,463 (GRCm38) |
A82T |
probably damaging |
Het |
Cyp2d11 |
C |
A |
15: 82,390,111 (GRCm38) |
M356I |
probably damaging |
Het |
Cyp2r1 |
C |
T |
7: 114,551,974 (GRCm38) |
R370K |
probably damaging |
Het |
Cyp2t4 |
G |
C |
7: 27,157,746 (GRCm38) |
G345R |
probably damaging |
Het |
Cyp3a59 |
A |
C |
5: 146,098,222 (GRCm38) |
N237H |
probably benign |
Het |
Cyp4a29 |
T |
G |
4: 115,248,496 (GRCm38) |
F132V |
probably benign |
Het |
Cyp4f15 |
G |
C |
17: 32,692,690 (GRCm38) |
|
probably null |
Het |
Cyp4f40 |
G |
A |
17: 32,674,002 (GRCm38) |
|
probably null |
Het |
D030056L22Rik |
A |
T |
19: 18,717,315 (GRCm38) |
S145C |
possibly damaging |
Het |
D230025D16Rik |
C |
T |
8: 105,231,172 (GRCm38) |
R37C |
probably damaging |
Het |
D7Ertd443e |
T |
G |
7: 134,294,982 (GRCm38) |
S154R |
probably benign |
Het |
Dab1 |
A |
C |
4: 104,479,232 (GRCm38) |
Q8H |
probably damaging |
Het |
Dag1 |
G |
C |
9: 108,208,668 (GRCm38) |
P425A |
possibly damaging |
Het |
Dapk2 |
T |
C |
9: 66,246,477 (GRCm38) |
F172L |
possibly damaging |
Het |
Daw1 |
A |
T |
1: 83,205,964 (GRCm38) |
K245M |
probably null |
Het |
Dbnl |
A |
T |
11: 5,796,797 (GRCm38) |
K176* |
probably null |
Het |
Dcaf13 |
C |
T |
15: 39,145,247 (GRCm38) |
R415C |
probably damaging |
Het |
Dcaf15 |
A |
C |
8: 84,102,781 (GRCm38) |
W111G |
probably damaging |
Het |
Dclk1 |
G |
T |
3: 55,500,105 (GRCm38) |
G235V |
probably damaging |
Het |
Dclre1c |
G |
T |
2: 3,438,080 (GRCm38) |
E92D |
possibly damaging |
Het |
Dda1 |
C |
G |
8: 71,474,495 (GRCm38) |
A4G |
probably damaging |
Het |
Ddb1 |
C |
A |
19: 10,619,230 (GRCm38) |
L438I |
probably damaging |
Het |
Ddit4l |
G |
C |
3: 137,626,362 (GRCm38) |
G163A |
probably benign |
Het |
Ddn |
T |
C |
15: 98,806,139 (GRCm38) |
E424G |
possibly damaging |
Het |
Ddx19b |
T |
G |
8: 111,015,575 (GRCm38) |
K176T |
probably benign |
Het |
Ddx23 |
A |
G |
15: 98,647,621 (GRCm38) |
V602A |
probably benign |
Het |
Ddx59 |
A |
C |
1: 136,432,451 (GRCm38) |
N401T |
possibly damaging |
Het |
Def8 |
A |
G |
8: 123,456,498 (GRCm38) |
R279G |
probably damaging |
Het |
Defb14 |
G |
T |
8: 19,195,184 (GRCm38) |
G59V |
probably damaging |
Het |
Defb8 |
A |
C |
8: 19,447,541 (GRCm38) |
L18R |
possibly damaging |
Het |
Defb9 |
A |
C |
8: 21,881,867 (GRCm38) |
F43L |
probably benign |
Het |
Dennd1a |
A |
G |
2: 37,800,692 (GRCm38) |
S799P |
probably benign |
Het |
Dennd2d |
C |
T |
3: 106,499,874 (GRCm38) |
R414* |
probably null |
Het |
Dennd4a |
G |
A |
9: 64,872,022 (GRCm38) |
A596T |
probably damaging |
Het |
Dennd5a |
T |
C |
7: 109,905,273 (GRCm38) |
K854E |
probably damaging |
Het |
Dennd5a |
T |
G |
7: 109,894,747 (GRCm38) |
D1250A |
possibly damaging |
Het |
Dera |
T |
G |
6: 137,837,118 (GRCm38) |
I99M |
possibly damaging |
Het |
Desi2 |
A |
G |
1: 178,187,944 (GRCm38) |
N10S |
probably benign |
Het |
Dgkg |
T |
G |
16: 22,469,328 (GRCm38) |
N763T |
probably damaging |
Het |
Dgkg |
A |
T |
16: 22,572,686 (GRCm38) |
S341T |
probably benign |
Het |
Dhh |
T |
C |
15: 98,894,909 (GRCm38) |
N157D |
probably benign |
Het |
Dhtkd1 |
C |
A |
2: 5,911,874 (GRCm38) |
A664S |
possibly damaging |
Het |
Dhx37 |
T |
C |
5: 125,416,591 (GRCm38) |
E968G |
possibly damaging |
Het |
Dhx57 |
A |
C |
17: 80,251,348 (GRCm38) |
L1061V |
probably damaging |
Het |
Dip2a |
T |
C |
10: 76,285,628 (GRCm38) |
K798R |
probably benign |
Het |
Disp3 |
G |
C |
4: 148,271,743 (GRCm38) |
A220G |
possibly damaging |
Het |
Dlg4 |
G |
A |
11: 70,031,130 (GRCm38) |
R66Q |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,158,094 (GRCm38) |
P992S |
probably damaging |
Het |
Dlgap2 |
C |
G |
8: 14,822,472 (GRCm38) |
A651G |
probably benign |
Het |
Dlx5 |
C |
A |
6: 6,879,607 (GRCm38) |
Q153H |
probably damaging |
Het |
Dmd |
A |
G |
X: 84,575,760 (GRCm38) |
T2614A |
probably benign |
Het |
Dmd |
C |
T |
X: 83,878,495 (GRCm38) |
S1457F |
possibly damaging |
Het |
Dmrt2 |
T |
G |
19: 25,678,642 (GRCm38) |
L535R |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 49,920,965 (GRCm38) |
N2546S |
probably benign |
Het |
Dnaaf3 |
G |
A |
7: 4,523,795 (GRCm38) |
R428W |
probably damaging |
Het |
Dnah1 |
T |
G |
14: 31,304,811 (GRCm38) |
K752T |
probably benign |
Het |
Dnah11 |
C |
A |
12: 117,982,969 (GRCm38) |
A3127S |
probably damaging |
Het |
Dnah11 |
G |
C |
12: 117,895,012 (GRCm38) |
T4121R |
probably damaging |
Het |
Dnah2 |
A |
C |
11: 69,430,793 (GRCm38) |
L3847R |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 120,086,297 (GRCm38) |
D164V |
probably benign |
Het |
Dnah3 |
T |
C |
7: 120,010,873 (GRCm38) |
K1769R |
probably null |
Het |
Dnah5 |
A |
C |
15: 28,384,230 (GRCm38) |
D3040A |
probably damaging |
Het |
Dnah5 |
G |
A |
15: 28,366,357 (GRCm38) |
G2739S |
probably null |
Het |
Dnah7a |
A |
C |
1: 53,468,643 (GRCm38) |
Y3090D |
probably damaging |
Het |
Dnajb12 |
C |
A |
10: 59,890,054 (GRCm38) |
P54T |
probably benign |
Het |
Dnajb8 |
G |
A |
6: 88,222,845 (GRCm38) |
G121D |
probably benign |
Het |
Dnajc6 |
G |
A |
4: 101,639,329 (GRCm38) |
V830M |
probably damaging |
Het |
Dnhd1 |
C |
G |
7: 105,712,727 (GRCm38) |
T3664S |
probably benign |
Het |
Dnmbp |
G |
A |
19: 43,902,122 (GRCm38) |
P402L |
probably benign |
Het |
Dnmbp |
G |
A |
19: 43,874,984 (GRCm38) |
A453V |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,804,547 (GRCm38) |
Y760C |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,532,347 (GRCm38) |
K1588R |
probably damaging |
Het |
Dock11 |
A |
G |
X: 36,002,533 (GRCm38) |
K718R |
probably benign |
Het |
Dock2 |
C |
A |
11: 34,695,212 (GRCm38) |
E548* |
probably null |
Het |
Dock2 |
A |
C |
11: 34,692,382 (GRCm38) |
L568R |
probably damaging |
Het |
Dock2 |
G |
A |
11: 34,438,300 (GRCm38) |
T211M |
probably benign |
Het |
Dock9 |
C |
T |
14: 121,555,275 (GRCm38) |
V1844M |
probably damaging |
Het |
Dopey2 |
C |
T |
16: 93,763,326 (GRCm38) |
T720I |
probably benign |
Het |
Dpf2 |
A |
C |
19: 5,902,444 (GRCm38) |
F289V |
probably damaging |
Het |
Dpy19l2 |
C |
T |
9: 24,660,824 (GRCm38) |
|
probably null |
Het |
Dsc2 |
C |
T |
18: 20,046,304 (GRCm38) |
E236K |
probably damaging |
Het |
Dscam |
A |
C |
16: 96,772,561 (GRCm38) |
F734V |
probably benign |
Het |
Dscc1 |
A |
C |
15: 55,080,317 (GRCm38) |
S386A |
possibly damaging |
Het |
Dusp27 |
A |
G |
1: 166,099,283 (GRCm38) |
L920P |
probably damaging |
Het |
Dync1h1 |
GAAA |
GAA |
12: 110,629,917 (GRCm38) |
|
probably null |
Het |
Dyrk3 |
A |
G |
1: 131,129,233 (GRCm38) |
L401P |
probably damaging |
Het |
Ecm1 |
T |
C |
3: 95,734,876 (GRCm38) |
I466V |
probably benign |
Het |
Eef2 |
G |
C |
10: 81,181,889 (GRCm38) |
G795A |
probably damaging |
Het |
Efcab6 |
A |
C |
15: 83,955,009 (GRCm38) |
L383R |
probably damaging |
Het |
Efl1 |
A |
C |
7: 82,692,850 (GRCm38) |
S489R |
probably benign |
Het |
Egfl8 |
C |
A |
17: 34,614,241 (GRCm38) |
G177V |
probably damaging |
Het |
Ehbp1l1 |
G |
C |
19: 5,716,287 (GRCm38) |
P399A |
possibly damaging |
Het |
Ehd2 |
G |
C |
7: 15,963,466 (GRCm38) |
A139G |
possibly damaging |
Het |
Eif3j1 |
T |
G |
2: 122,050,613 (GRCm38) |
F182C |
probably damaging |
Het |
Eif3k |
T |
C |
7: 28,974,599 (GRCm38) |
|
probably null |
Het |
Eif3m |
A |
C |
2: 105,013,256 (GRCm38) |
L127R |
probably damaging |
Het |
Elac1 |
T |
G |
18: 73,739,090 (GRCm38) |
D278A |
probably benign |
Het |
Ell2 |
TCTAGGTGGCC |
TC |
13: 75,761,873 (GRCm38) |
|
probably benign |
Het |
Elmod1 |
A |
C |
9: 53,919,614 (GRCm38) |
S263A |
probably benign |
Het |
Eme2 |
T |
A |
17: 24,894,567 (GRCm38) |
|
probably null |
Het |
Eml1 |
T |
G |
12: 108,537,459 (GRCm38) |
F772V |
possibly damaging |
Het |
Emsy |
G |
A |
7: 98,600,722 (GRCm38) |
P786L |
probably damaging |
Het |
Epb41l3 |
T |
G |
17: 69,253,522 (GRCm38) |
F355V |
probably damaging |
Het |
Epg5 |
C |
G |
18: 77,959,139 (GRCm38) |
A591G |
probably benign |
Het |
Epha4 |
A |
C |
1: 77,506,662 (GRCm38) |
S237A |
possibly damaging |
Het |
Epha5 |
G |
C |
5: 84,237,522 (GRCm38) |
H317D |
probably benign |
Het |
Ephb1 |
C |
T |
9: 101,984,145 (GRCm38) |
V607I |
probably damaging |
Het |
Ephx2 |
A |
G |
14: 66,107,318 (GRCm38) |
F168L |
probably benign |
Het |
Eps15l1 |
T |
G |
8: 72,386,901 (GRCm38) |
N249T |
probably damaging |
Het |
Ercc6l2 |
A |
G |
13: 63,853,728 (GRCm38) |
E567G |
possibly damaging |
Het |
Ermp1 |
G |
C |
19: 29,612,925 (GRCm38) |
S792R |
probably damaging |
Het |
Esp8 |
A |
G |
17: 40,530,045 (GRCm38) |
T66A |
possibly damaging |
Het |
Esr1 |
C |
G |
10: 4,712,667 (GRCm38) |
A95G |
possibly damaging |
Het |
Esrrg |
A |
T |
1: 188,150,218 (GRCm38) |
E224V |
probably benign |
Het |
Etaa1 |
T |
C |
11: 17,946,465 (GRCm38) |
T551A |
possibly damaging |
Het |
Etv5 |
C |
T |
16: 22,383,589 (GRCm38) |
E472K |
probably benign |
Het |
Eva1a |
TGCAGCGACAGCAGCGACAGC |
TGCAGCGACAGCAGCGACAGCAGCGACAGC |
6: 82,091,937 (GRCm38) |
|
probably benign |
Het |
Exoc3l4 |
G |
A |
12: 111,429,487 (GRCm38) |
D645N |
probably benign |
Het |
Eya4 |
T |
C |
10: 23,113,988 (GRCm38) |
Q513R |
probably damaging |
Het |
F11 |
C |
T |
8: 45,245,772 (GRCm38) |
G445D |
possibly damaging |
Het |
F13a1 |
C |
T |
13: 36,989,012 (GRCm38) |
W131* |
probably null |
Het |
F13b |
A |
C |
1: 139,508,202 (GRCm38) |
S249R |
probably benign |
Het |
F5 |
A |
C |
1: 164,154,385 (GRCm38) |
K73T |
probably benign |
Het |
F8 |
C |
T |
X: 75,323,149 (GRCm38) |
|
probably null |
Het |
Fam117a |
C |
G |
11: 95,371,524 (GRCm38) |
H151Q |
possibly damaging |
Het |
Fam186a |
T |
C |
15: 99,945,994 (GRCm38) |
S790G |
unknown |
Het |
Fam193a |
A |
T |
5: 34,420,895 (GRCm38) |
E244D |
probably benign |
Het |
Fam207a |
C |
A |
10: 77,490,031 (GRCm38) |
S168I |
probably damaging |
Het |
Fam71b |
G |
A |
11: 46,407,723 (GRCm38) |
R618K |
possibly damaging |
Het |
Fancd2 |
C |
G |
6: 113,581,422 (GRCm38) |
H1167D |
probably benign |
Het |
Far2 |
A |
C |
6: 148,138,658 (GRCm38) |
K29T |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,023,807 (GRCm38) |
I1963M |
possibly damaging |
Het |
Fat4 |
C |
G |
3: 38,887,050 (GRCm38) |
L31V |
possibly damaging |
Het |
Fat4 |
C |
G |
3: 38,958,492 (GRCm38) |
A2312G |
probably benign |
Het |
Fbln2 |
G |
A |
6: 91,233,346 (GRCm38) |
D91N |
probably damaging |
Het |
Fbn1 |
C |
T |
2: 125,350,288 (GRCm38) |
D1434N |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,293,860 (GRCm38) |
K71M |
possibly damaging |
Het |
Fbxw21 |
T |
C |
9: 109,145,537 (GRCm38) |
H305R |
probably benign |
Het |
Fgd4 |
T |
A |
16: 16,484,470 (GRCm38) |
K74* |
probably null |
Het |
Fgfr2 |
A |
T |
7: 130,169,799 (GRCm38) |
L596H |
probably damaging |
Het |
Fhl1 |
T |
A |
X: 56,779,491 (GRCm38) |
L10Q |
probably null |
Het |
Fig4 |
A |
C |
10: 41,253,731 (GRCm38) |
F498V |
probably damaging |
Het |
Fign |
A |
C |
2: 64,096,902 (GRCm38) |
S6R |
probably benign |
Het |
Filip1l |
G |
C |
16: 57,513,405 (GRCm38) |
S187T |
probably damaging |
Het |
Fitm2 |
C |
T |
2: 163,469,865 (GRCm38) |
E143K |
probably benign |
Het |
Flnb |
A |
C |
14: 7,905,871 (GRCm38) |
K1207T |
probably benign |
Het |
Flnc |
G |
A |
6: 29,457,151 (GRCm38) |
A2351T |
probably damaging |
Het |
Flt1 |
T |
C |
5: 147,681,649 (GRCm38) |
T261A |
possibly damaging |
Het |
Flt3 |
C |
G |
5: 147,349,564 (GRCm38) |
|
probably null |
Het |
Fmn1 |
A |
C |
2: 113,441,925 (GRCm38) |
|
probably benign |
Het |
Fmo9 |
A |
G |
1: 166,673,545 (GRCm38) |
|
probably null |
Het |
Fn1 |
A |
G |
1: 71,649,292 (GRCm38) |
I151T |
probably damaging |
Het |
Fndc1 |
T |
G |
17: 7,782,479 (GRCm38) |
E139A |
probably damaging |
Het |
Fndc3b |
G |
C |
3: 27,465,808 (GRCm38) |
C561W |
possibly damaging |
Het |
Fndc7 |
T |
C |
3: 108,883,500 (GRCm38) |
E70G |
probably damaging |
Het |
Folh1 |
T |
G |
7: 86,725,954 (GRCm38) |
K575T |
probably benign |
Het |
Foxc2 |
G |
C |
8: 121,117,150 (GRCm38) |
R179P |
probably damaging |
Het |
Foxc2 |
G |
C |
8: 121,116,959 (GRCm38) |
W115C |
possibly damaging |
Het |
Foxl1 |
G |
A |
8: 121,128,772 (GRCm38) |
E271K |
possibly damaging |
Het |
Foxred2 |
C |
T |
15: 77,952,003 (GRCm38) |
A385T |
probably damaging |
Het |
Fpr-rs4 |
G |
A |
17: 18,022,694 (GRCm38) |
R321K |
probably benign |
Het |
Fpr-rs4 |
T |
C |
17: 18,021,919 (GRCm38) |
S63P |
possibly damaging |
Het |
Fras1 |
A |
C |
5: 96,743,211 (GRCm38) |
Q2866H |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,758,142 (GRCm38) |
L3135P |
probably benign |
Het |
Frem1 |
C |
T |
4: 82,972,267 (GRCm38) |
E974K |
probably damaging |
Het |
Frem3 |
A |
C |
8: 80,615,426 (GRCm38) |
Q1449H |
probably benign |
Het |
Frmd6 |
A |
G |
12: 70,880,678 (GRCm38) |
Q144R |
probably benign |
Het |
Frmd7 |
T |
G |
X: 50,896,147 (GRCm38) |
N382T |
possibly damaging |
Het |
Frmpd1 |
C |
T |
4: 45,284,080 (GRCm38) |
P967L |
possibly damaging |
Het |
Frmpd4 |
G |
A |
X: 167,497,840 (GRCm38) |
T348M |
probably damaging |
Het |
Fryl |
A |
C |
5: 73,090,709 (GRCm38) |
L1022V |
probably damaging |
Het |
Fryl |
A |
C |
5: 73,090,738 (GRCm38) |
L1012R |
probably damaging |
Het |
Fsd1 |
T |
A |
17: 55,991,203 (GRCm38) |
L176H |
probably damaging |
Het |
Fsip2 |
G |
C |
2: 82,975,448 (GRCm38) |
E704Q |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,987,653 (GRCm38) |
S4577R |
possibly damaging |
Het |
Fsip2 |
A |
C |
2: 82,988,634 (GRCm38) |
K4904Q |
possibly damaging |
Het |
Fyb |
G |
A |
15: 6,658,540 (GRCm38) |
V794I |
probably benign |
Het |
Fzd10 |
T |
C |
5: 128,601,246 (GRCm38) |
L10P |
probably damaging |
Het |
Fzd7 |
G |
C |
1: 59,483,870 (GRCm38) |
G304A |
probably damaging |
Het |
Gadl1 |
A |
T |
9: 115,937,270 (GRCm38) |
I37L |
probably benign |
Het |
Gal3st1 |
C |
G |
11: 3,997,984 (GRCm38) |
P64A |
probably benign |
Het |
Gal3st2c |
A |
G |
1: 94,008,145 (GRCm38) |
H73R |
probably benign |
Het |
Galnt10 |
G |
A |
11: 57,721,331 (GRCm38) |
G66R |
possibly damaging |
Het |
Gbp2 |
G |
A |
3: 142,630,015 (GRCm38) |
D159N |
probably benign |
Het |
Gbp4 |
A |
T |
5: 105,120,997 (GRCm38) |
F430Y |
probably damaging |
Het |
Gbp9 |
C |
A |
5: 105,094,125 (GRCm38) |
G189W |
probably damaging |
Het |
Gclc |
G |
A |
9: 77,781,367 (GRCm38) |
|
probably null |
Het |
Gcm2 |
C |
A |
13: 41,102,792 (GRCm38) |
G494W |
probably damaging |
Het |
Gcnt2 |
C |
A |
13: 40,918,639 (GRCm38) |
P253T |
probably damaging |
Het |
Gdf10 |
C |
T |
14: 33,932,390 (GRCm38) |
R285C |
probably damaging |
Het |
Gdpd4 |
A |
G |
7: 97,966,309 (GRCm38) |
S114G |
probably damaging |
Het |
Gga1 |
C |
A |
15: 78,892,021 (GRCm38) |
D421E |
probably damaging |
Het |
Ggt5 |
T |
G |
10: 75,608,759 (GRCm38) |
F304V |
possibly damaging |
Het |
Gja3 |
A |
C |
14: 57,035,815 (GRCm38) |
L367V |
possibly damaging |
Het |
Gje1 |
A |
C |
10: 14,718,124 (GRCm38) |
F9V |
possibly damaging |
Het |
Glrb |
T |
G |
3: 80,845,234 (GRCm38) |
K407N |
possibly damaging |
Het |
Glyat |
A |
G |
19: 12,648,009 (GRCm38) |
T32A |
probably benign |
Het |
Gm10324 |
A |
G |
13: 66,122,394 (GRCm38) |
K458R |
probably damaging |
Het |
Gm10772 |
C |
A |
13: 66,227,356 (GRCm38) |
S73I |
probably benign |
Het |
Gm10784 |
T |
G |
13: 49,945,143 (GRCm38) |
|
noncoding transcript |
Het |
Gm1110 |
A |
C |
9: 26,913,310 (GRCm38) |
L145V |
probably benign |
Het |
Gm11559 |
C |
A |
11: 99,864,949 (GRCm38) |
C141* |
probably null |
Het |
Gm11639 |
A |
C |
11: 104,751,902 (GRCm38) |
K1117T |
probably damaging |
Het |
Gm12800 |
A |
G |
4: 101,909,118 (GRCm38) |
|
probably null |
Het |
Gm12800 |
A |
C |
4: 101,910,186 (GRCm38) |
I211L |
probably benign |
Het |
Gm13078 |
T |
C |
4: 143,727,033 (GRCm38) |
L237P |
probably damaging |
Het |
Gm13083 |
C |
A |
4: 143,615,232 (GRCm38) |
A77E |
possibly damaging |
Het |
Gm13089 |
T |
G |
4: 143,698,080 (GRCm38) |
Q264H |
probably benign |
Het |
Gm13101 |
C |
T |
4: 143,965,562 (GRCm38) |
E290K |
probably benign |
Het |
Gm13741 |
A |
T |
2: 87,656,421 (GRCm38) |
S167T |
probably damaging |
Het |
Gm13741 |
A |
C |
2: 87,656,877 (GRCm38) |
L15V |
probably benign |
Het |
Gm15127 |
A |
G |
X: 148,695,496 (GRCm38) |
T415A |
probably benign |
Het |
Gm156 |
T |
C |
6: 129,772,463 (GRCm38) |
|
probably null |
Het |
Gm15932 |
G |
C |
14: 55,575,840 (GRCm38) |
|
probably benign |
Het |
Gm1818 |
C |
A |
12: 48,556,124 (GRCm38) |
|
noncoding transcript |
Het |
Gm19965 |
T |
G |
1: 116,804,600 (GRCm38) |
F58V |
probably benign |
Het |
Gm2016 |
A |
C |
12: 87,876,934 (GRCm38) |
E117A |
possibly damaging |
Het |
Gm20939 |
T |
C |
17: 94,877,433 (GRCm38) |
F503S |
probably damaging |
Het |
Gm21834 |
T |
G |
17: 57,742,121 (GRCm38) |
E33D |
possibly damaging |
Het |
Gm266 |
T |
C |
12: 111,485,337 (GRCm38) |
E145G |
probably damaging |
Het |
Gm266 |
C |
G |
12: 111,485,172 (GRCm38) |
G200A |
probably damaging |
Het |
Gm364 |
A |
C |
X: 57,488,638 (GRCm38) |
I668L |
probably benign |
Het |
Gm4775 |
C |
G |
14: 106,100,965 (GRCm38) |
|
noncoding transcript |
Het |
Gm4788 |
T |
A |
1: 139,754,261 (GRCm38) |
Q199L |
probably damaging |
Het |
Gm4884 |
A |
G |
7: 41,042,876 (GRCm38) |
N90D |
possibly damaging |
Het |
Gm4981 |
T |
G |
10: 58,235,911 (GRCm38) |
E160D |
probably damaging |
Het |
Gm5114 |
T |
C |
7: 39,408,447 (GRCm38) |
K583E |
probably damaging |
Het |
Gm5152 |
T |
C |
5: 10,243,130 (GRCm38) |
|
probably benign |
Het |
Gm5565 |
G |
A |
5: 146,158,669 (GRCm38) |
T172I |
probably benign |
Het |
Gm6205 |
C |
A |
5: 94,683,833 (GRCm38) |
A233E |
probably benign |
Het |
Gm7173 |
C |
A |
X: 79,330,813 (GRCm38) |
L2544F |
probably damaging |
Het |
Gm7173 |
A |
T |
X: 79,330,814 (GRCm38) |
L2544* |
probably null |
Het |
Gm8267 |
T |
C |
14: 44,724,865 (GRCm38) |
K33E |
probably benign |
Het |
Gm8674 |
T |
C |
13: 49,901,248 (GRCm38) |
|
noncoding transcript |
Het |
Gm8674 |
C |
A |
13: 49,900,794 (GRCm38) |
|
noncoding transcript |
Het |
Gm904 |
A |
C |
13: 50,645,262 (GRCm38) |
K86Q |
probably damaging |
Het |
Gm9637 |
A |
G |
14: 19,401,731 (GRCm38) |
|
noncoding transcript |
Het |
Gm9758 |
C |
G |
5: 14,913,539 (GRCm38) |
V92L |
probably benign |
Het |
Gm9774 |
A |
G |
3: 92,429,090 (GRCm38) |
S102P |
probably damaging |
Het |
Gm9805 |
A |
G |
17: 22,689,871 (GRCm38) |
Y34C |
probably benign |
Het |
Gm9964 |
T |
C |
11: 79,296,408 (GRCm38) |
E71G |
unknown |
Het |
Gnal |
G |
A |
18: 67,191,403 (GRCm38) |
D210N |
probably damaging |
Het |
Gnas |
A |
G |
2: 174,298,373 (GRCm38) |
S112G |
probably benign |
Het |
Gnat3 |
A |
C |
5: 18,015,323 (GRCm38) |
S228R |
probably damaging |
Het |
Golgb1 |
A |
C |
16: 36,919,742 (GRCm38) |
E2814D |
probably damaging |
Het |
Gorab |
C |
G |
1: 163,386,323 (GRCm38) |
S346T |
possibly damaging |
Het |
Gorab |
C |
A |
1: 163,403,550 (GRCm38) |
E12* |
probably null |
Het |
Gpaa1 |
A |
G |
15: 76,332,542 (GRCm38) |
E142G |
possibly damaging |
Het |
Gpatch8 |
T |
A |
11: 102,480,945 (GRCm38) |
K589I |
unknown |
Het |
Gphb5 |
A |
C |
12: 75,415,807 (GRCm38) |
L3V |
unknown |
Het |
Gpr26 |
AC |
A |
7: 131,984,094 (GRCm38) |
|
probably null |
Het |
Gpr75 |
T |
G |
11: 30,891,139 (GRCm38) |
L15V |
probably benign |
Het |
Gprasp1 |
G |
T |
X: 135,799,441 (GRCm38) |
A128S |
possibly damaging |
Het |
Gpsm2 |
T |
C |
3: 108,700,760 (GRCm38) |
E234G |
probably damaging |
Het |
Grid1 |
G |
A |
14: 35,452,294 (GRCm38) |
R631H |
probably damaging |
Het |
Grm3 |
A |
C |
5: 9,570,183 (GRCm38) |
F354V |
probably damaging |
Het |
Grpel1 |
C |
T |
5: 36,470,614 (GRCm38) |
R80C |
probably damaging |
Het |
Gsdmd |
T |
G |
15: 75,863,474 (GRCm38) |
D22E |
probably benign |
Het |
Gtf2f2 |
C |
T |
14: 75,897,623 (GRCm38) |
G221S |
probably damaging |
Het |
Guca1a |
T |
C |
17: 47,400,410 (GRCm38) |
I4V |
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,743,981 (GRCm38) |
P406L |
probably benign |
Het |
Gykl1 |
T |
A |
18: 52,694,165 (GRCm38) |
Y148* |
probably null |
Het |
H2-T22 |
G |
A |
17: 36,041,638 (GRCm38) |
R132W |
probably benign |
Het |
Hao2 |
A |
C |
3: 98,875,352 (GRCm38) |
V340G |
probably damaging |
Het |
Hapln1 |
A |
G |
13: 89,601,498 (GRCm38) |
H54R |
probably benign |
Het |
Haus6 |
A |
C |
4: 86,602,874 (GRCm38) |
L176V |
possibly damaging |
Het |
Hc |
T |
G |
2: 35,008,249 (GRCm38) |
T1145P |
possibly damaging |
Het |
Hc |
T |
A |
2: 35,029,470 (GRCm38) |
D668V |
probably benign |
Het |
Hccs |
C |
G |
X: 169,313,612 (GRCm38) |
R199T |
probably damaging |
Het |
Hdac9 |
T |
G |
12: 34,407,789 (GRCm38) |
K255T |
probably damaging |
Het |
Hdlbp |
G |
A |
1: 93,431,354 (GRCm38) |
|
probably benign |
Het |
Heatr5a |
G |
A |
12: 51,891,404 (GRCm38) |
A1497V |
probably damaging |
Het |
Heatr5a |
T |
C |
12: 51,951,076 (GRCm38) |
T347A |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,295,503 (GRCm38) |
|
probably null |
Het |
Heph |
T |
A |
X: 96,466,031 (GRCm38) |
V130D |
probably damaging |
Het |
Hephl1 |
A |
T |
9: 15,053,721 (GRCm38) |
L1126H |
probably damaging |
Het |
Herc2 |
G |
T |
7: 56,226,589 (GRCm38) |
C4450F |
probably damaging |
Het |
Herc2 |
C |
A |
7: 56,215,432 (GRCm38) |
A4219D |
probably damaging |
Het |
Herc2 |
G |
A |
7: 56,087,341 (GRCm38) |
A183T |
probably benign |
Het |
Herc2 |
T |
G |
7: 56,215,381 (GRCm38) |
V4202G |
possibly damaging |
Het |
Herc2 |
G |
A |
7: 56,131,292 (GRCm38) |
G1235D |
probably benign |
Het |
Heyl |
GGAAGAAG |
GGAAG |
4: 123,240,181 (GRCm38) |
|
probably benign |
Het |
Hgf |
C |
T |
5: 16,618,919 (GRCm38) |
R705C |
probably damaging |
Het |
Hip1r |
A |
T |
5: 123,999,132 (GRCm38) |
|
probably null |
Het |
Hipk1 |
T |
C |
3: 103,764,544 (GRCm38) |
E413G |
possibly damaging |
Het |
Hipk3 |
G |
A |
2: 104,434,629 (GRCm38) |
S702F |
probably damaging |
Het |
Hmcn1 |
G |
T |
1: 150,648,937 (GRCm38) |
A3414D |
probably damaging |
Het |
Hmcn2 |
C |
A |
2: 31,459,064 (GRCm38) |
|
probably null |
Het |
Hmcn2 |
G |
T |
2: 31,381,067 (GRCm38) |
E1252D |
probably benign |
Het |
Hmg20b |
C |
G |
10: 81,346,573 (GRCm38) |
A310P |
probably damaging |
Het |
Hnrnpab |
T |
G |
11: 51,601,746 (GRCm38) |
|
probably benign |
Het |
Hoxa6 |
G |
C |
6: 52,206,545 (GRCm38) |
F173L |
possibly damaging |
Het |
Hoxc4 |
A |
T |
15: 103,034,763 (GRCm38) |
D14V |
probably damaging |
Het |
Hpdl |
G |
C |
4: 116,820,833 (GRCm38) |
P144A |
probably damaging |
Het |
Hsd3b6 |
T |
G |
3: 98,806,332 (GRCm38) |
K217T |
probably benign |
Het |
Hsf2 |
A |
T |
10: 57,496,168 (GRCm38) |
K72N |
probably damaging |
Het |
Hsf3 |
G |
T |
X: 96,320,316 (GRCm38) |
S193* |
probably null |
Het |
Hsf3 |
A |
T |
X: 96,320,317 (GRCm38) |
S250T |
possibly damaging |
Het |
Hspa13 |
C |
T |
16: 75,758,185 (GRCm38) |
G338S |
probably benign |
Het |
Hspa4l |
C |
G |
3: 40,766,993 (GRCm38) |
S282* |
probably null |
Het |
Hydin |
AGGG |
AGG |
8: 110,592,791 (GRCm38) |
|
probably null |
Het |
Hydin |
G |
T |
8: 110,586,048 (GRCm38) |
K4140N |
probably benign |
Het |
Hydin |
A |
G |
8: 110,299,973 (GRCm38) |
K108E |
probably benign |
Het |
I830077J02Rik |
C |
A |
3: 105,927,213 (GRCm38) |
A42S |
probably damaging |
Het |
Iars |
G |
A |
13: 49,721,088 (GRCm38) |
S746N |
probably benign |
Het |
Ifi203 |
A |
T |
1: 173,928,581 (GRCm38) |
|
probably benign |
Het |
Ifi206 |
T |
G |
1: 173,474,011 (GRCm38) |
E700D |
probably damaging |
Het |
Ifi209 |
A |
G |
1: 173,641,146 (GRCm38) |
K181E |
probably benign |
Het |
Ifi209 |
A |
C |
1: 173,637,407 (GRCm38) |
K34N |
probably damaging |
Het |
Ifi211 |
A |
T |
1: 173,907,660 (GRCm38) |
F68I |
possibly damaging |
Het |
Ifna16 |
C |
A |
4: 88,676,378 (GRCm38) |
S160I |
probably damaging |
Het |
Ift52 |
A |
C |
2: 163,023,358 (GRCm38) |
D43A |
possibly damaging |
Het |
Ighv13-2 |
G |
T |
12: 114,357,815 (GRCm38) |
Y82* |
probably null |
Het |
Ighv1-37 |
A |
T |
12: 114,896,624 (GRCm38) |
|
probably benign |
Het |
Ighv15-2 |
T |
G |
12: 114,564,804 (GRCm38) |
D43A |
probably damaging |
Het |
Ighv1-69 |
A |
C |
12: 115,623,253 (GRCm38) |
S87A |
probably benign |
Het |
Ighv5-9-1 |
C |
G |
12: 113,736,120 (GRCm38) |
C124S |
probably damaging |
Het |
Ighv7-4 |
A |
C |
12: 114,222,897 (GRCm38) |
V85G |
probably damaging |
Het |
Igkv12-98 |
C |
A |
6: 68,571,031 (GRCm38) |
T48N |
probably benign |
Het |
Igkv18-36 |
C |
A |
6: 69,992,499 (GRCm38) |
V104F |
probably damaging |
Het |
Igkv2-112 |
G |
A |
6: 68,220,647 (GRCm38) |
S101N |
possibly damaging |
Het |
Igkv5-48 |
C |
A |
6: 69,726,691 (GRCm38) |
G77W |
probably damaging |
Het |
Igsf10 |
C |
T |
3: 59,329,938 (GRCm38) |
V941I |
possibly damaging |
Het |
Ik |
C |
T |
18: 36,744,782 (GRCm38) |
R4* |
probably null |
Het |
Il11 |
G |
A |
7: 4,775,999 (GRCm38) |
S44F |
probably damaging |
Het |
Il18r1 |
C |
A |
1: 40,478,486 (GRCm38) |
S136Y |
probably damaging |
Het |
Il18r1 |
A |
C |
1: 40,474,751 (GRCm38) |
K39T |
probably damaging |
Het |
Il3ra |
G |
A |
14: 14,351,129 (GRCm38) |
R217Q |
probably benign |
Het |
Inpp4b |
G |
A |
8: 82,068,931 (GRCm38) |
|
probably null |
Het |
Inpp5f |
C |
G |
7: 128,694,949 (GRCm38) |
T381R |
probably benign |
Het |
Insm2 |
C |
G |
12: 55,599,797 (GRCm38) |
P109A |
probably damaging |
Het |
Ints11 |
G |
A |
4: 155,886,970 (GRCm38) |
D292N |
probably benign |
Het |
Ipo13 |
T |
C |
4: 117,904,680 (GRCm38) |
E441G |
probably benign |
Het |
Iqub |
C |
T |
6: 24,500,243 (GRCm38) |
|
probably null |
Het |
Itga2 |
G |
A |
13: 114,857,332 (GRCm38) |
P762S |
possibly damaging |
Het |
Itga7 |
T |
A |
10: 128,949,163 (GRCm38) |
I787N |
probably benign |
Het |
Itgb1 |
T |
G |
8: 128,713,369 (GRCm38) |
F180V |
probably damaging |
Het |
Itgb6 |
C |
T |
2: 60,620,211 (GRCm38) |
R628Q |
probably null |
Het |
Itk |
A |
C |
11: 46,353,862 (GRCm38) |
|
probably null |
Het |
Itpr3 |
C |
T |
17: 27,113,528 (GRCm38) |
S1782L |
possibly damaging |
Het |
Itsn2 |
A |
C |
12: 4,712,472 (GRCm38) |
S1578R |
probably damaging |
Het |
Izumo3 |
C |
T |
4: 92,146,933 (GRCm38) |
A16T |
probably damaging |
Het |
Jag1 |
C |
A |
2: 137,085,151 (GRCm38) |
W896L |
probably benign |
Het |
Jakmip1 |
A |
T |
5: 37,120,986 (GRCm38) |
I536F |
probably damaging |
Het |
Jmjd1c |
T |
C |
10: 67,238,174 (GRCm38) |
L1896P |
probably benign |
Het |
Jmy |
T |
A |
13: 93,441,081 (GRCm38) |
S860C |
probably damaging |
Het |
Jph2 |
G |
C |
2: 163,397,332 (GRCm38) |
S65R |
possibly damaging |
Het |
Jrk |
T |
C |
15: 74,707,394 (GRCm38) |
K14R |
unknown |
Het |
Kat6a |
C |
T |
8: 22,935,501 (GRCm38) |
R1021* |
probably null |
Het |
Kbtbd11 |
C |
G |
8: 15,027,839 (GRCm38) |
P146R |
probably damaging |
Het |
Kcna3 |
C |
A |
3: 107,036,953 (GRCm38) |
F177L |
probably damaging |
Het |
Kcna7 |
T |
G |
7: 45,406,959 (GRCm38) |
F200V |
probably benign |
Het |
Kcna7 |
A |
T |
7: 45,409,105 (GRCm38) |
K272M |
probably damaging |
Het |
Kcnb1 |
G |
C |
2: 167,188,061 (GRCm38) |
A188G |
probably benign |
Het |
Kcnb2 |
C |
T |
1: 15,711,028 (GRCm38) |
S708L |
probably benign |
Het |
Kcnb2 |
A |
C |
1: 15,710,091 (GRCm38) |
I396L |
probably benign |
Het |
Kcnh5 |
A |
C |
12: 74,965,295 (GRCm38) |
F617V |
possibly damaging |
Het |
Kcnh5 |
C |
T |
12: 74,897,761 (GRCm38) |
A905T |
probably benign |
Het |
Kcnh6 |
T |
G |
11: 106,009,048 (GRCm38) |
F48V |
probably damaging |
Het |
Kcnh7 |
G |
A |
2: 63,184,068 (GRCm38) |
R4C |
probably damaging |
Het |
Kcnh7 |
A |
C |
2: 62,736,103 (GRCm38) |
L828R |
probably damaging |
Het |
Kcnh8 |
A |
G |
17: 52,978,292 (GRCm38) |
S1097G |
probably benign |
Het |
Kcnh8 |
G |
C |
17: 52,725,890 (GRCm38) |
K68N |
probably damaging |
Het |
Kcnj15 |
A |
G |
16: 95,296,119 (GRCm38) |
K200R |
probably damaging |
Het |
Kcnk9 |
T |
A |
15: 72,546,015 (GRCm38) |
T89S |
possibly damaging |
Het |
Kcnn3 |
A |
T |
3: 89,667,130 (GRCm38) |
S650C |
probably damaging |
Het |
Kcnq5 |
G |
A |
1: 21,457,529 (GRCm38) |
P440L |
probably damaging |
Het |
Kcnt2 |
G |
A |
1: 140,584,158 (GRCm38) |
W1017* |
probably null |
Het |
Kcnt2 |
G |
T |
1: 140,573,646 (GRCm38) |
D917Y |
probably damaging |
Het |
Kctd19 |
A |
C |
8: 105,385,335 (GRCm38) |
L826R |
probably benign |
Het |
Kctd2 |
A |
G |
11: 115,421,987 (GRCm38) |
E115G |
possibly damaging |
Het |
Khdrbs2 |
T |
C |
1: 32,244,055 (GRCm38) |
|
probably benign |
Het |
Khsrp |
C |
T |
17: 57,024,249 (GRCm38) |
R443Q |
probably damaging |
Het |
Kif12 |
GGGGC |
GGGGCCTCCACCCGGCGGGC |
4: 63,171,423 (GRCm38) |
|
probably benign |
Het |
Kif18b |
T |
G |
11: 102,908,157 (GRCm38) |
K739N |
probably benign |
Het |
Kif20b |
G |
C |
19: 34,950,451 (GRCm38) |
E1038Q |
probably damaging |
Het |
Kif24 |
C |
A |
4: 41,395,091 (GRCm38) |
S594I |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,288,033 (GRCm38) |
Q1315H |
probably benign |
Het |
Klhl22 |
T |
G |
16: 17,776,543 (GRCm38) |
F179V |
possibly damaging |
Het |
Klhl26 |
T |
G |
8: 70,451,799 (GRCm38) |
E426A |
probably damaging |
Het |
Klhl41 |
A |
C |
2: 69,674,730 (GRCm38) |
K459T |
possibly damaging |
Het |
Klk1b1 |
A |
C |
7: 43,970,401 (GRCm38) |
K128T |
probably benign |
Het |
Klk1b26 |
A |
T |
7: 44,015,996 (GRCm38) |
Q109H |
probably benign |
Het |
Klk1b3 |
G |
A |
7: 44,200,305 (GRCm38) |
W38* |
probably null |
Het |
Klk6 |
T |
C |
7: 43,828,488 (GRCm38) |
S95P |
probably benign |
Het |
Klk9 |
G |
A |
7: 43,794,311 (GRCm38) |
G83D |
probably damaging |
Het |
Klra2 |
A |
C |
6: 131,228,290 (GRCm38) |
L196R |
probably damaging |
Het |
Kmt2b |
G |
T |
7: 30,585,251 (GRCm38) |
Q739K |
probably benign |
Het |
Kprp |
G |
A |
3: 92,825,057 (GRCm38) |
Q229* |
probably null |
Het |
Kptn |
T |
C |
7: 16,123,070 (GRCm38) |
L161P |
probably damaging |
Het |
Kri1 |
C |
A |
9: 21,274,122 (GRCm38) |
E639D |
probably benign |
Het |
Krt32 |
C |
T |
11: 100,088,216 (GRCm38) |
S4N |
probably benign |
Het |
Krt36 |
A |
T |
11: 100,104,189 (GRCm38) |
L186M |
possibly damaging |
Het |
Krt75 |
C |
G |
15: 101,573,665 (GRCm38) |
G56A |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,890,551 (GRCm38) |
L233P |
probably damaging |
Het |
Krt78 |
C |
T |
15: 101,947,331 (GRCm38) |
E682K |
possibly damaging |
Het |
Krtap6-3 |
G |
A |
16: 89,084,165 (GRCm38) |
C28Y |
unknown |
Het |
Ksr1 |
G |
C |
11: 79,044,879 (GRCm38) |
|
probably null |
Het |
Ksr2 |
A |
C |
5: 117,747,402 (GRCm38) |
T764P |
probably damaging |
Het |
Lama1 |
G |
T |
17: 67,810,171 (GRCm38) |
G2487V |
probably damaging |
Het |
Lama1 |
G |
A |
17: 67,771,082 (GRCm38) |
G1171S |
probably benign |
Het |
Lama1 |
G |
A |
17: 67,752,883 (GRCm38) |
D656N |
probably benign |
Het |
Large1 |
C |
T |
8: 72,912,103 (GRCm38) |
W282* |
probably null |
Het |
Lce1e |
A |
G |
3: 92,707,849 (GRCm38) |
C64R |
unknown |
Het |
Lce1f |
T |
C |
3: 92,719,254 (GRCm38) |
K32R |
unknown |
Het |
Lce1i |
C |
A |
3: 92,777,289 (GRCm38) |
|
probably null |
Het |
Lefty2 |
A |
T |
1: 180,897,715 (GRCm38) |
R337W |
probably damaging |
Het |
Lelp1 |
T |
A |
3: 92,135,598 (GRCm38) |
K48M |
unknown |
Het |
Lenep |
C |
G |
3: 89,402,569 (GRCm38) |
G24A |
probably damaging |
Het |
Lgr6 |
C |
T |
1: 134,988,071 (GRCm38) |
G313E |
possibly damaging |
Het |
Lhb |
A |
C |
7: 45,421,730 (GRCm38) |
|
probably null |
Het |
Lipo2 |
T |
C |
19: 33,721,685 (GRCm38) |
Y315C |
probably damaging |
Het |
Lmbr1 |
C |
A |
5: 29,323,816 (GRCm38) |
A110S |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,182,851 (GRCm38) |
S1377G |
probably benign |
Het |
Lpcat2b |
C |
T |
5: 107,433,311 (GRCm38) |
P169S |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,892,231 (GRCm38) |
F12S |
probably damaging |
Het |
Lrfn3 |
A |
C |
7: 30,360,201 (GRCm38) |
F200V |
probably damaging |
Het |
Lrif1 |
G |
A |
3: 106,732,570 (GRCm38) |
D324N |
probably benign |
Het |
Lrp1 |
G |
A |
10: 127,584,379 (GRCm38) |
R912C |
probably damaging |
Het |
Lrp10 |
A |
C |
14: 54,467,922 (GRCm38) |
T190P |
probably benign |
Het |
Lrpprc |
C |
T |
17: 84,770,500 (GRCm38) |
|
probably null |
Het |
Lrpprc |
G |
A |
17: 84,731,784 (GRCm38) |
Q923* |
probably null |
Het |
Lrrc18 |
C |
T |
14: 33,008,510 (GRCm38) |
A2V |
probably damaging |
Het |
Lrrc28 |
T |
G |
7: 67,529,631 (GRCm38) |
K329T |
possibly damaging |
Het |
Lrrc30 |
T |
C |
17: 67,631,695 (GRCm38) |
K297E |
possibly damaging |
Het |
Lrrc32 |
G |
A |
7: 98,499,060 (GRCm38) |
R349K |
probably benign |
Het |
Lrrc45 |
G |
T |
11: 120,720,231 (GRCm38) |
V572F |
probably damaging |
Het |
Lrrc52 |
C |
A |
1: 167,466,494 (GRCm38) |
G74V |
possibly damaging |
Het |
Lrrc63 |
C |
T |
14: 75,125,990 (GRCm38) |
E234K |
possibly damaging |
Het |
Lrrfip1 |
GAAGAACAAGAA |
GAAGAA |
1: 91,115,530 (GRCm38) |
|
probably benign |
Het |
Lrriq1 |
T |
A |
10: 103,202,446 (GRCm38) |
N832I |
probably damaging |
Het |
Lrrk2 |
T |
G |
15: 91,726,240 (GRCm38) |
V725G |
probably benign |
Het |
Ltbp4 |
C |
T |
7: 27,307,792 (GRCm38) |
A1364T |
probably damaging |
Het |
Luc7l |
T |
G |
17: 26,267,255 (GRCm38) |
L136R |
probably damaging |
Het |
Luc7l2 |
A |
C |
6: 38,603,369 (GRCm38) |
|
probably benign |
Het |
Lypd8 |
A |
C |
11: 58,386,730 (GRCm38) |
T113P |
possibly damaging |
Het |
Lyst |
A |
T |
13: 13,743,433 (GRCm38) |
Q3359H |
probably benign |
Het |
Lyzl1 |
A |
C |
18: 4,181,156 (GRCm38) |
K114T |
probably damaging |
Het |
Magel2 |
G |
T |
7: 62,378,977 (GRCm38) |
R543L |
possibly damaging |
Het |
Mak16 |
A |
G |
8: 31,166,095 (GRCm38) |
L120P |
probably damaging |
Het |
Man2b2 |
C |
T |
5: 36,815,356 (GRCm38) |
D605N |
possibly damaging |
Het |
Map10 |
CGGG |
CGG |
8: 125,671,931 (GRCm38) |
|
probably null |
Het |
Map1b |
T |
G |
13: 99,508,115 (GRCm38) |
E93D |
probably benign |
Het |
Map1s |
T |
G |
8: 70,916,449 (GRCm38) |
F881V |
possibly damaging |
Het |
Map3k3 |
G |
A |
11: 106,150,353 (GRCm38) |
D383N |
possibly damaging |
Het |
Map3k6 |
C |
G |
4: 133,245,066 (GRCm38) |
H318D |
probably damaging |
Het |
Mapk13 |
A |
G |
17: 28,777,533 (GRCm38) |
E245G |
possibly damaging |
Het |
Mapkapk5 |
C |
T |
5: 121,531,591 (GRCm38) |
E115K |
probably benign |
Het |
March10 |
C |
A |
11: 105,390,359 (GRCm38) |
G367W |
probably damaging |
Het |
Marveld3 |
G |
A |
8: 109,948,063 (GRCm38) |
R374C |
possibly damaging |
Het |
Mast4 |
T |
G |
13: 102,738,519 (GRCm38) |
K1255T |
probably damaging |
Het |
Maz |
GGCCCTG |
GG |
7: 127,024,474 (GRCm38) |
|
probably null |
Het |
Mcf2 |
T |
C |
X: 60,178,713 (GRCm38) |
H65R |
probably benign |
Het |
Mcm6 |
T |
G |
1: 128,344,298 (GRCm38) |
N454T |
probably damaging |
Het |
Mcpt4 |
T |
A |
14: 56,060,510 (GRCm38) |
R195* |
probably null |
Het |
Mdm1 |
A |
C |
10: 118,158,362 (GRCm38) |
K380N |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,994,547 (GRCm38) |
S286P |
probably benign |
Het |
Med13l |
C |
A |
5: 118,749,641 (GRCm38) |
T1660K |
probably damaging |
Het |
Med14 |
A |
C |
X: 12,677,606 (GRCm38) |
L1451R |
probably damaging |
Het |
Megf11 |
A |
T |
9: 64,660,476 (GRCm38) |
S416C |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,339,669 (GRCm38) |
E902K |
possibly damaging |
Het |
Mep1a |
C |
G |
17: 43,491,596 (GRCm38) |
W192C |
probably damaging |
Het |
Mfap3 |
T |
A |
11: 57,528,142 (GRCm38) |
F43I |
possibly damaging |
Het |
Mfhas1 |
C |
G |
8: 35,590,236 (GRCm38) |
P622A |
probably benign |
Het |
Mgam |
G |
C |
6: 40,643,060 (GRCm38) |
V28L |
probably benign |
Het |
Mgp |
T |
G |
6: 136,874,263 (GRCm38) |
|
probably null |
Het |
Micall2 |
A |
C |
5: 139,716,295 (GRCm38) |
L398V |
probably benign |
Het |
Micall2 |
T |
A |
5: 139,706,894 (GRCm38) |
K908M |
probably damaging |
Het |
Mill2 |
G |
A |
7: 18,856,399 (GRCm38) |
|
probably null |
Het |
Mir1966 |
C |
T |
8: 105,615,571 (GRCm38) |
R130* |
probably null |
Het |
Mkrn1 |
T |
A |
6: 39,400,456 (GRCm38) |
N282Y |
probably null |
Het |
Mkx |
C |
T |
18: 6,936,975 (GRCm38) |
A319T |
probably damaging |
Het |
Mn1 |
T |
A |
5: 111,418,280 (GRCm38) |
F39I |
possibly damaging |
Het |
Morc2b |
A |
T |
17: 33,136,086 (GRCm38) |
I904N |
possibly damaging |
Het |
Mpo |
T |
G |
11: 87,795,245 (GRCm38) |
F74V |
probably benign |
Het |
Mpv17l2 |
T |
G |
8: 70,759,410 (GRCm38) |
K139T |
probably damaging |
Het |
Mrgprb4 |
A |
G |
7: 48,198,682 (GRCm38) |
L166P |
possibly damaging |
Het |
Mrgprg |
C |
G |
7: 143,764,656 (GRCm38) |
A240P |
probably damaging |
Het |
Mrgprx1 |
T |
G |
7: 48,021,129 (GRCm38) |
K290T |
probably damaging |
Het |
Mroh5 |
G |
A |
15: 73,788,031 (GRCm38) |
A320V |
possibly damaging |
Het |
Mrpl1 |
T |
G |
5: 96,262,069 (GRCm38) |
M267R |
probably damaging |
Het |
Mrpl2 |
A |
G |
17: 46,647,478 (GRCm38) |
K62R |
probably null |
Het |
Mrps36 |
T |
G |
13: 100,739,133 (GRCm38) |
S58R |
possibly damaging |
Het |
Msantd3 |
A |
C |
4: 48,552,525 (GRCm38) |
D38A |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,133,200 (GRCm38) |
P547L |
probably benign |
Het |
Mta3 |
A |
G |
17: 83,762,914 (GRCm38) |
D16G |
probably benign |
Het |
Mtcl1 |
C |
T |
17: 66,343,728 (GRCm38) |
A1132T |
probably benign |
Het |
Mtf2 |
A |
G |
5: 108,087,329 (GRCm38) |
D139G |
probably damaging |
Het |
Mthfd1l |
T |
G |
10: 4,007,844 (GRCm38) |
F294V |
probably benign |
Het |
Mtus2 |
G |
A |
5: 148,303,263 (GRCm38) |
|
probably benign |
Het |
Muc4 |
A |
T |
16: 32,756,076 (GRCm38) |
|
probably benign |
Het |
Muc5ac |
A |
C |
7: 141,811,692 (GRCm38) |
T1984P |
possibly damaging |
Het |
Muc5ac |
C |
T |
7: 141,809,744 (GRCm38) |
|
probably benign |
Het |
Muc5b |
A |
G |
7: 141,862,214 (GRCm38) |
S2966G |
probably benign |
Het |
Mup3 |
G |
C |
4: 62,087,189 (GRCm38) |
L15V |
unknown |
Het |
Mvd |
G |
C |
8: 122,439,730 (GRCm38) |
A56G |
probably benign |
Het |
Mvk |
G |
T |
5: 114,458,934 (GRCm38) |
G321W |
probably damaging |
Het |
Mxra7 |
G |
T |
11: 116,804,606 (GRCm38) |
N157K |
probably benign |
Het |
Mybpc2 |
T |
C |
7: 44,516,503 (GRCm38) |
K256R |
possibly damaging |
Het |
Mybpc3 |
A |
G |
2: 91,135,359 (GRCm38) |
E1172G |
probably benign |
Het |
Myh11 |
AGG |
AG |
16: 14,269,262 (GRCm38) |
|
probably null |
Het |
Myh2 |
GTATTTATTTA |
GTATTTA |
11: 67,180,763 (GRCm38) |
|
probably benign |
Het |
Myh2 |
C |
T |
11: 67,191,449 (GRCm38) |
L1326F |
probably damaging |
Het |
Myh6 |
C |
T |
14: 54,956,997 (GRCm38) |
R725H |
probably damaging |
Het |
Myh8 |
A |
C |
11: 67,298,592 (GRCm38) |
K1198T |
probably damaging |
Het |
Myh9 |
A |
G |
15: 77,775,258 (GRCm38) |
L96P |
probably damaging |
Het |
Myo18b |
G |
A |
5: 112,692,943 (GRCm38) |
S2328L |
possibly damaging |
Het |
Myo18b |
C |
T |
5: 112,757,484 (GRCm38) |
E2083K |
probably benign |
Het |
Myo1d |
T |
G |
11: 80,674,898 (GRCm38) |
N367T |
probably benign |
Het |
Myo5b |
G |
C |
18: 74,744,749 (GRCm38) |
E1606D |
probably benign |
Het |
Myo5c |
C |
G |
9: 75,245,059 (GRCm38) |
S76R |
probably damaging |
Het |
Myrf |
C |
A |
19: 10,221,298 (GRCm38) |
Q195H |
probably damaging |
Het |
Nacc1 |
G |
C |
8: 84,673,286 (GRCm38) |
A434G |
probably damaging |
Het |
Naip2 |
A |
T |
13: 100,161,909 (GRCm38) |
Y540N |
probably benign |
Het |
Nap1l2 |
T |
G |
X: 103,185,196 (GRCm38) |
N372T |
probably damaging |
Het |
Nat8 |
G |
T |
6: 85,831,193 (GRCm38) |
|
probably benign |
Het |
Nav1 |
T |
C |
1: 135,470,724 (GRCm38) |
T707A |
probably benign |
Het |
Nbea |
G |
A |
3: 55,723,163 (GRCm38) |
T2251I |
probably benign |
Het |
Nbeal2 |
G |
C |
9: 110,632,372 (GRCm38) |
A1536G |
possibly damaging |
Het |
Ncapg |
T |
G |
5: 45,679,880 (GRCm38) |
L431R |
probably damaging |
Het |
Nck2 |
A |
C |
1: 43,554,383 (GRCm38) |
N250T |
possibly damaging |
Het |
Nckap5 |
G |
A |
1: 126,024,832 (GRCm38) |
R1264C |
possibly damaging |
Het |
Nckipsd |
G |
C |
9: 108,814,677 (GRCm38) |
K492N |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,067,788 (GRCm38) |
S597C |
unknown |
Het |
Ncor2 |
C |
T |
5: 125,086,840 (GRCm38) |
|
probably null |
Het |
Ndn |
T |
G |
7: 62,349,134 (GRCm38) |
F243V |
probably damaging |
Het |
Ndufs6 |
A |
G |
13: 73,328,436 (GRCm38) |
V4A |
probably benign |
Het |
Neb |
T |
A |
2: 52,308,567 (GRCm38) |
K423M |
probably damaging |
Het |
Neb |
G |
C |
2: 52,223,152 (GRCm38) |
P7A |
probably benign |
Het |
Neb |
C |
T |
2: 52,169,872 (GRCm38) |
V2321I |
possibly damaging |
Het |
Nedd4 |
G |
A |
9: 72,670,078 (GRCm38) |
V62M |
probably benign |
Het |
Nek7 |
C |
A |
1: 138,515,625 (GRCm38) |
V197L |
probably null |
Het |
Nelfcd |
GTT |
GT |
2: 174,426,494 (GRCm38) |
|
probably null |
Het |
Nell2 |
A |
T |
15: 95,435,097 (GRCm38) |
L194M |
probably damaging |
Het |
Neurod6 |
G |
A |
6: 55,679,362 (GRCm38) |
Q97* |
probably null |
Het |
Nfkbiz |
G |
C |
16: 55,816,438 (GRCm38) |
A500G |
probably damaging |
Het |
Nfkbiz |
T |
C |
16: 55,818,236 (GRCm38) |
Y287C |
probably damaging |
Het |
Nfrkb |
A |
C |
9: 31,411,333 (GRCm38) |
S900R |
possibly damaging |
Het |
Nipbl |
T |
A |
15: 8,307,882 (GRCm38) |
E2065D |
probably damaging |
Het |
Nkapl |
C |
G |
13: 21,468,303 (GRCm38) |
G47R |
unknown |
Het |
Nlrc5 |
A |
G |
8: 94,504,464 (GRCm38) |
D1275G |
possibly damaging |
Het |
Nlrp12 |
T |
C |
7: 3,222,537 (GRCm38) |
K1034R |
probably benign |
Het |
Nlrp14 |
T |
G |
7: 107,186,622 (GRCm38) |
L635R |
probably damaging |
Het |
Nlrp3 |
G |
C |
11: 59,551,860 (GRCm38) |
S746T |
possibly damaging |
Het |
Nlrp4a |
T |
C |
7: 26,454,163 (GRCm38) |
V713A |
probably benign |
Het |
Nlrp4c |
A |
C |
7: 6,066,636 (GRCm38) |
K512T |
probably damaging |
Het |
Nlrp4f |
C |
T |
13: 65,194,302 (GRCm38) |
E510K |
probably benign |
Het |
Nlrp4g |
T |
G |
9: 124,349,201 (GRCm38) |
|
noncoding transcript |
Het |
Nlrp5 |
T |
C |
7: 23,417,586 (GRCm38) |
L245P |
probably damaging |
Het |
Nlrp5 |
G |
A |
7: 23,404,167 (GRCm38) |
E20K |
possibly damaging |
Het |
Nlrp9b |
T |
G |
7: 20,023,743 (GRCm38) |
F302V |
probably benign |
Het |
Nme8 |
T |
A |
13: 19,688,957 (GRCm38) |
E172D |
possibly damaging |
Het |
Nnt |
G |
A |
13: 119,338,446 (GRCm38) |
S649L |
probably damaging |
Het |
Nod2 |
G |
C |
8: 88,664,146 (GRCm38) |
Q345H |
probably damaging |
Het |
Nol4 |
C |
T |
18: 22,921,902 (GRCm38) |
S157N |
probably damaging |
Het |
Nolc1 |
G |
T |
19: 46,083,098 (GRCm38) |
|
probably benign |
Het |
Notch1 |
T |
G |
2: 26,477,115 (GRCm38) |
D680A |
probably damaging |
Het |
Notch3 |
C |
G |
17: 32,158,652 (GRCm38) |
G150A |
possibly damaging |
Het |
Notch4 |
C |
T |
17: 34,587,915 (GRCm38) |
P1942L |
probably damaging |
Het |
Nr3c2 |
C |
A |
8: 76,908,632 (GRCm38) |
Q121K |
possibly damaging |
Het |
Nr4a2 |
C |
T |
2: 57,111,614 (GRCm38) |
G213S |
probably damaging |
Het |
Nrg1 |
G |
C |
8: 31,918,005 (GRCm38) |
L67V |
possibly damaging |
Het |
Nrxn1 |
T |
A |
17: 90,059,505 (GRCm38) |
D31V |
probably damaging |
Het |
Nsd1 |
A |
C |
13: 55,213,848 (GRCm38) |
S210R |
possibly damaging |
Het |
Nsd2 |
T |
C |
5: 33,855,738 (GRCm38) |
|
probably null |
Het |
Nsd3 |
CCTTCT |
CCT |
8: 25,641,002 (GRCm38) |
|
probably benign |
Het |
Nsun2 |
A |
T |
13: 69,615,465 (GRCm38) |
K103M |
probably damaging |
Het |
Ntn5 |
G |
C |
7: 45,694,203 (GRCm38) |
G322A |
probably damaging |
Het |
Nudt4 |
C |
T |
10: 95,552,515 (GRCm38) |
G60S |
probably benign |
Het |
Nup214 |
T |
C |
2: 32,011,223 (GRCm38) |
F940L |
probably benign |
Het |
Nxpe5 |
G |
A |
5: 138,240,914 (GRCm38) |
|
probably null |
Het |
Nxph2 |
G |
T |
2: 23,400,217 (GRCm38) |
A194S |
probably benign |
Het |
Oaz1 |
C |
G |
10: 80,826,829 (GRCm38) |
R24G |
possibly damaging |
Het |
Obox2 |
A |
G |
7: 15,397,338 (GRCm38) |
K123R |
possibly damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Oca2 |
G |
T |
7: 56,330,375 (GRCm38) |
K609N |
probably null |
Het |
Ocln |
G |
A |
13: 100,535,052 (GRCm38) |
R266* |
probably null |
Het |
Ocstamp |
C |
A |
2: 165,395,918 (GRCm38) |
Q475H |
possibly damaging |
Het |
Odf1 |
A |
G |
15: 38,219,674 (GRCm38) |
Y82C |
probably benign |
Het |
Ogdh |
A |
C |
11: 6,355,427 (GRCm38) |
D978A |
probably benign |
Het |
Olfm3 |
G |
T |
3: 114,904,668 (GRCm38) |
|
probably benign |
Het |
Olfm5 |
T |
G |
7: 104,154,150 (GRCm38) |
S294R |
probably damaging |
Het |
Olfr1014 |
T |
G |
2: 85,777,122 (GRCm38) |
D179E |
probably damaging |
Het |
Olfr1026 |
T |
G |
2: 85,923,798 (GRCm38) |
F177V |
probably damaging |
Het |
Olfr103 |
A |
C |
17: 37,336,705 (GRCm38) |
F176V |
probably damaging |
Het |
Olfr1033 |
T |
C |
2: 86,041,719 (GRCm38) |
S135P |
probably damaging |
Het |
Olfr1036 |
G |
T |
2: 86,075,323 (GRCm38) |
E194D |
possibly damaging |
Het |
Olfr1037 |
C |
T |
2: 86,084,982 (GRCm38) |
S265N |
probably benign |
Het |
Olfr1047 |
C |
A |
2: 86,228,222 (GRCm38) |
V250F |
probably damaging |
Het |
Olfr1056 |
A |
T |
2: 86,355,893 (GRCm38) |
I163N |
probably benign |
Het |
Olfr1058 |
T |
C |
2: 86,385,756 (GRCm38) |
I221V |
probably benign |
Het |
Olfr1058 |
T |
G |
2: 86,386,179 (GRCm38) |
K80Q |
probably damaging |
Het |
Olfr1080 |
C |
T |
2: 86,553,966 (GRCm38) |
A53T |
probably benign |
Het |
Olfr1093 |
A |
G |
2: 86,786,473 (GRCm38) |
K248E |
probably damaging |
Het |
Olfr1099 |
T |
G |
2: 86,958,666 (GRCm38) |
K264T |
probably benign |
Het |
Olfr1106 |
A |
C |
2: 87,048,433 (GRCm38) |
L268V |
probably benign |
Het |
Olfr1113 |
T |
G |
2: 87,213,778 (GRCm38) |
I295M |
possibly damaging |
Het |
Olfr1116 |
G |
T |
2: 87,269,575 (GRCm38) |
G265* |
probably null |
Het |
Olfr1124 |
A |
G |
2: 87,435,159 (GRCm38) |
Y224C |
probably damaging |
Het |
Olfr1129 |
T |
C |
2: 87,575,680 (GRCm38) |
S199P |
possibly damaging |
Het |
Olfr1140 |
G |
T |
2: 87,746,489 (GRCm38) |
A98S |
probably damaging |
Het |
Olfr1145 |
C |
A |
2: 87,810,746 (GRCm38) |
L309I |
probably damaging |
Het |
Olfr1153 |
G |
A |
2: 87,896,633 (GRCm38) |
A145T |
probably benign |
Het |
Olfr1154 |
A |
C |
2: 87,903,584 (GRCm38) |
F31V |
possibly damaging |
Het |
Olfr1155 |
G |
A |
2: 87,943,448 (GRCm38) |
P60L |
probably damaging |
Het |
Olfr116 |
G |
T |
17: 37,624,429 (GRCm38) |
L69M |
probably damaging |
Het |
Olfr1193 |
T |
G |
2: 88,678,664 (GRCm38) |
F263V |
probably damaging |
Het |
Olfr1198 |
A |
C |
2: 88,746,578 (GRCm38) |
F103L |
probably damaging |
Het |
Olfr120 |
T |
A |
17: 37,726,092 (GRCm38) |
F23I |
probably damaging |
Het |
Olfr1215 |
C |
A |
2: 89,001,838 (GRCm38) |
G150V |
possibly damaging |
Het |
Olfr1259 |
A |
G |
2: 89,943,770 (GRCm38) |
V115A |
probably benign |
Het |
Olfr1276 |
T |
G |
2: 111,257,859 (GRCm38) |
V248G |
possibly damaging |
Het |
Olfr1287 |
T |
C |
2: 111,449,457 (GRCm38) |
F106L |
probably benign |
Het |
Olfr1294 |
A |
C |
2: 111,537,814 (GRCm38) |
I158M |
possibly damaging |
Het |
Olfr1329 |
A |
C |
4: 118,916,588 (GRCm38) |
L293R |
probably damaging |
Het |
Olfr1341 |
A |
G |
4: 118,710,226 (GRCm38) |
K273R |
probably benign |
Het |
Olfr1387 |
T |
G |
11: 49,460,456 (GRCm38) |
L259R |
probably damaging |
Het |
Olfr1412 |
T |
A |
1: 92,588,551 (GRCm38) |
S74T |
probably damaging |
Het |
Olfr1424 |
T |
C |
19: 12,059,129 (GRCm38) |
T208A |
probably benign |
Het |
Olfr1431 |
A |
C |
19: 12,210,490 (GRCm38) |
K308T |
possibly damaging |
Het |
Olfr1432 |
C |
A |
19: 12,229,224 (GRCm38) |
W107C |
probably damaging |
Het |
Olfr1440 |
A |
C |
19: 12,394,299 (GRCm38) |
K12T |
probably benign |
Het |
Olfr1444 |
T |
C |
19: 12,862,284 (GRCm38) |
C170R |
probably damaging |
Het |
Olfr1453 |
A |
C |
19: 13,028,027 (GRCm38) |
F101V |
probably benign |
Het |
Olfr146 |
A |
C |
9: 39,018,789 (GRCm38) |
F251V |
probably damaging |
Het |
Olfr1471 |
T |
C |
19: 13,445,849 (GRCm38) |
V279A |
possibly damaging |
Het |
Olfr1480 |
T |
G |
19: 13,529,852 (GRCm38) |
F104V |
possibly damaging |
Het |
Olfr1489 |
C |
A |
19: 13,633,453 (GRCm38) |
A114E |
probably damaging |
Het |
Olfr1495 |
C |
A |
19: 13,768,416 (GRCm38) |
P25T |
probably benign |
Het |
Olfr1499 |
A |
C |
19: 13,815,548 (GRCm38) |
L14R |
probably damaging |
Het |
Olfr1509 |
C |
A |
14: 52,451,209 (GRCm38) |
F265L |
probably benign |
Het |
Olfr152 |
G |
T |
2: 87,782,628 (GRCm38) |
L29F |
probably damaging |
Het |
Olfr154 |
C |
T |
2: 85,663,616 (GRCm38) |
V273I |
probably benign |
Het |
Olfr16 |
T |
A |
1: 172,957,324 (GRCm38) |
F176L |
probably damaging |
Het |
Olfr166 |
T |
C |
16: 19,487,048 (GRCm38) |
L70P |
possibly damaging |
Het |
Olfr23 |
G |
A |
11: 73,941,138 (GRCm38) |
M297I |
probably benign |
Het |
Olfr231 |
C |
T |
1: 174,117,315 (GRCm38) |
A234T |
probably benign |
Het |
Olfr299 |
T |
A |
7: 86,465,746 (GRCm38) |
F112I |
possibly damaging |
Het |
Olfr340 |
T |
G |
2: 36,452,906 (GRCm38) |
F107C |
possibly damaging |
Het |
Olfr357 |
A |
C |
2: 36,997,705 (GRCm38) |
K298N |
possibly damaging |
Het |
Olfr364-ps1 |
T |
G |
2: 37,146,385 (GRCm38) |
F58V |
probably benign |
Het |
Olfr373 |
T |
G |
8: 72,100,517 (GRCm38) |
F252L |
probably benign |
Het |
Olfr378 |
T |
C |
11: 73,425,105 (GRCm38) |
S293G |
probably benign |
Het |
Olfr410 |
A |
T |
11: 74,334,692 (GRCm38) |
F180I |
probably damaging |
Het |
Olfr417 |
G |
A |
1: 174,369,744 (GRCm38) |
V276I |
probably benign |
Het |
Olfr430 |
C |
T |
1: 174,069,949 (GRCm38) |
S217F |
probably damaging |
Het |
Olfr477 |
G |
A |
7: 107,990,731 (GRCm38) |
R122H |
probably benign |
Het |
Olfr480 |
C |
A |
7: 108,066,327 (GRCm38) |
C127F |
probably damaging |
Het |
Olfr498 |
T |
A |
7: 108,465,371 (GRCm38) |
F16I |
probably benign |
Het |
Olfr502 |
A |
C |
7: 108,523,398 (GRCm38) |
F184C |
probably damaging |
Het |
Olfr512 |
T |
G |
7: 108,713,538 (GRCm38) |
F50V |
probably benign |
Het |
Olfr513 |
T |
G |
7: 108,755,104 (GRCm38) |
L83V |
probably benign |
Het |
Olfr514 |
A |
C |
7: 108,825,896 (GRCm38) |
Y34* |
probably null |
Het |
Olfr519 |
G |
T |
7: 108,893,773 (GRCm38) |
F211L |
probably damaging |
Het |
Olfr536 |
A |
C |
7: 140,503,805 (GRCm38) |
V218G |
probably benign |
Het |
Olfr59 |
T |
C |
11: 74,288,835 (GRCm38) |
L63P |
probably damaging |
Het |
Olfr591 |
A |
G |
7: 103,172,806 (GRCm38) |
L277P |
possibly damaging |
Het |
Olfr60 |
A |
G |
7: 140,345,804 (GRCm38) |
F62L |
probably benign |
Het |
Olfr61 |
A |
G |
7: 140,638,220 (GRCm38) |
K173R |
probably benign |
Het |
Olfr615 |
G |
C |
7: 103,561,390 (GRCm38) |
L304F |
probably damaging |
Het |
Olfr615 |
A |
G |
7: 103,561,059 (GRCm38) |
K194R |
probably benign |
Het |
Olfr625-ps1 |
T |
G |
7: 103,683,186 (GRCm38) |
I156S |
probably benign |
Het |
Olfr643 |
A |
C |
7: 104,059,316 (GRCm38) |
S95R |
possibly damaging |
Het |
Olfr663 |
T |
C |
7: 104,704,493 (GRCm38) |
Y309H |
probably benign |
Het |
Olfr667 |
G |
T |
7: 104,916,666 (GRCm38) |
A210E |
probably benign |
Het |
Olfr67 |
T |
G |
7: 103,787,365 (GRCm38) |
K304T |
probably damaging |
Het |
Olfr672 |
C |
A |
7: 104,996,454 (GRCm38) |
G150V |
probably benign |
Het |
Olfr693 |
T |
G |
7: 106,678,457 (GRCm38) |
S10R |
probably benign |
Het |
Olfr697 |
A |
T |
7: 106,741,143 (GRCm38) |
S264T |
probably benign |
Het |
Olfr706 |
T |
A |
7: 106,886,296 (GRCm38) |
I174F |
probably damaging |
Het |
Olfr714 |
C |
A |
7: 107,074,405 (GRCm38) |
D192E |
possibly damaging |
Het |
Olfr716 |
A |
C |
7: 107,148,212 (GRCm38) |
S299R |
probably benign |
Het |
Olfr742 |
T |
C |
14: 50,515,527 (GRCm38) |
F108L |
possibly damaging |
Het |
Olfr77 |
T |
A |
9: 19,920,712 (GRCm38) |
F168I |
probably damaging |
Het |
Olfr770 |
T |
G |
10: 129,133,075 (GRCm38) |
K231T |
probably benign |
Het |
Olfr807 |
A |
C |
10: 129,755,339 (GRCm38) |
I37S |
possibly damaging |
Het |
Olfr815 |
T |
C |
10: 129,902,683 (GRCm38) |
E9G |
possibly damaging |
Het |
Olfr821 |
A |
C |
10: 130,033,788 (GRCm38) |
K54T |
probably damaging |
Het |
Olfr832 |
G |
A |
9: 18,945,421 (GRCm38) |
V258I |
possibly damaging |
Het |
Olfr847 |
G |
A |
9: 19,375,684 (GRCm38) |
L66F |
probably damaging |
Het |
Olfr866 |
A |
G |
9: 20,027,279 (GRCm38) |
S220P |
probably damaging |
Het |
Olfr877 |
A |
C |
9: 37,855,318 (GRCm38) |
S167R |
probably benign |
Het |
Olfr888 |
T |
C |
9: 38,109,586 (GRCm38) |
V295A |
probably damaging |
Het |
Olfr895 |
T |
C |
9: 38,268,612 (GRCm38) |
L33S |
probably damaging |
Het |
Olfr910 |
T |
C |
9: 38,539,149 (GRCm38) |
F85L |
probably damaging |
Het |
Olfr911-ps1 |
T |
G |
9: 38,523,859 (GRCm38) |
N42K |
probably damaging |
Het |
Olfr945 |
G |
A |
9: 39,257,871 (GRCm38) |
S270L |
probably benign |
Het |
Olfr980 |
A |
G |
9: 40,006,596 (GRCm38) |
S118P |
probably damaging |
Het |
Omg |
G |
C |
11: 79,502,320 (GRCm38) |
N237K |
possibly damaging |
Het |
Oog3 |
A |
G |
4: 144,159,636 (GRCm38) |
F131L |
probably benign |
Het |
Oog3 |
T |
A |
4: 144,158,307 (GRCm38) |
N353I |
probably benign |
Het |
Orc2 |
A |
C |
1: 58,476,516 (GRCm38) |
F230V |
probably benign |
Het |
Osbpl3 |
A |
G |
6: 50,297,097 (GRCm38) |
F846L |
probably damaging |
Het |
Pabpc1l |
G |
C |
2: 164,032,324 (GRCm38) |
|
probably null |
Het |
Pah |
C |
T |
10: 87,571,291 (GRCm38) |
S303F |
probably damaging |
Het |
Paip2b |
T |
G |
6: 83,808,882 (GRCm38) |
N122T |
probably benign |
Het |
Pak4 |
G |
T |
7: 28,565,228 (GRCm38) |
T83N |
probably damaging |
Het |
Pamr1 |
C |
A |
2: 102,634,446 (GRCm38) |
F313L |
possibly damaging |
Het |
Papln |
C |
G |
12: 83,776,376 (GRCm38) |
P396A |
probably benign |
Het |
Papss1 |
C |
G |
3: 131,642,967 (GRCm38) |
H559Q |
possibly damaging |
Het |
Parp14 |
C |
G |
16: 35,841,586 (GRCm38) |
D1360H |
probably damaging |
Het |
Pask |
C |
T |
1: 93,316,801 (GRCm38) |
S1166N |
probably damaging |
Het |
Pbk |
T |
A |
14: 65,813,948 (GRCm38) |
V145D |
probably damaging |
Het |
Pbrm1 |
G |
A |
14: 31,110,454 (GRCm38) |
R1443Q |
possibly damaging |
Het |
Pcbp3 |
C |
A |
10: 76,763,323 (GRCm38) |
Q326H |
probably benign |
Het |
Pcdh1 |
G |
C |
18: 38,198,067 (GRCm38) |
R767G |
probably damaging |
Het |
Pcdh17 |
A |
G |
14: 84,448,274 (GRCm38) |
K727R |
possibly damaging |
Het |
Pcdha2 |
G |
T |
18: 36,941,121 (GRCm38) |
G602C |
probably damaging |
Het |
Pcdha6 |
G |
A |
18: 36,969,217 (GRCm38) |
A488T |
probably damaging |
Het |
Pcdhac1 |
G |
T |
18: 37,092,190 (GRCm38) |
L685F |
probably damaging |
Het |
Pcdhac1 |
G |
T |
18: 37,092,566 (GRCm38) |
A811S |
probably damaging |
Het |
Pcdhb21 |
A |
G |
18: 37,514,541 (GRCm38) |
E241G |
probably benign |
Het |
Pcdhb22 |
A |
C |
18: 37,519,345 (GRCm38) |
T289P |
probably benign |
Het |
Pcdhb6 |
T |
A |
18: 37,335,146 (GRCm38) |
D373E |
probably damaging |
Het |
Pcdhga11 |
G |
C |
18: 37,756,184 (GRCm38) |
G82R |
probably damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,163,330 (GRCm38) |
P222L |
possibly damaging |
Het |
Pcnx2 |
T |
G |
8: 125,866,018 (GRCm38) |
S736R |
probably damaging |
Het |
Pcnx2 |
C |
T |
8: 125,826,928 (GRCm38) |
E1151K |
probably damaging |
Het |
Pcsk5 |
A |
G |
19: 17,463,374 (GRCm38) |
L1284P |
probably damaging |
Het |
Pdgfra |
C |
T |
5: 75,166,577 (GRCm38) |
S145F |
probably benign |
Het |
Pdrg1 |
C |
T |
2: 153,014,037 (GRCm38) |
A46T |
probably damaging |
Het |
Pds5a |
A |
C |
5: 65,618,986 (GRCm38) |
I88M |
probably damaging |
Het |
Pdzk1 |
A |
G |
3: 96,854,557 (GRCm38) |
N162D |
probably benign |
Het |
Pelp1 |
A |
G |
11: 70,396,890 (GRCm38) |
L402P |
probably damaging |
Het |
Pet2 |
A |
G |
X: 89,406,337 (GRCm38) |
V62A |
probably benign |
Het |
Pex1 |
G |
A |
5: 3,606,075 (GRCm38) |
A301T |
probably benign |
Het |
Pex6 |
A |
T |
17: 46,712,222 (GRCm38) |
Q241H |
possibly damaging |
Het |
Pgm3 |
A |
G |
9: 86,564,707 (GRCm38) |
F253L |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,760,931 (GRCm38) |
R367Q |
possibly damaging |
Het |
Pi4kb |
T |
G |
3: 94,984,509 (GRCm38) |
F179V |
probably damaging |
Het |
Pid1 |
T |
G |
1: 84,116,014 (GRCm38) |
N51T |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,069,994 (GRCm38) |
G1525D |
probably damaging |
Het |
Piga |
A |
C |
X: 164,422,909 (GRCm38) |
K88N |
probably damaging |
Het |
Pigo |
G |
C |
4: 43,019,409 (GRCm38) |
P970A |
probably damaging |
Het |
Pik3r6 |
G |
A |
11: 68,525,602 (GRCm38) |
V6M |
probably damaging |
Het |
Piwil4 |
G |
A |
9: 14,734,517 (GRCm38) |
H142Y |
probably damaging |
Het |
Pkd1 |
T |
G |
17: 24,565,605 (GRCm38) |
L375R |
probably benign |
Het |
Pkd2 |
T |
G |
5: 104,498,861 (GRCm38) |
L780V |
probably damaging |
Het |
Pkdcc |
A |
G |
17: 83,222,150 (GRCm38) |
E380G |
probably damaging |
Het |
Pla2g12a |
C |
T |
3: 129,890,380 (GRCm38) |
S136F |
probably benign |
Het |
Pla2g2c |
T |
C |
4: 138,734,286 (GRCm38) |
F22S |
probably damaging |
Het |
Pla2g4c |
A |
T |
7: 13,329,753 (GRCm38) |
Q48H |
probably benign |
Het |
Plb1 |
T |
G |
5: 32,310,847 (GRCm38) |
F503V |
probably damaging |
Het |
Plb1 |
C |
T |
5: 32,310,917 (GRCm38) |
S526L |
probably benign |
Het |
Plcb1 |
A |
C |
2: 135,220,846 (GRCm38) |
E27D |
probably benign |
Het |
Plcl2 |
C |
A |
17: 50,606,992 (GRCm38) |
P343H |
probably damaging |
Het |
Pld1 |
A |
C |
3: 28,029,243 (GRCm38) |
I171L |
probably benign |
Het |
Plod2 |
T |
G |
9: 92,603,035 (GRCm38) |
F551V |
probably benign |
Het |
Plxna2 |
A |
G |
1: 194,764,539 (GRCm38) |
N786D |
probably benign |
Het |
Plxna2 |
A |
C |
1: 194,644,441 (GRCm38) |
I228L |
possibly damaging |
Het |
Plxnd1 |
C |
A |
6: 115,967,510 (GRCm38) |
S1033I |
probably benign |
Het |
Pmfbp1 |
A |
C |
8: 109,513,944 (GRCm38) |
E219D |
probably damaging |
Het |
Pml |
G |
T |
9: 58,234,590 (GRCm38) |
L320M |
probably damaging |
Het |
Pnisr |
C |
G |
4: 21,873,684 (GRCm38) |
R476G |
probably benign |
Het |
Pnliprp2 |
G |
A |
19: 58,762,325 (GRCm38) |
A149T |
probably damaging |
Het |
Pnp |
T |
G |
14: 50,951,495 (GRCm38) |
D248E |
probably benign |
Het |
Pnpla5 |
A |
G |
15: 84,123,071 (GRCm38) |
S15P |
probably damaging |
Het |
Pogz |
T |
A |
3: 94,879,076 (GRCm38) |
F992I |
probably damaging |
Het |
Pole |
C |
T |
5: 110,327,865 (GRCm38) |
L1847F |
possibly damaging |
Het |
Polr2b |
T |
G |
5: 77,342,722 (GRCm38) |
I903S |
possibly damaging |
Het |
Polr2b |
G |
A |
5: 77,345,401 (GRCm38) |
G1077S |
probably damaging |
Het |
Polr3a |
A |
C |
14: 24,479,724 (GRCm38) |
V266G |
probably damaging |
Het |
Pop1 |
C |
G |
15: 34,499,319 (GRCm38) |
A10G |
probably damaging |
Het |
Pop7 |
T |
C |
5: 137,502,011 (GRCm38) |
Y20C |
probably damaging |
Het |
Postn |
A |
T |
3: 54,375,127 (GRCm38) |
D503V |
probably benign |
Het |
Pou4f2 |
C |
G |
8: 78,435,601 (GRCm38) |
Q124H |
probably benign |
Het |
Ppl |
G |
A |
16: 5,089,507 (GRCm38) |
R975W |
probably damaging |
Het |
Ppp1cc |
C |
T |
5: 122,172,753 (GRCm38) |
S182F |
possibly damaging |
Het |
Ppp1r10 |
ACATGATGTCCCTAGCCAT |
ACAT |
17: 35,930,767 (GRCm38) |
|
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,352,588 (GRCm38) |
L126P |
probably damaging |
Het |
Ppp2r1b |
A |
C |
9: 50,866,911 (GRCm38) |
E309D |
probably damaging |
Het |
Prdm1 |
G |
A |
10: 44,441,925 (GRCm38) |
R301W |
probably damaging |
Het |
Prg2 |
G |
T |
2: 84,982,265 (GRCm38) |
K106N |
possibly damaging |
Het |
Prkg2 |
A |
T |
5: 99,024,804 (GRCm38) |
H17Q |
probably benign |
Het |
Prob1 |
G |
C |
18: 35,652,769 (GRCm38) |
P811A |
possibly damaging |
Het |
Prox1 |
G |
C |
1: 190,161,999 (GRCm38) |
A83G |
probably damaging |
Het |
Prr23a1 |
G |
A |
9: 98,843,347 (GRCm38) |
R254Q |
possibly damaging |
Het |
Prr27 |
G |
A |
5: 87,842,646 (GRCm38) |
R31H |
probably damaging |
Het |
Prr30 |
G |
C |
14: 101,198,140 (GRCm38) |
Q329E |
probably benign |
Het |
Prrc2b |
G |
A |
2: 32,216,732 (GRCm38) |
R1582K |
probably damaging |
Het |
Prrc2b |
C |
A |
2: 32,214,429 (GRCm38) |
N1306K |
probably benign |
Het |
Prrx1 |
A |
C |
1: 163,261,877 (GRCm38) |
L127R |
probably damaging |
Het |
Prss36 |
G |
A |
7: 127,934,537 (GRCm38) |
R32* |
probably null |
Het |
Prss53 |
C |
T |
7: 127,887,398 (GRCm38) |
W352* |
probably null |
Het |
Psd3 |
T |
C |
8: 67,906,260 (GRCm38) |
|
silent |
Het |
Psg17 |
G |
A |
7: 18,816,910 (GRCm38) |
T340I |
probably benign |
Het |
Psg25 |
T |
A |
7: 18,529,591 (GRCm38) |
R102S |
probably benign |
Het |
Psmd11 |
A |
ATC |
11: 80,471,550 (GRCm38) |
|
probably null |
Het |
Ptcra |
G |
C |
17: 46,763,595 (GRCm38) |
A7G |
probably damaging |
Het |
Pten |
C |
T |
19: 32,776,051 (GRCm38) |
A39V |
probably damaging |
Het |
Pten |
A |
C |
19: 32,799,998 (GRCm38) |
T131P |
probably damaging |
Het |
Ptgfrn |
T |
G |
3: 101,056,437 (GRCm38) |
T620P |
probably damaging |
Het |
Ptprn |
T |
A |
1: 75,260,620 (GRCm38) |
M20L |
possibly damaging |
Het |
Ptprq |
C |
T |
10: 107,699,672 (GRCm38) |
A411T |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 162,238,121 (GRCm38) |
S253P |
possibly damaging |
Het |
Rab3gap2 |
A |
T |
1: 185,281,677 (GRCm38) |
L1173F |
probably damaging |
Het |
Rac1 |
C |
A |
5: 143,514,719 (GRCm38) |
A59S |
probably damaging |
Het |
Rad21 |
T |
G |
15: 51,982,626 (GRCm38) |
K16T |
probably damaging |
Het |
Rad21l |
C |
T |
2: 151,668,019 (GRCm38) |
R54Q |
probably damaging |
Het |
Rad9b |
A |
G |
5: 122,333,372 (GRCm38) |
F210L |
possibly damaging |
Het |
Raet1e |
A |
C |
10: 22,181,951 (GRCm38) |
T206P |
possibly damaging |
Het |
Ralgapa2 |
T |
G |
2: 146,434,905 (GRCm38) |
S472R |
probably benign |
Het |
Ranbp2 |
A |
T |
10: 58,492,893 (GRCm38) |
Q2871H |
probably benign |
Het |
Ranbp2 |
GGT |
GGTTTGTGCTCCGT |
10: 58,477,983 (GRCm38) |
|
probably null |
Het |
Ranbp2 |
AGTTTGTGCTCGGT |
AGTTTGTGCTCGGTTTGTGCTCGGT |
10: 58,477,972 (GRCm38) |
|
probably null |
Het |
Rapgefl1 |
C |
G |
11: 98,845,895 (GRCm38) |
P285R |
probably damaging |
Het |
Rasgrp4 |
A |
C |
7: 29,150,536 (GRCm38) |
|
probably benign |
Het |
Rassf7 |
C |
G |
7: 141,217,145 (GRCm38) |
S90R |
probably damaging |
Het |
Rassf8 |
A |
C |
6: 145,816,616 (GRCm38) |
E371A |
probably benign |
Het |
Rassf8 |
A |
G |
6: 145,815,482 (GRCm38) |
Q178R |
probably benign |
Het |
Rb1cc1 |
AT |
ATT |
1: 6,249,018 (GRCm38) |
|
probably null |
Het |
Rbm12b1 |
G |
T |
4: 12,146,079 (GRCm38) |
V684L |
probably benign |
Het |
Rdh16f1 |
A |
C |
10: 127,788,833 (GRCm38) |
K180T |
probably damaging |
Het |
Rec8 |
A |
T |
14: 55,625,147 (GRCm38) |
K553M |
probably damaging |
Het |
Reg1 |
G |
T |
6: 78,426,918 (GRCm38) |
E23* |
probably null |
Het |
Rergl |
C |
A |
6: 139,493,426 (GRCm38) |
E135* |
probably null |
Het |
Resp18 |
T |
C |
1: 75,278,291 (GRCm38) |
K6R |
possibly damaging |
Het |
Rev3l |
C |
A |
10: 39,824,318 (GRCm38) |
Q1604K |
probably benign |
Het |
Rfc3 |
C |
T |
5: 151,644,862 (GRCm38) |
R213H |
probably benign |
Het |
Rfwd3 |
C |
A |
8: 111,297,606 (GRCm38) |
G28V |
probably benign |
Het |
Rfx3 |
G |
A |
19: 27,837,450 (GRCm38) |
S169F |
probably damaging |
Het |
Rfx8 |
T |
G |
1: 39,682,966 (GRCm38) |
E286D |
possibly damaging |
Het |
Rgl1 |
G |
A |
1: 152,675,020 (GRCm38) |
|
probably benign |
Het |
Rgs11 |
G |
C |
17: 26,205,772 (GRCm38) |
Q218H |
probably benign |
Het |
Rgs7 |
T |
C |
1: 175,084,020 (GRCm38) |
E345G |
possibly damaging |
Het |
Rims1 |
C |
G |
1: 22,288,586 (GRCm38) |
A1258P |
probably damaging |
Het |
Rint1 |
A |
G |
5: 23,805,314 (GRCm38) |
N174D |
probably benign |
Het |
Ripk3 |
T |
G |
14: 55,787,926 (GRCm38) |
E60D |
possibly damaging |
Het |
Rnf146 |
G |
A |
10: 29,347,572 (GRCm38) |
A106V |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,477,254 (GRCm38) |
K4705R |
possibly damaging |
Het |
Rnmt |
C |
T |
18: 68,307,674 (GRCm38) |
S136L |
probably benign |
Het |
Rp1l1 |
T |
G |
14: 64,030,378 (GRCm38) |
F1138V |
probably benign |
Het |
Rp1l1 |
C |
T |
14: 64,028,758 (GRCm38) |
H598Y |
possibly damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,270,120 (GRCm38) |
F109I |
possibly damaging |
Het |
Rpgrip1l |
T |
G |
8: 91,260,975 (GRCm38) |
K818T |
possibly damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,220,179 (GRCm38) |
*1265R |
probably null |
Het |
Rpl12 |
T |
A |
2: 32,963,019 (GRCm38) |
I82N |
possibly damaging |
Het |
Rpl13a |
G |
C |
7: 45,127,513 (GRCm38) |
A24G |
probably damaging |
Het |
Rpp14 |
A |
C |
14: 8,090,539 (GRCm38) |
E154D |
probably benign |
Het |
Rps19 |
G |
C |
7: 24,886,107 (GRCm38) |
|
probably benign |
Het |
Rptn |
C |
A |
3: 93,397,427 (GRCm38) |
P689H |
probably benign |
Het |
Rrbp1 |
C |
A |
2: 143,974,486 (GRCm38) |
G741V |
probably damaging |
Het |
Rreb1 |
G |
A |
13: 37,948,937 (GRCm38) |
R1696K |
probably benign |
Het |
Rsl1d1 |
C |
T |
16: 11,202,385 (GRCm38) |
G59R |
possibly damaging |
Het |
Rtl1 |
T |
A |
12: 109,592,319 (GRCm38) |
T1029S |
probably benign |
Het |
Runx1 |
C |
T |
16: 92,605,792 (GRCm38) |
A421T |
probably damaging |
Het |
Runx1t1 |
G |
A |
4: 13,865,892 (GRCm38) |
R380Q |
possibly damaging |
Het |
Rxfp1 |
C |
T |
3: 79,705,704 (GRCm38) |
G20R |
probably damaging |
Het |
Ryr3 |
C |
A |
2: 112,900,916 (GRCm38) |
G683V |
probably damaging |
Het |
S100a13 |
C |
G |
3: 90,515,942 (GRCm38) |
S80C |
probably damaging |
Het |
Samd1 |
CGAGGAGGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGAGGA |
8: 83,998,996 (GRCm38) |
|
probably benign |
Het |
Satb1 |
C |
G |
17: 51,782,939 (GRCm38) |
Q293H |
probably damaging |
Het |
Satb1 |
G |
A |
17: 51,782,952 (GRCm38) |
S289F |
probably damaging |
Het |
Sbno1 |
G |
T |
5: 124,404,304 (GRCm38) |
P308T |
probably damaging |
Het |
Sbno1 |
T |
G |
5: 124,393,958 (GRCm38) |
K719N |
possibly damaging |
Het |
Sbpl |
A |
C |
17: 23,953,544 (GRCm38) |
F134V |
probably damaging |
Het |
Sbsn |
G |
T |
7: 30,751,751 (GRCm38) |
E64* |
probably null |
Het |
Scaf8 |
T |
G |
17: 3,162,983 (GRCm38) |
|
probably benign |
Het |
Scap |
A |
G |
9: 110,372,336 (GRCm38) |
N131S |
probably damaging |
Het |
Scarf1 |
C |
T |
11: 75,525,490 (GRCm38) |
A586V |
probably damaging |
Het |
Scd1 |
C |
A |
19: 44,397,923 (GRCm38) |
S355I |
probably benign |
Het |
Scgb2b26 |
A |
C |
7: 33,944,367 (GRCm38) |
F49L |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,755,242 (GRCm38) |
F1436L |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,713,951 (GRCm38) |
E399K |
probably damaging |
Het |
Scrib |
G |
A |
15: 76,048,231 (GRCm38) |
P1560S |
probably damaging |
Het |
Sctr |
GT |
G |
1: 120,036,406 (GRCm38) |
|
probably null |
Het |
Sec16a |
G |
A |
2: 26,439,093 (GRCm38) |
S970F |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,558,024 (GRCm38) |
|
probably null |
Het |
Sec23a |
A |
G |
12: 59,004,576 (GRCm38) |
F94L |
probably benign |
Het |
Sel1l3 |
C |
A |
5: 53,116,196 (GRCm38) |
A1081S |
probably damaging |
Het |
Selenok |
G |
A |
14: 29,973,444 (GRCm38) |
G93E |
probably damaging |
Het |
Selenov |
G |
A |
7: 28,290,668 (GRCm38) |
T137I |
possibly damaging |
Het |
Sema3b |
A |
C |
9: 107,599,034 (GRCm38) |
|
probably null |
Het |
Sema3e |
G |
A |
5: 14,226,456 (GRCm38) |
S285N |
probably damaging |
Het |
Sema5b |
T |
G |
16: 35,660,590 (GRCm38) |
F815V |
probably damaging |
Het |
Serac1 |
G |
A |
17: 6,048,918 (GRCm38) |
P533S |
probably damaging |
Het |
Serpina1a |
C |
A |
12: 103,854,667 (GRCm38) |
|
probably null |
Het |
Serpinb3b |
T |
G |
1: 107,157,751 (GRCm38) |
T87P |
probably damaging |
Het |
Serpinb6c |
G |
A |
13: 33,893,923 (GRCm38) |
P155S |
probably benign |
Het |
Serpinb6c |
A |
G |
13: 33,893,872 (GRCm38) |
F172L |
probably damaging |
Het |
Serpinb6d |
T |
C |
13: 33,671,254 (GRCm38) |
F304L |
possibly damaging |
Het |
Sertad4 |
G |
T |
1: 192,847,031 (GRCm38) |
T159N |
probably damaging |
Het |
Setbp1 |
G |
C |
18: 78,859,594 (GRCm38) |
P286R |
probably damaging |
Het |
Sez6 |
T |
G |
11: 77,973,197 (GRCm38) |
F502V |
possibly damaging |
Het |
Sez6l |
T |
G |
5: 112,440,915 (GRCm38) |
Q644P |
probably damaging |
Het |
Sfmbt2 |
A |
C |
2: 10,579,183 (GRCm38) |
T784P |
probably damaging |
Het |
Sgo2b |
T |
G |
8: 63,928,422 (GRCm38) |
T459P |
possibly damaging |
Het |
Sgo2b |
C |
A |
8: 63,927,005 (GRCm38) |
G931V |
probably damaging |
Het |
Sgtb |
T |
C |
13: 104,131,939 (GRCm38) |
L118P |
probably damaging |
Het |
Shank1 |
C |
T |
7: 44,352,166 (GRCm38) |
A1103V |
unknown |
Het |
Siglech |
A |
G |
7: 55,768,994 (GRCm38) |
I182V |
possibly damaging |
Het |
Sirpa |
C |
A |
2: 129,618,535 (GRCm38) |
A54D |
probably damaging |
Het |
Slamf1 |
T |
G |
1: 171,799,592 (GRCm38) |
V334G |
probably damaging |
Het |
Slc14a2 |
T |
G |
18: 78,195,780 (GRCm38) |
K208T |
probably damaging |
Het |
Slc15a1 |
A |
G |
14: 121,491,044 (GRCm38) |
L65P |
probably damaging |
Het |
Slc15a1 |
C |
T |
14: 121,480,054 (GRCm38) |
R272Q |
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,772,445 (GRCm38) |
M179T |
probably benign |
Het |
Slc1a5 |
C |
T |
7: 16,797,669 (GRCm38) |
P533L |
probably damaging |
Het |
Slc22a12 |
G |
A |
19: 6,538,463 (GRCm38) |
H342Y |
possibly damaging |
Het |
Slc22a2 |
G |
A |
17: 12,614,776 (GRCm38) |
E448K |
probably benign |
Het |
Slc22a28 |
A |
C |
19: 8,062,398 (GRCm38) |
S537A |
probably damaging |
Het |
Slc22a3 |
A |
T |
17: 12,425,681 (GRCm38) |
C472* |
probably null |
Het |
Slc22a30 |
C |
A |
19: 8,335,775 (GRCm38) |
V549F |
probably damaging |
Het |
Slc22a6 |
A |
G |
19: 8,621,833 (GRCm38) |
D276G |
probably benign |
Het |
Slc23a1 |
T |
C |
18: 35,624,508 (GRCm38) |
N237D |
probably benign |
Het |
Slc25a1 |
C |
G |
16: 17,927,206 (GRCm38) |
G130A |
probably benign |
Het |
Slc28a1 |
C |
G |
7: 81,138,168 (GRCm38) |
P268A |
probably damaging |
Het |
Slc2a6 |
G |
A |
2: 27,021,987 (GRCm38) |
P420L |
probably damaging |
Het |
Slc35a4 |
A |
C |
18: 36,683,093 (GRCm38) |
*325Y |
probably null |
Het |
Slc48a1 |
C |
A |
15: 97,790,681 (GRCm38) |
Y74* |
probably null |
Het |
Slc4a10 |
T |
G |
2: 62,228,571 (GRCm38) |
L141V |
probably damaging |
Het |
Slc4a8 |
C |
G |
15: 100,761,951 (GRCm38) |
P8A |
probably benign |
Het |
Slc6a19 |
C |
T |
13: 73,689,730 (GRCm38) |
E217K |
possibly damaging |
Het |
Slc6a5 |
C |
G |
7: 49,911,857 (GRCm38) |
P46A |
probably benign |
Het |
Slc7a14 |
G |
C |
3: 31,223,999 (GRCm38) |
L486V |
probably benign |
Het |
Slco2a1 |
C |
A |
9: 103,079,527 (GRCm38) |
L513M |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,302,353 (GRCm38) |
Y1308C |
probably damaging |
Het |
Slurp2 |
C |
A |
15: 74,743,101 (GRCm38) |
V64L |
probably damaging |
Het |
Smad5 |
A |
T |
13: 56,728,628 (GRCm38) |
R258S |
probably benign |
Het |
Smarcc2 |
G |
C |
10: 128,461,434 (GRCm38) |
G65A |
probably damaging |
Het |
Smco1 |
A |
T |
16: 32,273,215 (GRCm38) |
D37V |
probably damaging |
Het |
Smg1 |
A |
C |
7: 118,154,635 (GRCm38) |
|
probably benign |
Het |
Smg1 |
C |
A |
7: 118,168,661 (GRCm38) |
E1665* |
probably null |
Het |
Smg1 |
A |
G |
7: 118,178,399 (GRCm38) |
L1358P |
possibly damaging |
Het |
Snx15 |
T |
C |
19: 6,121,411 (GRCm38) |
E211G |
probably damaging |
Het |
Snx5 |
C |
T |
2: 144,252,491 (GRCm38) |
R373Q |
probably benign |
Het |
Sod2 |
T |
A |
17: 13,013,538 (GRCm38) |
L150H |
probably damaging |
Het |
Sorcs1 |
C |
G |
19: 50,222,143 (GRCm38) |
Q761H |
probably benign |
Het |
Sox12 |
C |
G |
2: 152,397,465 (GRCm38) |
W78C |
probably damaging |
Het |
Sox17 |
G |
T |
1: 4,492,302 (GRCm38) |
S160Y |
probably damaging |
Het |
Sp9 |
G |
C |
2: 73,273,230 (GRCm38) |
A43P |
possibly damaging |
Het |
Spag17 |
A |
G |
3: 100,095,630 (GRCm38) |
K1890R |
probably benign |
Het |
Speer4b |
C |
G |
5: 27,497,941 (GRCm38) |
E188D |
probably benign |
Het |
Speer4f1 |
A |
C |
5: 17,479,479 (GRCm38) |
E168D |
probably damaging |
Het |
Spen |
C |
A |
4: 141,477,976 (GRCm38) |
E1113D |
unknown |
Het |
Spen |
T |
C |
4: 141,477,977 (GRCm38) |
E1113G |
unknown |
Het |
Sphkap |
T |
A |
1: 83,276,608 (GRCm38) |
N1140I |
probably damaging |
Het |
Sphkap |
T |
G |
1: 83,278,604 (GRCm38) |
T475P |
probably damaging |
Het |
Spinkl |
G |
C |
18: 44,174,559 (GRCm38) |
L12V |
probably damaging |
Het |
Spire1 |
C |
A |
18: 67,495,152 (GRCm38) |
R509L |
possibly damaging |
Het |
Spon1 |
G |
A |
7: 113,766,386 (GRCm38) |
A20T |
possibly damaging |
Het |
Srd5a3 |
T |
C |
5: 76,149,821 (GRCm38) |
F33L |
possibly damaging |
Het |
Srebf2 |
T |
G |
15: 82,194,921 (GRCm38) |
F783L |
probably benign |
Het |
Srp68 |
TCCGCCGCCGCCGCCGC |
TCCGCCGCCGCCGCCGCCGCCGC |
11: 116,274,035 (GRCm38) |
|
probably benign |
Het |
Ssbp4 |
A |
C |
8: 70,599,835 (GRCm38) |
|
probably benign |
Het |
Ssc5d |
A |
C |
7: 4,928,434 (GRCm38) |
E213D |
probably damaging |
Het |
Ssh2 |
C |
A |
11: 77,449,495 (GRCm38) |
T491N |
probably damaging |
Het |
Ssrp1 |
G |
A |
2: 85,040,653 (GRCm38) |
R211H |
probably damaging |
Het |
Ssxb3 |
T |
G |
X: 8,589,188 (GRCm38) |
S5R |
probably benign |
Het |
Stam |
C |
A |
2: 14,139,090 (GRCm38) |
S397* |
probably null |
Het |
Stambpl1 |
A |
T |
19: 34,226,627 (GRCm38) |
N39I |
probably damaging |
Het |
Stap2 |
G |
C |
17: 55,999,748 (GRCm38) |
A275G |
probably benign |
Het |
Stard4 |
G |
T |
18: 33,203,717 (GRCm38) |
Q182K |
probably benign |
Het |
Stard4 |
T |
C |
18: 33,203,720 (GRCm38) |
S181G |
probably benign |
Het |
Stil |
T |
G |
4: 115,006,693 (GRCm38) |
L44R |
probably damaging |
Het |
Stk31 |
G |
T |
6: 49,417,188 (GRCm38) |
|
probably null |
Het |
Ston2 |
T |
G |
12: 91,649,067 (GRCm38) |
N189T |
possibly damaging |
Het |
Stxbp5l |
T |
G |
16: 37,204,489 (GRCm38) |
Q582H |
probably benign |
Het |
Sult2a1 |
T |
C |
7: 13,801,414 (GRCm38) |
Q238R |
probably benign |
Het |
Sult2a1 |
T |
C |
7: 13,804,036 (GRCm38) |
I187M |
probably benign |
Het |
Sult2a1 |
A |
T |
7: 13,801,435 (GRCm38) |
F231Y |
probably benign |
Het |
Sult2a6 |
T |
C |
7: 14,225,894 (GRCm38) |
Q238R |
probably benign |
Het |
Sycp2 |
T |
G |
2: 178,374,367 (GRCm38) |
E767D |
probably benign |
Het |
Sycp2 |
C |
T |
2: 178,381,934 (GRCm38) |
V430I |
probably benign |
Het |
Syna |
C |
T |
5: 134,558,529 (GRCm38) |
R522Q |
probably benign |
Het |
Syne4 |
C |
G |
7: 30,316,336 (GRCm38) |
S125C |
probably damaging |
Het |
Syngap1 |
A |
C |
17: 26,961,576 (GRCm38) |
D653A |
probably damaging |
Het |
Synm |
A |
C |
7: 67,751,886 (GRCm38) |
L285V |
probably damaging |
Het |
Synpo2l |
T |
G |
14: 20,665,967 (GRCm38) |
E183D |
probably damaging |
Het |
Syt10 |
C |
T |
15: 89,841,639 (GRCm38) |
G44D |
probably benign |
Het |
Szrd1 |
C |
A |
4: 141,118,587 (GRCm38) |
R99L |
probably damaging |
Het |
Taar9 |
G |
C |
10: 24,108,965 (GRCm38) |
C190W |
probably damaging |
Het |
Tab2 |
A |
T |
10: 7,920,266 (GRCm38) |
S77T |
possibly damaging |
Het |
Taf1a |
G |
T |
1: 183,404,460 (GRCm38) |
R291M |
possibly damaging |
Het |
Taf5l |
C |
A |
8: 123,997,338 (GRCm38) |
G581* |
probably null |
Het |
Tars |
G |
T |
15: 11,391,884 (GRCm38) |
P255H |
probably benign |
Het |
Tas1r2 |
C |
T |
4: 139,660,424 (GRCm38) |
A398V |
possibly damaging |
Het |
Tas2r109 |
T |
C |
6: 132,980,301 (GRCm38) |
Q222R |
probably benign |
Het |
Tas2r115 |
G |
T |
6: 132,737,081 (GRCm38) |
C302* |
probably null |
Het |
Tas2r116 |
A |
G |
6: 132,855,948 (GRCm38) |
N171D |
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,275,393 (GRCm38) |
|
probably null |
Het |
Tbc1d13 |
T |
C |
2: 30,134,872 (GRCm38) |
|
probably null |
Het |
Tbc1d4 |
A |
C |
14: 101,452,423 (GRCm38) |
V1049G |
probably damaging |
Het |
Tbc1d5 |
C |
A |
17: 50,963,696 (GRCm38) |
R169I |
probably damaging |
Het |
Tbxa2r |
G |
C |
10: 81,333,215 (GRCm38) |
G246A |
probably damaging |
Het |
Tcaim |
A |
C |
9: 122,833,657 (GRCm38) |
K430T |
probably benign |
Het |
Tchh |
C |
T |
3: 93,445,682 (GRCm38) |
Q810* |
probably null |
Het |
Tcp10a |
G |
C |
17: 7,326,449 (GRCm38) |
A58P |
probably damaging |
Het |
Tctn1 |
C |
G |
5: 122,251,641 (GRCm38) |
A273P |
probably damaging |
Het |
Tctn3 |
A |
C |
19: 40,607,346 (GRCm38) |
F332V |
possibly damaging |
Het |
Tdrd6 |
T |
G |
17: 43,626,518 (GRCm38) |
E1213A |
probably benign |
Het |
Tead4 |
G |
C |
6: 128,270,904 (GRCm38) |
R57G |
probably damaging |
Het |
Teddm1a |
G |
A |
1: 153,892,026 (GRCm38) |
G79R |
probably benign |
Het |
Tekt5 |
G |
A |
16: 10,358,377 (GRCm38) |
R435W |
probably damaging |
Het |
Tenm1 |
G |
A |
X: 42,899,835 (GRCm38) |
P290S |
probably damaging |
Het |
Tenm2 |
C |
T |
11: 36,273,267 (GRCm38) |
A384T |
probably damaging |
Het |
Terf2 |
A |
G |
8: 107,081,223 (GRCm38) |
L240P |
probably damaging |
Het |
Tex13c2 |
A |
T |
X: 42,490,562 (GRCm38) |
S211C |
probably damaging |
Het |
Tex15 |
A |
C |
8: 33,571,315 (GRCm38) |
K532Q |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 33,571,810 (GRCm38) |
I697V |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 33,574,870 (GRCm38) |
N1443D |
probably benign |
Het |
Them6 |
G |
A |
15: 74,721,569 (GRCm38) |
R92H |
probably benign |
Het |
Thsd1 |
G |
A |
8: 22,252,219 (GRCm38) |
R301H |
probably damaging |
Het |
Thumpd3 |
C |
G |
6: 113,056,030 (GRCm38) |
T243S |
probably benign |
Het |
Tiam2 |
C |
T |
17: 3,415,019 (GRCm38) |
S341F |
probably benign |
Het |
Tie1 |
A |
G |
4: 118,484,429 (GRCm38) |
C229R |
probably damaging |
Het |
Timm44 |
C |
T |
8: 4,268,004 (GRCm38) |
E135K |
probably benign |
Het |
Tlr11 |
T |
G |
14: 50,362,338 (GRCm38) |
F594V |
possibly damaging |
Het |
Tlr4 |
G |
A |
4: 66,929,082 (GRCm38) |
D149N |
probably benign |
Het |
Tm9sf3 |
A |
G |
19: 41,232,378 (GRCm38) |
Y382H |
probably damaging |
Het |
Tmc3 |
A |
C |
7: 83,603,468 (GRCm38) |
K359T |
probably damaging |
Het |
Tmem132a |
G |
A |
19: 10,858,935 (GRCm38) |
R744C |
probably damaging |
Het |
Tmem132c |
G |
A |
5: 127,504,921 (GRCm38) |
S400N |
probably benign |
Het |
Tmem189 |
G |
C |
2: 167,644,864 (GRCm38) |
Y198* |
probably null |
Het |
Tmem198 |
C |
A |
1: 75,480,262 (GRCm38) |
Q11K |
probably benign |
Het |
Tmem219 |
G |
C |
7: 126,891,674 (GRCm38) |
P198A |
possibly damaging |
Het |
Tmem246 |
A |
G |
4: 49,587,135 (GRCm38) |
L11P |
probably damaging |
Het |
Tmem270 |
A |
C |
5: 134,906,656 (GRCm38) |
L15R |
probably damaging |
Het |
Tmem39a |
C |
A |
16: 38,575,778 (GRCm38) |
F124L |
possibly damaging |
Het |
Tmem39b |
C |
G |
4: 129,692,477 (GRCm38) |
A4P |
probably benign |
Het |
Tmem45b |
A |
G |
9: 31,428,027 (GRCm38) |
F131L |
probably damaging |
Het |
Tmppe |
G |
A |
9: 114,405,077 (GRCm38) |
R148H |
probably benign |
Het |
Tmprss4 |
T |
A |
9: 45,175,465 (GRCm38) |
N333Y |
probably damaging |
Het |
Tnni3k |
G |
C |
3: 154,939,670 (GRCm38) |
A526G |
probably damaging |
Het |
Tnpo1 |
C |
G |
13: 98,860,670 (GRCm38) |
G417A |
probably benign |
Het |
Tnpo3 |
C |
G |
6: 29,565,843 (GRCm38) |
G504A |
probably benign |
Het |
Tnr |
T |
C |
1: 159,895,095 (GRCm38) |
F1037L |
probably benign |
Het |
Tnrc6b |
C |
T |
15: 80,927,690 (GRCm38) |
R813* |
probably null |
Het |
Togaram2 |
A |
G |
17: 71,714,280 (GRCm38) |
K687R |
possibly damaging |
Het |
Tox |
C |
A |
4: 6,688,450 (GRCm38) |
R519M |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,094,782 (GRCm38) |
D656G |
probably damaging |
Het |
Trank1 |
G |
A |
9: 111,364,710 (GRCm38) |
D601N |
probably damaging |
Het |
Trav13d-4 |
C |
G |
14: 53,073,170 (GRCm38) |
T76S |
probably benign |
Het |
Trav16n |
C |
T |
14: 53,351,573 (GRCm38) |
A101V |
possibly damaging |
Het |
Trav5-4 |
A |
G |
14: 53,704,239 (GRCm38) |
E23G |
possibly damaging |
Het |
Trav8d-2 |
T |
G |
14: 53,042,808 (GRCm38) |
L85R |
probably damaging |
Het |
Tril |
G |
A |
6: 53,818,920 (GRCm38) |
T439M |
probably benign |
Het |
Trim30a |
C |
A |
7: 104,435,654 (GRCm38) |
W116C |
probably damaging |
Het |
Trim30b |
C |
A |
7: 104,366,100 (GRCm38) |
S27I |
probably damaging |
Het |
Trim42 |
T |
G |
9: 97,369,622 (GRCm38) |
N75H |
probably benign |
Het |
Trim43c |
A |
C |
9: 88,842,935 (GRCm38) |
|
probably null |
Het |
Trim45 |
A |
C |
3: 100,925,640 (GRCm38) |
E396D |
probably benign |
Het |
Trim5 |
C |
T |
7: 104,266,225 (GRCm38) |
A294T |
possibly damaging |
Het |
Trim67 |
A |
G |
8: 124,817,041 (GRCm38) |
Q380R |
probably damaging |
Het |
Triml1 |
T |
A |
8: 43,130,398 (GRCm38) |
I389F |
probably damaging |
Het |
Trip12 |
A |
C |
1: 84,766,168 (GRCm38) |
N500K |
probably damaging |
Het |
Trip4 |
G |
A |
9: 65,864,415 (GRCm38) |
R278* |
probably null |
Het |
Trp53bp1 |
T |
C |
2: 121,253,645 (GRCm38) |
K247E |
probably benign |
Het |
Trp63 |
G |
A |
16: 25,763,313 (GRCm38) |
R37K |
probably benign |
Het |
Trpm7 |
G |
T |
2: 126,797,281 (GRCm38) |
A1711E |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,834,197 (GRCm38) |
K2802R |
probably benign |
Het |
Tspan5 |
G |
C |
3: 138,898,326 (GRCm38) |
W228C |
possibly damaging |
Het |
Tssk4 |
A |
G |
14: 55,650,923 (GRCm38) |
K83R |
probably damaging |
Het |
Ttbk1 |
C |
A |
17: 46,446,325 (GRCm38) |
A1128S |
probably benign |
Het |
Ttc16 |
C |
A |
2: 32,769,333 (GRCm38) |
L251F |
probably damaging |
Het |
Ttc23l |
C |
A |
15: 10,533,667 (GRCm38) |
R263S |
probably damaging |
Het |
Ttc28 |
G |
C |
5: 111,286,315 (GRCm38) |
G2405A |
probably benign |
Het |
Ttc30b |
T |
G |
2: 75,937,982 (GRCm38) |
E142D |
probably benign |
Het |
Ttc39c |
G |
T |
18: 12,686,963 (GRCm38) |
M15I |
possibly damaging |
Het |
Ttll1 |
C |
T |
15: 83,498,189 (GRCm38) |
V201I |
probably damaging |
Het |
Ttll12 |
T |
C |
15: 83,582,078 (GRCm38) |
Q394R |
probably damaging |
Het |
Ttll2 |
T |
G |
17: 7,351,526 (GRCm38) |
D334A |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,738,687 (GRCm38) |
E25541D |
possibly damaging |
Het |
Ttn |
C |
G |
2: 76,746,951 (GRCm38) |
E24533Q |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,752,230 (GRCm38) |
A14446E |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,752,519 (GRCm38) |
W20931R |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,787,269 (GRCm38) |
K14540T |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,848,325 (GRCm38) |
|
probably benign |
Het |
Tubal3 |
A |
C |
13: 3,933,511 (GRCm38) |
E430D |
probably benign |
Het |
Tubb3 |
G |
C |
8: 123,421,534 (GRCm38) |
G402A |
probably damaging |
Het |
Tubd1 |
G |
A |
11: 86,549,470 (GRCm38) |
G107S |
probably damaging |
Het |
Tubd1 |
A |
T |
11: 86,555,167 (GRCm38) |
K211M |
probably damaging |
Het |
Tubgcp5 |
G |
A |
7: 55,815,101 (GRCm38) |
G577S |
probably benign |
Het |
Tulp2 |
A |
C |
7: 45,521,986 (GRCm38) |
K404T |
probably damaging |
Het |
Tyro3 |
T |
G |
2: 119,809,467 (GRCm38) |
I377S |
probably benign |
Het |
Ube4b |
A |
G |
4: 149,335,125 (GRCm38) |
I1042T |
possibly damaging |
Het |
Ubl4b |
T |
G |
3: 107,554,403 (GRCm38) |
E180D |
unknown |
Het |
Ubqln5 |
T |
A |
7: 104,128,971 (GRCm38) |
K215N |
possibly damaging |
Het |
Ubqlnl |
A |
G |
7: 104,149,993 (GRCm38) |
V99A |
probably damaging |
Het |
Ubr3 |
A |
G |
2: 69,922,367 (GRCm38) |
T322A |
probably benign |
Het |
Uggt1 |
A |
C |
1: 36,174,191 (GRCm38) |
F861C |
probably damaging |
Het |
Ugt1a10 |
T |
C |
1: 88,055,842 (GRCm38) |
F121L |
probably benign |
Het |
Umps |
CCTGACTGA |
CCTGA |
16: 33,966,825 (GRCm38) |
|
probably null |
Het |
Unc13a |
C |
A |
8: 71,654,803 (GRCm38) |
|
probably null |
Het |
Unc5c |
T |
G |
3: 141,733,900 (GRCm38) |
L111V |
probably damaging |
Het |
Unc79 |
C |
A |
12: 103,021,012 (GRCm38) |
H187N |
probably damaging |
Het |
Unc80 |
C |
G |
1: 66,646,451 (GRCm38) |
P2245A |
possibly damaging |
Het |
Ush2a |
A |
C |
1: 188,947,004 (GRCm38) |
N4803T |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,911,983 (GRCm38) |
L4514P |
probably benign |
Het |
Usp17lb |
G |
A |
7: 104,841,129 (GRCm38) |
P197L |
probably benign |
Het |
Usp43 |
C |
A |
11: 67,856,040 (GRCm38) |
R942L |
probably benign |
Het |
Usp51 |
C |
T |
X: 153,008,223 (GRCm38) |
P271L |
probably benign |
Het |
Usp51 |
C |
T |
X: 153,008,222 (GRCm38) |
P271S |
probably benign |
Het |
Vmn1r12 |
T |
G |
6: 57,158,981 (GRCm38) |
L21R |
probably damaging |
Het |
Vmn1r176 |
C |
T |
7: 23,835,173 (GRCm38) |
R185H |
probably benign |
Het |
Vmn1r179 |
A |
G |
7: 23,928,482 (GRCm38) |
I33V |
probably benign |
Het |
Vmn1r188 |
T |
C |
13: 22,088,280 (GRCm38) |
W135R |
probably damaging |
Het |
Vmn1r212 |
A |
C |
13: 22,883,762 (GRCm38) |
F134V |
probably damaging |
Het |
Vmn1r229 |
C |
A |
17: 20,815,065 (GRCm38) |
L191M |
probably damaging |
Het |
Vmn1r232 |
C |
A |
17: 20,913,838 (GRCm38) |
V167F |
probably benign |
Het |
Vmn1r4 |
G |
A |
6: 56,957,065 (GRCm38) |
V185M |
possibly damaging |
Het |
Vmn1r46 |
A |
G |
6: 89,976,741 (GRCm38) |
R191G |
probably damaging |
Het |
Vmn1r72 |
T |
G |
7: 11,670,173 (GRCm38) |
N116T |
probably benign |
Het |
Vmn1r78 |
A |
C |
7: 12,152,714 (GRCm38) |
K84T |
probably damaging |
Het |
Vmn2r10 |
A |
G |
5: 108,996,113 (GRCm38) |
F657S |
probably damaging |
Het |
Vmn2r101 |
C |
A |
17: 19,588,975 (GRCm38) |
A122D |
possibly damaging |
Het |
Vmn2r103 |
C |
A |
17: 19,795,047 (GRCm38) |
S483Y |
probably benign |
Het |
Vmn2r108 |
C |
T |
17: 20,471,113 (GRCm38) |
V383M |
probably benign |
Het |
Vmn2r110 |
T |
G |
17: 20,583,680 (GRCm38) |
H211P |
probably damaging |
Het |
Vmn2r112 |
C |
G |
17: 22,605,078 (GRCm38) |
S438C |
possibly damaging |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,290,932 (GRCm38) |
|
probably null |
Het |
Vmn2r12 |
G |
T |
5: 109,092,780 (GRCm38) |
H156N |
probably benign |
Het |
Vmn2r16 |
TA |
T |
5: 109,363,913 (GRCm38) |
|
probably null |
Het |
Vmn2r16 |
A |
C |
5: 109,340,515 (GRCm38) |
Q418P |
probably benign |
Het |
Vmn2r19 |
T |
G |
6: 123,308,339 (GRCm38) |
L3V |
probably benign |
Het |
Vmn2r23 |
A |
C |
6: 123,742,108 (GRCm38) |
T807P |
probably damaging |
Het |
Vmn2r24 |
A |
C |
6: 123,804,196 (GRCm38) |
S454R |
probably benign |
Het |
Vmn2r45 |
T |
A |
7: 8,471,485 (GRCm38) |
E848V |
probably benign |
Het |
Vmn2r5 |
T |
G |
3: 64,509,542 (GRCm38) |
N65T |
probably benign |
Het |
Vmn2r50 |
G |
T |
7: 10,046,159 (GRCm38) |
L432I |
probably benign |
Het |
Vmn2r50 |
G |
C |
7: 10,037,500 (GRCm38) |
T758R |
possibly damaging |
Het |
Vmn2r59 |
G |
T |
7: 42,012,414 (GRCm38) |
A659E |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 42,299,964 (GRCm38) |
T603A |
possibly damaging |
Het |
Vmn2r63 |
G |
A |
7: 42,928,559 (GRCm38) |
T185I |
probably benign |
Het |
Vmn2r65 |
C |
A |
7: 84,943,265 (GRCm38) |
|
probably null |
Het |
Vmn2r70 |
A |
C |
7: 85,564,760 (GRCm38) |
L395V |
possibly damaging |
Het |
Vmn2r79 |
T |
G |
7: 87,002,341 (GRCm38) |
F316C |
probably damaging |
Het |
Vmn2r8 |
A |
C |
5: 108,801,998 (GRCm38) |
F328V |
probably damaging |
Het |
Vmn2r82 |
T |
G |
10: 79,356,622 (GRCm38) |
F11C |
probably damaging |
Het |
Vmn2r87 |
C |
A |
10: 130,472,314 (GRCm38) |
R685M |
probably damaging |
Het |
Vmn2r90 |
C |
A |
17: 17,733,617 (GRCm38) |
A681E |
probably damaging |
Het |
Vmn2r93 |
A |
C |
17: 18,326,403 (GRCm38) |
K846Q |
probably damaging |
Het |
Vmn2r95 |
C |
A |
17: 18,440,401 (GRCm38) |
F358L |
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,597,366 (GRCm38) |
L594I |
possibly damaging |
Het |
Vmn2r99 |
C |
A |
17: 19,379,301 (GRCm38) |
Q416K |
probably benign |
Het |
Vmo1 |
T |
A |
11: 70,513,817 (GRCm38) |
L119F |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,913,975 (GRCm38) |
S1256P |
probably damaging |
Het |
Vwa8 |
C |
T |
14: 78,982,246 (GRCm38) |
A478V |
probably benign |
Het |
Washc4 |
C |
G |
10: 83,576,741 (GRCm38) |
A749G |
probably benign |
Het |
Wbp2 |
T |
A |
11: 116,086,913 (GRCm38) |
K5* |
probably null |
Het |
Wdcp |
A |
C |
12: 4,850,825 (GRCm38) |
K227T |
probably damaging |
Het |
Wdr13 |
A |
C |
X: 8,125,622 (GRCm38) |
F369V |
probably damaging |
Het |
Wdr13 |
C |
A |
X: 8,125,624 (GRCm38) |
S460I |
probably damaging |
Het |
Wdr3 |
T |
G |
3: 100,144,344 (GRCm38) |
K663T |
probably benign |
Het |
Wdr36 |
T |
G |
18: 32,866,012 (GRCm38) |
|
probably null |
Het |
Wdr53 |
T |
A |
16: 32,252,298 (GRCm38) |
S154T |
probably damaging |
Het |
Wdr5b |
G |
A |
16: 36,042,443 (GRCm38) |
A311T |
probably damaging |
Het |
Wdr64 |
A |
T |
1: 175,705,985 (GRCm38) |
Q62H |
possibly damaging |
Het |
Wdr82 |
A |
C |
9: 106,184,800 (GRCm38) |
I221L |
probably benign |
Het |
Wnt5a |
C |
T |
14: 28,522,728 (GRCm38) |
R311C |
probably damaging |
Het |
Wrap53 |
G |
A |
11: 69,578,498 (GRCm38) |
S144F |
probably damaging |
Het |
Wsb2 |
C |
A |
5: 117,377,506 (GRCm38) |
P392Q |
probably damaging |
Het |
Wwc1 |
T |
G |
11: 35,883,482 (GRCm38) |
N317T |
possibly damaging |
Het |
Wwp2 |
G |
A |
8: 107,555,087 (GRCm38) |
E303K |
probably damaging |
Het |
Xdh |
C |
T |
17: 73,886,428 (GRCm38) |
S1291N |
probably benign |
Het |
Xirp1 |
T |
G |
9: 120,016,907 (GRCm38) |
Q970P |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,513,321 (GRCm38) |
T1969A |
probably benign |
Het |
Xpot |
A |
C |
10: 121,601,323 (GRCm38) |
I830S |
probably damaging |
Het |
Xylb |
T |
A |
9: 119,381,614 (GRCm38) |
L388M |
probably benign |
Het |
Ylpm1 |
G |
A |
12: 85,030,155 (GRCm38) |
R760K |
possibly damaging |
Het |
Zadh2 |
G |
A |
18: 84,094,927 (GRCm38) |
V243I |
probably damaging |
Het |
Zbtb34 |
C |
G |
2: 33,411,108 (GRCm38) |
E474Q |
probably damaging |
Het |
Zc3h12b |
A |
C |
X: 95,899,442 (GRCm38) |
K116T |
probably damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,945,466 (GRCm38) |
|
probably null |
Het |
Zfat |
G |
A |
15: 68,187,101 (GRCm38) |
A195V |
probably benign |
Het |
Zfhx2 |
T |
G |
14: 55,074,180 (GRCm38) |
Q352H |
possibly damaging |
Het |
Zfhx3 |
A |
C |
8: 108,951,357 (GRCm38) |
K3013T |
possibly damaging |
Het |
Zfp106 |
G |
T |
2: 120,530,490 (GRCm38) |
L1047I |
probably damaging |
Het |
Zfp109 |
A |
G |
7: 24,228,935 (GRCm38) |
F358L |
probably benign |
Het |
Zfp157 |
T |
C |
5: 138,457,199 (GRCm38) |
L553P |
probably damaging |
Het |
Zfp273 |
A |
T |
13: 67,825,394 (GRCm38) |
I214F |
possibly damaging |
Het |
Zfp326 |
T |
A |
5: 105,888,630 (GRCm38) |
Y136N |
probably damaging |
Het |
Zfp386 |
G |
A |
12: 116,054,773 (GRCm38) |
E21K |
possibly damaging |
Het |
Zfp42 |
C |
G |
8: 43,295,805 (GRCm38) |
V220L |
probably benign |
Het |
Zfp507 |
C |
G |
7: 35,794,277 (GRCm38) |
S447T |
possibly damaging |
Het |
Zfp518b |
C |
A |
5: 38,674,293 (GRCm38) |
S123I |
probably damaging |
Het |
Zfp541 |
A |
C |
7: 16,079,795 (GRCm38) |
K791T |
probably benign |
Het |
Zfp553 |
G |
T |
7: 127,235,498 (GRCm38) |
G75V |
probably damaging |
Het |
Zfp57 |
T |
C |
17: 37,010,138 (GRCm38) |
F295L |
probably damaging |
Het |
Zfp593 |
G |
C |
4: 134,245,442 (GRCm38) |
A21G |
probably benign |
Het |
Zfp598 |
CCAT |
CCATCAT |
17: 24,680,210 (GRCm38) |
|
probably benign |
Het |
Zfp638 |
A |
C |
6: 83,944,811 (GRCm38) |
K640T |
probably damaging |
Het |
Zfp648 |
T |
C |
1: 154,204,520 (GRCm38) |
F142L |
probably benign |
Het |
Zfp729b |
C |
T |
13: 67,593,070 (GRCm38) |
E359K |
possibly damaging |
Het |
Zfp775 |
G |
A |
6: 48,620,688 (GRCm38) |
E499K |
probably damaging |
Het |
Zfp868 |
TTAT |
TT |
8: 69,611,910 (GRCm38) |
|
probably null |
Het |
Zfp959 |
A |
G |
17: 55,898,135 (GRCm38) |
R391G |
probably damaging |
Het |
Zfp976 |
T |
G |
7: 42,612,760 (GRCm38) |
E551A |
possibly damaging |
Het |
Zfx |
A |
C |
X: 94,079,443 (GRCm38) |
L585V |
probably damaging |
Het |
Zglp1 |
C |
T |
9: 21,067,000 (GRCm38) |
R27Q |
possibly damaging |
Het |
Zhx3 |
GGAAG |
GG |
2: 160,779,755 (GRCm38) |
|
probably benign |
Het |
Zic2 |
A |
T |
14: 122,478,675 (GRCm38) |
H403L |
probably damaging |
Het |
Zim1 |
T |
G |
7: 6,677,659 (GRCm38) |
N335T |
possibly damaging |
Het |
Zkscan3 |
T |
C |
13: 21,388,565 (GRCm38) |
K299R |
possibly damaging |
Het |
Zkscan4 |
T |
G |
13: 21,483,897 (GRCm38) |
L173V |
probably damaging |
Het |
Zmiz2 |
A |
T |
11: 6,399,603 (GRCm38) |
H421L |
probably damaging |
Het |
Zmynd15 |
A |
C |
11: 70,461,135 (GRCm38) |
K60T |
possibly damaging |
Het |
Zmynd8 |
A |
C |
2: 165,828,171 (GRCm38) |
L481R |
probably benign |
Het |
Zpbp |
C |
A |
11: 11,408,568 (GRCm38) |
R233L |
probably damaging |
Het |
Zscan18 |
G |
A |
7: 12,775,093 (GRCm38) |
|
probably benign |
Het |
Zscan18 |
G |
T |
7: 12,775,067 (GRCm38) |
Q169K |
probably benign |
Het |
Zscan26 |
T |
G |
13: 21,445,463 (GRCm38) |
K290T |
probably damaging |
Het |
|