Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
T |
C |
11: 109,679,547 (GRCm39) |
|
probably benign |
Het |
6430571L13Rik |
T |
A |
9: 107,219,707 (GRCm39) |
D53E |
possibly damaging |
Het |
A2ml1 |
T |
A |
6: 128,527,736 (GRCm39) |
N1018I |
probably damaging |
Het |
Abi3 |
C |
A |
11: 95,727,937 (GRCm39) |
A85S |
probably benign |
Het |
Acsl5 |
A |
T |
19: 55,272,904 (GRCm39) |
M340L |
probably benign |
Het |
Adam29 |
T |
A |
8: 56,324,612 (GRCm39) |
H614L |
probably benign |
Het |
Adgrg6 |
A |
T |
10: 14,312,628 (GRCm39) |
S720T |
probably damaging |
Het |
Adrb2 |
G |
T |
18: 62,312,441 (GRCm39) |
A128E |
probably damaging |
Het |
Afap1l1 |
T |
C |
18: 61,872,291 (GRCm39) |
E510G |
probably benign |
Het |
Angel1 |
A |
G |
12: 86,764,487 (GRCm39) |
|
probably null |
Het |
Aox3 |
T |
G |
1: 58,211,458 (GRCm39) |
I1005S |
possibly damaging |
Het |
Apc |
C |
A |
18: 34,451,507 (GRCm39) |
P2767Q |
probably damaging |
Het |
Apob |
T |
G |
12: 8,066,193 (GRCm39) |
D4387E |
probably benign |
Het |
Apobr |
T |
C |
7: 126,185,827 (GRCm39) |
V446A |
possibly damaging |
Het |
Arhgap28 |
A |
T |
17: 68,203,108 (GRCm39) |
|
probably null |
Het |
Aspm |
G |
T |
1: 139,419,339 (GRCm39) |
K3001N |
probably damaging |
Het |
Asxl3 |
G |
T |
18: 22,655,937 (GRCm39) |
V1316F |
probably benign |
Het |
Atp2a1 |
T |
A |
7: 126,046,162 (GRCm39) |
|
probably null |
Het |
Bach1 |
A |
G |
16: 87,526,359 (GRCm39) |
D607G |
possibly damaging |
Het |
Batf3 |
A |
G |
1: 190,832,935 (GRCm39) |
D27G |
probably damaging |
Het |
Baz1a |
G |
T |
12: 55,022,055 (GRCm39) |
Q76K |
probably damaging |
Het |
Bdnf |
G |
A |
2: 109,553,883 (GRCm39) |
V86M |
probably benign |
Het |
Birc7 |
A |
G |
2: 180,573,098 (GRCm39) |
I172V |
probably benign |
Het |
Bod1l |
A |
C |
5: 41,988,880 (GRCm39) |
V409G |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,364,563 (GRCm39) |
E337V |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,612,520 (GRCm39) |
F287L |
possibly damaging |
Het |
Ces1e |
A |
G |
8: 93,950,671 (GRCm39) |
Y37H |
probably benign |
Het |
Clasrp |
A |
T |
7: 19,318,418 (GRCm39) |
|
probably benign |
Het |
Clec2d |
T |
A |
6: 129,160,090 (GRCm39) |
S35T |
probably damaging |
Het |
Cntn4 |
T |
A |
6: 106,639,539 (GRCm39) |
D556E |
probably benign |
Het |
Cntnap5c |
A |
T |
17: 58,349,422 (GRCm39) |
D245V |
probably benign |
Het |
Col5a1 |
T |
A |
2: 27,818,255 (GRCm39) |
L160* |
probably null |
Het |
Col6a6 |
T |
C |
9: 105,654,943 (GRCm39) |
E926G |
probably benign |
Het |
Cpsf2 |
T |
A |
12: 101,951,490 (GRCm39) |
H142Q |
probably benign |
Het |
Cr2 |
A |
C |
1: 194,853,419 (GRCm39) |
S20A |
possibly damaging |
Het |
Ct45a |
G |
A |
X: 55,590,399 (GRCm39) |
P134L |
probably benign |
Het |
Cyp2j5 |
A |
T |
4: 96,547,749 (GRCm39) |
H164Q |
probably benign |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,703,811 (GRCm39) |
V1124M |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,323,838 (GRCm39) |
H1182R |
probably damaging |
Het |
Dnah2 |
A |
T |
11: 69,368,509 (GRCm39) |
S1709T |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,560,844 (GRCm39) |
V776A |
probably damaging |
Het |
Emc3 |
T |
C |
6: 113,492,992 (GRCm39) |
T220A |
probably benign |
Het |
Entpd1 |
A |
C |
19: 40,715,769 (GRCm39) |
N312T |
probably benign |
Het |
Fam8a1 |
A |
T |
13: 46,824,699 (GRCm39) |
I229F |
probably damaging |
Het |
Fancc |
G |
A |
13: 63,465,205 (GRCm39) |
P501S |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,702,751 (GRCm39) |
R1704G |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,819,302 (GRCm39) |
I5012V |
probably benign |
Het |
Glce |
T |
C |
9: 61,968,282 (GRCm39) |
T290A |
probably benign |
Het |
Gns |
G |
A |
10: 121,219,349 (GRCm39) |
|
probably null |
Het |
Gsdma2 |
A |
G |
11: 98,542,810 (GRCm39) |
N190S |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,415,887 (GRCm39) |
S563T |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,674,470 (GRCm39) |
|
probably null |
Het |
Jup |
A |
T |
11: 100,267,589 (GRCm39) |
M578K |
probably benign |
Het |
Kir3dl1 |
G |
A |
X: 135,434,594 (GRCm39) |
|
probably null |
Het |
Krt75 |
A |
G |
15: 101,482,025 (GRCm39) |
F81S |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Maged2 |
T |
A |
X: 149,594,830 (GRCm39) |
N176Y |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,333,382 (GRCm39) |
C1354* |
probably null |
Het |
Mup7 |
A |
C |
4: 60,069,742 (GRCm39) |
V74G |
possibly damaging |
Het |
Naca |
A |
G |
10: 127,877,031 (GRCm39) |
|
probably benign |
Het |
Nav3 |
T |
G |
10: 109,659,325 (GRCm39) |
Y764S |
probably damaging |
Het |
Nkpd1 |
A |
T |
7: 19,257,099 (GRCm39) |
T293S |
probably benign |
Het |
Numb |
A |
G |
12: 83,842,614 (GRCm39) |
Y510H |
probably damaging |
Het |
Nynrin |
T |
G |
14: 56,105,492 (GRCm39) |
L834R |
probably damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or2ak5 |
G |
T |
11: 58,611,347 (GRCm39) |
H176N |
probably benign |
Het |
Or8g18 |
T |
A |
9: 39,149,162 (GRCm39) |
N186I |
possibly damaging |
Het |
Otog |
T |
C |
7: 45,920,797 (GRCm39) |
V1000A |
possibly damaging |
Het |
Pafah1b3 |
A |
G |
7: 24,996,554 (GRCm39) |
V43A |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 82,030,450 (GRCm39) |
Y1775C |
possibly damaging |
Het |
Phka1 |
G |
A |
X: 101,564,437 (GRCm39) |
R1074C |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,111,765 (GRCm39) |
Y1570F |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,152,329 (GRCm39) |
K2588E |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,794,549 (GRCm39) |
T2079A |
probably damaging |
Het |
Plekhd1 |
G |
T |
12: 80,764,075 (GRCm39) |
Q212H |
probably damaging |
Het |
Plekhh1 |
C |
T |
12: 79,087,359 (GRCm39) |
R16* |
probably null |
Het |
Polm |
C |
A |
11: 5,786,207 (GRCm39) |
R120L |
probably damaging |
Het |
Ptpn22 |
T |
C |
3: 103,767,721 (GRCm39) |
M1T |
probably null |
Het |
Ptprh |
G |
A |
7: 4,567,271 (GRCm39) |
L534F |
probably benign |
Het |
Rabl6 |
C |
T |
2: 25,482,778 (GRCm39) |
|
probably null |
Het |
Rap2a |
A |
G |
14: 120,716,403 (GRCm39) |
S89G |
probably damaging |
Het |
Rara |
A |
T |
11: 98,862,406 (GRCm39) |
|
probably null |
Het |
Reck |
A |
G |
4: 43,930,295 (GRCm39) |
D623G |
probably benign |
Het |
Relt |
A |
T |
7: 100,498,023 (GRCm39) |
L237Q |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,329,598 (GRCm39) |
|
probably null |
Het |
Rtn4rl2 |
T |
G |
2: 84,710,763 (GRCm39) |
Y167S |
probably damaging |
Het |
Sec24c |
C |
T |
14: 20,738,505 (GRCm39) |
R353C |
probably damaging |
Het |
Slc35g2 |
T |
C |
9: 100,435,495 (GRCm39) |
S59G |
probably benign |
Het |
Smarcd2 |
A |
T |
11: 106,158,241 (GRCm39) |
M107K |
probably benign |
Het |
Snrnp200 |
A |
G |
2: 127,063,734 (GRCm39) |
N638D |
possibly damaging |
Het |
Sntb1 |
A |
G |
15: 55,506,179 (GRCm39) |
S465P |
probably benign |
Het |
Sp4 |
A |
G |
12: 118,263,314 (GRCm39) |
L244P |
probably damaging |
Het |
Sulf1 |
A |
G |
1: 12,887,716 (GRCm39) |
|
probably null |
Het |
Tbc1d17 |
T |
C |
7: 44,492,509 (GRCm39) |
T385A |
probably benign |
Het |
Tbx10 |
C |
A |
19: 4,047,873 (GRCm39) |
D206E |
probably benign |
Het |
Tcea2 |
C |
T |
2: 181,329,431 (GRCm39) |
P275S |
probably damaging |
Het |
Tns3 |
C |
A |
11: 8,443,121 (GRCm39) |
R414L |
probably benign |
Het |
Trip11 |
T |
C |
12: 101,852,235 (GRCm39) |
R610G |
possibly damaging |
Het |
Ugt2b1 |
T |
C |
5: 87,073,720 (GRCm39) |
K213R |
probably null |
Het |
Unc80 |
A |
G |
1: 66,647,601 (GRCm39) |
S1514G |
probably benign |
Het |
Usp7 |
G |
T |
16: 8,511,778 (GRCm39) |
Q867K |
possibly damaging |
Het |
Vim |
T |
C |
2: 13,579,463 (GRCm39) |
V74A |
probably benign |
Het |
Vmn1r234 |
A |
G |
17: 21,450,007 (GRCm39) |
Y307C |
probably benign |
Het |
Vmn2r74 |
A |
T |
7: 85,610,517 (GRCm39) |
Y58* |
probably null |
Het |
Wdr36 |
C |
A |
18: 32,983,584 (GRCm39) |
A445E |
probably damaging |
Het |
Xpo5 |
T |
A |
17: 46,532,359 (GRCm39) |
W465R |
probably damaging |
Het |
Zscan4d |
T |
A |
7: 10,898,946 (GRCm39) |
R110S |
probably damaging |
Het |
|
Other mutations in Smg1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Smg1
|
APN |
7 |
117,797,494 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00481:Smg1
|
APN |
7 |
117,810,017 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL00503:Smg1
|
APN |
7 |
117,784,706 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00927:Smg1
|
APN |
7 |
117,739,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01333:Smg1
|
APN |
7 |
117,762,601 (GRCm39) |
splice site |
probably benign |
|
IGL01344:Smg1
|
APN |
7 |
117,790,059 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01397:Smg1
|
APN |
7 |
117,762,444 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01403:Smg1
|
APN |
7 |
117,757,355 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01573:Smg1
|
APN |
7 |
117,767,185 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01872:Smg1
|
APN |
7 |
117,748,167 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02010:Smg1
|
APN |
7 |
117,785,369 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02158:Smg1
|
APN |
7 |
117,812,169 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02268:Smg1
|
APN |
7 |
117,781,764 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02314:Smg1
|
APN |
7 |
117,753,932 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02552:Smg1
|
APN |
7 |
117,795,117 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02577:Smg1
|
APN |
7 |
117,802,345 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02859:Smg1
|
APN |
7 |
117,748,156 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02890:Smg1
|
APN |
7 |
117,784,724 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02892:Smg1
|
APN |
7 |
117,767,178 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03119:Smg1
|
APN |
7 |
117,794,336 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03123:Smg1
|
APN |
7 |
117,756,404 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03128:Smg1
|
APN |
7 |
117,802,282 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03184:Smg1
|
APN |
7 |
117,779,603 (GRCm39) |
missense |
possibly damaging |
0.86 |
PIT4508001:Smg1
|
UTSW |
7 |
117,784,764 (GRCm39) |
missense |
unknown |
|
R0010:Smg1
|
UTSW |
7 |
117,771,082 (GRCm39) |
utr 3 prime |
probably benign |
|
R0010:Smg1
|
UTSW |
7 |
117,771,082 (GRCm39) |
utr 3 prime |
probably benign |
|
R0025:Smg1
|
UTSW |
7 |
117,811,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0025:Smg1
|
UTSW |
7 |
117,811,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0098:Smg1
|
UTSW |
7 |
117,744,690 (GRCm39) |
missense |
probably benign |
0.02 |
R0139:Smg1
|
UTSW |
7 |
117,751,898 (GRCm39) |
critical splice donor site |
probably null |
|
R0371:Smg1
|
UTSW |
7 |
117,767,523 (GRCm39) |
utr 3 prime |
probably benign |
|
R0415:Smg1
|
UTSW |
7 |
117,781,691 (GRCm39) |
missense |
probably benign |
0.34 |
R0416:Smg1
|
UTSW |
7 |
117,783,684 (GRCm39) |
splice site |
probably benign |
|
R0423:Smg1
|
UTSW |
7 |
117,776,103 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0600:Smg1
|
UTSW |
7 |
117,759,606 (GRCm39) |
utr 3 prime |
probably benign |
|
R0627:Smg1
|
UTSW |
7 |
117,767,084 (GRCm39) |
utr 3 prime |
probably benign |
|
R0727:Smg1
|
UTSW |
7 |
117,765,645 (GRCm39) |
utr 3 prime |
probably benign |
|
R0729:Smg1
|
UTSW |
7 |
117,745,512 (GRCm39) |
utr 3 prime |
probably benign |
|
R0841:Smg1
|
UTSW |
7 |
117,742,524 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1114:Smg1
|
UTSW |
7 |
117,759,013 (GRCm39) |
utr 3 prime |
probably benign |
|
R1256:Smg1
|
UTSW |
7 |
117,802,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1298:Smg1
|
UTSW |
7 |
117,767,434 (GRCm39) |
utr 3 prime |
probably benign |
|
R1370:Smg1
|
UTSW |
7 |
117,758,975 (GRCm39) |
utr 3 prime |
probably benign |
|
R1591:Smg1
|
UTSW |
7 |
117,756,142 (GRCm39) |
utr 3 prime |
probably benign |
|
R1736:Smg1
|
UTSW |
7 |
117,765,190 (GRCm39) |
splice site |
probably null |
|
R1755:Smg1
|
UTSW |
7 |
117,802,287 (GRCm39) |
nonsense |
probably null |
|
R1765:Smg1
|
UTSW |
7 |
117,738,938 (GRCm39) |
missense |
probably benign |
0.03 |
R1789:Smg1
|
UTSW |
7 |
117,745,021 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1845:Smg1
|
UTSW |
7 |
117,753,845 (GRCm39) |
utr 3 prime |
probably benign |
|
R1908:Smg1
|
UTSW |
7 |
117,753,422 (GRCm39) |
utr 3 prime |
probably benign |
|
R1909:Smg1
|
UTSW |
7 |
117,753,422 (GRCm39) |
utr 3 prime |
probably benign |
|
R1942:Smg1
|
UTSW |
7 |
117,757,326 (GRCm39) |
utr 3 prime |
probably benign |
|
R2064:Smg1
|
UTSW |
7 |
117,756,090 (GRCm39) |
utr 3 prime |
probably benign |
|
R2072:Smg1
|
UTSW |
7 |
117,762,389 (GRCm39) |
utr 3 prime |
probably benign |
|
R2154:Smg1
|
UTSW |
7 |
117,757,299 (GRCm39) |
utr 3 prime |
probably benign |
|
R2895:Smg1
|
UTSW |
7 |
117,788,366 (GRCm39) |
utr 3 prime |
probably benign |
|
R2915:Smg1
|
UTSW |
7 |
117,810,102 (GRCm39) |
splice site |
probably benign |
|
R3416:Smg1
|
UTSW |
7 |
117,748,076 (GRCm39) |
utr 3 prime |
probably benign |
|
R3417:Smg1
|
UTSW |
7 |
117,748,076 (GRCm39) |
utr 3 prime |
probably benign |
|
R3873:Smg1
|
UTSW |
7 |
117,753,885 (GRCm39) |
utr 3 prime |
probably benign |
|
R4082:Smg1
|
UTSW |
7 |
117,759,469 (GRCm39) |
utr 3 prime |
probably benign |
|
R4230:Smg1
|
UTSW |
7 |
117,747,956 (GRCm39) |
critical splice donor site |
probably null |
|
R4304:Smg1
|
UTSW |
7 |
117,738,741 (GRCm39) |
missense |
probably benign |
0.03 |
R4549:Smg1
|
UTSW |
7 |
117,758,906 (GRCm39) |
utr 3 prime |
probably benign |
|
R4571:Smg1
|
UTSW |
7 |
117,738,688 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4638:Smg1
|
UTSW |
7 |
117,795,149 (GRCm39) |
utr 3 prime |
probably benign |
|
R4642:Smg1
|
UTSW |
7 |
117,753,487 (GRCm39) |
utr 3 prime |
probably benign |
|
R4656:Smg1
|
UTSW |
7 |
117,812,174 (GRCm39) |
missense |
probably benign |
0.00 |
R4754:Smg1
|
UTSW |
7 |
117,755,954 (GRCm39) |
utr 3 prime |
probably benign |
|
R4798:Smg1
|
UTSW |
7 |
117,779,697 (GRCm39) |
missense |
probably benign |
0.32 |
R4906:Smg1
|
UTSW |
7 |
117,751,631 (GRCm39) |
utr 3 prime |
probably benign |
|
R4978:Smg1
|
UTSW |
7 |
117,753,470 (GRCm39) |
utr 3 prime |
probably benign |
|
R4989:Smg1
|
UTSW |
7 |
117,807,274 (GRCm39) |
missense |
probably benign |
|
R4989:Smg1
|
UTSW |
7 |
117,757,323 (GRCm39) |
utr 3 prime |
probably benign |
|
R5026:Smg1
|
UTSW |
7 |
117,792,768 (GRCm39) |
utr 3 prime |
probably benign |
|
R5124:Smg1
|
UTSW |
7 |
117,812,235 (GRCm39) |
missense |
probably benign |
0.00 |
R5318:Smg1
|
UTSW |
7 |
117,759,427 (GRCm39) |
utr 3 prime |
probably benign |
|
R5356:Smg1
|
UTSW |
7 |
117,794,356 (GRCm39) |
utr 3 prime |
probably benign |
|
R5404:Smg1
|
UTSW |
7 |
117,806,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Smg1
|
UTSW |
7 |
117,745,294 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5441:Smg1
|
UTSW |
7 |
117,794,304 (GRCm39) |
utr 3 prime |
probably benign |
|
R5490:Smg1
|
UTSW |
7 |
117,738,659 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5541:Smg1
|
UTSW |
7 |
117,756,386 (GRCm39) |
utr 3 prime |
probably benign |
|
R5564:Smg1
|
UTSW |
7 |
117,789,042 (GRCm39) |
utr 3 prime |
probably benign |
|
R5580:Smg1
|
UTSW |
7 |
117,748,125 (GRCm39) |
utr 3 prime |
probably benign |
|
R5600:Smg1
|
UTSW |
7 |
117,767,107 (GRCm39) |
utr 3 prime |
probably benign |
|
R5628:Smg1
|
UTSW |
7 |
117,753,924 (GRCm39) |
utr 3 prime |
probably benign |
|
R5646:Smg1
|
UTSW |
7 |
117,811,782 (GRCm39) |
missense |
probably benign |
0.42 |
R5656:Smg1
|
UTSW |
7 |
117,753,887 (GRCm39) |
utr 3 prime |
probably benign |
|
R5660:Smg1
|
UTSW |
7 |
117,742,570 (GRCm39) |
missense |
probably benign |
0.33 |
R5706:Smg1
|
UTSW |
7 |
117,744,813 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5786:Smg1
|
UTSW |
7 |
117,812,120 (GRCm39) |
missense |
probably benign |
0.12 |
R5890:Smg1
|
UTSW |
7 |
117,789,809 (GRCm39) |
utr 3 prime |
probably benign |
|
R5912:Smg1
|
UTSW |
7 |
117,753,809 (GRCm39) |
utr 3 prime |
probably benign |
|
R5977:Smg1
|
UTSW |
7 |
117,740,580 (GRCm39) |
utr 3 prime |
probably benign |
|
R5993:Smg1
|
UTSW |
7 |
117,739,732 (GRCm39) |
missense |
probably benign |
0.33 |
R6161:Smg1
|
UTSW |
7 |
117,762,553 (GRCm39) |
utr 3 prime |
probably benign |
|
R6187:Smg1
|
UTSW |
7 |
117,788,386 (GRCm39) |
utr 3 prime |
probably benign |
|
R6264:Smg1
|
UTSW |
7 |
117,765,310 (GRCm39) |
utr 3 prime |
probably benign |
|
R6331:Smg1
|
UTSW |
7 |
117,753,500 (GRCm39) |
utr 3 prime |
probably benign |
|
R6561:Smg1
|
UTSW |
7 |
117,765,300 (GRCm39) |
utr 3 prime |
probably benign |
|
R6571:Smg1
|
UTSW |
7 |
117,783,737 (GRCm39) |
utr 3 prime |
probably benign |
|
R6736:Smg1
|
UTSW |
7 |
117,756,389 (GRCm39) |
utr 3 prime |
probably benign |
|
R6752:Smg1
|
UTSW |
7 |
117,762,539 (GRCm39) |
utr 3 prime |
probably benign |
|
R6777:Smg1
|
UTSW |
7 |
117,788,340 (GRCm39) |
utr 3 prime |
probably benign |
|
R6788:Smg1
|
UTSW |
7 |
117,783,794 (GRCm39) |
utr 3 prime |
probably benign |
|
R6883:Smg1
|
UTSW |
7 |
117,767,403 (GRCm39) |
utr 3 prime |
probably benign |
|
R6991:Smg1
|
UTSW |
7 |
117,767,091 (GRCm39) |
utr 3 prime |
probably benign |
|
R7056:Smg1
|
UTSW |
7 |
117,745,623 (GRCm39) |
splice site |
probably benign |
|
R7058:Smg1
|
UTSW |
7 |
117,797,502 (GRCm39) |
utr 3 prime |
probably benign |
|
R7100:Smg1
|
UTSW |
7 |
117,783,743 (GRCm39) |
missense |
unknown |
|
R7133:Smg1
|
UTSW |
7 |
117,752,131 (GRCm39) |
missense |
unknown |
|
R7221:Smg1
|
UTSW |
7 |
117,782,020 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7229:Smg1
|
UTSW |
7 |
117,776,178 (GRCm39) |
missense |
probably benign |
0.03 |
R7293:Smg1
|
UTSW |
7 |
117,765,322 (GRCm39) |
missense |
unknown |
|
R7361:Smg1
|
UTSW |
7 |
117,784,200 (GRCm39) |
missense |
unknown |
|
R7438:Smg1
|
UTSW |
7 |
117,795,116 (GRCm39) |
missense |
unknown |
|
R7686:Smg1
|
UTSW |
7 |
117,767,081 (GRCm39) |
missense |
unknown |
|
R7798:Smg1
|
UTSW |
7 |
117,771,162 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7908:Smg1
|
UTSW |
7 |
117,785,357 (GRCm39) |
missense |
unknown |
|
R7923:Smg1
|
UTSW |
7 |
117,742,545 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7978:Smg1
|
UTSW |
7 |
117,792,878 (GRCm39) |
missense |
unknown |
|
R7997:Smg1
|
UTSW |
7 |
117,772,365 (GRCm39) |
missense |
unknown |
|
R7997:Smg1
|
UTSW |
7 |
117,772,364 (GRCm39) |
missense |
unknown |
|
R8025:Smg1
|
UTSW |
7 |
117,806,212 (GRCm39) |
nonsense |
probably null |
|
R8056:Smg1
|
UTSW |
7 |
117,759,589 (GRCm39) |
missense |
unknown |
|
R8061:Smg1
|
UTSW |
7 |
117,751,610 (GRCm39) |
missense |
unknown |
|
R8095:Smg1
|
UTSW |
7 |
117,772,285 (GRCm39) |
missense |
unknown |
|
R8198:Smg1
|
UTSW |
7 |
117,744,829 (GRCm39) |
missense |
probably benign |
0.03 |
R8399:Smg1
|
UTSW |
7 |
117,789,794 (GRCm39) |
missense |
unknown |
|
R8445:Smg1
|
UTSW |
7 |
117,736,200 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8519:Smg1
|
UTSW |
7 |
117,770,982 (GRCm39) |
utr 3 prime |
probably benign |
|
R8817:Smg1
|
UTSW |
7 |
117,758,887 (GRCm39) |
missense |
unknown |
|
R8832:Smg1
|
UTSW |
7 |
117,739,006 (GRCm39) |
missense |
probably benign |
0.33 |
R8855:Smg1
|
UTSW |
7 |
117,806,122 (GRCm39) |
missense |
unknown |
|
R8866:Smg1
|
UTSW |
7 |
117,806,122 (GRCm39) |
missense |
unknown |
|
R8946:Smg1
|
UTSW |
7 |
117,751,900 (GRCm39) |
missense |
probably null |
|
R8954:Smg1
|
UTSW |
7 |
117,806,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8967:Smg1
|
UTSW |
7 |
117,765,739 (GRCm39) |
missense |
unknown |
|
R9072:Smg1
|
UTSW |
7 |
117,783,032 (GRCm39) |
missense |
unknown |
|
R9090:Smg1
|
UTSW |
7 |
117,811,786 (GRCm39) |
missense |
unknown |
|
R9156:Smg1
|
UTSW |
7 |
117,753,884 (GRCm39) |
missense |
unknown |
|
R9198:Smg1
|
UTSW |
7 |
117,795,179 (GRCm39) |
missense |
unknown |
|
R9240:Smg1
|
UTSW |
7 |
117,739,031 (GRCm39) |
missense |
probably benign |
0.18 |
R9271:Smg1
|
UTSW |
7 |
117,811,786 (GRCm39) |
missense |
unknown |
|
R9289:Smg1
|
UTSW |
7 |
117,744,639 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9378:Smg1
|
UTSW |
7 |
117,777,998 (GRCm39) |
nonsense |
probably null |
|
R9396:Smg1
|
UTSW |
7 |
117,807,303 (GRCm39) |
missense |
unknown |
|
R9469:Smg1
|
UTSW |
7 |
117,739,774 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9539:Smg1
|
UTSW |
7 |
117,744,976 (GRCm39) |
missense |
probably benign |
0.03 |
R9549:Smg1
|
UTSW |
7 |
117,795,254 (GRCm39) |
missense |
unknown |
|
R9563:Smg1
|
UTSW |
7 |
117,812,208 (GRCm39) |
missense |
unknown |
|
R9564:Smg1
|
UTSW |
7 |
117,812,208 (GRCm39) |
missense |
unknown |
|
R9597:Smg1
|
UTSW |
7 |
117,812,270 (GRCm39) |
missense |
unknown |
|
R9643:Smg1
|
UTSW |
7 |
117,755,933 (GRCm39) |
missense |
unknown |
|
R9703:Smg1
|
UTSW |
7 |
117,739,744 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9730:Smg1
|
UTSW |
7 |
117,783,004 (GRCm39) |
missense |
unknown |
|
Z1088:Smg1
|
UTSW |
7 |
117,777,622 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1088:Smg1
|
UTSW |
7 |
117,767,884 (GRCm39) |
nonsense |
probably null |
|
Z1088:Smg1
|
UTSW |
7 |
117,753,858 (GRCm39) |
utr 3 prime |
probably benign |
|
Z1176:Smg1
|
UTSW |
7 |
117,806,130 (GRCm39) |
missense |
unknown |
|
Z1176:Smg1
|
UTSW |
7 |
117,806,110 (GRCm39) |
missense |
unknown |
|
Z1177:Smg1
|
UTSW |
7 |
117,812,256 (GRCm39) |
missense |
unknown |
|
Z1177:Smg1
|
UTSW |
7 |
117,767,831 (GRCm39) |
missense |
probably null |
|
|