Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
C |
4: 53,042,376 (GRCm39) |
R1899G |
probably damaging |
Het |
Abca6 |
C |
T |
11: 110,132,407 (GRCm39) |
G296D |
probably damaging |
Het |
Abcb5 |
A |
T |
12: 118,854,284 (GRCm39) |
|
probably null |
Het |
Adam28 |
T |
G |
14: 68,870,657 (GRCm39) |
T339P |
probably damaging |
Het |
Adam34l |
T |
A |
8: 44,079,189 (GRCm39) |
H345L |
probably damaging |
Het |
Adcy10 |
C |
G |
1: 165,345,943 (GRCm39) |
Q331E |
probably damaging |
Het |
Aldh1a2 |
A |
T |
9: 71,160,196 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
A |
6: 85,673,639 (GRCm39) |
I3078N |
probably damaging |
Het |
Amtn |
A |
T |
5: 88,528,139 (GRCm39) |
N71Y |
probably damaging |
Het |
Arhgef18 |
A |
T |
8: 3,438,753 (GRCm39) |
Y370F |
probably benign |
Het |
Arid4a |
T |
C |
12: 71,121,862 (GRCm39) |
S748P |
probably benign |
Het |
Atp2b1 |
C |
A |
10: 98,852,842 (GRCm39) |
Q108K |
possibly damaging |
Het |
Bcdin3d |
T |
C |
15: 99,368,830 (GRCm39) |
D123G |
probably benign |
Het |
Capn15 |
A |
G |
17: 26,184,410 (GRCm39) |
S24P |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,896,754 (GRCm39) |
S1550R |
possibly damaging |
Het |
Ccdc7a |
C |
T |
8: 129,559,091 (GRCm39) |
V1174M |
probably damaging |
Het |
Cd22 |
T |
A |
7: 30,575,578 (GRCm39) |
I155F |
probably damaging |
Het |
Ceacam3 |
T |
C |
7: 16,895,863 (GRCm39) |
I611T |
possibly damaging |
Het |
Chrna1 |
C |
T |
2: 73,397,180 (GRCm39) |
D370N |
possibly damaging |
Het |
Dlg2 |
C |
A |
7: 92,093,716 (GRCm39) |
|
probably null |
Het |
Dll4 |
A |
T |
2: 119,164,276 (GRCm39) |
|
probably null |
Het |
Eif5b |
T |
C |
1: 38,058,108 (GRCm39) |
S137P |
probably benign |
Het |
Epn2 |
A |
T |
11: 61,424,467 (GRCm39) |
M250K |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,161,283 (GRCm39) |
Q3149L |
probably damaging |
Het |
Fbxl13 |
G |
A |
5: 21,761,812 (GRCm39) |
S341F |
probably benign |
Het |
Gm5141 |
A |
T |
13: 62,922,597 (GRCm39) |
C191S |
probably damaging |
Het |
Gm5150 |
C |
T |
3: 16,044,815 (GRCm39) |
G137S |
probably damaging |
Het |
Gpr75 |
C |
T |
11: 30,841,529 (GRCm39) |
R145W |
probably damaging |
Het |
Heatr5b |
G |
A |
17: 79,060,502 (GRCm39) |
H2058Y |
probably benign |
Het |
Ina |
G |
A |
19: 47,012,000 (GRCm39) |
E473K |
probably benign |
Het |
Irx6 |
T |
C |
8: 93,402,700 (GRCm39) |
S22P |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,394,933 (GRCm39) |
M32K |
probably damaging |
Het |
Jmjd1c |
T |
A |
10: 67,061,795 (GRCm39) |
S1383T |
probably benign |
Het |
Lclat1 |
T |
A |
17: 73,468,828 (GRCm39) |
S3T |
probably damaging |
Het |
Llgl1 |
G |
A |
11: 60,600,486 (GRCm39) |
V612M |
probably damaging |
Het |
Mios |
A |
G |
6: 8,231,239 (GRCm39) |
R708G |
probably benign |
Het |
Mphosph8 |
T |
C |
14: 56,925,943 (GRCm39) |
L636P |
probably damaging |
Het |
Mrgpra2b |
T |
A |
7: 47,113,893 (GRCm39) |
N254Y |
probably damaging |
Het |
Myo7a |
C |
T |
7: 97,722,374 (GRCm39) |
V1184M |
probably benign |
Het |
Myog |
G |
A |
1: 134,218,226 (GRCm39) |
D145N |
probably benign |
Het |
Nat10 |
T |
A |
2: 103,570,231 (GRCm39) |
I371F |
possibly damaging |
Het |
Neb |
A |
T |
2: 52,057,656 (GRCm39) |
Y229* |
probably null |
Het |
Nlrp6 |
T |
A |
7: 140,507,422 (GRCm39) |
I896K |
possibly damaging |
Het |
Or11g7 |
A |
T |
14: 50,691,042 (GRCm39) |
I178L |
possibly damaging |
Het |
Or52p2 |
G |
A |
7: 102,237,878 (GRCm39) |
A24V |
probably benign |
Het |
Or5an11 |
T |
C |
19: 12,246,070 (GRCm39) |
S159P |
probably damaging |
Het |
Pate5 |
T |
A |
9: 35,755,351 (GRCm39) |
K3* |
probably null |
Het |
Pcdhgc5 |
A |
C |
18: 37,954,301 (GRCm39) |
E525A |
probably damaging |
Het |
Pira1 |
T |
A |
7: 3,741,930 (GRCm39) |
Y150F |
probably benign |
Het |
Pkd2 |
C |
A |
5: 104,607,790 (GRCm39) |
D96E |
probably benign |
Het |
Prtg |
A |
G |
9: 72,815,138 (GRCm39) |
D1022G |
probably damaging |
Het |
Ptpn13 |
T |
C |
5: 103,689,150 (GRCm39) |
M981T |
probably benign |
Het |
Rc3h2 |
C |
A |
2: 37,299,482 (GRCm39) |
A183S |
probably damaging |
Het |
Rorb |
A |
T |
19: 18,937,856 (GRCm39) |
I270N |
probably damaging |
Het |
Rpgrip1 |
C |
T |
14: 52,378,646 (GRCm39) |
R524W |
probably damaging |
Het |
Slc25a10 |
T |
C |
11: 120,386,031 (GRCm39) |
V124A |
probably damaging |
Het |
Slc40a1 |
T |
A |
1: 45,958,107 (GRCm39) |
I109F |
probably damaging |
Het |
Spen |
G |
A |
4: 141,202,820 (GRCm39) |
R1936W |
probably damaging |
Het |
St6gal2 |
T |
A |
17: 55,789,514 (GRCm39) |
Y183N |
probably benign |
Het |
Tas2r122 |
C |
T |
6: 132,688,626 (GRCm39) |
W89* |
probably null |
Het |
Tbxas1 |
T |
A |
6: 38,929,079 (GRCm39) |
|
probably benign |
Het |
Tia1 |
T |
A |
6: 86,397,360 (GRCm39) |
I111N |
probably damaging |
Het |
Tlr9 |
T |
A |
9: 106,101,198 (GRCm39) |
L163H |
probably damaging |
Het |
Tnn |
C |
T |
1: 159,942,289 (GRCm39) |
V806M |
probably damaging |
Het |
Traf5 |
G |
A |
1: 191,731,887 (GRCm39) |
A318V |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,219,482 (GRCm39) |
M1K |
probably null |
Het |
Utp25 |
G |
T |
1: 192,810,684 (GRCm39) |
D106E |
probably benign |
Het |
Vmn1r192 |
T |
A |
13: 22,372,000 (GRCm39) |
R73S |
probably benign |
Het |
Vmn1r71 |
T |
C |
7: 10,482,331 (GRCm39) |
Y53C |
probably benign |
Het |
Vmn2r34 |
T |
A |
7: 7,686,582 (GRCm39) |
N372Y |
probably damaging |
Het |
Wbp2 |
A |
T |
11: 115,970,579 (GRCm39) |
S229R |
probably damaging |
Het |
Wdr18 |
C |
T |
10: 79,801,115 (GRCm39) |
T176I |
probably damaging |
Het |
|
Other mutations in Svil |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Svil
|
APN |
18 |
5,099,045 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00840:Svil
|
APN |
18 |
5,063,555 (GRCm39) |
missense |
probably benign |
|
IGL01329:Svil
|
APN |
18 |
5,064,501 (GRCm39) |
missense |
probably benign |
|
IGL01446:Svil
|
APN |
18 |
5,062,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Svil
|
APN |
18 |
5,092,899 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02223:Svil
|
APN |
18 |
5,105,879 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Svil
|
APN |
18 |
5,118,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Svil
|
APN |
18 |
5,118,369 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02479:Svil
|
APN |
18 |
5,099,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02560:Svil
|
APN |
18 |
5,049,379 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02652:Svil
|
APN |
18 |
5,114,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Svil
|
APN |
18 |
5,056,150 (GRCm39) |
nonsense |
probably null |
|
R3779_Svil_985
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R5433_Svil_176
|
UTSW |
18 |
5,059,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R6062_Svil_873
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
BB012:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03055:Svil
|
UTSW |
18 |
5,108,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Svil
|
UTSW |
18 |
5,063,286 (GRCm39) |
missense |
probably benign |
0.14 |
R0029:Svil
|
UTSW |
18 |
5,063,286 (GRCm39) |
missense |
probably benign |
0.14 |
R0266:Svil
|
UTSW |
18 |
5,099,063 (GRCm39) |
splice site |
probably benign |
|
R0281:Svil
|
UTSW |
18 |
5,094,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Svil
|
UTSW |
18 |
5,046,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Svil
|
UTSW |
18 |
5,064,566 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Svil
|
UTSW |
18 |
5,117,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Svil
|
UTSW |
18 |
5,099,443 (GRCm39) |
missense |
probably benign |
0.00 |
R0894:Svil
|
UTSW |
18 |
5,097,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1053:Svil
|
UTSW |
18 |
5,056,690 (GRCm39) |
missense |
probably benign |
0.16 |
R1065:Svil
|
UTSW |
18 |
5,063,777 (GRCm39) |
splice site |
probably benign |
|
R1080:Svil
|
UTSW |
18 |
5,058,147 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1199:Svil
|
UTSW |
18 |
5,059,217 (GRCm39) |
splice site |
probably benign |
|
R1472:Svil
|
UTSW |
18 |
5,048,950 (GRCm39) |
missense |
probably benign |
0.09 |
R1480:Svil
|
UTSW |
18 |
5,057,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Svil
|
UTSW |
18 |
5,046,817 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1626:Svil
|
UTSW |
18 |
5,117,099 (GRCm39) |
critical splice donor site |
probably null |
|
R1691:Svil
|
UTSW |
18 |
5,056,336 (GRCm39) |
missense |
probably benign |
0.06 |
R1812:Svil
|
UTSW |
18 |
5,097,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Svil
|
UTSW |
18 |
5,063,383 (GRCm39) |
missense |
probably benign |
0.01 |
R1842:Svil
|
UTSW |
18 |
5,062,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Svil
|
UTSW |
18 |
5,094,640 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1945:Svil
|
UTSW |
18 |
5,117,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Svil
|
UTSW |
18 |
5,099,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Svil
|
UTSW |
18 |
5,099,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Svil
|
UTSW |
18 |
5,046,640 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R2398:Svil
|
UTSW |
18 |
5,060,613 (GRCm39) |
splice site |
probably null |
|
R3076:Svil
|
UTSW |
18 |
5,116,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Svil
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R3779:Svil
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R3797:Svil
|
UTSW |
18 |
5,060,534 (GRCm39) |
missense |
probably benign |
0.29 |
R4077:Svil
|
UTSW |
18 |
5,063,522 (GRCm39) |
missense |
probably benign |
0.03 |
R4350:Svil
|
UTSW |
18 |
5,118,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Svil
|
UTSW |
18 |
5,046,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4488:Svil
|
UTSW |
18 |
5,049,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Svil
|
UTSW |
18 |
5,088,813 (GRCm39) |
missense |
probably damaging |
0.99 |
R4825:Svil
|
UTSW |
18 |
5,114,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Svil
|
UTSW |
18 |
5,108,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Svil
|
UTSW |
18 |
5,095,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Svil
|
UTSW |
18 |
5,054,025 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4990:Svil
|
UTSW |
18 |
5,056,810 (GRCm39) |
missense |
probably benign |
0.05 |
R4991:Svil
|
UTSW |
18 |
5,056,810 (GRCm39) |
missense |
probably benign |
0.05 |
R5061:Svil
|
UTSW |
18 |
5,048,954 (GRCm39) |
missense |
probably benign |
0.02 |
R5271:Svil
|
UTSW |
18 |
5,062,329 (GRCm39) |
missense |
probably benign |
0.45 |
R5362:Svil
|
UTSW |
18 |
5,057,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Svil
|
UTSW |
18 |
5,059,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R5677:Svil
|
UTSW |
18 |
5,046,823 (GRCm39) |
nonsense |
probably null |
|
R5850:Svil
|
UTSW |
18 |
5,098,900 (GRCm39) |
splice site |
probably null |
|
R5868:Svil
|
UTSW |
18 |
5,056,854 (GRCm39) |
splice site |
probably null |
|
R5871:Svil
|
UTSW |
18 |
5,103,669 (GRCm39) |
splice site |
probably null |
|
R5876:Svil
|
UTSW |
18 |
5,082,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6061:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6066:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Svil
|
UTSW |
18 |
5,108,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Svil
|
UTSW |
18 |
5,108,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R6117:Svil
|
UTSW |
18 |
5,116,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Svil
|
UTSW |
18 |
5,057,432 (GRCm39) |
missense |
probably benign |
0.13 |
R6418:Svil
|
UTSW |
18 |
5,040,171 (GRCm39) |
missense |
probably benign |
0.26 |
R6441:Svil
|
UTSW |
18 |
5,049,323 (GRCm39) |
missense |
probably benign |
|
R6446:Svil
|
UTSW |
18 |
5,057,323 (GRCm39) |
missense |
probably benign |
0.09 |
R6545:Svil
|
UTSW |
18 |
5,108,621 (GRCm39) |
missense |
probably benign |
0.00 |
R6692:Svil
|
UTSW |
18 |
5,082,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R6730:Svil
|
UTSW |
18 |
5,049,311 (GRCm39) |
missense |
probably benign |
0.17 |
R6763:Svil
|
UTSW |
18 |
5,056,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R6870:Svil
|
UTSW |
18 |
5,063,231 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6916:Svil
|
UTSW |
18 |
5,114,682 (GRCm39) |
utr 3 prime |
probably benign |
|
R7134:Svil
|
UTSW |
18 |
5,116,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Svil
|
UTSW |
18 |
5,092,937 (GRCm39) |
missense |
probably benign |
0.01 |
R7213:Svil
|
UTSW |
18 |
5,094,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R7249:Svil
|
UTSW |
18 |
5,062,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R7249:Svil
|
UTSW |
18 |
5,056,270 (GRCm39) |
missense |
probably benign |
0.01 |
R7421:Svil
|
UTSW |
18 |
5,056,109 (GRCm39) |
missense |
probably benign |
0.18 |
R7571:Svil
|
UTSW |
18 |
5,114,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Svil
|
UTSW |
18 |
5,095,188 (GRCm39) |
missense |
probably benign |
0.16 |
R7645:Svil
|
UTSW |
18 |
5,099,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
R8113:Svil
|
UTSW |
18 |
5,062,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Svil
|
UTSW |
18 |
5,108,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Svil
|
UTSW |
18 |
5,064,566 (GRCm39) |
missense |
probably benign |
0.03 |
R8491:Svil
|
UTSW |
18 |
5,106,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Svil
|
UTSW |
18 |
5,060,366 (GRCm39) |
intron |
probably benign |
|
R8774:Svil
|
UTSW |
18 |
5,049,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Svil
|
UTSW |
18 |
5,049,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8780:Svil
|
UTSW |
18 |
5,063,449 (GRCm39) |
missense |
probably benign |
0.00 |
R8787:Svil
|
UTSW |
18 |
5,059,332 (GRCm39) |
nonsense |
probably null |
|
R8790:Svil
|
UTSW |
18 |
5,056,098 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8974:Svil
|
UTSW |
18 |
5,099,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9029:Svil
|
UTSW |
18 |
5,056,239 (GRCm39) |
missense |
probably benign |
|
R9072:Svil
|
UTSW |
18 |
5,097,500 (GRCm39) |
missense |
probably benign |
0.23 |
R9073:Svil
|
UTSW |
18 |
5,097,500 (GRCm39) |
missense |
probably benign |
0.23 |
R9079:Svil
|
UTSW |
18 |
5,056,308 (GRCm39) |
missense |
probably benign |
0.31 |
R9181:Svil
|
UTSW |
18 |
5,090,833 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9363:Svil
|
UTSW |
18 |
5,037,155 (GRCm39) |
missense |
probably benign |
0.02 |
R9377:Svil
|
UTSW |
18 |
5,057,294 (GRCm39) |
missense |
probably benign |
0.06 |
R9381:Svil
|
UTSW |
18 |
5,099,013 (GRCm39) |
missense |
probably benign |
0.06 |
R9389:Svil
|
UTSW |
18 |
5,090,811 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9566:Svil
|
UTSW |
18 |
5,099,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R9607:Svil
|
UTSW |
18 |
5,058,126 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9716:Svil
|
UTSW |
18 |
5,062,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Svil
|
UTSW |
18 |
5,049,062 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Svil
|
UTSW |
18 |
5,062,317 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Svil
|
UTSW |
18 |
5,062,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|