Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,843,386 (GRCm39) |
Y946F |
probably benign |
Het |
Abcb4 |
T |
G |
5: 8,984,240 (GRCm39) |
W657G |
probably benign |
Het |
Adcy1 |
T |
C |
11: 7,088,279 (GRCm39) |
|
probably benign |
Het |
Arap3 |
A |
G |
18: 38,124,047 (GRCm39) |
V351A |
probably benign |
Het |
Bpifb9b |
A |
C |
2: 154,153,201 (GRCm39) |
Y89S |
probably benign |
Het |
Carns1 |
C |
T |
19: 4,223,083 (GRCm39) |
C47Y |
probably benign |
Het |
Chd5 |
C |
T |
4: 152,445,050 (GRCm39) |
H344Y |
probably damaging |
Het |
Ctnna2 |
T |
C |
6: 76,957,807 (GRCm39) |
T481A |
probably benign |
Het |
Cyth1 |
T |
A |
11: 118,073,072 (GRCm39) |
D264V |
probably damaging |
Het |
Dph1 |
C |
A |
11: 75,071,461 (GRCm39) |
L311F |
probably benign |
Het |
Eif3l |
A |
G |
15: 78,961,142 (GRCm39) |
D65G |
probably damaging |
Het |
Gtf2a1l |
T |
A |
17: 88,976,146 (GRCm39) |
F3Y |
probably benign |
Het |
Hcn4 |
A |
T |
9: 58,766,748 (GRCm39) |
T770S |
unknown |
Het |
Hydin |
A |
T |
8: 111,139,908 (GRCm39) |
I726F |
possibly damaging |
Het |
Klf2 |
A |
G |
8: 73,072,940 (GRCm39) |
I7V |
probably benign |
Het |
Ltn1 |
A |
T |
16: 87,212,662 (GRCm39) |
L633H |
probably damaging |
Het |
Ncoa3 |
A |
G |
2: 165,893,313 (GRCm39) |
D206G |
probably benign |
Het |
Nlrp4a |
T |
G |
7: 26,149,138 (GRCm39) |
D248E |
probably benign |
Het |
Nyap1 |
A |
G |
5: 137,733,746 (GRCm39) |
I429T |
probably damaging |
Het |
Or1j10 |
T |
A |
2: 36,267,072 (GRCm39) |
C95S |
probably damaging |
Het |
Or2p2 |
G |
A |
13: 21,256,982 (GRCm39) |
T163I |
probably damaging |
Het |
Or2t6 |
T |
A |
14: 14,175,732 (GRCm38) |
M117L |
possibly damaging |
Het |
Or51g1 |
A |
G |
7: 102,633,537 (GRCm39) |
M278T |
probably benign |
Het |
Or8s16 |
A |
G |
15: 98,211,237 (GRCm39) |
S65P |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,296,254 (GRCm39) |
E1322G |
probably damaging |
Het |
Plcxd2 |
A |
T |
16: 45,792,689 (GRCm39) |
F217I |
probably benign |
Het |
Plxna4 |
A |
T |
6: 32,162,346 (GRCm39) |
I1389N |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,174,091 (GRCm39) |
Y239C |
probably benign |
Het |
Psma6 |
A |
G |
12: 55,458,996 (GRCm39) |
E126G |
probably benign |
Het |
R3hcc1l |
T |
A |
19: 42,551,141 (GRCm39) |
V46E |
probably damaging |
Het |
Rap1gds1 |
G |
T |
3: 138,663,240 (GRCm39) |
H320N |
probably damaging |
Het |
Sdhaf3 |
A |
G |
6: 7,038,992 (GRCm39) |
M105V |
probably damaging |
Het |
Slc22a26 |
T |
A |
19: 7,765,613 (GRCm39) |
N345I |
probably benign |
Het |
Sncaip |
T |
C |
18: 53,028,027 (GRCm39) |
I412T |
possibly damaging |
Het |
Spag5 |
C |
T |
11: 78,212,157 (GRCm39) |
Q1062* |
probably null |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Szrd1 |
A |
G |
4: 140,867,057 (GRCm39) |
|
probably benign |
Het |
Tns2 |
C |
A |
15: 102,016,231 (GRCm39) |
|
probably benign |
Het |
Trcg1 |
C |
A |
9: 57,149,511 (GRCm39) |
S361* |
probably null |
Het |
Tshz3 |
T |
C |
7: 36,468,583 (GRCm39) |
F191L |
probably damaging |
Het |
Ttc39a |
T |
C |
4: 109,280,090 (GRCm39) |
V124A |
probably damaging |
Het |
Ttf1 |
T |
C |
2: 28,964,023 (GRCm39) |
I633T |
probably damaging |
Het |
Zfp691 |
A |
G |
4: 119,027,704 (GRCm39) |
F176S |
probably damaging |
Het |
|
Other mutations in Sorcs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Sorcs1
|
APN |
19 |
50,178,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Sorcs1
|
APN |
19 |
50,164,566 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01125:Sorcs1
|
APN |
19 |
50,216,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01320:Sorcs1
|
APN |
19 |
50,276,517 (GRCm39) |
splice site |
probably benign |
|
IGL01445:Sorcs1
|
APN |
19 |
50,141,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01682:Sorcs1
|
APN |
19 |
50,169,944 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01799:Sorcs1
|
APN |
19 |
50,218,647 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02044:Sorcs1
|
APN |
19 |
50,276,597 (GRCm39) |
splice site |
probably benign |
|
IGL02111:Sorcs1
|
APN |
19 |
50,218,683 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02364:Sorcs1
|
APN |
19 |
50,322,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02378:Sorcs1
|
APN |
19 |
50,171,109 (GRCm39) |
nonsense |
probably null |
|
IGL02498:Sorcs1
|
APN |
19 |
50,666,606 (GRCm39) |
missense |
probably benign |
|
IGL02939:Sorcs1
|
APN |
19 |
50,666,368 (GRCm39) |
nonsense |
probably null |
|
IGL02942:Sorcs1
|
APN |
19 |
50,463,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Sorcs1
|
APN |
19 |
50,248,194 (GRCm39) |
nonsense |
probably null |
|
IGL03230:Sorcs1
|
APN |
19 |
50,230,531 (GRCm39) |
missense |
probably damaging |
1.00 |
P0033:Sorcs1
|
UTSW |
19 |
50,141,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R0109:Sorcs1
|
UTSW |
19 |
50,367,329 (GRCm39) |
splice site |
probably benign |
|
R0115:Sorcs1
|
UTSW |
19 |
50,624,891 (GRCm39) |
intron |
probably benign |
|
R0242:Sorcs1
|
UTSW |
19 |
50,216,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Sorcs1
|
UTSW |
19 |
50,216,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Sorcs1
|
UTSW |
19 |
50,301,480 (GRCm39) |
splice site |
probably null |
|
R0481:Sorcs1
|
UTSW |
19 |
50,624,891 (GRCm39) |
intron |
probably benign |
|
R0581:Sorcs1
|
UTSW |
19 |
50,241,139 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0669:Sorcs1
|
UTSW |
19 |
50,230,380 (GRCm39) |
splice site |
probably benign |
|
R0980:Sorcs1
|
UTSW |
19 |
50,220,761 (GRCm39) |
missense |
probably benign |
0.04 |
R1158:Sorcs1
|
UTSW |
19 |
50,132,598 (GRCm39) |
unclassified |
probably benign |
|
R1519:Sorcs1
|
UTSW |
19 |
50,241,025 (GRCm39) |
missense |
probably benign |
0.05 |
R1669:Sorcs1
|
UTSW |
19 |
50,463,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R1779:Sorcs1
|
UTSW |
19 |
50,163,481 (GRCm39) |
splice site |
probably benign |
|
R1783:Sorcs1
|
UTSW |
19 |
50,216,747 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1927:Sorcs1
|
UTSW |
19 |
50,210,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Sorcs1
|
UTSW |
19 |
50,221,082 (GRCm39) |
missense |
probably damaging |
0.96 |
R1936:Sorcs1
|
UTSW |
19 |
50,221,082 (GRCm39) |
missense |
probably damaging |
0.96 |
R2109:Sorcs1
|
UTSW |
19 |
50,666,630 (GRCm39) |
missense |
probably benign |
|
R2206:Sorcs1
|
UTSW |
19 |
50,218,655 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2207:Sorcs1
|
UTSW |
19 |
50,218,655 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3031:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3032:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3107:Sorcs1
|
UTSW |
19 |
50,199,088 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3508:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R3738:Sorcs1
|
UTSW |
19 |
50,139,659 (GRCm39) |
missense |
probably benign |
0.03 |
R4127:Sorcs1
|
UTSW |
19 |
50,210,597 (GRCm39) |
missense |
probably benign |
0.29 |
R4212:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R4213:Sorcs1
|
UTSW |
19 |
50,213,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R4385:Sorcs1
|
UTSW |
19 |
50,178,599 (GRCm39) |
missense |
probably benign |
0.01 |
R4424:Sorcs1
|
UTSW |
19 |
50,367,379 (GRCm39) |
missense |
probably damaging |
0.97 |
R4603:Sorcs1
|
UTSW |
19 |
50,301,402 (GRCm39) |
critical splice donor site |
probably null |
|
R4679:Sorcs1
|
UTSW |
19 |
50,171,107 (GRCm39) |
missense |
probably benign |
|
R4780:Sorcs1
|
UTSW |
19 |
50,132,419 (GRCm39) |
unclassified |
probably benign |
|
R4781:Sorcs1
|
UTSW |
19 |
50,171,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Sorcs1
|
UTSW |
19 |
50,218,740 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4823:Sorcs1
|
UTSW |
19 |
50,666,578 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4883:Sorcs1
|
UTSW |
19 |
50,220,741 (GRCm39) |
missense |
probably benign |
0.00 |
R5091:Sorcs1
|
UTSW |
19 |
50,248,190 (GRCm39) |
critical splice donor site |
probably null |
|
R5105:Sorcs1
|
UTSW |
19 |
50,213,579 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5437:Sorcs1
|
UTSW |
19 |
50,241,040 (GRCm39) |
missense |
probably benign |
0.19 |
R5574:Sorcs1
|
UTSW |
19 |
50,210,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5734:Sorcs1
|
UTSW |
19 |
50,171,213 (GRCm39) |
missense |
probably benign |
0.04 |
R6045:Sorcs1
|
UTSW |
19 |
50,178,555 (GRCm39) |
nonsense |
probably null |
|
R6091:Sorcs1
|
UTSW |
19 |
50,276,539 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6119:Sorcs1
|
UTSW |
19 |
50,276,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R6226:Sorcs1
|
UTSW |
19 |
50,169,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Sorcs1
|
UTSW |
19 |
50,132,562 (GRCm39) |
missense |
probably benign |
0.00 |
R6378:Sorcs1
|
UTSW |
19 |
50,213,615 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6782:Sorcs1
|
UTSW |
19 |
50,164,560 (GRCm39) |
nonsense |
probably null |
|
R6792:Sorcs1
|
UTSW |
19 |
50,666,606 (GRCm39) |
missense |
probably benign |
|
R6891:Sorcs1
|
UTSW |
19 |
50,213,557 (GRCm39) |
nonsense |
probably null |
|
R7151:Sorcs1
|
UTSW |
19 |
50,301,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Sorcs1
|
UTSW |
19 |
50,178,480 (GRCm39) |
missense |
probably benign |
0.06 |
R7356:Sorcs1
|
UTSW |
19 |
50,163,595 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7471:Sorcs1
|
UTSW |
19 |
50,250,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Sorcs1
|
UTSW |
19 |
50,141,550 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7503:Sorcs1
|
UTSW |
19 |
50,141,490 (GRCm39) |
missense |
probably benign |
|
R7506:Sorcs1
|
UTSW |
19 |
50,171,112 (GRCm39) |
nonsense |
probably null |
|
R7573:Sorcs1
|
UTSW |
19 |
50,141,234 (GRCm39) |
nonsense |
probably null |
|
R7867:Sorcs1
|
UTSW |
19 |
50,218,698 (GRCm39) |
nonsense |
probably null |
|
R7911:Sorcs1
|
UTSW |
19 |
50,132,470 (GRCm39) |
missense |
unknown |
|
R8032:Sorcs1
|
UTSW |
19 |
50,463,846 (GRCm39) |
missense |
probably benign |
0.28 |
R8063:Sorcs1
|
UTSW |
19 |
50,132,415 (GRCm39) |
missense |
unknown |
|
R8463:Sorcs1
|
UTSW |
19 |
50,248,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Sorcs1
|
UTSW |
19 |
50,367,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R8724:Sorcs1
|
UTSW |
19 |
50,139,658 (GRCm39) |
missense |
probably benign |
0.33 |
R8926:Sorcs1
|
UTSW |
19 |
50,241,096 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9160:Sorcs1
|
UTSW |
19 |
50,213,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:Sorcs1
|
UTSW |
19 |
50,220,753 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9203:Sorcs1
|
UTSW |
19 |
50,250,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Sorcs1
|
UTSW |
19 |
50,141,300 (GRCm39) |
missense |
probably benign |
0.17 |
R9398:Sorcs1
|
UTSW |
19 |
50,213,651 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9430:Sorcs1
|
UTSW |
19 |
50,199,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Sorcs1
|
UTSW |
19 |
50,666,521 (GRCm39) |
missense |
probably benign |
0.04 |
R9511:Sorcs1
|
UTSW |
19 |
50,666,521 (GRCm39) |
missense |
probably benign |
0.04 |
R9744:Sorcs1
|
UTSW |
19 |
50,215,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Sorcs1
|
UTSW |
19 |
50,248,190 (GRCm39) |
critical splice donor site |
probably null |
|
X0024:Sorcs1
|
UTSW |
19 |
50,171,201 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1088:Sorcs1
|
UTSW |
19 |
50,210,581 (GRCm39) |
missense |
probably benign |
0.16 |
Z1177:Sorcs1
|
UTSW |
19 |
50,322,037 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sorcs1
|
UTSW |
19 |
50,215,180 (GRCm39) |
missense |
probably null |
1.00 |
|