Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ccdc18 |
G |
A |
5: 108,328,391 (GRCm39) |
S697N |
probably benign |
Het |
Cyp2c29 |
A |
G |
19: 39,313,434 (GRCm39) |
D310G |
probably damaging |
Het |
Cyp4f13 |
G |
A |
17: 33,160,138 (GRCm39) |
H79Y |
probably benign |
Het |
Dtna |
T |
C |
18: 23,730,545 (GRCm39) |
S311P |
probably benign |
Het |
Dynlrb2 |
A |
G |
8: 117,241,572 (GRCm39) |
T39A |
probably benign |
Het |
Erc2 |
T |
C |
14: 27,762,478 (GRCm39) |
I747T |
probably damaging |
Het |
Herc6 |
G |
A |
6: 57,596,534 (GRCm39) |
M491I |
probably damaging |
Het |
Klra3 |
A |
T |
6: 130,304,107 (GRCm39) |
I195N |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,605,285 (GRCm39) |
I1080V |
probably benign |
Het |
Pls1 |
A |
G |
9: 95,643,475 (GRCm39) |
V508A |
possibly damaging |
Het |
Prdm10 |
C |
A |
9: 31,241,165 (GRCm39) |
|
probably benign |
Het |
Rnase1 |
T |
A |
14: 51,383,003 (GRCm39) |
Y117F |
probably benign |
Het |
S100pbp |
A |
T |
4: 129,075,901 (GRCm39) |
N141K |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,014,629 (GRCm39) |
|
probably null |
Het |
Slc2a2 |
G |
A |
3: 28,772,890 (GRCm39) |
A228T |
possibly damaging |
Het |
Smurf2 |
A |
G |
11: 106,743,462 (GRCm39) |
Y182H |
probably benign |
Het |
Snx2 |
T |
A |
18: 53,349,472 (GRCm39) |
M411K |
possibly damaging |
Het |
Stx17 |
T |
C |
4: 48,158,955 (GRCm39) |
S90P |
possibly damaging |
Het |
Stxbp5l |
A |
T |
16: 37,028,462 (GRCm39) |
S534T |
possibly damaging |
Het |
Tacc2 |
A |
G |
7: 130,360,898 (GRCm39) |
D2730G |
probably damaging |
Het |
Timm8b |
A |
G |
9: 50,516,294 (GRCm39) |
D49G |
possibly damaging |
Het |
Ufd1 |
G |
T |
16: 18,646,468 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp974 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01805:Zfp974
|
APN |
7 |
27,611,689 (GRCm39) |
splice site |
probably benign |
|
IGL02313:Zfp974
|
APN |
7 |
27,611,678 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02449:Zfp974
|
APN |
7 |
27,611,152 (GRCm39) |
missense |
probably benign |
|
R0362:Zfp974
|
UTSW |
7 |
27,626,819 (GRCm39) |
splice site |
probably benign |
|
R0372:Zfp974
|
UTSW |
7 |
27,620,120 (GRCm39) |
critical splice donor site |
probably null |
|
R0379:Zfp974
|
UTSW |
7 |
27,610,357 (GRCm39) |
missense |
probably damaging |
0.98 |
R0699:Zfp974
|
UTSW |
7 |
27,611,416 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0791:Zfp974
|
UTSW |
7 |
27,609,510 (GRCm39) |
nonsense |
probably null |
|
R1411:Zfp974
|
UTSW |
7 |
27,610,634 (GRCm39) |
missense |
probably benign |
0.00 |
R1567:Zfp974
|
UTSW |
7 |
27,610,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R1747:Zfp974
|
UTSW |
7 |
27,610,506 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1837:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1838:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1839:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2311:Zfp974
|
UTSW |
7 |
27,609,866 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4006:Zfp974
|
UTSW |
7 |
27,611,677 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4303:Zfp974
|
UTSW |
7 |
27,609,657 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4541:Zfp974
|
UTSW |
7 |
27,625,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R4771:Zfp974
|
UTSW |
7 |
27,625,733 (GRCm39) |
missense |
probably damaging |
0.96 |
R4889:Zfp974
|
UTSW |
7 |
27,610,244 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5332:Zfp974
|
UTSW |
7 |
27,625,715 (GRCm39) |
missense |
probably benign |
0.01 |
R5537:Zfp974
|
UTSW |
7 |
27,611,671 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5906:Zfp974
|
UTSW |
7 |
27,610,230 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5908:Zfp974
|
UTSW |
7 |
27,610,382 (GRCm39) |
missense |
probably benign |
0.01 |
R6419:Zfp974
|
UTSW |
7 |
27,610,940 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6654:Zfp974
|
UTSW |
7 |
27,625,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6731:Zfp974
|
UTSW |
7 |
27,611,074 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7162:Zfp974
|
UTSW |
7 |
27,610,944 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7316:Zfp974
|
UTSW |
7 |
27,609,863 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7484:Zfp974
|
UTSW |
7 |
27,611,559 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7663:Zfp974
|
UTSW |
7 |
27,611,110 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7664:Zfp974
|
UTSW |
7 |
27,610,137 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8052:Zfp974
|
UTSW |
7 |
27,610,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Zfp974
|
UTSW |
7 |
27,610,361 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8700:Zfp974
|
UTSW |
7 |
27,609,472 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8938:Zfp974
|
UTSW |
7 |
27,610,311 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8972:Zfp974
|
UTSW |
7 |
27,610,589 (GRCm39) |
missense |
probably benign |
0.06 |
R9212:Zfp974
|
UTSW |
7 |
27,610,052 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9236:Zfp974
|
UTSW |
7 |
27,610,342 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9335:Zfp974
|
UTSW |
7 |
27,611,476 (GRCm39) |
missense |
probably benign |
0.02 |
R9436:Zfp974
|
UTSW |
7 |
27,611,094 (GRCm39) |
missense |
probably benign |
0.24 |
R9740:Zfp974
|
UTSW |
7 |
27,610,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|