Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amer3 |
A |
T |
1: 34,627,470 (GRCm39) |
T570S |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,370,110 (GRCm39) |
K20I |
possibly damaging |
Het |
Bmp10 |
G |
A |
6: 87,410,740 (GRCm39) |
E178K |
probably benign |
Het |
Brca1 |
T |
A |
11: 101,417,372 (GRCm39) |
H254L |
possibly damaging |
Het |
Cdon |
C |
T |
9: 35,415,485 (GRCm39) |
S1241L |
possibly damaging |
Het |
Cnst |
C |
A |
1: 179,407,051 (GRCm39) |
P33T |
possibly damaging |
Het |
Dnhd1 |
A |
G |
7: 105,369,331 (GRCm39) |
Y4318C |
probably damaging |
Het |
Fst |
C |
T |
13: 114,590,815 (GRCm39) |
|
probably benign |
Het |
Gapvd1 |
A |
G |
2: 34,596,814 (GRCm39) |
L714P |
probably damaging |
Het |
Hectd4 |
T |
G |
5: 121,491,758 (GRCm39) |
L3732R |
possibly damaging |
Het |
Lox |
A |
G |
18: 52,661,891 (GRCm39) |
Y171H |
probably damaging |
Het |
Magi3 |
T |
A |
3: 103,922,374 (GRCm39) |
K1448* |
probably null |
Het |
Med12l |
T |
A |
3: 58,945,159 (GRCm39) |
I128N |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,781,673 (GRCm39) |
T791A |
possibly damaging |
Het |
Prrt4 |
A |
G |
6: 29,169,950 (GRCm39) |
V834A |
possibly damaging |
Het |
Ptprz1 |
A |
G |
6: 23,001,728 (GRCm39) |
S1273G |
probably benign |
Het |
Slc13a4 |
A |
C |
6: 35,248,597 (GRCm39) |
F517V |
probably damaging |
Het |
Treh |
T |
C |
9: 44,596,602 (GRCm39) |
V452A |
probably benign |
Het |
Vmn2r83 |
T |
A |
10: 79,314,931 (GRCm39) |
M393K |
probably damaging |
Het |
Zfp931 |
T |
C |
2: 177,709,984 (GRCm39) |
N134S |
probably benign |
Het |
|
Other mutations in Farp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Farp1
|
APN |
14 |
121,474,561 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01017:Farp1
|
APN |
14 |
121,510,186 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02309:Farp1
|
APN |
14 |
121,480,928 (GRCm39) |
missense |
probably benign |
|
IGL02376:Farp1
|
APN |
14 |
121,510,268 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03018:Farp1
|
APN |
14 |
121,339,581 (GRCm39) |
missense |
probably benign |
|
IGL03400:Farp1
|
APN |
14 |
121,444,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0034:Farp1
|
UTSW |
14 |
121,492,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0046:Farp1
|
UTSW |
14 |
121,492,925 (GRCm39) |
missense |
probably benign |
0.00 |
R0046:Farp1
|
UTSW |
14 |
121,492,925 (GRCm39) |
missense |
probably benign |
0.00 |
R0219:Farp1
|
UTSW |
14 |
121,481,012 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0359:Farp1
|
UTSW |
14 |
121,492,808 (GRCm39) |
splice site |
probably benign |
|
R0616:Farp1
|
UTSW |
14 |
121,514,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R0653:Farp1
|
UTSW |
14 |
121,471,258 (GRCm39) |
critical splice donor site |
probably null |
|
R0710:Farp1
|
UTSW |
14 |
121,474,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Farp1
|
UTSW |
14 |
121,494,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Farp1
|
UTSW |
14 |
121,492,908 (GRCm39) |
missense |
probably benign |
0.16 |
R1953:Farp1
|
UTSW |
14 |
121,492,894 (GRCm39) |
missense |
probably benign |
|
R1958:Farp1
|
UTSW |
14 |
121,456,787 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2891:Farp1
|
UTSW |
14 |
121,494,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R3121:Farp1
|
UTSW |
14 |
121,460,138 (GRCm39) |
splice site |
probably benign |
|
R4005:Farp1
|
UTSW |
14 |
121,513,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R4257:Farp1
|
UTSW |
14 |
121,492,891 (GRCm39) |
missense |
probably benign |
0.00 |
R4559:Farp1
|
UTSW |
14 |
121,510,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Farp1
|
UTSW |
14 |
121,513,716 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4739:Farp1
|
UTSW |
14 |
121,476,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Farp1
|
UTSW |
14 |
121,514,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Farp1
|
UTSW |
14 |
121,513,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5379:Farp1
|
UTSW |
14 |
121,494,169 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5463:Farp1
|
UTSW |
14 |
121,472,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5466:Farp1
|
UTSW |
14 |
121,472,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5467:Farp1
|
UTSW |
14 |
121,472,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5511:Farp1
|
UTSW |
14 |
121,474,584 (GRCm39) |
missense |
probably damaging |
0.98 |
R5520:Farp1
|
UTSW |
14 |
121,472,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Farp1
|
UTSW |
14 |
121,513,716 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5639:Farp1
|
UTSW |
14 |
121,512,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5954:Farp1
|
UTSW |
14 |
121,460,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R6765:Farp1
|
UTSW |
14 |
121,460,066 (GRCm39) |
missense |
probably benign |
0.00 |
R7469:Farp1
|
UTSW |
14 |
121,512,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Farp1
|
UTSW |
14 |
121,472,589 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7660:Farp1
|
UTSW |
14 |
121,514,334 (GRCm39) |
missense |
probably benign |
0.00 |
R7752:Farp1
|
UTSW |
14 |
121,495,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Farp1
|
UTSW |
14 |
121,513,665 (GRCm39) |
missense |
probably benign |
0.12 |
R7911:Farp1
|
UTSW |
14 |
121,479,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Farp1
|
UTSW |
14 |
121,479,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R8078:Farp1
|
UTSW |
14 |
121,513,712 (GRCm39) |
missense |
probably benign |
0.04 |
R8113:Farp1
|
UTSW |
14 |
121,513,008 (GRCm39) |
missense |
probably benign |
0.35 |
R8116:Farp1
|
UTSW |
14 |
121,471,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Farp1
|
UTSW |
14 |
121,479,855 (GRCm39) |
missense |
probably benign |
|
R9103:Farp1
|
UTSW |
14 |
121,509,104 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9190:Farp1
|
UTSW |
14 |
121,492,988 (GRCm39) |
missense |
probably damaging |
0.97 |
R9193:Farp1
|
UTSW |
14 |
121,518,281 (GRCm39) |
missense |
probably benign |
0.34 |
R9581:Farp1
|
UTSW |
14 |
121,480,841 (GRCm39) |
missense |
probably benign |
0.09 |
RF024:Farp1
|
UTSW |
14 |
121,474,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|