Other mutations in this stock |
Total: 21 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,557,349 (GRCm39) |
A115T |
probably benign |
Het |
AY358078 |
A |
G |
14: 52,042,147 (GRCm39) |
Y174C |
unknown |
Het |
Bod1l |
A |
T |
5: 41,984,463 (GRCm39) |
V529E |
probably benign |
Het |
Ccn2 |
T |
C |
10: 24,472,732 (GRCm39) |
M214T |
probably damaging |
Het |
Cfap57 |
T |
A |
4: 118,467,922 (GRCm39) |
I272L |
probably benign |
Het |
Cnr1 |
A |
G |
4: 33,944,514 (GRCm39) |
K301E |
probably damaging |
Het |
Elavl1 |
A |
T |
8: 4,339,802 (GRCm39) |
L260H |
probably damaging |
Het |
Ercc6 |
A |
G |
14: 32,248,274 (GRCm39) |
Y275C |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 8,007,847 (GRCm39) |
S96P |
probably damaging |
Het |
Hykk |
G |
A |
9: 54,853,418 (GRCm39) |
G247S |
probably benign |
Het |
Ky |
T |
C |
9: 102,414,990 (GRCm39) |
|
probably null |
Het |
Mcu |
A |
C |
10: 59,290,766 (GRCm39) |
|
probably null |
Het |
Or2y17 |
T |
G |
11: 49,231,476 (GRCm39) |
L39R |
probably damaging |
Het |
Or5w11 |
T |
C |
2: 87,459,118 (GRCm39) |
C104R |
possibly damaging |
Het |
Ppp4r3a |
C |
T |
12: 101,008,878 (GRCm39) |
R667Q |
probably damaging |
Het |
Ptprj |
T |
C |
2: 90,301,473 (GRCm39) |
T220A |
probably benign |
Het |
St18 |
T |
A |
1: 6,914,348 (GRCm39) |
C766* |
probably null |
Het |
St8sia4 |
C |
T |
1: 95,581,463 (GRCm39) |
R93H |
probably damaging |
Het |
Tcim |
G |
C |
8: 24,928,726 (GRCm39) |
R63G |
probably damaging |
Het |
Xylb |
T |
C |
9: 119,217,813 (GRCm39) |
S488P |
possibly damaging |
Het |
Zhx3 |
T |
C |
2: 160,623,948 (GRCm39) |
D73G |
probably damaging |
Het |
|
Other mutations in Brinp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Brinp3
|
APN |
1 |
146,777,512 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00503:Brinp3
|
APN |
1 |
146,776,905 (GRCm39) |
missense |
probably benign |
|
IGL01702:Brinp3
|
APN |
1 |
146,627,735 (GRCm39) |
splice site |
probably benign |
|
IGL01728:Brinp3
|
APN |
1 |
146,707,289 (GRCm39) |
splice site |
probably null |
|
IGL01733:Brinp3
|
APN |
1 |
146,390,541 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01937:Brinp3
|
APN |
1 |
146,776,878 (GRCm39) |
missense |
probably benign |
|
IGL02020:Brinp3
|
APN |
1 |
146,777,865 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02082:Brinp3
|
APN |
1 |
146,627,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Brinp3
|
APN |
1 |
146,776,860 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02366:Brinp3
|
APN |
1 |
146,577,481 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02565:Brinp3
|
APN |
1 |
146,777,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02999:Brinp3
|
APN |
1 |
146,577,587 (GRCm39) |
splice site |
probably null |
|
IGL03099:Brinp3
|
APN |
1 |
146,777,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4283001:Brinp3
|
UTSW |
1 |
146,777,161 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4418001:Brinp3
|
UTSW |
1 |
146,777,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R0021:Brinp3
|
UTSW |
1 |
146,777,189 (GRCm39) |
missense |
probably benign |
0.04 |
R0021:Brinp3
|
UTSW |
1 |
146,777,189 (GRCm39) |
missense |
probably benign |
0.04 |
R0266:Brinp3
|
UTSW |
1 |
146,558,418 (GRCm39) |
nonsense |
probably null |
|
R1468:Brinp3
|
UTSW |
1 |
146,777,700 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:Brinp3
|
UTSW |
1 |
146,777,700 (GRCm39) |
missense |
probably benign |
0.01 |
R1522:Brinp3
|
UTSW |
1 |
146,777,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R1596:Brinp3
|
UTSW |
1 |
146,390,520 (GRCm39) |
missense |
probably benign |
|
R1898:Brinp3
|
UTSW |
1 |
146,776,987 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2036:Brinp3
|
UTSW |
1 |
146,577,579 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2224:Brinp3
|
UTSW |
1 |
146,777,658 (GRCm39) |
nonsense |
probably null |
|
R2272:Brinp3
|
UTSW |
1 |
146,777,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2291:Brinp3
|
UTSW |
1 |
146,776,812 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2880:Brinp3
|
UTSW |
1 |
146,777,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R3918:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3939:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3940:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3941:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3942:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R4095:Brinp3
|
UTSW |
1 |
146,777,430 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4783:Brinp3
|
UTSW |
1 |
146,603,378 (GRCm39) |
intron |
probably benign |
|
R5009:Brinp3
|
UTSW |
1 |
146,776,787 (GRCm39) |
missense |
probably benign |
0.25 |
R5034:Brinp3
|
UTSW |
1 |
146,603,458 (GRCm39) |
intron |
probably benign |
|
R5166:Brinp3
|
UTSW |
1 |
146,777,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5372:Brinp3
|
UTSW |
1 |
146,707,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R5472:Brinp3
|
UTSW |
1 |
146,777,197 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5651:Brinp3
|
UTSW |
1 |
146,577,537 (GRCm39) |
missense |
probably benign |
0.01 |
R5681:Brinp3
|
UTSW |
1 |
146,777,484 (GRCm39) |
missense |
probably benign |
0.12 |
R6351:Brinp3
|
UTSW |
1 |
146,777,323 (GRCm39) |
missense |
probably damaging |
0.96 |
R6470:Brinp3
|
UTSW |
1 |
146,777,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R6499:Brinp3
|
UTSW |
1 |
146,777,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7078:Brinp3
|
UTSW |
1 |
146,390,627 (GRCm39) |
nonsense |
probably null |
|
R7223:Brinp3
|
UTSW |
1 |
146,776,812 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7322:Brinp3
|
UTSW |
1 |
146,558,426 (GRCm39) |
nonsense |
probably null |
|
R7347:Brinp3
|
UTSW |
1 |
146,777,824 (GRCm39) |
missense |
probably benign |
0.22 |
R7375:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7412:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7532:Brinp3
|
UTSW |
1 |
146,777,139 (GRCm39) |
missense |
probably damaging |
0.98 |
R7562:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7576:Brinp3
|
UTSW |
1 |
146,777,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R7723:Brinp3
|
UTSW |
1 |
146,577,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Brinp3
|
UTSW |
1 |
146,558,332 (GRCm39) |
missense |
probably damaging |
0.98 |
R7793:Brinp3
|
UTSW |
1 |
146,622,306 (GRCm39) |
missense |
probably benign |
0.20 |
R8334:Brinp3
|
UTSW |
1 |
146,777,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R8401:Brinp3
|
UTSW |
1 |
146,777,184 (GRCm39) |
missense |
probably benign |
0.17 |
R9205:Brinp3
|
UTSW |
1 |
146,777,827 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9328:Brinp3
|
UTSW |
1 |
146,707,455 (GRCm39) |
missense |
probably damaging |
0.98 |
R9602:Brinp3
|
UTSW |
1 |
146,622,234 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Brinp3
|
UTSW |
1 |
146,777,524 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Brinp3
|
UTSW |
1 |
146,777,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|