Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
T |
1: 71,331,605 (GRCm39) |
M1315K |
probably benign |
Het |
Abcc4 |
C |
T |
14: 118,868,449 (GRCm39) |
V168I |
probably benign |
Het |
Add3 |
T |
A |
19: 53,215,038 (GRCm39) |
L71Q |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,051,247 (GRCm39) |
|
probably null |
Het |
Angpt1 |
A |
G |
15: 42,375,737 (GRCm39) |
L173P |
probably damaging |
Het |
Crls1 |
T |
A |
2: 132,703,165 (GRCm39) |
M205K |
possibly damaging |
Het |
Cspg4b |
T |
C |
13: 113,504,427 (GRCm39) |
V1852A |
probably benign |
Het |
Dhtkd1 |
A |
T |
2: 5,916,662 (GRCm39) |
N671K |
probably damaging |
Het |
Dmbt1 |
A |
T |
7: 130,642,920 (GRCm39) |
D246V |
probably damaging |
Het |
Dolk |
G |
A |
2: 30,175,820 (GRCm39) |
A75V |
probably damaging |
Het |
Dtna |
T |
A |
18: 23,779,287 (GRCm39) |
V623E |
probably damaging |
Het |
Elavl3 |
T |
C |
9: 21,947,622 (GRCm39) |
T106A |
probably benign |
Het |
Ergic1 |
T |
C |
17: 26,843,652 (GRCm39) |
C41R |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,160,187 (GRCm39) |
I3309F |
possibly damaging |
Het |
Fbn1 |
C |
A |
2: 125,207,559 (GRCm39) |
R978L |
possibly damaging |
Het |
Fzd6 |
A |
T |
15: 38,894,559 (GRCm39) |
S242C |
possibly damaging |
Het |
Galntl6 |
T |
A |
8: 58,926,004 (GRCm39) |
H87L |
probably benign |
Het |
Gatad2a |
T |
C |
8: 70,388,591 (GRCm39) |
E32G |
probably damaging |
Het |
Gemin6 |
T |
G |
17: 80,535,178 (GRCm39) |
V46G |
probably damaging |
Het |
Gm11541 |
G |
T |
11: 94,594,944 (GRCm39) |
H41Q |
unknown |
Het |
Has3 |
A |
G |
8: 107,600,579 (GRCm39) |
T14A |
probably damaging |
Het |
Kmt2b |
A |
G |
7: 30,279,869 (GRCm39) |
L1377P |
probably damaging |
Het |
Lcorl |
T |
C |
5: 45,891,069 (GRCm39) |
N428S |
probably benign |
Het |
Lipo5 |
A |
T |
19: 33,445,284 (GRCm39) |
V95D |
unknown |
Het |
Lrp1 |
A |
T |
10: 127,391,593 (GRCm39) |
V2942D |
probably benign |
Het |
Map1a |
T |
C |
2: 121,136,143 (GRCm39) |
S2082P |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,890,723 (GRCm39) |
S852G |
possibly damaging |
Het |
Mlh3 |
A |
T |
12: 85,316,147 (GRCm39) |
L13* |
probably null |
Het |
Ncam2 |
C |
T |
16: 81,231,766 (GRCm39) |
R77* |
probably null |
Het |
Nlrp9c |
T |
A |
7: 26,081,791 (GRCm39) |
N645I |
possibly damaging |
Het |
Or12d17 |
T |
A |
17: 37,778,003 (GRCm39) |
L302Q |
unknown |
Het |
Or12e7 |
T |
C |
2: 87,288,109 (GRCm39) |
I200T |
probably benign |
Het |
Or14j7 |
T |
A |
17: 38,235,383 (GRCm39) |
*309K |
probably null |
Het |
Or7e166 |
C |
A |
9: 19,624,994 (GRCm39) |
Y290* |
probably null |
Het |
Or8g52 |
A |
T |
9: 39,630,892 (GRCm39) |
Y123F |
possibly damaging |
Het |
Pex12 |
A |
G |
11: 83,187,090 (GRCm39) |
V286A |
possibly damaging |
Het |
Phax |
C |
T |
18: 56,717,382 (GRCm39) |
T275I |
probably damaging |
Het |
Phf21b |
A |
G |
15: 84,676,006 (GRCm39) |
V335A |
probably benign |
Het |
Psg18 |
A |
T |
7: 18,083,273 (GRCm39) |
L173H |
probably damaging |
Het |
Rab3ip |
T |
C |
10: 116,754,834 (GRCm39) |
T209A |
possibly damaging |
Het |
Ralgapb |
T |
C |
2: 158,274,705 (GRCm39) |
V202A |
probably damaging |
Het |
Rpn2 |
T |
C |
2: 157,165,187 (GRCm39) |
L611P |
probably damaging |
Het |
Runx2 |
T |
G |
17: 45,035,749 (GRCm39) |
T148P |
probably damaging |
Het |
Sbpl |
C |
A |
17: 24,173,623 (GRCm39) |
D50Y |
probably damaging |
Het |
Sfn |
T |
C |
4: 133,328,915 (GRCm39) |
R56G |
probably damaging |
Het |
Spata31g1 |
T |
C |
4: 42,972,125 (GRCm39) |
V486A |
possibly damaging |
Het |
Tas2r138 |
C |
T |
6: 40,589,914 (GRCm39) |
A111T |
probably benign |
Het |
Tasp1 |
A |
T |
2: 139,850,709 (GRCm39) |
S105T |
probably damaging |
Het |
Tmem225 |
T |
G |
9: 40,062,002 (GRCm39) |
H205Q |
possibly damaging |
Het |
Tmprss7 |
A |
G |
16: 45,481,267 (GRCm39) |
S640P |
probably damaging |
Het |
Utp4 |
G |
A |
8: 107,644,265 (GRCm39) |
A535T |
possibly damaging |
Het |
Vmn1r203 |
A |
T |
13: 22,708,273 (GRCm39) |
D18V |
probably benign |
Het |
Vmn2r58 |
A |
G |
7: 41,522,069 (GRCm39) |
L9P |
probably benign |
Het |
Zcchc2 |
T |
A |
1: 105,957,984 (GRCm39) |
C420* |
probably null |
Het |
Zfp804a |
A |
G |
2: 82,088,934 (GRCm39) |
D921G |
probably benign |
Het |
|
Other mutations in Scn5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Scn5a
|
APN |
9 |
119,315,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00480:Scn5a
|
APN |
9 |
119,346,604 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00542:Scn5a
|
APN |
9 |
119,321,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00852:Scn5a
|
APN |
9 |
119,366,748 (GRCm39) |
missense |
probably benign |
0.26 |
IGL00895:Scn5a
|
APN |
9 |
119,342,170 (GRCm39) |
splice site |
probably null |
|
IGL00905:Scn5a
|
APN |
9 |
119,365,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Scn5a
|
APN |
9 |
119,391,507 (GRCm39) |
nonsense |
probably null |
|
IGL01396:Scn5a
|
APN |
9 |
119,363,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01402:Scn5a
|
APN |
9 |
119,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01404:Scn5a
|
APN |
9 |
119,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01487:Scn5a
|
APN |
9 |
119,391,689 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
IGL01612:Scn5a
|
APN |
9 |
119,315,091 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02134:Scn5a
|
APN |
9 |
119,314,958 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02434:Scn5a
|
APN |
9 |
119,362,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02698:Scn5a
|
APN |
9 |
119,350,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Scn5a
|
APN |
9 |
119,358,076 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02746:Scn5a
|
APN |
9 |
119,379,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Scn5a
|
APN |
9 |
119,324,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Scn5a
|
APN |
9 |
119,341,248 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03188:Scn5a
|
APN |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03268:Scn5a
|
APN |
9 |
119,350,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03287:Scn5a
|
APN |
9 |
119,318,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Scn5a
|
APN |
9 |
119,366,702 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4142001:Scn5a
|
UTSW |
9 |
119,315,324 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Scn5a
|
UTSW |
9 |
119,363,636 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0026:Scn5a
|
UTSW |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Scn5a
|
UTSW |
9 |
119,321,113 (GRCm39) |
critical splice donor site |
probably null |
|
R0044:Scn5a
|
UTSW |
9 |
119,321,113 (GRCm39) |
critical splice donor site |
probably null |
|
R0267:Scn5a
|
UTSW |
9 |
119,372,201 (GRCm39) |
missense |
probably damaging |
0.98 |
R0313:Scn5a
|
UTSW |
9 |
119,363,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Scn5a
|
UTSW |
9 |
119,351,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R0364:Scn5a
|
UTSW |
9 |
119,351,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R0369:Scn5a
|
UTSW |
9 |
119,362,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Scn5a
|
UTSW |
9 |
119,379,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Scn5a
|
UTSW |
9 |
119,368,706 (GRCm39) |
missense |
probably damaging |
0.96 |
R1163:Scn5a
|
UTSW |
9 |
119,362,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Scn5a
|
UTSW |
9 |
119,362,727 (GRCm39) |
critical splice donor site |
probably null |
|
R1469:Scn5a
|
UTSW |
9 |
119,362,727 (GRCm39) |
critical splice donor site |
probably null |
|
R1470:Scn5a
|
UTSW |
9 |
119,365,541 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1470:Scn5a
|
UTSW |
9 |
119,365,541 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1530:Scn5a
|
UTSW |
9 |
119,324,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Scn5a
|
UTSW |
9 |
119,362,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Scn5a
|
UTSW |
9 |
119,315,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Scn5a
|
UTSW |
9 |
119,350,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Scn5a
|
UTSW |
9 |
119,391,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1607:Scn5a
|
UTSW |
9 |
119,315,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Scn5a
|
UTSW |
9 |
119,391,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Scn5a
|
UTSW |
9 |
119,350,243 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1785:Scn5a
|
UTSW |
9 |
119,350,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Scn5a
|
UTSW |
9 |
119,358,085 (GRCm39) |
missense |
probably benign |
|
R1956:Scn5a
|
UTSW |
9 |
119,346,479 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2006:Scn5a
|
UTSW |
9 |
119,365,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Scn5a
|
UTSW |
9 |
119,314,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R2083:Scn5a
|
UTSW |
9 |
119,321,189 (GRCm39) |
missense |
probably benign |
0.45 |
R2180:Scn5a
|
UTSW |
9 |
119,345,117 (GRCm39) |
missense |
probably benign |
|
R2216:Scn5a
|
UTSW |
9 |
119,342,151 (GRCm39) |
missense |
probably benign |
|
R2216:Scn5a
|
UTSW |
9 |
119,314,678 (GRCm39) |
missense |
probably benign |
0.37 |
R2320:Scn5a
|
UTSW |
9 |
119,359,022 (GRCm39) |
critical splice donor site |
probably null |
|
R2377:Scn5a
|
UTSW |
9 |
119,368,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Scn5a
|
UTSW |
9 |
119,362,751 (GRCm39) |
missense |
probably benign |
0.05 |
R3113:Scn5a
|
UTSW |
9 |
119,314,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R3769:Scn5a
|
UTSW |
9 |
119,381,142 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4133:Scn5a
|
UTSW |
9 |
119,315,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4164:Scn5a
|
UTSW |
9 |
119,324,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Scn5a
|
UTSW |
9 |
119,379,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Scn5a
|
UTSW |
9 |
119,358,051 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4734:Scn5a
|
UTSW |
9 |
119,368,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R4829:Scn5a
|
UTSW |
9 |
119,363,773 (GRCm39) |
missense |
probably benign |
0.00 |
R4867:Scn5a
|
UTSW |
9 |
119,379,737 (GRCm39) |
nonsense |
probably null |
|
R5055:Scn5a
|
UTSW |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Scn5a
|
UTSW |
9 |
119,365,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Scn5a
|
UTSW |
9 |
119,363,073 (GRCm39) |
missense |
probably benign |
0.25 |
R5424:Scn5a
|
UTSW |
9 |
119,330,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Scn5a
|
UTSW |
9 |
119,324,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Scn5a
|
UTSW |
9 |
119,389,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Scn5a
|
UTSW |
9 |
119,359,118 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5726:Scn5a
|
UTSW |
9 |
119,362,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5800:Scn5a
|
UTSW |
9 |
119,330,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5826:Scn5a
|
UTSW |
9 |
119,350,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Scn5a
|
UTSW |
9 |
119,391,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6101:Scn5a
|
UTSW |
9 |
119,351,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R6162:Scn5a
|
UTSW |
9 |
119,351,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R6375:Scn5a
|
UTSW |
9 |
119,372,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Scn5a
|
UTSW |
9 |
119,315,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6464:Scn5a
|
UTSW |
9 |
119,363,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6794:Scn5a
|
UTSW |
9 |
119,364,955 (GRCm39) |
missense |
probably damaging |
0.98 |
R6799:Scn5a
|
UTSW |
9 |
119,324,688 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6850:Scn5a
|
UTSW |
9 |
119,330,815 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6858:Scn5a
|
UTSW |
9 |
119,321,156 (GRCm39) |
missense |
probably benign |
0.11 |
R6861:Scn5a
|
UTSW |
9 |
119,359,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Scn5a
|
UTSW |
9 |
119,315,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Scn5a
|
UTSW |
9 |
119,315,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Scn5a
|
UTSW |
9 |
119,314,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Scn5a
|
UTSW |
9 |
119,318,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R7145:Scn5a
|
UTSW |
9 |
119,315,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Scn5a
|
UTSW |
9 |
119,372,451 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7238:Scn5a
|
UTSW |
9 |
119,320,610 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7266:Scn5a
|
UTSW |
9 |
119,391,626 (GRCm39) |
missense |
probably benign |
0.37 |
R7348:Scn5a
|
UTSW |
9 |
119,364,899 (GRCm39) |
missense |
probably benign |
0.00 |
R7399:Scn5a
|
UTSW |
9 |
119,315,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7453:Scn5a
|
UTSW |
9 |
119,351,656 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7495:Scn5a
|
UTSW |
9 |
119,372,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R7681:Scn5a
|
UTSW |
9 |
119,359,043 (GRCm39) |
missense |
probably benign |
0.01 |
R7729:Scn5a
|
UTSW |
9 |
119,324,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R7791:Scn5a
|
UTSW |
9 |
119,372,402 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7794:Scn5a
|
UTSW |
9 |
119,358,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R7873:Scn5a
|
UTSW |
9 |
119,327,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R7951:Scn5a
|
UTSW |
9 |
119,358,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Scn5a
|
UTSW |
9 |
119,391,611 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8306:Scn5a
|
UTSW |
9 |
119,350,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Scn5a
|
UTSW |
9 |
119,365,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R8390:Scn5a
|
UTSW |
9 |
119,368,604 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8536:Scn5a
|
UTSW |
9 |
119,368,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Scn5a
|
UTSW |
9 |
119,363,766 (GRCm39) |
missense |
probably benign |
|
R9000:Scn5a
|
UTSW |
9 |
119,321,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9015:Scn5a
|
UTSW |
9 |
119,381,142 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9272:Scn5a
|
UTSW |
9 |
119,315,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9394:Scn5a
|
UTSW |
9 |
119,324,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R9448:Scn5a
|
UTSW |
9 |
119,381,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R9511:Scn5a
|
UTSW |
9 |
119,351,611 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Scn5a
|
UTSW |
9 |
119,315,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R9593:Scn5a
|
UTSW |
9 |
119,315,839 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Scn5a
|
UTSW |
9 |
119,346,835 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Scn5a
|
UTSW |
9 |
119,314,735 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn5a
|
UTSW |
9 |
119,362,997 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Scn5a
|
UTSW |
9 |
119,351,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|