Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts18 |
C |
A |
8: 114,425,656 (GRCm39) |
C1202F |
probably damaging |
Het |
Ago2 |
C |
T |
15: 72,995,182 (GRCm39) |
V466I |
probably benign |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Aptx |
A |
T |
4: 40,695,143 (GRCm39) |
|
probably null |
Het |
Aurka |
A |
T |
2: 172,205,688 (GRCm39) |
D123E |
possibly damaging |
Het |
Btaf1 |
T |
C |
19: 36,926,508 (GRCm39) |
I60T |
possibly damaging |
Het |
Ccdc154 |
A |
T |
17: 25,383,067 (GRCm39) |
|
probably null |
Het |
Cct5 |
T |
C |
15: 31,598,148 (GRCm39) |
N55S |
probably benign |
Het |
Cntnap3 |
A |
G |
13: 64,929,559 (GRCm39) |
S547P |
probably damaging |
Het |
Efl1 |
T |
A |
7: 82,320,909 (GRCm39) |
I114N |
probably damaging |
Het |
Gprin1 |
T |
C |
13: 54,886,465 (GRCm39) |
D603G |
probably benign |
Het |
Il16 |
A |
G |
7: 83,337,371 (GRCm39) |
S115P |
probably benign |
Het |
Kalrn |
C |
A |
16: 34,134,562 (GRCm39) |
V401L |
probably benign |
Het |
Kcnq4 |
T |
A |
4: 120,561,623 (GRCm39) |
K482I |
possibly damaging |
Het |
L3mbtl3 |
C |
T |
10: 26,218,515 (GRCm39) |
A114T |
unknown |
Het |
Lig1 |
G |
A |
7: 13,045,032 (GRCm39) |
|
probably benign |
Het |
Lnx1 |
G |
A |
5: 74,780,924 (GRCm39) |
T199M |
probably damaging |
Het |
Mapk13 |
A |
G |
17: 28,995,557 (GRCm39) |
|
probably benign |
Het |
Mfsd2b |
A |
T |
12: 4,916,538 (GRCm39) |
|
probably null |
Het |
Mrpl3 |
A |
G |
9: 104,934,264 (GRCm39) |
D137G |
probably benign |
Het |
Muc15 |
A |
G |
2: 110,562,044 (GRCm39) |
D160G |
probably benign |
Het |
Myh4 |
T |
C |
11: 67,137,369 (GRCm39) |
|
probably null |
Het |
Nipa2 |
T |
G |
7: 55,582,680 (GRCm39) |
N355T |
probably benign |
Het |
Or11h4 |
A |
T |
14: 50,974,315 (GRCm39) |
Y101* |
probably null |
Het |
Or2v2 |
T |
C |
11: 49,004,536 (GRCm39) |
N6D |
probably damaging |
Het |
Or51a43 |
A |
G |
7: 103,717,945 (GRCm39) |
S98P |
possibly damaging |
Het |
Or5p60 |
T |
C |
7: 107,723,841 (GRCm39) |
T210A |
probably benign |
Het |
Pfkm |
G |
T |
15: 98,021,124 (GRCm39) |
|
probably null |
Het |
Ppip5k1 |
A |
G |
2: 121,157,327 (GRCm39) |
|
probably benign |
Het |
Ppp1r18 |
A |
G |
17: 36,178,857 (GRCm39) |
D244G |
possibly damaging |
Het |
Rimoc1 |
A |
G |
15: 4,018,187 (GRCm39) |
Y163H |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,351,632 (GRCm39) |
I783N |
probably damaging |
Het |
Snx1 |
A |
G |
9: 66,001,734 (GRCm39) |
W307R |
probably damaging |
Het |
Spata31g1 |
A |
G |
4: 42,971,225 (GRCm39) |
Y186C |
possibly damaging |
Het |
Stk11ip |
G |
A |
1: 75,511,079 (GRCm39) |
V928M |
probably benign |
Het |
Tgm4 |
A |
G |
9: 122,874,101 (GRCm39) |
M114V |
probably null |
Het |
Trpm2 |
G |
A |
10: 77,754,743 (GRCm39) |
R1248C |
probably benign |
Het |
Txnrd1 |
T |
C |
10: 82,720,880 (GRCm39) |
I347T |
possibly damaging |
Het |
Unc5a |
A |
G |
13: 55,147,316 (GRCm39) |
S106G |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,254,612 (GRCm39) |
M691V |
probably benign |
Het |
Zfp58 |
T |
A |
13: 67,639,528 (GRCm39) |
Q321L |
probably benign |
Het |
|
Other mutations in Scn2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Scn2a
|
APN |
2 |
65,594,784 (GRCm39) |
missense |
probably benign |
|
IGL00159:Scn2a
|
APN |
2 |
65,573,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00418:Scn2a
|
APN |
2 |
65,594,866 (GRCm39) |
missense |
probably benign |
0.43 |
IGL00753:Scn2a
|
APN |
2 |
65,514,207 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00770:Scn2a
|
APN |
2 |
65,566,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00774:Scn2a
|
APN |
2 |
65,566,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00847:Scn2a
|
APN |
2 |
65,501,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:Scn2a
|
APN |
2 |
65,548,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01329:Scn2a
|
APN |
2 |
65,547,852 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01537:Scn2a
|
APN |
2 |
65,546,219 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01672:Scn2a
|
APN |
2 |
65,582,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Scn2a
|
APN |
2 |
65,532,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02028:Scn2a
|
APN |
2 |
65,594,002 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02142:Scn2a
|
APN |
2 |
65,546,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Scn2a
|
APN |
2 |
65,560,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02183:Scn2a
|
APN |
2 |
65,501,947 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02341:Scn2a
|
APN |
2 |
65,518,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Scn2a
|
APN |
2 |
65,514,228 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02530:Scn2a
|
APN |
2 |
65,560,522 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02621:Scn2a
|
APN |
2 |
65,579,223 (GRCm39) |
splice site |
probably benign |
|
IGL02652:Scn2a
|
APN |
2 |
65,532,382 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02966:Scn2a
|
APN |
2 |
65,532,188 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03329:Scn2a
|
APN |
2 |
65,594,973 (GRCm39) |
missense |
probably benign |
|
IGL03336:Scn2a
|
APN |
2 |
65,519,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Scn2a
|
APN |
2 |
65,594,557 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Scn2a
|
UTSW |
2 |
65,546,074 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4362001:Scn2a
|
UTSW |
2 |
65,514,182 (GRCm39) |
missense |
probably benign |
0.09 |
PIT4403001:Scn2a
|
UTSW |
2 |
65,542,252 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Scn2a
|
UTSW |
2 |
65,518,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0021:Scn2a
|
UTSW |
2 |
65,500,859 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0141:Scn2a
|
UTSW |
2 |
65,542,160 (GRCm39) |
missense |
probably benign |
0.01 |
R0240:Scn2a
|
UTSW |
2 |
65,566,118 (GRCm39) |
missense |
probably benign |
0.32 |
R0240:Scn2a
|
UTSW |
2 |
65,566,118 (GRCm39) |
missense |
probably benign |
0.32 |
R0335:Scn2a
|
UTSW |
2 |
65,512,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0508:Scn2a
|
UTSW |
2 |
65,548,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R0558:Scn2a
|
UTSW |
2 |
65,542,269 (GRCm39) |
missense |
probably benign |
0.26 |
R0600:Scn2a
|
UTSW |
2 |
65,532,177 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0667:Scn2a
|
UTSW |
2 |
65,582,340 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1178:Scn2a
|
UTSW |
2 |
65,517,123 (GRCm39) |
splice site |
probably benign |
|
R1244:Scn2a
|
UTSW |
2 |
65,593,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1386:Scn2a
|
UTSW |
2 |
65,519,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Scn2a
|
UTSW |
2 |
65,532,335 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1440:Scn2a
|
UTSW |
2 |
65,594,938 (GRCm39) |
missense |
probably benign |
|
R1448:Scn2a
|
UTSW |
2 |
65,514,189 (GRCm39) |
missense |
probably benign |
0.17 |
R1460:Scn2a
|
UTSW |
2 |
65,532,187 (GRCm39) |
missense |
probably damaging |
0.96 |
R1553:Scn2a
|
UTSW |
2 |
65,544,180 (GRCm39) |
nonsense |
probably null |
|
R1642:Scn2a
|
UTSW |
2 |
65,514,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Scn2a
|
UTSW |
2 |
65,501,111 (GRCm39) |
splice site |
probably null |
|
R1981:Scn2a
|
UTSW |
2 |
65,520,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Scn2a
|
UTSW |
2 |
65,512,427 (GRCm39) |
missense |
probably null |
1.00 |
R2068:Scn2a
|
UTSW |
2 |
65,582,417 (GRCm39) |
missense |
probably benign |
0.14 |
R2125:Scn2a
|
UTSW |
2 |
65,582,423 (GRCm39) |
nonsense |
probably null |
|
R2126:Scn2a
|
UTSW |
2 |
65,582,423 (GRCm39) |
nonsense |
probably null |
|
R2876:Scn2a
|
UTSW |
2 |
65,546,241 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2878:Scn2a
|
UTSW |
2 |
65,518,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Scn2a
|
UTSW |
2 |
65,579,129 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3749:Scn2a
|
UTSW |
2 |
65,544,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Scn2a
|
UTSW |
2 |
65,544,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3765:Scn2a
|
UTSW |
2 |
65,513,054 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3850:Scn2a
|
UTSW |
2 |
65,512,375 (GRCm39) |
missense |
probably benign |
0.14 |
R4585:Scn2a
|
UTSW |
2 |
65,573,395 (GRCm39) |
splice site |
probably null |
|
R4586:Scn2a
|
UTSW |
2 |
65,573,395 (GRCm39) |
splice site |
probably null |
|
R4588:Scn2a
|
UTSW |
2 |
65,544,111 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4622:Scn2a
|
UTSW |
2 |
65,582,371 (GRCm39) |
missense |
probably benign |
0.04 |
R5108:Scn2a
|
UTSW |
2 |
65,518,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R5161:Scn2a
|
UTSW |
2 |
65,594,935 (GRCm39) |
missense |
probably benign |
0.00 |
R5235:Scn2a
|
UTSW |
2 |
65,582,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5464:Scn2a
|
UTSW |
2 |
65,532,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Scn2a
|
UTSW |
2 |
65,537,639 (GRCm39) |
nonsense |
probably null |
|
R5630:Scn2a
|
UTSW |
2 |
65,556,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Scn2a
|
UTSW |
2 |
65,547,928 (GRCm39) |
missense |
probably benign |
0.27 |
R5730:Scn2a
|
UTSW |
2 |
65,512,882 (GRCm39) |
nonsense |
probably null |
|
R5734:Scn2a
|
UTSW |
2 |
65,548,066 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5779:Scn2a
|
UTSW |
2 |
65,594,827 (GRCm39) |
missense |
probably benign |
0.00 |
R6133:Scn2a
|
UTSW |
2 |
65,573,448 (GRCm39) |
missense |
probably benign |
0.35 |
R6547:Scn2a
|
UTSW |
2 |
65,546,241 (GRCm39) |
missense |
probably benign |
0.29 |
R6549:Scn2a
|
UTSW |
2 |
65,595,018 (GRCm39) |
missense |
probably benign |
0.05 |
R6818:Scn2a
|
UTSW |
2 |
65,519,013 (GRCm39) |
nonsense |
probably null |
|
R6999:Scn2a
|
UTSW |
2 |
65,512,453 (GRCm39) |
missense |
probably benign |
|
R7069:Scn2a
|
UTSW |
2 |
65,594,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Scn2a
|
UTSW |
2 |
65,558,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7125:Scn2a
|
UTSW |
2 |
65,594,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7178:Scn2a
|
UTSW |
2 |
65,579,197 (GRCm39) |
nonsense |
probably null |
|
R7179:Scn2a
|
UTSW |
2 |
65,532,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Scn2a
|
UTSW |
2 |
65,578,663 (GRCm39) |
missense |
probably benign |
0.01 |
R7227:Scn2a
|
UTSW |
2 |
65,582,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R7269:Scn2a
|
UTSW |
2 |
65,594,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Scn2a
|
UTSW |
2 |
65,512,850 (GRCm39) |
nonsense |
probably null |
|
R7388:Scn2a
|
UTSW |
2 |
65,518,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Scn2a
|
UTSW |
2 |
65,532,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R7619:Scn2a
|
UTSW |
2 |
65,546,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7695:Scn2a
|
UTSW |
2 |
65,542,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R7735:Scn2a
|
UTSW |
2 |
65,594,013 (GRCm39) |
missense |
probably benign |
0.40 |
R7911:Scn2a
|
UTSW |
2 |
65,512,427 (GRCm39) |
missense |
probably null |
1.00 |
R8096:Scn2a
|
UTSW |
2 |
65,594,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R8172:Scn2a
|
UTSW |
2 |
65,520,672 (GRCm39) |
missense |
probably benign |
0.01 |
R8220:Scn2a
|
UTSW |
2 |
65,520,620 (GRCm39) |
missense |
probably benign |
0.01 |
R8333:Scn2a
|
UTSW |
2 |
65,514,191 (GRCm39) |
missense |
probably benign |
0.01 |
R8416:Scn2a
|
UTSW |
2 |
65,511,345 (GRCm39) |
missense |
probably benign |
0.00 |
R8850:Scn2a
|
UTSW |
2 |
65,518,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Scn2a
|
UTSW |
2 |
65,546,002 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8977:Scn2a
|
UTSW |
2 |
65,594,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R8992:Scn2a
|
UTSW |
2 |
65,594,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Scn2a
|
UTSW |
2 |
65,511,346 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Scn2a
|
UTSW |
2 |
65,548,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9355:Scn2a
|
UTSW |
2 |
65,594,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Scn2a
|
UTSW |
2 |
65,595,163 (GRCm39) |
missense |
probably benign |
|
R9529:Scn2a
|
UTSW |
2 |
65,594,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R9567:Scn2a
|
UTSW |
2 |
65,518,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Scn2a
|
UTSW |
2 |
65,560,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Scn2a
|
UTSW |
2 |
65,566,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Scn2a
|
UTSW |
2 |
65,579,149 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9761:Scn2a
|
UTSW |
2 |
65,566,030 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scn2a
|
UTSW |
2 |
65,582,212 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1177:Scn2a
|
UTSW |
2 |
65,548,079 (GRCm39) |
missense |
probably benign |
0.07 |
|