Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy9 |
A |
G |
16: 4,236,658 (GRCm39) |
V14A |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,873,643 (GRCm39) |
N59K |
probably damaging |
Het |
Ano4 |
T |
C |
10: 88,863,114 (GRCm39) |
Y286C |
probably damaging |
Het |
Arhgap21 |
G |
A |
2: 20,885,543 (GRCm39) |
H545Y |
possibly damaging |
Het |
Arid1a |
T |
A |
4: 133,414,937 (GRCm39) |
S1152C |
unknown |
Het |
Cfap73 |
T |
C |
5: 120,768,258 (GRCm39) |
T167A |
probably benign |
Het |
Ctbs |
A |
T |
3: 146,165,254 (GRCm39) |
|
probably null |
Het |
Dmgdh |
T |
A |
13: 93,857,123 (GRCm39) |
N742K |
probably benign |
Het |
Dmxl1 |
T |
C |
18: 50,011,313 (GRCm39) |
S1157P |
probably benign |
Het |
Dnm3 |
T |
C |
1: 162,305,352 (GRCm39) |
N14S |
probably damaging |
Het |
Dpp4 |
C |
T |
2: 62,217,439 (GRCm39) |
V53I |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,718,246 (GRCm39) |
N329S |
probably damaging |
Het |
Fbxw25 |
A |
G |
9: 109,480,699 (GRCm39) |
V327A |
probably benign |
Het |
Gsg1 |
T |
A |
6: 135,214,612 (GRCm39) |
Q299L |
probably damaging |
Het |
Igsf23 |
A |
G |
7: 19,678,673 (GRCm39) |
L39P |
probably damaging |
Het |
Il17rd |
A |
G |
14: 26,821,488 (GRCm39) |
R261G |
possibly damaging |
Het |
Krt75 |
C |
T |
15: 101,479,503 (GRCm39) |
D276N |
probably benign |
Het |
Lox |
T |
C |
18: 52,660,031 (GRCm39) |
T268A |
possibly damaging |
Het |
Mroh4 |
T |
C |
15: 74,481,568 (GRCm39) |
S825G |
probably benign |
Het |
Nlrp9c |
T |
C |
7: 26,084,850 (GRCm39) |
D243G |
probably damaging |
Het |
Or10a5 |
T |
C |
7: 106,636,018 (GRCm39) |
Y219H |
probably damaging |
Het |
Or1x6 |
T |
A |
11: 50,939,564 (GRCm39) |
V210E |
probably damaging |
Het |
Picalm |
C |
A |
7: 89,825,916 (GRCm39) |
T131N |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,160,522 (GRCm39) |
L781H |
probably damaging |
Het |
Proz |
A |
T |
8: 13,123,451 (GRCm39) |
I241F |
possibly damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,304,454 (GRCm39) |
D67G |
probably damaging |
Het |
Rnf213 |
T |
A |
11: 119,333,097 (GRCm39) |
C2769S |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Snrnp70 |
A |
T |
7: 45,036,843 (GRCm39) |
D100E |
probably damaging |
Het |
Triobp |
T |
A |
15: 78,850,566 (GRCm39) |
L240Q |
possibly damaging |
Het |
Vmn2r5 |
A |
G |
3: 64,398,637 (GRCm39) |
S781P |
probably damaging |
Het |
Zfp451 |
A |
G |
1: 33,842,675 (GRCm39) |
|
probably benign |
Het |
Zfta |
C |
T |
19: 7,398,712 (GRCm39) |
R243* |
probably null |
Het |
|
Other mutations in Scn8a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Scn8a
|
APN |
15 |
100,853,413 (GRCm39) |
unclassified |
probably benign |
|
IGL00979:Scn8a
|
APN |
15 |
100,853,287 (GRCm39) |
unclassified |
probably benign |
|
IGL01339:Scn8a
|
APN |
15 |
100,930,082 (GRCm39) |
missense |
probably benign |
|
IGL01992:Scn8a
|
APN |
15 |
100,866,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Scn8a
|
APN |
15 |
100,927,453 (GRCm39) |
splice site |
probably null |
|
IGL02311:Scn8a
|
APN |
15 |
100,911,164 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02404:Scn8a
|
APN |
15 |
100,937,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Scn8a
|
APN |
15 |
100,911,357 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02690:Scn8a
|
APN |
15 |
100,868,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Scn8a
|
APN |
15 |
100,905,943 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03084:Scn8a
|
APN |
15 |
100,915,053 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Scn8a
|
APN |
15 |
100,872,496 (GRCm39) |
missense |
probably benign |
|
IGL03224:Scn8a
|
APN |
15 |
100,933,520 (GRCm39) |
missense |
probably damaging |
1.00 |
dan
|
UTSW |
15 |
100,933,505 (GRCm39) |
nonsense |
probably null |
|
nymph
|
UTSW |
15 |
100,933,527 (GRCm39) |
missense |
probably damaging |
1.00 |
Tremord
|
UTSW |
15 |
100,911,385 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Scn8a
|
UTSW |
15 |
100,937,820 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4280001:Scn8a
|
UTSW |
15 |
100,855,370 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4508001:Scn8a
|
UTSW |
15 |
100,927,573 (GRCm39) |
missense |
probably damaging |
0.98 |
R0010:Scn8a
|
UTSW |
15 |
100,911,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Scn8a
|
UTSW |
15 |
100,911,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Scn8a
|
UTSW |
15 |
100,916,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R0412:Scn8a
|
UTSW |
15 |
100,906,187 (GRCm39) |
splice site |
probably benign |
|
R0538:Scn8a
|
UTSW |
15 |
100,933,505 (GRCm39) |
nonsense |
probably null |
|
R0539:Scn8a
|
UTSW |
15 |
100,914,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Scn8a
|
UTSW |
15 |
100,933,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Scn8a
|
UTSW |
15 |
100,870,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R0945:Scn8a
|
UTSW |
15 |
100,913,668 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0967:Scn8a
|
UTSW |
15 |
100,933,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Scn8a
|
UTSW |
15 |
100,938,043 (GRCm39) |
missense |
probably benign |
0.06 |
R1283:Scn8a
|
UTSW |
15 |
100,867,052 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1368:Scn8a
|
UTSW |
15 |
100,933,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Scn8a
|
UTSW |
15 |
100,927,696 (GRCm39) |
missense |
probably benign |
0.01 |
R1669:Scn8a
|
UTSW |
15 |
100,909,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Scn8a
|
UTSW |
15 |
100,853,409 (GRCm39) |
nonsense |
probably null |
|
R1735:Scn8a
|
UTSW |
15 |
100,913,742 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1773:Scn8a
|
UTSW |
15 |
100,937,496 (GRCm39) |
missense |
probably damaging |
0.97 |
R1940:Scn8a
|
UTSW |
15 |
100,868,085 (GRCm39) |
missense |
probably benign |
0.22 |
R1996:Scn8a
|
UTSW |
15 |
100,922,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Scn8a
|
UTSW |
15 |
100,916,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R2251:Scn8a
|
UTSW |
15 |
100,914,987 (GRCm39) |
missense |
probably benign |
0.02 |
R2516:Scn8a
|
UTSW |
15 |
100,867,043 (GRCm39) |
missense |
probably benign |
0.05 |
R2917:Scn8a
|
UTSW |
15 |
100,937,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3417:Scn8a
|
UTSW |
15 |
100,869,549 (GRCm39) |
splice site |
probably benign |
|
R3896:Scn8a
|
UTSW |
15 |
100,933,379 (GRCm39) |
missense |
probably benign |
|
R4024:Scn8a
|
UTSW |
15 |
100,937,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Scn8a
|
UTSW |
15 |
100,911,294 (GRCm39) |
nonsense |
probably null |
|
R4193:Scn8a
|
UTSW |
15 |
100,869,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R4212:Scn8a
|
UTSW |
15 |
100,854,954 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4358:Scn8a
|
UTSW |
15 |
100,838,014 (GRCm39) |
missense |
probably benign |
0.00 |
R4396:Scn8a
|
UTSW |
15 |
100,870,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4428:Scn8a
|
UTSW |
15 |
100,881,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R4452:Scn8a
|
UTSW |
15 |
100,854,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4631:Scn8a
|
UTSW |
15 |
100,914,384 (GRCm39) |
nonsense |
probably null |
|
R4693:Scn8a
|
UTSW |
15 |
100,913,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Scn8a
|
UTSW |
15 |
100,938,352 (GRCm39) |
missense |
probably benign |
0.07 |
R4777:Scn8a
|
UTSW |
15 |
100,913,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4949:Scn8a
|
UTSW |
15 |
100,927,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R4997:Scn8a
|
UTSW |
15 |
100,854,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R5246:Scn8a
|
UTSW |
15 |
100,908,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Scn8a
|
UTSW |
15 |
100,872,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5875:Scn8a
|
UTSW |
15 |
100,870,703 (GRCm39) |
nonsense |
probably null |
|
R6031:Scn8a
|
UTSW |
15 |
100,881,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Scn8a
|
UTSW |
15 |
100,881,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6057:Scn8a
|
UTSW |
15 |
100,872,548 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6114:Scn8a
|
UTSW |
15 |
100,938,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R6362:Scn8a
|
UTSW |
15 |
100,837,996 (GRCm39) |
splice site |
probably null |
|
R6535:Scn8a
|
UTSW |
15 |
100,857,588 (GRCm39) |
intron |
probably benign |
|
R6677:Scn8a
|
UTSW |
15 |
100,866,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6687:Scn8a
|
UTSW |
15 |
100,872,508 (GRCm39) |
missense |
probably benign |
0.12 |
R6701:Scn8a
|
UTSW |
15 |
100,937,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R6719:Scn8a
|
UTSW |
15 |
100,908,896 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6769:Scn8a
|
UTSW |
15 |
100,933,445 (GRCm39) |
missense |
probably benign |
|
R6786:Scn8a
|
UTSW |
15 |
100,930,096 (GRCm39) |
missense |
probably benign |
0.00 |
R6849:Scn8a
|
UTSW |
15 |
100,853,468 (GRCm39) |
splice site |
probably null |
|
R7108:Scn8a
|
UTSW |
15 |
100,937,659 (GRCm39) |
missense |
probably benign |
0.01 |
R7215:Scn8a
|
UTSW |
15 |
100,927,711 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7217:Scn8a
|
UTSW |
15 |
100,868,108 (GRCm39) |
missense |
probably benign |
0.00 |
R7219:Scn8a
|
UTSW |
15 |
100,866,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R7356:Scn8a
|
UTSW |
15 |
100,855,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Scn8a
|
UTSW |
15 |
100,853,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R7816:Scn8a
|
UTSW |
15 |
100,908,917 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7985:Scn8a
|
UTSW |
15 |
100,914,843 (GRCm39) |
splice site |
probably null |
|
R8112:Scn8a
|
UTSW |
15 |
100,927,718 (GRCm39) |
missense |
probably benign |
0.27 |
R8263:Scn8a
|
UTSW |
15 |
100,881,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R8305:Scn8a
|
UTSW |
15 |
100,938,387 (GRCm39) |
missense |
probably benign |
0.01 |
R8489:Scn8a
|
UTSW |
15 |
100,867,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Scn8a
|
UTSW |
15 |
100,900,030 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9034:Scn8a
|
UTSW |
15 |
100,927,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R9050:Scn8a
|
UTSW |
15 |
100,906,161 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9240:Scn8a
|
UTSW |
15 |
100,915,068 (GRCm39) |
nonsense |
probably null |
|
R9249:Scn8a
|
UTSW |
15 |
100,914,456 (GRCm39) |
missense |
probably benign |
0.00 |
R9462:Scn8a
|
UTSW |
15 |
100,930,159 (GRCm39) |
missense |
|
|
R9599:Scn8a
|
UTSW |
15 |
100,911,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Scn8a
|
UTSW |
15 |
100,834,407 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9653:Scn8a
|
UTSW |
15 |
100,937,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Scn8a
|
UTSW |
15 |
100,933,332 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Scn8a
|
UTSW |
15 |
100,937,962 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Scn8a
|
UTSW |
15 |
100,937,961 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scn8a
|
UTSW |
15 |
100,931,399 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn8a
|
UTSW |
15 |
100,938,103 (GRCm39) |
missense |
probably benign |
0.00 |
|