Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
T |
C |
16: 20,176,128 (GRCm39) |
T1228A |
probably damaging |
Het |
Actg2 |
A |
T |
6: 83,489,989 (GRCm39) |
I370N |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,557,137 (GRCm39) |
T330A |
possibly damaging |
Het |
Atrip |
C |
T |
9: 108,903,057 (GRCm39) |
A6T |
possibly damaging |
Het |
Bms1 |
G |
A |
6: 118,360,767 (GRCm39) |
R1234C |
probably benign |
Het |
Cacnb2 |
A |
T |
2: 14,989,230 (GRCm39) |
T487S |
probably benign |
Het |
Cert1 |
T |
C |
13: 96,767,284 (GRCm39) |
F478S |
probably damaging |
Het |
Esco2 |
A |
T |
14: 66,068,914 (GRCm39) |
V132E |
probably damaging |
Het |
Gjb5 |
A |
T |
4: 127,250,033 (GRCm39) |
L37Q |
probably damaging |
Het |
Gm8020 |
T |
A |
14: 42,324,234 (GRCm39) |
Y24F |
|
Het |
H2bc8 |
CTCGACCATCACGTC |
CTC |
13: 23,755,867 (GRCm39) |
|
probably benign |
Het |
H2-Q6 |
T |
C |
17: 35,644,796 (GRCm39) |
L195P |
probably damaging |
Het |
Hc |
T |
C |
2: 34,874,816 (GRCm39) |
T1602A |
probably damaging |
Het |
Hcrtr2 |
A |
T |
9: 76,153,662 (GRCm39) |
Y243* |
probably null |
Het |
Itga3 |
T |
C |
11: 94,946,719 (GRCm39) |
H730R |
probably benign |
Het |
Kif1a |
A |
T |
1: 92,974,451 (GRCm39) |
L866Q |
probably damaging |
Het |
Krt81 |
A |
T |
15: 101,360,606 (GRCm39) |
L127Q |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,719,223 (GRCm39) |
I2262T |
probably damaging |
Het |
Mxd3 |
A |
T |
13: 55,473,707 (GRCm39) |
D170E |
probably benign |
Het |
Myh2 |
A |
G |
11: 67,076,331 (GRCm39) |
M811V |
probably benign |
Het |
Naa16 |
A |
T |
14: 79,606,527 (GRCm39) |
D335E |
probably benign |
Het |
Nkd1 |
A |
G |
8: 89,249,028 (GRCm39) |
T58A |
probably benign |
Het |
Ogfrl1 |
T |
A |
1: 23,409,351 (GRCm39) |
R292* |
probably null |
Het |
Or52e2 |
T |
A |
7: 102,804,520 (GRCm39) |
M145L |
probably benign |
Het |
Or5w13 |
G |
A |
2: 87,524,059 (GRCm39) |
H56Y |
probably damaging |
Het |
Pom121l12 |
A |
G |
11: 14,549,689 (GRCm39) |
R132G |
possibly damaging |
Het |
Prss46 |
A |
G |
9: 110,680,484 (GRCm39) |
K210E |
probably damaging |
Het |
Shisa9 |
G |
A |
16: 12,085,344 (GRCm39) |
V318I |
probably benign |
Het |
Slc41a2 |
T |
G |
10: 83,090,744 (GRCm39) |
H480P |
probably damaging |
Het |
Slc45a1 |
C |
A |
4: 150,722,892 (GRCm39) |
A331S |
probably benign |
Het |
Smg1 |
A |
T |
7: 117,784,764 (GRCm39) |
F885I |
unknown |
Het |
Speer4f1 |
T |
C |
5: 17,685,412 (GRCm39) |
S236P |
unknown |
Het |
Zfp326 |
A |
T |
5: 106,062,556 (GRCm39) |
Q475L |
probably benign |
Het |
Zzef1 |
T |
G |
11: 72,786,002 (GRCm39) |
V2058G |
probably benign |
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 |
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 |
|
R6739:Scn8a
|
UTSW |
15 |
100,913,836 (GRCm39) |
missense |
possibly damaging |
0.82 |
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 |
|