Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
G |
A |
8: 120,886,723 (GRCm39) |
E342K |
possibly damaging |
Het |
9430015G10Rik |
T |
G |
4: 156,203,649 (GRCm39) |
V34G |
probably damaging |
Het |
Alkbh3 |
T |
C |
2: 93,838,437 (GRCm39) |
S44G |
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,439,555 (GRCm39) |
C613S |
probably benign |
Het |
Aplp2 |
G |
A |
9: 31,072,645 (GRCm39) |
R488C |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,387,095 (GRCm39) |
N1463S |
probably benign |
Het |
Atxn2l |
A |
T |
7: 126,100,441 (GRCm39) |
L125Q |
probably damaging |
Het |
Cd3d |
A |
G |
9: 44,897,634 (GRCm39) |
K172E |
probably benign |
Het |
Chd7 |
T |
A |
4: 8,805,234 (GRCm39) |
D764E |
probably benign |
Het |
Col19a1 |
T |
C |
1: 24,569,089 (GRCm39) |
I220V |
unknown |
Het |
Cpq |
T |
C |
15: 33,497,493 (GRCm39) |
I411T |
probably benign |
Het |
Crybg2 |
C |
A |
4: 133,792,844 (GRCm39) |
H160N |
probably benign |
Het |
Cryl1 |
A |
T |
14: 57,513,013 (GRCm39) |
C285S |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,909,365 (GRCm39) |
D1326G |
probably damaging |
Het |
Dgkh |
A |
G |
14: 78,962,459 (GRCm39) |
V24A |
probably benign |
Het |
Dnajb4 |
A |
C |
3: 151,892,154 (GRCm39) |
S226R |
probably benign |
Het |
Dnm3 |
A |
T |
1: 161,819,622 (GRCm39) |
I850N |
possibly damaging |
Het |
Dtna |
G |
T |
18: 23,758,253 (GRCm39) |
|
probably null |
Het |
Efcab6 |
G |
T |
15: 83,834,125 (GRCm39) |
D494E |
probably benign |
Het |
Fam169a |
G |
T |
13: 97,263,196 (GRCm39) |
E550* |
probably null |
Het |
Fbxw7 |
A |
G |
3: 84,832,988 (GRCm39) |
N10S |
probably benign |
Het |
Flrt2 |
T |
C |
12: 95,747,528 (GRCm39) |
F622S |
probably damaging |
Het |
Gprc5d |
G |
A |
6: 135,093,355 (GRCm39) |
T184I |
possibly damaging |
Het |
Grem2 |
A |
G |
1: 174,664,693 (GRCm39) |
V52A |
probably damaging |
Het |
Gtf3c2 |
G |
T |
5: 31,327,533 (GRCm39) |
T310N |
probably damaging |
Het |
H2-T13 |
T |
A |
17: 36,394,770 (GRCm39) |
N51I |
probably damaging |
Het |
Hyou1 |
A |
G |
9: 44,295,759 (GRCm39) |
D338G |
possibly damaging |
Het |
Ifna6 |
T |
C |
4: 88,745,971 (GRCm39) |
S107P |
probably benign |
Het |
Kif14 |
G |
T |
1: 136,399,191 (GRCm39) |
G451C |
probably benign |
Het |
Kit |
T |
A |
5: 75,798,019 (GRCm39) |
F436I |
probably damaging |
Het |
Lonp2 |
G |
A |
8: 87,440,636 (GRCm39) |
C751Y |
probably damaging |
Het |
Lonrf1 |
C |
A |
8: 36,716,375 (GRCm39) |
G87C |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,309,687 (GRCm39) |
|
probably null |
Het |
Lrrc37 |
G |
T |
11: 103,505,738 (GRCm39) |
Q2077K |
probably benign |
Het |
Mkln1 |
A |
G |
6: 31,469,584 (GRCm39) |
H598R |
probably damaging |
Het |
Mmaa |
T |
C |
8: 79,994,774 (GRCm39) |
H344R |
probably benign |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Myh7b |
T |
G |
2: 155,462,323 (GRCm39) |
L342R |
probably damaging |
Het |
Or12e8 |
A |
G |
2: 87,187,871 (GRCm39) |
N28D |
probably benign |
Het |
Or2h2b-ps1 |
C |
T |
17: 37,480,847 (GRCm39) |
G129R |
probably damaging |
Het |
Or4f4-ps1 |
T |
A |
2: 111,330,497 (GRCm39) |
I300K |
probably damaging |
Het |
Or7e178 |
A |
T |
9: 20,225,319 (GRCm39) |
V299E |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,416,444 (GRCm39) |
Y1668F |
possibly damaging |
Het |
Pfn4 |
C |
T |
12: 4,824,414 (GRCm39) |
T47I |
possibly damaging |
Het |
Pklr |
T |
C |
3: 89,048,649 (GRCm39) |
L104P |
probably damaging |
Het |
Plcxd2 |
A |
G |
16: 45,800,693 (GRCm39) |
V177A |
probably benign |
Het |
Pramel16 |
T |
C |
4: 143,675,822 (GRCm39) |
S335G |
probably benign |
Het |
Prdm10 |
G |
T |
9: 31,268,528 (GRCm39) |
A826S |
probably damaging |
Het |
Prrt4 |
A |
G |
6: 29,177,455 (GRCm39) |
S105P |
probably benign |
Het |
Prss51 |
T |
A |
14: 64,334,937 (GRCm39) |
V164E |
probably damaging |
Het |
Psap |
T |
C |
10: 60,135,634 (GRCm39) |
V360A |
probably damaging |
Het |
Psg22 |
T |
C |
7: 18,452,267 (GRCm39) |
|
probably null |
Het |
Qrfprl |
A |
G |
6: 65,418,357 (GRCm39) |
H23R |
|
Het |
Rad51 |
A |
G |
2: 118,962,071 (GRCm39) |
Q206R |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,664,874 (GRCm39) |
K277R |
probably benign |
Het |
Rassf2 |
T |
A |
2: 131,847,297 (GRCm39) |
T103S |
probably benign |
Het |
Rbm15b |
T |
A |
9: 106,763,142 (GRCm39) |
H342L |
possibly damaging |
Het |
Rsf1 |
G |
GACCGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Scaf8 |
T |
C |
17: 3,237,909 (GRCm39) |
F561L |
probably damaging |
Het |
Scn1a |
G |
A |
2: 66,134,004 (GRCm39) |
A130V |
probably benign |
Het |
Slc39a14 |
T |
A |
14: 70,551,124 (GRCm39) |
R183W |
probably damaging |
Het |
Slfn1 |
A |
T |
11: 83,012,089 (GRCm39) |
K68N |
possibly damaging |
Het |
Slx4ip |
A |
G |
2: 136,909,914 (GRCm39) |
D303G |
probably damaging |
Het |
Snx17 |
T |
A |
5: 31,352,804 (GRCm39) |
F101Y |
probably damaging |
Het |
Spata31e3 |
T |
G |
13: 50,401,131 (GRCm39) |
R398S |
probably benign |
Het |
Specc1l |
C |
A |
10: 75,066,642 (GRCm39) |
N30K |
probably benign |
Het |
Spmip2 |
A |
G |
3: 79,313,167 (GRCm39) |
I80M |
probably damaging |
Het |
Tbx19 |
A |
G |
1: 164,966,768 (GRCm39) |
S369P |
probably benign |
Het |
Usp17ld |
T |
C |
7: 102,899,489 (GRCm39) |
H481R |
probably damaging |
Het |
Wnt2 |
A |
G |
6: 17,990,036 (GRCm39) |
L287P |
probably benign |
Het |
Zfhx4 |
G |
T |
3: 5,462,016 (GRCm39) |
M1230I |
probably damaging |
Het |
Zfp1 |
T |
C |
8: 112,396,794 (GRCm39) |
C272R |
not run |
Het |
Zfp458 |
A |
G |
13: 67,407,664 (GRCm39) |
S64P |
possibly damaging |
Het |
|
Other mutations in Scn7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Scn7a
|
APN |
2 |
66,513,671 (GRCm39) |
splice site |
probably benign |
|
IGL00432:Scn7a
|
APN |
2 |
66,572,326 (GRCm39) |
nonsense |
probably null |
|
IGL00720:Scn7a
|
APN |
2 |
66,506,388 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL00783:Scn7a
|
APN |
2 |
66,522,908 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00784:Scn7a
|
APN |
2 |
66,522,908 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00926:Scn7a
|
APN |
2 |
66,514,475 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00963:Scn7a
|
APN |
2 |
66,534,289 (GRCm39) |
splice site |
probably benign |
|
IGL01099:Scn7a
|
APN |
2 |
66,514,582 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Scn7a
|
APN |
2 |
66,582,604 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01538:Scn7a
|
APN |
2 |
66,534,196 (GRCm39) |
missense |
probably benign |
|
IGL01624:Scn7a
|
APN |
2 |
66,582,269 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01794:Scn7a
|
APN |
2 |
66,505,853 (GRCm39) |
missense |
probably benign |
|
IGL02100:Scn7a
|
APN |
2 |
66,505,843 (GRCm39) |
makesense |
probably null |
|
IGL02326:Scn7a
|
APN |
2 |
66,530,392 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02472:Scn7a
|
APN |
2 |
66,582,658 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02528:Scn7a
|
APN |
2 |
66,530,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02798:Scn7a
|
APN |
2 |
66,544,219 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03026:Scn7a
|
APN |
2 |
66,506,442 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03071:Scn7a
|
APN |
2 |
66,530,291 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03080:Scn7a
|
APN |
2 |
66,528,160 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03180:Scn7a
|
APN |
2 |
66,506,578 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03337:Scn7a
|
APN |
2 |
66,506,304 (GRCm39) |
missense |
probably benign |
0.00 |
alert
|
UTSW |
2 |
66,510,590 (GRCm39) |
nonsense |
probably null |
|
glimmer
|
UTSW |
2 |
66,574,047 (GRCm39) |
missense |
probably damaging |
0.96 |
Uptick
|
UTSW |
2 |
66,530,393 (GRCm39) |
nonsense |
probably null |
|
PIT4514001:Scn7a
|
UTSW |
2 |
66,514,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Scn7a
|
UTSW |
2 |
66,518,139 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0076:Scn7a
|
UTSW |
2 |
66,544,381 (GRCm39) |
missense |
probably benign |
0.04 |
R0230:Scn7a
|
UTSW |
2 |
66,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Scn7a
|
UTSW |
2 |
66,506,084 (GRCm39) |
missense |
probably benign |
0.05 |
R0846:Scn7a
|
UTSW |
2 |
66,527,944 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1237:Scn7a
|
UTSW |
2 |
66,510,639 (GRCm39) |
missense |
probably damaging |
0.98 |
R1282:Scn7a
|
UTSW |
2 |
66,531,193 (GRCm39) |
missense |
probably damaging |
0.98 |
R1467:Scn7a
|
UTSW |
2 |
66,519,902 (GRCm39) |
missense |
probably benign |
0.01 |
R1467:Scn7a
|
UTSW |
2 |
66,519,902 (GRCm39) |
missense |
probably benign |
0.01 |
R1501:Scn7a
|
UTSW |
2 |
66,530,507 (GRCm39) |
missense |
probably benign |
0.37 |
R1672:Scn7a
|
UTSW |
2 |
66,527,944 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1690:Scn7a
|
UTSW |
2 |
66,506,287 (GRCm39) |
missense |
probably damaging |
0.99 |
R1712:Scn7a
|
UTSW |
2 |
66,535,447 (GRCm39) |
missense |
probably benign |
0.05 |
R1758:Scn7a
|
UTSW |
2 |
66,531,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R1758:Scn7a
|
UTSW |
2 |
66,510,527 (GRCm39) |
missense |
probably benign |
0.00 |
R1775:Scn7a
|
UTSW |
2 |
66,511,299 (GRCm39) |
missense |
probably benign |
0.02 |
R1848:Scn7a
|
UTSW |
2 |
66,514,357 (GRCm39) |
critical splice donor site |
probably null |
|
R1851:Scn7a
|
UTSW |
2 |
66,510,635 (GRCm39) |
missense |
probably benign |
|
R1919:Scn7a
|
UTSW |
2 |
66,530,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Scn7a
|
UTSW |
2 |
66,506,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Scn7a
|
UTSW |
2 |
66,506,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Scn7a
|
UTSW |
2 |
66,514,633 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1998:Scn7a
|
UTSW |
2 |
66,513,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R2008:Scn7a
|
UTSW |
2 |
66,518,091 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2038:Scn7a
|
UTSW |
2 |
66,567,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Scn7a
|
UTSW |
2 |
66,506,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Scn7a
|
UTSW |
2 |
66,528,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R2163:Scn7a
|
UTSW |
2 |
66,506,300 (GRCm39) |
missense |
probably damaging |
0.97 |
R2421:Scn7a
|
UTSW |
2 |
66,556,646 (GRCm39) |
splice site |
probably benign |
|
R2446:Scn7a
|
UTSW |
2 |
66,523,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R2922:Scn7a
|
UTSW |
2 |
66,530,551 (GRCm39) |
splice site |
probably benign |
|
R3015:Scn7a
|
UTSW |
2 |
66,530,240 (GRCm39) |
missense |
probably benign |
0.08 |
R3034:Scn7a
|
UTSW |
2 |
66,513,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R3419:Scn7a
|
UTSW |
2 |
66,531,239 (GRCm39) |
frame shift |
probably null |
|
R3429:Scn7a
|
UTSW |
2 |
66,531,239 (GRCm39) |
frame shift |
probably null |
|
R3430:Scn7a
|
UTSW |
2 |
66,531,239 (GRCm39) |
frame shift |
probably null |
|
R3434:Scn7a
|
UTSW |
2 |
66,505,847 (GRCm39) |
missense |
probably benign |
0.01 |
R3803:Scn7a
|
UTSW |
2 |
66,510,590 (GRCm39) |
nonsense |
probably null |
|
R3831:Scn7a
|
UTSW |
2 |
66,528,028 (GRCm39) |
missense |
probably damaging |
0.96 |
R3833:Scn7a
|
UTSW |
2 |
66,528,028 (GRCm39) |
missense |
probably damaging |
0.96 |
R4017:Scn7a
|
UTSW |
2 |
66,572,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Scn7a
|
UTSW |
2 |
66,572,345 (GRCm39) |
missense |
probably benign |
0.00 |
R4245:Scn7a
|
UTSW |
2 |
66,572,345 (GRCm39) |
missense |
probably benign |
0.00 |
R4276:Scn7a
|
UTSW |
2 |
66,514,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R4307:Scn7a
|
UTSW |
2 |
66,506,099 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4327:Scn7a
|
UTSW |
2 |
66,567,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Scn7a
|
UTSW |
2 |
66,506,780 (GRCm39) |
missense |
probably benign |
0.00 |
R4721:Scn7a
|
UTSW |
2 |
66,514,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Scn7a
|
UTSW |
2 |
66,531,228 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4781:Scn7a
|
UTSW |
2 |
66,534,104 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4792:Scn7a
|
UTSW |
2 |
66,556,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Scn7a
|
UTSW |
2 |
66,530,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Scn7a
|
UTSW |
2 |
66,506,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5729:Scn7a
|
UTSW |
2 |
66,572,301 (GRCm39) |
critical splice donor site |
probably null |
|
R5777:Scn7a
|
UTSW |
2 |
66,522,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5785:Scn7a
|
UTSW |
2 |
66,527,912 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5821:Scn7a
|
UTSW |
2 |
66,574,047 (GRCm39) |
missense |
probably damaging |
0.96 |
R5830:Scn7a
|
UTSW |
2 |
66,544,395 (GRCm39) |
nonsense |
probably null |
|
R5877:Scn7a
|
UTSW |
2 |
66,530,217 (GRCm39) |
nonsense |
probably null |
|
R5881:Scn7a
|
UTSW |
2 |
66,505,870 (GRCm39) |
missense |
probably benign |
0.01 |
R5967:Scn7a
|
UTSW |
2 |
66,506,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Scn7a
|
UTSW |
2 |
66,556,558 (GRCm39) |
nonsense |
probably null |
|
R6077:Scn7a
|
UTSW |
2 |
66,527,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Scn7a
|
UTSW |
2 |
66,534,244 (GRCm39) |
missense |
probably benign |
|
R6242:Scn7a
|
UTSW |
2 |
66,531,110 (GRCm39) |
missense |
probably benign |
0.00 |
R6264:Scn7a
|
UTSW |
2 |
66,505,870 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6291:Scn7a
|
UTSW |
2 |
66,530,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R6544:Scn7a
|
UTSW |
2 |
66,514,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6770:Scn7a
|
UTSW |
2 |
66,559,528 (GRCm39) |
splice site |
probably null |
|
R6997:Scn7a
|
UTSW |
2 |
66,534,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Scn7a
|
UTSW |
2 |
66,572,303 (GRCm39) |
missense |
probably null |
1.00 |
R7126:Scn7a
|
UTSW |
2 |
66,587,630 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7129:Scn7a
|
UTSW |
2 |
66,530,537 (GRCm39) |
missense |
probably benign |
0.14 |
R7176:Scn7a
|
UTSW |
2 |
66,506,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Scn7a
|
UTSW |
2 |
66,518,139 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7276:Scn7a
|
UTSW |
2 |
66,587,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Scn7a
|
UTSW |
2 |
66,522,898 (GRCm39) |
nonsense |
probably null |
|
R7421:Scn7a
|
UTSW |
2 |
66,505,876 (GRCm39) |
missense |
probably benign |
0.07 |
R7488:Scn7a
|
UTSW |
2 |
66,587,574 (GRCm39) |
missense |
probably benign |
0.16 |
R7636:Scn7a
|
UTSW |
2 |
66,574,172 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7685:Scn7a
|
UTSW |
2 |
66,506,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7813:Scn7a
|
UTSW |
2 |
66,506,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Scn7a
|
UTSW |
2 |
66,506,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7914:Scn7a
|
UTSW |
2 |
66,530,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R7953:Scn7a
|
UTSW |
2 |
66,587,670 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7970:Scn7a
|
UTSW |
2 |
66,506,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Scn7a
|
UTSW |
2 |
66,522,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R8121:Scn7a
|
UTSW |
2 |
66,531,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R8172:Scn7a
|
UTSW |
2 |
66,506,191 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8209:Scn7a
|
UTSW |
2 |
66,531,204 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8226:Scn7a
|
UTSW |
2 |
66,531,204 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8288:Scn7a
|
UTSW |
2 |
66,506,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R8431:Scn7a
|
UTSW |
2 |
66,534,164 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8678:Scn7a
|
UTSW |
2 |
66,574,041 (GRCm39) |
splice site |
probably benign |
|
R8745:Scn7a
|
UTSW |
2 |
66,510,526 (GRCm39) |
missense |
probably benign |
|
R8781:Scn7a
|
UTSW |
2 |
66,567,775 (GRCm39) |
missense |
probably benign |
0.03 |
R8848:Scn7a
|
UTSW |
2 |
66,530,393 (GRCm39) |
nonsense |
probably null |
|
R8878:Scn7a
|
UTSW |
2 |
66,506,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8943:Scn7a
|
UTSW |
2 |
66,525,206 (GRCm39) |
synonymous |
silent |
|
R8991:Scn7a
|
UTSW |
2 |
66,514,588 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9147:Scn7a
|
UTSW |
2 |
66,514,507 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9148:Scn7a
|
UTSW |
2 |
66,514,507 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9402:Scn7a
|
UTSW |
2 |
66,510,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Scn7a
|
UTSW |
2 |
66,582,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9546:Scn7a
|
UTSW |
2 |
66,582,603 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9715:Scn7a
|
UTSW |
2 |
66,519,902 (GRCm39) |
missense |
possibly damaging |
0.93 |
X0060:Scn7a
|
UTSW |
2 |
66,520,026 (GRCm39) |
missense |
probably benign |
0.01 |
X0066:Scn7a
|
UTSW |
2 |
66,510,536 (GRCm39) |
missense |
probably benign |
|
Z1088:Scn7a
|
UTSW |
2 |
66,544,295 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Scn7a
|
UTSW |
2 |
66,582,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|