Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
C |
T |
11: 100,410,583 (GRCm39) |
V132I |
probably benign |
Het |
Adgrb3 |
A |
T |
1: 25,133,081 (GRCm39) |
L1335* |
probably null |
Het |
Adgre5 |
A |
G |
8: 84,454,595 (GRCm39) |
S301P |
probably benign |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Aldh1b1 |
A |
G |
4: 45,802,525 (GRCm39) |
Y21C |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Ankrd7 |
T |
A |
6: 18,868,071 (GRCm39) |
S112R |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,382,058 (GRCm39) |
|
probably null |
Het |
Atp4a |
G |
A |
7: 30,415,344 (GRCm39) |
M321I |
probably benign |
Het |
C2cd4d |
A |
T |
3: 94,271,615 (GRCm39) |
R294W |
probably damaging |
Het |
Carns1 |
T |
C |
19: 4,220,875 (GRCm39) |
I352V |
probably benign |
Het |
Cdh17 |
T |
A |
4: 11,803,969 (GRCm39) |
S547R |
probably benign |
Het |
Cdyl2 |
G |
T |
8: 117,316,129 (GRCm39) |
N286K |
probably damaging |
Het |
Fam186a |
C |
A |
15: 99,840,584 (GRCm39) |
V1887L |
possibly damaging |
Het |
Fat4 |
C |
T |
3: 39,056,951 (GRCm39) |
R4216C |
probably damaging |
Het |
Fcamr |
T |
C |
1: 130,740,663 (GRCm39) |
W361R |
probably damaging |
Het |
Helz2 |
G |
A |
2: 180,874,831 (GRCm39) |
P1888S |
probably benign |
Het |
Itih1 |
A |
T |
14: 30,651,833 (GRCm39) |
F840L |
possibly damaging |
Het |
Kansl2 |
T |
C |
15: 98,429,312 (GRCm39) |
D146G |
probably benign |
Het |
Kcnk18 |
T |
C |
19: 59,223,746 (GRCm39) |
V297A |
probably damaging |
Het |
Kif1a |
T |
C |
1: 92,982,618 (GRCm39) |
T720A |
possibly damaging |
Het |
Kl |
C |
G |
5: 150,876,466 (GRCm39) |
F95L |
probably damaging |
Het |
Large2 |
C |
T |
2: 92,196,915 (GRCm39) |
R423K |
probably benign |
Het |
Lgals3bp |
A |
G |
11: 118,290,568 (GRCm39) |
V13A |
probably damaging |
Het |
Lrrd1 |
A |
G |
5: 3,900,837 (GRCm39) |
I381V |
probably benign |
Het |
Mastl |
A |
T |
2: 23,045,806 (GRCm39) |
I23N |
probably damaging |
Het |
Mettl23 |
T |
C |
11: 116,739,728 (GRCm39) |
V1A |
possibly damaging |
Het |
Mindy2 |
A |
G |
9: 70,538,363 (GRCm39) |
V324A |
probably damaging |
Het |
Mtmr4 |
T |
A |
11: 87,501,845 (GRCm39) |
L633Q |
probably damaging |
Het |
Myh1 |
G |
A |
11: 67,102,273 (GRCm39) |
E855K |
probably damaging |
Het |
Nin |
C |
T |
12: 70,066,006 (GRCm39) |
A2026T |
probably damaging |
Het |
Nova2 |
G |
A |
7: 18,691,794 (GRCm39) |
A244T |
unknown |
Het |
Or2w1 |
A |
T |
13: 21,317,463 (GRCm39) |
I173F |
probably benign |
Het |
Otulin |
T |
C |
15: 27,611,696 (GRCm39) |
T166A |
probably benign |
Het |
P2ry14 |
T |
A |
3: 59,022,798 (GRCm39) |
R230W |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,162,073 (GRCm39) |
E83G |
probably damaging |
Het |
Raet1e |
C |
A |
10: 22,057,887 (GRCm39) |
T218N |
possibly damaging |
Het |
Rsf1 |
GCGGCGGC |
GCGGCGGCGTCGGCGGC |
7: 97,229,135 (GRCm39) |
|
probably benign |
Het |
Safb |
G |
A |
17: 56,909,956 (GRCm39) |
|
probably benign |
Het |
Slc16a4 |
A |
G |
3: 107,208,381 (GRCm39) |
D297G |
possibly damaging |
Het |
Tcf7l2 |
A |
T |
19: 55,905,868 (GRCm39) |
K278* |
probably null |
Het |
Tesmin |
T |
C |
19: 3,439,260 (GRCm39) |
V104A |
possibly damaging |
Het |
Tiam1 |
A |
G |
16: 89,594,918 (GRCm39) |
|
probably null |
Het |
Tmc4 |
T |
C |
7: 3,670,526 (GRCm39) |
T522A |
probably damaging |
Het |
Tmprss3 |
T |
A |
17: 31,408,141 (GRCm39) |
I274F |
possibly damaging |
Het |
Topbp1 |
A |
G |
9: 103,210,189 (GRCm39) |
K916E |
probably damaging |
Het |
Trdv1 |
A |
G |
14: 54,119,513 (GRCm39) |
D58G |
probably benign |
Het |
Ube2g2 |
G |
T |
10: 77,458,139 (GRCm39) |
|
probably benign |
Het |
Unc5d |
G |
T |
8: 29,165,335 (GRCm39) |
Q747K |
possibly damaging |
Het |
Xpo6 |
A |
G |
7: 125,709,124 (GRCm39) |
V819A |
possibly damaging |
Het |
Zan |
T |
A |
5: 137,412,559 (GRCm39) |
|
probably benign |
Het |
Zfp317 |
T |
A |
9: 19,558,184 (GRCm39) |
W133R |
probably benign |
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 |
|
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 |
R7711:Scn7a
|
UTSW |
2 |
66,531,221 (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 |
|