Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
T |
11: 94,252,062 (GRCm39) |
H840Q |
probably benign |
Het |
Amotl2 |
C |
T |
9: 102,605,767 (GRCm39) |
R540C |
probably damaging |
Het |
Brpf1 |
A |
G |
6: 113,294,115 (GRCm39) |
E605G |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,694,199 (GRCm39) |
I865V |
probably benign |
Het |
Cdh24 |
A |
T |
14: 54,876,046 (GRCm39) |
F199I |
probably damaging |
Het |
Cdk9 |
A |
G |
2: 32,600,521 (GRCm39) |
V27A |
probably damaging |
Het |
Cfap69 |
G |
T |
5: 5,690,230 (GRCm39) |
|
probably null |
Het |
Cyp2d11 |
G |
T |
15: 82,273,498 (GRCm39) |
L458I |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,408,138 (GRCm39) |
E1898G |
probably damaging |
Het |
Dennd4b |
G |
T |
3: 90,178,177 (GRCm39) |
L456F |
probably damaging |
Het |
Dgat1 |
T |
C |
15: 76,395,786 (GRCm39) |
T66A |
probably benign |
Het |
Dock10 |
C |
A |
1: 80,583,881 (GRCm39) |
|
probably null |
Het |
Fam110b |
A |
G |
4: 5,799,578 (GRCm39) |
D332G |
possibly damaging |
Het |
Fem1al |
A |
C |
11: 29,773,994 (GRCm39) |
Y488D |
probably benign |
Het |
Frmd4b |
G |
A |
6: 97,273,347 (GRCm39) |
P628S |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,753,529 (GRCm39) |
H852Q |
probably benign |
Het |
Il17ra |
T |
C |
6: 120,450,751 (GRCm39) |
V116A |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,232,460 (GRCm39) |
I173T |
probably benign |
Het |
Kctd14 |
A |
T |
7: 97,107,074 (GRCm39) |
M110L |
probably benign |
Het |
Krt6a |
T |
G |
15: 101,602,637 (GRCm39) |
Y16S |
probably benign |
Het |
Lamc2 |
T |
C |
1: 153,006,502 (GRCm39) |
N883S |
probably benign |
Het |
Larp4b |
C |
T |
13: 9,195,486 (GRCm39) |
T195M |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,375,398 (GRCm39) |
L4432P |
probably damaging |
Het |
Mei4 |
T |
C |
9: 81,772,252 (GRCm39) |
S22P |
probably damaging |
Het |
Mep1a |
T |
C |
17: 43,802,527 (GRCm39) |
Q166R |
probably damaging |
Het |
Mroh2b |
C |
A |
15: 4,980,612 (GRCm39) |
|
probably null |
Het |
Myoc |
T |
G |
1: 162,476,220 (GRCm39) |
L308R |
probably damaging |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Or1j21 |
A |
T |
2: 36,684,155 (GRCm39) |
R302S |
probably null |
Het |
Or2t6 |
T |
A |
14: 14,175,725 (GRCm38) |
Y119F |
probably damaging |
Het |
Or4c101 |
C |
G |
2: 88,389,985 (GRCm39) |
S57R |
probably damaging |
Het |
Pdilt |
T |
A |
7: 119,087,217 (GRCm39) |
T478S |
probably damaging |
Het |
Pias1 |
T |
C |
9: 62,827,769 (GRCm39) |
K222E |
probably damaging |
Het |
Prss16 |
A |
C |
13: 22,193,613 (GRCm39) |
L61V |
possibly damaging |
Het |
Pttg1ip2 |
C |
A |
5: 5,502,019 (GRCm39) |
W144C |
probably benign |
Het |
Pvr |
G |
A |
7: 19,644,551 (GRCm39) |
Q328* |
probably null |
Het |
Ranbp3 |
A |
G |
17: 57,017,865 (GRCm39) |
D481G |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
G |
T |
2: 112,508,435 (GRCm39) |
D3419E |
probably damaging |
Het |
Sh3pxd2a |
T |
C |
19: 47,266,864 (GRCm39) |
K242E |
probably damaging |
Het |
Slc34a2 |
A |
G |
5: 53,226,848 (GRCm39) |
D657G |
probably benign |
Het |
Stard9 |
T |
A |
2: 120,532,533 (GRCm39) |
I2930K |
probably benign |
Het |
Syna |
T |
C |
5: 134,588,112 (GRCm39) |
D279G |
probably benign |
Het |
Tfr2 |
T |
C |
5: 137,577,292 (GRCm39) |
F415L |
probably benign |
Het |
Tmem97 |
T |
A |
11: 78,433,586 (GRCm39) |
Y103F |
probably damaging |
Het |
Tmem97 |
A |
T |
11: 78,433,587 (GRCm39) |
Y103N |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,310 (GRCm39) |
D289V |
probably damaging |
Het |
Zbtb1 |
T |
G |
12: 76,433,206 (GRCm39) |
D397E |
probably benign |
Het |
Zc3h18 |
T |
C |
8: 123,140,677 (GRCm39) |
S847P |
probably benign |
Het |
Zfp382 |
G |
A |
7: 29,833,144 (GRCm39) |
G265E |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,369,740 (GRCm39) |
L39S |
probably damaging |
Het |
Zfp729a |
G |
T |
13: 67,767,440 (GRCm39) |
P930T |
probably benign |
Het |
|
Other mutations in Scn1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:Scn1a
|
APN |
2 |
66,165,875 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00650:Scn1a
|
APN |
2 |
66,111,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00658:Scn1a
|
APN |
2 |
66,116,382 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00823:Scn1a
|
APN |
2 |
66,155,279 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00907:Scn1a
|
APN |
2 |
66,158,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Scn1a
|
APN |
2 |
66,156,304 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01401:Scn1a
|
APN |
2 |
66,119,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01503:Scn1a
|
APN |
2 |
66,152,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01575:Scn1a
|
APN |
2 |
66,103,580 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01598:Scn1a
|
APN |
2 |
66,132,829 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01613:Scn1a
|
APN |
2 |
66,116,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01796:Scn1a
|
APN |
2 |
66,162,645 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Scn1a
|
APN |
2 |
66,153,704 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02171:Scn1a
|
APN |
2 |
66,103,543 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02335:Scn1a
|
APN |
2 |
66,108,005 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02406:Scn1a
|
APN |
2 |
66,156,380 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02436:Scn1a
|
APN |
2 |
66,181,497 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02507:Scn1a
|
APN |
2 |
66,108,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02646:Scn1a
|
APN |
2 |
66,129,962 (GRCm39) |
splice site |
probably null |
|
IGL02729:Scn1a
|
APN |
2 |
66,129,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Scn1a
|
APN |
2 |
66,148,421 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02740:Scn1a
|
APN |
2 |
66,155,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Scn1a
|
APN |
2 |
66,161,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:Scn1a
|
APN |
2 |
66,155,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03163:Scn1a
|
APN |
2 |
66,148,418 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03229:Scn1a
|
APN |
2 |
66,130,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Scn1a
|
APN |
2 |
66,107,920 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03393:Scn1a
|
APN |
2 |
66,148,362 (GRCm39) |
missense |
probably benign |
0.19 |
BB008:Scn1a
|
UTSW |
2 |
66,148,156 (GRCm39) |
missense |
probably damaging |
0.99 |
BB018:Scn1a
|
UTSW |
2 |
66,148,156 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4791001:Scn1a
|
UTSW |
2 |
66,103,626 (GRCm39) |
missense |
probably benign |
0.18 |
R0053:Scn1a
|
UTSW |
2 |
66,130,119 (GRCm39) |
missense |
probably benign |
0.05 |
R0053:Scn1a
|
UTSW |
2 |
66,130,119 (GRCm39) |
missense |
probably benign |
0.05 |
R0107:Scn1a
|
UTSW |
2 |
66,154,977 (GRCm39) |
missense |
probably benign |
0.07 |
R0141:Scn1a
|
UTSW |
2 |
66,119,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Scn1a
|
UTSW |
2 |
66,104,269 (GRCm39) |
missense |
probably damaging |
0.98 |
R0517:Scn1a
|
UTSW |
2 |
66,132,751 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0532:Scn1a
|
UTSW |
2 |
66,148,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R0746:Scn1a
|
UTSW |
2 |
66,181,470 (GRCm39) |
missense |
probably benign |
0.25 |
R0755:Scn1a
|
UTSW |
2 |
66,151,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R0830:Scn1a
|
UTSW |
2 |
66,130,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R0846:Scn1a
|
UTSW |
2 |
66,155,099 (GRCm39) |
missense |
probably benign |
0.43 |
R0918:Scn1a
|
UTSW |
2 |
66,153,651 (GRCm39) |
splice site |
probably null |
|
R1055:Scn1a
|
UTSW |
2 |
66,168,340 (GRCm39) |
missense |
probably benign |
0.08 |
R1432:Scn1a
|
UTSW |
2 |
66,152,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Scn1a
|
UTSW |
2 |
66,162,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Scn1a
|
UTSW |
2 |
66,161,629 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1567:Scn1a
|
UTSW |
2 |
66,103,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Scn1a
|
UTSW |
2 |
66,148,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Scn1a
|
UTSW |
2 |
66,152,620 (GRCm39) |
missense |
probably benign |
0.06 |
R1834:Scn1a
|
UTSW |
2 |
66,154,961 (GRCm39) |
missense |
probably benign |
0.00 |
R1834:Scn1a
|
UTSW |
2 |
66,154,960 (GRCm39) |
missense |
probably benign |
0.04 |
R1860:Scn1a
|
UTSW |
2 |
66,148,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R1871:Scn1a
|
UTSW |
2 |
66,148,369 (GRCm39) |
missense |
probably damaging |
0.98 |
R1909:Scn1a
|
UTSW |
2 |
66,161,696 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1967:Scn1a
|
UTSW |
2 |
66,158,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Scn1a
|
UTSW |
2 |
66,161,615 (GRCm39) |
missense |
probably benign |
0.02 |
R2291:Scn1a
|
UTSW |
2 |
66,119,312 (GRCm39) |
missense |
probably benign |
0.44 |
R2302:Scn1a
|
UTSW |
2 |
66,108,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Scn1a
|
UTSW |
2 |
66,158,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2418:Scn1a
|
UTSW |
2 |
66,104,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R2517:Scn1a
|
UTSW |
2 |
66,104,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Scn1a
|
UTSW |
2 |
66,103,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R3083:Scn1a
|
UTSW |
2 |
66,129,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R3903:Scn1a
|
UTSW |
2 |
66,148,476 (GRCm39) |
missense |
probably benign |
0.08 |
R3909:Scn1a
|
UTSW |
2 |
66,104,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Scn1a
|
UTSW |
2 |
66,107,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R3935:Scn1a
|
UTSW |
2 |
66,158,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R3936:Scn1a
|
UTSW |
2 |
66,158,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R4043:Scn1a
|
UTSW |
2 |
66,156,380 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4429:Scn1a
|
UTSW |
2 |
66,181,329 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4495:Scn1a
|
UTSW |
2 |
66,111,146 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4662:Scn1a
|
UTSW |
2 |
66,181,332 (GRCm39) |
missense |
probably benign |
0.23 |
R4834:Scn1a
|
UTSW |
2 |
66,158,866 (GRCm39) |
nonsense |
probably null |
|
R4873:Scn1a
|
UTSW |
2 |
66,158,820 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4875:Scn1a
|
UTSW |
2 |
66,158,820 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5099:Scn1a
|
UTSW |
2 |
66,108,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Scn1a
|
UTSW |
2 |
66,108,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R5435:Scn1a
|
UTSW |
2 |
66,103,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5449:Scn1a
|
UTSW |
2 |
66,151,346 (GRCm39) |
missense |
probably damaging |
0.96 |
R5519:Scn1a
|
UTSW |
2 |
66,162,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Scn1a
|
UTSW |
2 |
66,154,977 (GRCm39) |
missense |
probably benign |
0.07 |
R5556:Scn1a
|
UTSW |
2 |
66,155,141 (GRCm39) |
missense |
probably benign |
0.00 |
R5587:Scn1a
|
UTSW |
2 |
66,103,425 (GRCm39) |
missense |
probably benign |
0.01 |
R5972:Scn1a
|
UTSW |
2 |
66,181,454 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5992:Scn1a
|
UTSW |
2 |
66,165,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Scn1a
|
UTSW |
2 |
66,107,962 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6233:Scn1a
|
UTSW |
2 |
66,107,962 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6328:Scn1a
|
UTSW |
2 |
66,103,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6417:Scn1a
|
UTSW |
2 |
66,103,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R6420:Scn1a
|
UTSW |
2 |
66,103,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R6421:Scn1a
|
UTSW |
2 |
66,103,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R6461:Scn1a
|
UTSW |
2 |
66,156,466 (GRCm39) |
missense |
probably null |
0.01 |
R6701:Scn1a
|
UTSW |
2 |
66,168,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R6717:Scn1a
|
UTSW |
2 |
66,162,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6834:Scn1a
|
UTSW |
2 |
66,158,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6918:Scn1a
|
UTSW |
2 |
66,162,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R6953:Scn1a
|
UTSW |
2 |
66,149,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6996:Scn1a
|
UTSW |
2 |
66,118,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Scn1a
|
UTSW |
2 |
66,148,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7109:Scn1a
|
UTSW |
2 |
66,181,286 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7115:Scn1a
|
UTSW |
2 |
66,154,962 (GRCm39) |
nonsense |
probably null |
|
R7239:Scn1a
|
UTSW |
2 |
66,108,000 (GRCm39) |
splice site |
probably null |
|
R7434:Scn1a
|
UTSW |
2 |
66,103,389 (GRCm39) |
missense |
probably benign |
|
R7646:Scn1a
|
UTSW |
2 |
66,118,102 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7711:Scn1a
|
UTSW |
2 |
66,134,004 (GRCm39) |
missense |
probably benign |
|
R7879:Scn1a
|
UTSW |
2 |
66,116,349 (GRCm39) |
nonsense |
probably null |
|
R7931:Scn1a
|
UTSW |
2 |
66,148,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R7962:Scn1a
|
UTSW |
2 |
66,158,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R8025:Scn1a
|
UTSW |
2 |
66,148,557 (GRCm39) |
missense |
probably benign |
0.02 |
R8055:Scn1a
|
UTSW |
2 |
66,149,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Scn1a
|
UTSW |
2 |
66,132,809 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8167:Scn1a
|
UTSW |
2 |
66,155,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R8339:Scn1a
|
UTSW |
2 |
66,116,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Scn1a
|
UTSW |
2 |
66,152,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R8516:Scn1a
|
UTSW |
2 |
66,156,478 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8559:Scn1a
|
UTSW |
2 |
66,118,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R8726:Scn1a
|
UTSW |
2 |
66,133,983 (GRCm39) |
missense |
probably benign |
|
R8733:Scn1a
|
UTSW |
2 |
66,154,944 (GRCm39) |
missense |
probably benign |
|
R8779:Scn1a
|
UTSW |
2 |
66,181,257 (GRCm39) |
critical splice donor site |
probably benign |
|
R8841:Scn1a
|
UTSW |
2 |
66,156,466 (GRCm39) |
missense |
probably benign |
0.09 |
R8916:Scn1a
|
UTSW |
2 |
66,108,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R8919:Scn1a
|
UTSW |
2 |
66,168,330 (GRCm39) |
missense |
probably benign |
0.16 |
R9040:Scn1a
|
UTSW |
2 |
66,148,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R9086:Scn1a
|
UTSW |
2 |
66,181,358 (GRCm39) |
missense |
probably benign |
0.01 |
R9176:Scn1a
|
UTSW |
2 |
66,103,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Scn1a
|
UTSW |
2 |
66,130,099 (GRCm39) |
missense |
probably benign |
0.10 |
R9275:Scn1a
|
UTSW |
2 |
66,130,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R9365:Scn1a
|
UTSW |
2 |
66,148,465 (GRCm39) |
missense |
probably benign |
0.10 |
R9478:Scn1a
|
UTSW |
2 |
66,156,493 (GRCm39) |
missense |
probably benign |
0.01 |
R9560:Scn1a
|
UTSW |
2 |
66,158,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Scn1a
|
UTSW |
2 |
66,152,687 (GRCm39) |
missense |
probably benign |
0.02 |
R9624:Scn1a
|
UTSW |
2 |
66,153,766 (GRCm39) |
missense |
probably benign |
|
Z1176:Scn1a
|
UTSW |
2 |
66,156,472 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Scn1a
|
UTSW |
2 |
66,155,296 (GRCm39) |
critical splice acceptor site |
probably null |
|
|