Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp10b |
A |
G |
11: 43,107,391 (GRCm39) |
|
probably benign |
Het |
AY761185 |
A |
T |
8: 21,434,546 (GRCm39) |
|
probably benign |
Het |
BC048671 |
G |
A |
6: 90,282,076 (GRCm39) |
V78I |
probably benign |
Het |
Cadm1 |
C |
T |
9: 47,710,712 (GRCm39) |
T205I |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,322,318 (GRCm39) |
I413V |
possibly damaging |
Het |
Cblb |
C |
T |
16: 51,963,164 (GRCm39) |
T369I |
probably damaging |
Het |
Ccdc54 |
T |
A |
16: 50,410,597 (GRCm39) |
N223I |
probably benign |
Het |
Cdc25c |
A |
G |
18: 34,868,488 (GRCm39) |
V294A |
probably benign |
Het |
Cep170 |
A |
T |
1: 176,609,946 (GRCm39) |
S122T |
possibly damaging |
Het |
Chd1 |
A |
G |
17: 15,967,451 (GRCm39) |
N849D |
probably damaging |
Het |
Cspg4b |
T |
C |
13: 113,505,023 (GRCm39) |
W2051R |
probably benign |
Het |
Dst |
A |
G |
1: 34,333,631 (GRCm39) |
|
probably null |
Het |
Fbxw9 |
T |
A |
8: 85,791,083 (GRCm39) |
L250Q |
probably damaging |
Het |
Fry |
C |
A |
5: 150,384,842 (GRCm39) |
|
probably benign |
Het |
Gm19993 |
A |
G |
1: 19,905,272 (GRCm39) |
|
|
Het |
Gpr75 |
A |
T |
11: 30,842,571 (GRCm39) |
Q492L |
possibly damaging |
Het |
Hc |
C |
T |
2: 34,947,287 (GRCm39) |
E76K |
probably benign |
Het |
Hivep2 |
T |
C |
10: 14,007,865 (GRCm39) |
C1488R |
probably damaging |
Het |
Inava |
C |
T |
1: 136,155,288 (GRCm39) |
V106I |
probably benign |
Het |
Insr |
A |
G |
8: 3,205,683 (GRCm39) |
S1369P |
probably damaging |
Het |
Insrr |
A |
C |
3: 87,707,759 (GRCm39) |
D67A |
probably damaging |
Het |
Irf2 |
T |
A |
8: 47,271,886 (GRCm39) |
Y158N |
probably benign |
Het |
Izumo3 |
A |
T |
4: 92,033,267 (GRCm39) |
Y110N |
probably damaging |
Het |
Katnbl1 |
A |
G |
2: 112,234,586 (GRCm39) |
R23G |
probably benign |
Het |
Kif7 |
A |
G |
7: 79,351,927 (GRCm39) |
V945A |
probably benign |
Het |
Lamb2 |
T |
A |
9: 108,363,936 (GRCm39) |
C987* |
probably null |
Het |
Mmp14 |
T |
A |
14: 54,676,109 (GRCm39) |
|
probably benign |
Het |
Mycbpap |
A |
G |
11: 94,402,562 (GRCm39) |
Y258H |
probably damaging |
Het |
Nav3 |
A |
G |
10: 109,602,778 (GRCm39) |
|
probably benign |
Het |
Nr5a1 |
C |
T |
2: 38,584,178 (GRCm39) |
G414R |
probably damaging |
Het |
Parp10 |
T |
A |
15: 76,126,446 (GRCm39) |
L247F |
probably damaging |
Het |
Pcsk6 |
C |
T |
7: 65,633,451 (GRCm39) |
|
probably benign |
Het |
Pgap3 |
A |
T |
11: 98,281,924 (GRCm39) |
V129D |
probably benign |
Het |
Plcb1 |
A |
G |
2: 135,136,835 (GRCm39) |
E310G |
probably benign |
Het |
Plin3 |
T |
C |
17: 56,586,892 (GRCm39) |
D385G |
probably damaging |
Het |
Pole |
A |
T |
5: 110,441,206 (GRCm39) |
D220V |
probably damaging |
Het |
Resf1 |
T |
A |
6: 149,229,088 (GRCm39) |
D711E |
probably benign |
Het |
Rufy1 |
A |
T |
11: 50,292,292 (GRCm39) |
M499K |
probably benign |
Het |
Sf3b1 |
G |
A |
1: 55,039,532 (GRCm39) |
Q698* |
probably null |
Het |
Shprh |
A |
T |
10: 11,070,116 (GRCm39) |
|
probably null |
Het |
Snd1 |
C |
A |
6: 28,745,334 (GRCm39) |
|
probably benign |
Het |
Stab1 |
C |
T |
14: 30,862,644 (GRCm39) |
A2260T |
possibly damaging |
Het |
Strn |
T |
C |
17: 78,964,363 (GRCm39) |
H687R |
possibly damaging |
Het |
Tgfb3 |
A |
T |
12: 86,124,603 (GRCm39) |
I35N |
probably damaging |
Het |
Tnks2 |
T |
C |
19: 36,852,765 (GRCm39) |
S166P |
probably damaging |
Het |
Ttll9 |
A |
T |
2: 152,804,426 (GRCm39) |
|
probably benign |
Het |
Tyw5 |
G |
A |
1: 57,440,597 (GRCm39) |
T55M |
probably damaging |
Het |
Usp19 |
A |
G |
9: 108,374,369 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
T |
5: 101,992,480 (GRCm39) |
M3384K |
probably damaging |
Het |
Zfp13 |
A |
T |
17: 23,795,122 (GRCm39) |
I483N |
probably damaging |
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 |
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 |
R1525:Scn1a
|
UTSW |
2 |
66,149,806 (GRCm39) |
nonsense |
probably null |
|
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 |
|
|