Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
T |
A |
7: 43,147,288 (GRCm39) |
I315F |
possibly damaging |
Het |
Aadacl2fm3 |
T |
A |
3: 59,784,632 (GRCm39) |
D368E |
probably benign |
Het |
Acin1 |
G |
A |
14: 54,902,337 (GRCm39) |
T485I |
probably benign |
Het |
Adamts2 |
A |
T |
11: 50,670,541 (GRCm39) |
I552F |
probably damaging |
Het |
Anapc11 |
T |
A |
11: 120,490,112 (GRCm39) |
N9K |
probably benign |
Het |
Arhgef18 |
A |
T |
8: 3,403,636 (GRCm39) |
|
probably benign |
Het |
Atp9b |
T |
C |
18: 80,890,398 (GRCm39) |
T314A |
|
Het |
Birc6 |
T |
A |
17: 74,950,389 (GRCm39) |
I3214N |
probably damaging |
Het |
Catsperb |
A |
G |
12: 101,557,714 (GRCm39) |
I762V |
probably benign |
Het |
Cblb |
T |
A |
16: 51,986,365 (GRCm39) |
M536K |
probably benign |
Het |
Ccdc85c |
C |
A |
12: 108,240,759 (GRCm39) |
A212S |
unknown |
Het |
Cdh23 |
T |
A |
10: 60,150,162 (GRCm39) |
D2561V |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,173,472 (GRCm39) |
Y1672F |
probably damaging |
Het |
Cep83 |
T |
C |
10: 94,564,579 (GRCm39) |
S173P |
possibly damaging |
Het |
Ctc1 |
C |
T |
11: 68,918,584 (GRCm39) |
P530S |
probably damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,167,484 (GRCm39) |
|
probably null |
Het |
Dnah7b |
A |
T |
1: 46,292,671 (GRCm39) |
I3019F |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,230,258 (GRCm39) |
D349G |
probably damaging |
Het |
Ehd2 |
C |
G |
7: 15,697,917 (GRCm39) |
G107R |
probably damaging |
Het |
Epha3 |
A |
T |
16: 63,388,804 (GRCm39) |
W816R |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,404,840 (GRCm39) |
S69C |
probably null |
Het |
Fbxo43 |
A |
G |
15: 36,151,917 (GRCm39) |
F600S |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,455,921 (GRCm39) |
D2117V |
probably damaging |
Het |
Gas2l3 |
T |
A |
10: 89,262,342 (GRCm39) |
T127S |
probably damaging |
Het |
Gli3 |
T |
G |
13: 15,900,228 (GRCm39) |
L1205R |
probably benign |
Het |
Gm17093 |
A |
T |
14: 44,758,139 (GRCm39) |
I107F |
|
Het |
Gm7298 |
T |
A |
6: 121,761,414 (GRCm39) |
C1323* |
probably null |
Het |
H2-D1 |
A |
G |
17: 35,485,741 (GRCm39) |
T89A |
|
Het |
Hira |
T |
G |
16: 18,715,259 (GRCm39) |
D52E |
probably benign |
Het |
Ighv6-6 |
G |
C |
12: 114,398,525 (GRCm39) |
Y80* |
probably null |
Het |
Kat6b |
C |
T |
14: 21,719,953 (GRCm39) |
T1435I |
probably damaging |
Het |
Kcna1 |
C |
A |
6: 126,620,443 (GRCm39) |
|
probably benign |
Het |
Kif24 |
C |
A |
4: 41,392,957 (GRCm39) |
R1284L |
possibly damaging |
Het |
Kremen2 |
A |
C |
17: 23,962,314 (GRCm39) |
C173G |
probably damaging |
Het |
Krtap24-1 |
G |
C |
16: 88,408,707 (GRCm39) |
Q140E |
probably benign |
Het |
Lrrc66 |
C |
A |
5: 73,786,952 (GRCm39) |
G133* |
probably null |
Het |
Mast1 |
C |
A |
8: 85,647,987 (GRCm39) |
R498L |
probably damaging |
Het |
Myom3 |
T |
C |
4: 135,534,504 (GRCm39) |
I1231T |
possibly damaging |
Het |
Nid2 |
G |
A |
14: 19,860,131 (GRCm39) |
V1350I |
possibly damaging |
Het |
Or4f59 |
A |
T |
2: 111,872,789 (GRCm39) |
V196D |
possibly damaging |
Het |
Or8j3c |
A |
G |
2: 86,253,484 (GRCm39) |
C179R |
probably damaging |
Het |
Or9r3 |
T |
C |
10: 129,948,350 (GRCm39) |
Q103R |
probably damaging |
Het |
Pde4a |
A |
G |
9: 21,117,469 (GRCm39) |
D577G |
possibly damaging |
Het |
Pde4d |
T |
A |
13: 109,578,855 (GRCm39) |
N36K |
probably benign |
Het |
Plekhg1 |
A |
T |
10: 3,907,452 (GRCm39) |
S845C |
|
Het |
Plekhg1 |
G |
A |
10: 3,907,453 (GRCm39) |
S845N |
|
Het |
Plod1 |
C |
T |
4: 148,004,658 (GRCm39) |
D481N |
probably damaging |
Het |
Plxna4 |
T |
A |
6: 32,493,981 (GRCm39) |
M212L |
probably damaging |
Het |
Ppip5k1 |
C |
A |
2: 121,173,282 (GRCm39) |
E464* |
probably null |
Het |
Raph1 |
T |
A |
1: 60,529,270 (GRCm39) |
M664L |
unknown |
Het |
Rbm11 |
A |
C |
16: 75,395,673 (GRCm39) |
M115L |
probably benign |
Het |
Rerg |
T |
C |
6: 137,034,869 (GRCm39) |
H45R |
possibly damaging |
Het |
Rnf43 |
A |
G |
11: 87,618,232 (GRCm39) |
E47G |
probably benign |
Het |
Rsph1 |
A |
G |
17: 31,496,260 (GRCm39) |
|
probably benign |
Het |
Safb |
A |
G |
17: 56,892,286 (GRCm39) |
E42G |
unknown |
Het |
Sdf4 |
T |
G |
4: 156,093,379 (GRCm39) |
V237G |
possibly damaging |
Het |
Slc44a2 |
C |
A |
9: 21,258,068 (GRCm39) |
H439Q |
possibly damaging |
Het |
Smg7 |
A |
T |
1: 152,720,123 (GRCm39) |
N761K |
possibly damaging |
Het |
Snrpb2 |
A |
G |
2: 142,910,284 (GRCm39) |
E114G |
probably benign |
Het |
Spmip11 |
A |
G |
15: 98,486,548 (GRCm39) |
H106R |
probably benign |
Het |
Ssh1 |
T |
C |
5: 114,090,051 (GRCm39) |
D346G |
possibly damaging |
Het |
Svopl |
T |
A |
6: 37,993,979 (GRCm39) |
I351F |
probably damaging |
Het |
Tgfb2 |
A |
G |
1: 186,422,942 (GRCm39) |
S136P |
possibly damaging |
Het |
Thsd7a |
A |
T |
6: 12,317,400 (GRCm39) |
L1636* |
probably null |
Het |
Tmc2 |
A |
G |
2: 130,083,488 (GRCm39) |
T482A |
probably benign |
Het |
Tnk2 |
C |
A |
16: 32,499,080 (GRCm39) |
P798T |
probably damaging |
Het |
Trim5 |
T |
C |
7: 103,927,630 (GRCm39) |
Y170C |
probably damaging |
Het |
Ttll10 |
T |
C |
4: 156,129,213 (GRCm39) |
M310V |
probably null |
Het |
Unc13c |
T |
A |
9: 73,643,985 (GRCm39) |
T1160S |
probably damaging |
Het |
Usp25 |
A |
T |
16: 76,904,819 (GRCm39) |
D795V |
probably damaging |
Het |
Usp28 |
T |
A |
9: 48,949,148 (GRCm39) |
V914E |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,547,558 (GRCm39) |
C1627* |
probably null |
Het |
Vmn1r28 |
C |
A |
6: 58,243,052 (GRCm39) |
F298L |
noncoding transcript |
Het |
Vps29 |
T |
C |
5: 122,500,877 (GRCm39) |
S69P |
possibly damaging |
Het |
Zfp703 |
T |
A |
8: 27,469,782 (GRCm39) |
L482H |
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 |
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 |
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 |
|
|