Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
C |
T |
8: 60,993,158 (GRCm39) |
T373I |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,241,653 (GRCm39) |
L1172P |
possibly damaging |
Het |
Abcg2 |
A |
G |
6: 58,661,326 (GRCm39) |
Y459C |
probably benign |
Het |
AC125199.3 |
T |
C |
16: 88,609,061 (GRCm39) |
N4D |
possibly damaging |
Het |
Acad8 |
A |
G |
9: 26,910,785 (GRCm39) |
M3T |
probably benign |
Het |
Acsbg3 |
A |
C |
17: 57,189,218 (GRCm39) |
I209L |
probably benign |
Het |
Adcyap1r1 |
C |
T |
6: 55,474,080 (GRCm39) |
T472I |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,840,671 (GRCm39) |
K1890N |
possibly damaging |
Het |
Asic1 |
G |
A |
15: 99,569,826 (GRCm39) |
C49Y |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,498,547 (GRCm39) |
N215S |
probably damaging |
Het |
C87436 |
A |
G |
6: 86,422,774 (GRCm39) |
Y116C |
probably damaging |
Het |
Car5a |
T |
C |
8: 122,671,519 (GRCm39) |
D5G |
probably benign |
Het |
Ccdc169 |
T |
C |
3: 55,058,368 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
A |
G |
1: 121,426,970 (GRCm39) |
R586G |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,238,007 (GRCm39) |
V131A |
probably damaging |
Het |
Cox5a |
A |
G |
9: 57,436,329 (GRCm39) |
D60G |
possibly damaging |
Het |
Cpne6 |
A |
T |
14: 55,750,104 (GRCm39) |
E78D |
probably benign |
Het |
Cyp2u1 |
T |
C |
3: 131,089,114 (GRCm39) |
E390G |
probably damaging |
Het |
Dab2 |
C |
A |
15: 6,465,271 (GRCm39) |
N707K |
|
Het |
Dock10 |
A |
T |
1: 80,483,147 (GRCm39) |
D2101E |
probably benign |
Het |
Duoxa2 |
G |
A |
2: 122,132,357 (GRCm39) |
|
probably null |
Het |
Eif4a3 |
T |
C |
11: 119,190,758 (GRCm39) |
D22G |
probably benign |
Het |
Fhip1b |
T |
C |
7: 105,037,477 (GRCm39) |
T369A |
possibly damaging |
Het |
Fubp3 |
A |
G |
2: 31,482,476 (GRCm39) |
|
probably null |
Het |
Gm10330 |
A |
G |
12: 23,829,887 (GRCm39) |
L98P |
probably benign |
Het |
Gm5108 |
A |
G |
5: 68,134,299 (GRCm39) |
*102W |
probably null |
Het |
Gpr149 |
A |
C |
3: 62,438,478 (GRCm39) |
S560A |
probably damaging |
Het |
Haspin |
T |
C |
11: 73,027,430 (GRCm39) |
D553G |
probably benign |
Het |
Hsf1 |
C |
T |
15: 76,382,051 (GRCm39) |
H104Y |
probably benign |
Het |
Ifi203 |
T |
C |
1: 173,756,494 (GRCm39) |
T430A |
unknown |
Het |
Itih2 |
G |
A |
2: 10,102,822 (GRCm39) |
Q771* |
probably null |
Het |
Kazald1 |
T |
A |
19: 45,065,395 (GRCm39) |
L92Q |
probably damaging |
Het |
Krt19 |
T |
C |
11: 100,031,980 (GRCm39) |
E324G |
probably damaging |
Het |
Lrrc28 |
A |
T |
7: 67,268,833 (GRCm39) |
V79E |
possibly damaging |
Het |
Ltn1 |
T |
A |
16: 87,178,381 (GRCm39) |
Q1616L |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,158,843 (GRCm39) |
K408E |
probably benign |
Het |
Nalcn |
A |
T |
14: 123,561,284 (GRCm39) |
M738K |
probably benign |
Het |
Ncoa4 |
T |
C |
14: 31,894,848 (GRCm39) |
L125P |
probably damaging |
Het |
Ncor2 |
G |
T |
5: 125,106,253 (GRCm39) |
R810S |
|
Het |
Neb |
C |
T |
2: 52,127,141 (GRCm39) |
G348D |
|
Het |
Nfat5 |
T |
A |
8: 108,095,228 (GRCm39) |
F1156L |
probably damaging |
Het |
Oit3 |
G |
A |
10: 59,277,468 (GRCm39) |
T13I |
unknown |
Het |
Opa1 |
A |
C |
16: 29,424,340 (GRCm39) |
Q230P |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,044,064 (GRCm39) |
I282T |
probably damaging |
Het |
Or52k2 |
T |
A |
7: 102,253,711 (GRCm39) |
I50N |
probably damaging |
Het |
Or5p66 |
A |
G |
7: 107,886,289 (GRCm39) |
F15L |
probably damaging |
Het |
Or5w12 |
A |
C |
2: 87,502,567 (GRCm39) |
L48W |
probably damaging |
Het |
Or6c5b |
G |
T |
10: 129,246,082 (GRCm39) |
M282I |
probably benign |
Het |
Parpbp |
T |
C |
10: 87,946,189 (GRCm39) |
H410R |
probably null |
Het |
Pex5l |
A |
G |
3: 33,007,333 (GRCm39) |
V481A |
probably damaging |
Het |
Plekhh3 |
C |
A |
11: 101,057,225 (GRCm39) |
R344L |
probably benign |
Het |
Prrc2b |
T |
C |
2: 32,104,953 (GRCm39) |
V1477A |
probably benign |
Het |
Ptp4a2 |
G |
A |
4: 129,738,945 (GRCm39) |
G94S |
possibly damaging |
Het |
Ptprk |
T |
A |
10: 28,359,203 (GRCm39) |
Y598* |
probably null |
Het |
Rfx5 |
C |
A |
3: 94,864,475 (GRCm39) |
T207N |
probably damaging |
Het |
Rnase2b |
A |
G |
14: 51,400,347 (GRCm39) |
T143A |
possibly damaging |
Het |
Shank2 |
C |
A |
7: 143,965,265 (GRCm39) |
P958T |
probably damaging |
Het |
Slc13a1 |
A |
G |
6: 24,108,194 (GRCm39) |
I294T |
probably damaging |
Het |
Slc4a8 |
A |
T |
15: 100,712,421 (GRCm39) |
E1084D |
probably benign |
Het |
Smurf1 |
T |
A |
5: 144,820,422 (GRCm39) |
R549* |
probably null |
Het |
Spmip10 |
T |
C |
18: 56,725,537 (GRCm39) |
F66L |
probably damaging |
Het |
Sprr2b |
T |
C |
3: 92,225,032 (GRCm39) |
C93R |
unknown |
Het |
Tcn2 |
G |
T |
11: 3,873,569 (GRCm39) |
S259Y |
probably damaging |
Het |
Tent4a |
G |
T |
13: 69,651,828 (GRCm39) |
T531N |
possibly damaging |
Het |
Tle1 |
A |
G |
4: 72,076,525 (GRCm39) |
S168P |
possibly damaging |
Het |
Tnfrsf1b |
C |
T |
4: 144,950,150 (GRCm39) |
G264D |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,823,088 (GRCm39) |
N118K |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,626,930 (GRCm39) |
|
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,443,796 (GRCm39) |
|
probably benign |
Het |
Ttk |
A |
G |
9: 83,721,322 (GRCm39) |
E69G |
probably damaging |
Het |
Tulp3 |
T |
C |
6: 128,310,966 (GRCm39) |
D87G |
probably benign |
Het |
Usp38 |
C |
T |
8: 81,708,479 (GRCm39) |
G1033D |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,693,775 (GRCm39) |
N707K |
probably benign |
Het |
Vipas39 |
T |
A |
12: 87,305,858 (GRCm39) |
R112* |
probably null |
Het |
Vmn1r185 |
A |
C |
7: 26,311,206 (GRCm39) |
S100A |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,990,223 (GRCm39) |
M156V |
probably benign |
Het |
Vmn1r3 |
G |
A |
4: 3,184,863 (GRCm39) |
T148I |
probably benign |
Het |
Wdr41 |
G |
A |
13: 95,151,620 (GRCm39) |
R260H |
probably benign |
Het |
Wdr90 |
G |
A |
17: 26,076,146 (GRCm39) |
R104C |
|
Het |
Wnk2 |
A |
T |
13: 49,221,711 (GRCm39) |
H1183Q |
possibly damaging |
Het |
Zfp667 |
A |
T |
7: 6,308,256 (GRCm39) |
H308L |
possibly damaging |
Het |
Zfp952 |
A |
G |
17: 33,220,628 (GRCm39) |
N18D |
possibly 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 |
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 |
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 |
|
|