Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot8 |
T |
C |
2: 164,795,059 (GRCm38) |
D257G |
probably damaging |
Het |
Adamtsl1 |
T |
C |
4: 86,336,878 (GRCm38) |
V736A |
probably benign |
Het |
Anln |
A |
G |
9: 22,364,046 (GRCm38) |
L521S |
probably damaging |
Het |
Arfgap2 |
T |
G |
2: 91,270,282 (GRCm38) |
S311A |
probably benign |
Het |
Brdt |
A |
T |
5: 107,348,503 (GRCm38) |
E160D |
probably benign |
Het |
Ccdc187 |
A |
G |
2: 26,276,203 (GRCm38) |
I738T |
probably damaging |
Het |
Cd59a |
G |
C |
2: 104,104,205 (GRCm38) |
G6A |
probably damaging |
Het |
Cd5l |
C |
T |
3: 87,368,608 (GRCm38) |
P295L |
probably benign |
Het |
Cdhr17 |
T |
C |
5: 16,812,185 (GRCm38) |
|
noncoding transcript |
Het |
Cnot1 |
A |
G |
8: 95,741,921 (GRCm38) |
S1432P |
probably benign |
Het |
Cnot8 |
T |
A |
11: 58,114,051 (GRCm38) |
I192N |
probably damaging |
Het |
Col4a1 |
G |
T |
8: 11,207,409 (GRCm38) |
|
probably null |
Het |
Cuta |
A |
G |
17: 26,939,327 (GRCm38) |
L11P |
possibly damaging |
Het |
Cyp2c39 |
G |
A |
19: 39,568,019 (GRCm38) |
R433H |
probably damaging |
Het |
Cyp4a12b |
T |
A |
4: 115,414,543 (GRCm38) |
Y150* |
probably null |
Het |
Dcaf15 |
G |
A |
8: 84,099,105 (GRCm38) |
A291V |
probably benign |
Het |
Dcstamp |
A |
T |
15: 39,754,735 (GRCm38) |
H180L |
possibly damaging |
Het |
Egfr |
A |
G |
11: 16,889,964 (GRCm38) |
I659M |
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,214,598 (GRCm38) |
E560G |
possibly damaging |
Het |
Gm5111 |
A |
T |
6: 48,589,592 (GRCm38) |
|
probably benign |
Het |
Gm7945 |
T |
C |
14: 41,382,823 (GRCm38) |
T214A |
unknown |
Het |
Gpi1 |
T |
C |
7: 34,220,745 (GRCm38) |
T168A |
possibly damaging |
Het |
Gys2 |
T |
C |
6: 142,459,408 (GRCm38) |
I218V |
probably benign |
Het |
Gzmf |
T |
A |
14: 56,206,492 (GRCm38) |
I74L |
probably benign |
Het |
Hacl1 |
G |
A |
14: 31,635,771 (GRCm38) |
A70V |
probably damaging |
Het |
Herc2 |
T |
A |
7: 56,197,072 (GRCm38) |
L3590* |
probably null |
Het |
Idh2 |
GGTCCCAG |
GG |
7: 80,098,329 (GRCm38) |
|
probably benign |
Het |
Igfals |
G |
T |
17: 24,881,365 (GRCm38) |
V477F |
possibly damaging |
Het |
Igkv8-28 |
A |
T |
6: 70,143,890 (GRCm38) |
V23E |
probably benign |
Het |
Isg20l2 |
T |
A |
3: 87,932,088 (GRCm38) |
V202E |
probably damaging |
Het |
Jakmip2 |
A |
G |
18: 43,575,534 (GRCm38) |
I288T |
probably benign |
Het |
Kansl3 |
A |
G |
1: 36,365,605 (GRCm38) |
V88A |
probably benign |
Het |
Kcna3 |
A |
G |
3: 107,037,950 (GRCm38) |
T510A |
possibly damaging |
Het |
Map2k5 |
G |
T |
9: 63,338,098 (GRCm38) |
L140I |
probably benign |
Het |
Map3k19 |
A |
G |
1: 127,822,599 (GRCm38) |
I1005T |
possibly damaging |
Het |
Mmp25 |
G |
A |
17: 23,630,794 (GRCm38) |
A541V |
possibly damaging |
Het |
Ms4a14 |
T |
A |
19: 11,304,020 (GRCm38) |
E391D |
probably benign |
Het |
Mtrf1l |
A |
G |
10: 5,815,550 (GRCm38) |
|
probably null |
Het |
Myom1 |
A |
G |
17: 71,126,137 (GRCm38) |
N1591S |
probably damaging |
Het |
Nos1 |
G |
A |
5: 117,936,570 (GRCm38) |
V1060M |
probably benign |
Het |
Nsun5 |
C |
T |
5: 135,371,531 (GRCm38) |
T142M |
probably damaging |
Het |
Odc1 |
A |
G |
12: 17,550,654 (GRCm38) |
E430G |
probably benign |
Het |
Or8g36 |
C |
A |
9: 39,510,809 (GRCm38) |
V304F |
probably benign |
Het |
P2ry12 |
T |
C |
3: 59,217,907 (GRCm38) |
I116V |
probably null |
Het |
Patl1 |
T |
A |
19: 11,920,331 (GRCm38) |
V94E |
probably damaging |
Het |
Plin3 |
A |
T |
17: 56,281,488 (GRCm38) |
Y255* |
probably null |
Het |
Pou6f1 |
T |
C |
15: 100,579,946 (GRCm38) |
T439A |
probably damaging |
Het |
Prdm13 |
T |
C |
4: 21,678,366 (GRCm38) |
K708R |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,829,404 (GRCm38) |
S916P |
possibly damaging |
Het |
Rab34 |
T |
A |
11: 78,191,202 (GRCm38) |
|
probably null |
Het |
Rps7 |
A |
G |
12: 28,635,594 (GRCm38) |
S21P |
possibly damaging |
Het |
Sesn3 |
A |
G |
9: 14,321,163 (GRCm38) |
Y244C |
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,761,611 (GRCm38) |
F284L |
probably benign |
Het |
Slc25a44 |
C |
T |
3: 88,420,911 (GRCm38) |
G72D |
probably damaging |
Het |
Slco6d1 |
A |
G |
1: 98,499,863 (GRCm38) |
T640A |
probably benign |
Het |
Sspo |
A |
T |
6: 48,462,191 (GRCm38) |
E1591V |
possibly damaging |
Het |
Tbata |
C |
A |
10: 61,175,865 (GRCm38) |
T60K |
possibly damaging |
Het |
Tbc1d2 |
T |
A |
4: 46,637,692 (GRCm38) |
T185S |
possibly damaging |
Het |
Tlcd4 |
T |
A |
3: 121,235,059 (GRCm38) |
I60F |
possibly damaging |
Het |
Tmem87a |
A |
G |
2: 120,404,021 (GRCm38) |
S14P |
possibly damaging |
Het |
Tnnt2 |
C |
A |
1: 135,850,554 (GRCm38) |
|
probably null |
Het |
Trex1 |
A |
G |
9: 109,058,641 (GRCm38) |
V94A |
probably benign |
Het |
Ubtfl1 |
A |
C |
9: 18,409,296 (GRCm38) |
D40A |
possibly damaging |
Het |
Zc3hav1 |
A |
T |
6: 38,333,000 (GRCm38) |
Y296N |
probably benign |
Het |
Zfp521 |
T |
A |
18: 13,844,627 (GRCm38) |
N910Y |
probably damaging |
Het |
Zfp53 |
A |
G |
17: 21,508,713 (GRCm38) |
E336G |
possibly damaging |
Het |
|
Other mutations in Scn9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00514:Scn9a
|
APN |
2 |
66,563,601 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00570:Scn9a
|
APN |
2 |
66,484,142 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00809:Scn9a
|
APN |
2 |
66,483,935 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00977:Scn9a
|
APN |
2 |
66,484,301 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01120:Scn9a
|
APN |
2 |
66,526,972 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01134:Scn9a
|
APN |
2 |
66,504,968 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01300:Scn9a
|
APN |
2 |
66,488,053 (GRCm38) |
nonsense |
probably null |
|
IGL01452:Scn9a
|
APN |
2 |
66,527,072 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01531:Scn9a
|
APN |
2 |
66,537,378 (GRCm38) |
missense |
probably benign |
0.11 |
IGL01572:Scn9a
|
APN |
2 |
66,493,886 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01645:Scn9a
|
APN |
2 |
66,487,642 (GRCm38) |
missense |
possibly damaging |
0.62 |
IGL01823:Scn9a
|
APN |
2 |
66,484,042 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01965:Scn9a
|
APN |
2 |
66,484,433 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02127:Scn9a
|
APN |
2 |
66,494,826 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02127:Scn9a
|
APN |
2 |
66,547,135 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02166:Scn9a
|
APN |
2 |
66,493,103 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02183:Scn9a
|
APN |
2 |
66,484,611 (GRCm38) |
splice site |
probably benign |
|
IGL02640:Scn9a
|
APN |
2 |
66,536,096 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02685:Scn9a
|
APN |
2 |
66,537,293 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02798:Scn9a
|
APN |
2 |
66,540,559 (GRCm38) |
missense |
possibly damaging |
0.52 |
IGL02832:Scn9a
|
APN |
2 |
66,568,029 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03008:Scn9a
|
APN |
2 |
66,562,511 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03270:Scn9a
|
APN |
2 |
66,484,014 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03408:Scn9a
|
APN |
2 |
66,526,747 (GRCm38) |
missense |
probably benign |
0.00 |
BB007:Scn9a
|
UTSW |
2 |
66,504,849 (GRCm38) |
missense |
probably damaging |
0.99 |
BB017:Scn9a
|
UTSW |
2 |
66,504,849 (GRCm38) |
missense |
probably damaging |
0.99 |
R0039:Scn9a
|
UTSW |
2 |
66,562,444 (GRCm38) |
missense |
probably damaging |
0.98 |
R0173:Scn9a
|
UTSW |
2 |
66,533,093 (GRCm38) |
missense |
probably damaging |
1.00 |
R0323:Scn9a
|
UTSW |
2 |
66,568,131 (GRCm38) |
missense |
probably damaging |
1.00 |
R0344:Scn9a
|
UTSW |
2 |
66,505,010 (GRCm38) |
missense |
probably damaging |
0.99 |
R0421:Scn9a
|
UTSW |
2 |
66,543,277 (GRCm38) |
missense |
probably benign |
|
R0465:Scn9a
|
UTSW |
2 |
66,526,996 (GRCm38) |
missense |
probably damaging |
1.00 |
R0514:Scn9a
|
UTSW |
2 |
66,483,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R0599:Scn9a
|
UTSW |
2 |
66,526,799 (GRCm38) |
missense |
probably damaging |
0.96 |
R0627:Scn9a
|
UTSW |
2 |
66,537,377 (GRCm38) |
missense |
probably benign |
0.00 |
R0644:Scn9a
|
UTSW |
2 |
66,533,061 (GRCm38) |
critical splice donor site |
probably null |
|
R0653:Scn9a
|
UTSW |
2 |
66,533,377 (GRCm38) |
missense |
probably damaging |
1.00 |
R0685:Scn9a
|
UTSW |
2 |
66,483,499 (GRCm38) |
missense |
probably benign |
0.02 |
R0718:Scn9a
|
UTSW |
2 |
66,547,112 (GRCm38) |
missense |
probably damaging |
1.00 |
R0827:Scn9a
|
UTSW |
2 |
66,536,124 (GRCm38) |
nonsense |
probably null |
|
R0890:Scn9a
|
UTSW |
2 |
66,483,735 (GRCm38) |
missense |
probably damaging |
1.00 |
R1139:Scn9a
|
UTSW |
2 |
66,504,997 (GRCm38) |
missense |
probably benign |
0.02 |
R1385:Scn9a
|
UTSW |
2 |
66,563,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R1398:Scn9a
|
UTSW |
2 |
66,484,586 (GRCm38) |
missense |
probably benign |
0.11 |
R1496:Scn9a
|
UTSW |
2 |
66,526,888 (GRCm38) |
missense |
probably benign |
|
R1511:Scn9a
|
UTSW |
2 |
66,526,813 (GRCm38) |
missense |
probably benign |
0.01 |
R1517:Scn9a
|
UTSW |
2 |
66,505,027 (GRCm38) |
splice site |
probably benign |
|
R1564:Scn9a
|
UTSW |
2 |
66,484,304 (GRCm38) |
missense |
probably damaging |
1.00 |
R1634:Scn9a
|
UTSW |
2 |
66,488,017 (GRCm38) |
missense |
probably damaging |
1.00 |
R1662:Scn9a
|
UTSW |
2 |
66,483,459 (GRCm38) |
missense |
probably benign |
0.00 |
R1695:Scn9a
|
UTSW |
2 |
66,504,876 (GRCm38) |
nonsense |
probably null |
|
R1709:Scn9a
|
UTSW |
2 |
66,483,506 (GRCm38) |
missense |
probably damaging |
1.00 |
R1741:Scn9a
|
UTSW |
2 |
66,487,594 (GRCm38) |
missense |
probably damaging |
0.99 |
R1755:Scn9a
|
UTSW |
2 |
66,501,716 (GRCm38) |
missense |
probably benign |
0.38 |
R1914:Scn9a
|
UTSW |
2 |
66,566,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R1962:Scn9a
|
UTSW |
2 |
66,484,311 (GRCm38) |
missense |
probably damaging |
1.00 |
R1970:Scn9a
|
UTSW |
2 |
66,515,380 (GRCm38) |
missense |
probably damaging |
0.97 |
R2017:Scn9a
|
UTSW |
2 |
66,515,321 (GRCm38) |
missense |
probably damaging |
0.99 |
R2092:Scn9a
|
UTSW |
2 |
66,533,376 (GRCm38) |
missense |
probably damaging |
0.99 |
R2105:Scn9a
|
UTSW |
2 |
66,568,183 (GRCm38) |
missense |
probably benign |
0.25 |
R2114:Scn9a
|
UTSW |
2 |
66,484,052 (GRCm38) |
missense |
probably damaging |
1.00 |
R2115:Scn9a
|
UTSW |
2 |
66,484,052 (GRCm38) |
missense |
probably damaging |
1.00 |
R2128:Scn9a
|
UTSW |
2 |
66,526,654 (GRCm38) |
missense |
probably damaging |
1.00 |
R2157:Scn9a
|
UTSW |
2 |
66,536,325 (GRCm38) |
missense |
probably damaging |
1.00 |
R2162:Scn9a
|
UTSW |
2 |
66,534,229 (GRCm38) |
missense |
probably damaging |
0.98 |
R2350:Scn9a
|
UTSW |
2 |
66,504,968 (GRCm38) |
missense |
probably damaging |
1.00 |
R3694:Scn9a
|
UTSW |
2 |
66,562,405 (GRCm38) |
missense |
probably benign |
|
R3771:Scn9a
|
UTSW |
2 |
66,483,648 (GRCm38) |
missense |
probably benign |
0.26 |
R3772:Scn9a
|
UTSW |
2 |
66,483,648 (GRCm38) |
missense |
probably benign |
0.26 |
R3773:Scn9a
|
UTSW |
2 |
66,483,648 (GRCm38) |
missense |
probably benign |
0.26 |
R3922:Scn9a
|
UTSW |
2 |
66,526,873 (GRCm38) |
missense |
possibly damaging |
0.88 |
R3926:Scn9a
|
UTSW |
2 |
66,526,873 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4258:Scn9a
|
UTSW |
2 |
66,565,054 (GRCm38) |
intron |
probably benign |
|
R4385:Scn9a
|
UTSW |
2 |
66,484,556 (GRCm38) |
missense |
probably damaging |
1.00 |
R4415:Scn9a
|
UTSW |
2 |
66,526,693 (GRCm38) |
missense |
probably damaging |
1.00 |
R4570:Scn9a
|
UTSW |
2 |
66,483,558 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4682:Scn9a
|
UTSW |
2 |
66,547,018 (GRCm38) |
missense |
probably benign |
|
R4783:Scn9a
|
UTSW |
2 |
66,540,623 (GRCm38) |
missense |
probably benign |
0.01 |
R4822:Scn9a
|
UTSW |
2 |
66,483,749 (GRCm38) |
missense |
possibly damaging |
0.55 |
R4829:Scn9a
|
UTSW |
2 |
66,551,713 (GRCm38) |
missense |
probably benign |
|
R4908:Scn9a
|
UTSW |
2 |
66,526,743 (GRCm38) |
missense |
probably benign |
0.03 |
R4983:Scn9a
|
UTSW |
2 |
66,566,270 (GRCm38) |
missense |
probably benign |
0.02 |
R5047:Scn9a
|
UTSW |
2 |
66,562,480 (GRCm38) |
missense |
probably damaging |
1.00 |
R5100:Scn9a
|
UTSW |
2 |
66,534,119 (GRCm38) |
missense |
probably damaging |
1.00 |
R5140:Scn9a
|
UTSW |
2 |
66,565,167 (GRCm38) |
missense |
possibly damaging |
0.81 |
R5398:Scn9a
|
UTSW |
2 |
66,488,043 (GRCm38) |
missense |
probably damaging |
1.00 |
R5557:Scn9a
|
UTSW |
2 |
66,547,103 (GRCm38) |
missense |
probably damaging |
0.99 |
R5582:Scn9a
|
UTSW |
2 |
66,565,029 (GRCm38) |
intron |
probably benign |
|
R6108:Scn9a
|
UTSW |
2 |
66,484,049 (GRCm38) |
missense |
probably damaging |
1.00 |
R6115:Scn9a
|
UTSW |
2 |
66,563,629 (GRCm38) |
missense |
possibly damaging |
0.70 |
R6143:Scn9a
|
UTSW |
2 |
66,487,524 (GRCm38) |
missense |
probably benign |
0.00 |
R6335:Scn9a
|
UTSW |
2 |
66,568,264 (GRCm38) |
start codon destroyed |
possibly damaging |
0.91 |
R6429:Scn9a
|
UTSW |
2 |
66,526,963 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6632:Scn9a
|
UTSW |
2 |
66,483,502 (GRCm38) |
missense |
probably benign |
0.23 |
R6681:Scn9a
|
UTSW |
2 |
66,563,342 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6830:Scn9a
|
UTSW |
2 |
66,568,029 (GRCm38) |
missense |
probably damaging |
1.00 |
R7102:Scn9a
|
UTSW |
2 |
66,549,015 (GRCm38) |
missense |
probably damaging |
1.00 |
R7186:Scn9a
|
UTSW |
2 |
66,534,223 (GRCm38) |
missense |
probably damaging |
1.00 |
R7243:Scn9a
|
UTSW |
2 |
66,540,530 (GRCm38) |
missense |
probably damaging |
1.00 |
R7311:Scn9a
|
UTSW |
2 |
66,484,404 (GRCm38) |
missense |
possibly damaging |
0.54 |
R7328:Scn9a
|
UTSW |
2 |
66,484,587 (GRCm38) |
missense |
probably benign |
|
R7386:Scn9a
|
UTSW |
2 |
66,540,550 (GRCm38) |
missense |
probably damaging |
1.00 |
R7438:Scn9a
|
UTSW |
2 |
66,547,187 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7483:Scn9a
|
UTSW |
2 |
66,533,348 (GRCm38) |
missense |
probably damaging |
0.99 |
R7485:Scn9a
|
UTSW |
2 |
66,534,217 (GRCm38) |
missense |
probably damaging |
1.00 |
R7526:Scn9a
|
UTSW |
2 |
66,483,646 (GRCm38) |
missense |
probably benign |
|
R7617:Scn9a
|
UTSW |
2 |
66,540,549 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7642:Scn9a
|
UTSW |
2 |
66,536,236 (GRCm38) |
missense |
probably benign |
0.02 |
R7653:Scn9a
|
UTSW |
2 |
66,527,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R7747:Scn9a
|
UTSW |
2 |
66,484,298 (GRCm38) |
missense |
probably damaging |
1.00 |
R7823:Scn9a
|
UTSW |
2 |
66,483,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R7864:Scn9a
|
UTSW |
2 |
66,484,560 (GRCm38) |
missense |
possibly damaging |
0.73 |
R7890:Scn9a
|
UTSW |
2 |
66,543,112 (GRCm38) |
missense |
probably benign |
0.00 |
R7930:Scn9a
|
UTSW |
2 |
66,504,849 (GRCm38) |
missense |
probably damaging |
0.99 |
R7975:Scn9a
|
UTSW |
2 |
66,484,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R8057:Scn9a
|
UTSW |
2 |
66,515,430 (GRCm38) |
missense |
probably benign |
0.06 |
R8145:Scn9a
|
UTSW |
2 |
66,487,410 (GRCm38) |
missense |
probably damaging |
1.00 |
R8163:Scn9a
|
UTSW |
2 |
66,484,401 (GRCm38) |
missense |
probably damaging |
1.00 |
R8165:Scn9a
|
UTSW |
2 |
66,540,530 (GRCm38) |
missense |
probably damaging |
1.00 |
R8342:Scn9a
|
UTSW |
2 |
66,536,282 (GRCm38) |
missense |
probably benign |
|
R8345:Scn9a
|
UTSW |
2 |
66,494,622 (GRCm38) |
missense |
probably damaging |
0.96 |
R8464:Scn9a
|
UTSW |
2 |
66,566,281 (GRCm38) |
missense |
probably damaging |
0.99 |
R8467:Scn9a
|
UTSW |
2 |
66,501,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R8698:Scn9a
|
UTSW |
2 |
66,536,284 (GRCm38) |
missense |
probably benign |
0.00 |
R8810:Scn9a
|
UTSW |
2 |
66,501,666 (GRCm38) |
missense |
probably damaging |
1.00 |
R8822:Scn9a
|
UTSW |
2 |
66,540,635 (GRCm38) |
missense |
probably damaging |
0.99 |
R8829:Scn9a
|
UTSW |
2 |
66,483,617 (GRCm38) |
missense |
probably benign |
|
R9009:Scn9a
|
UTSW |
2 |
66,508,583 (GRCm38) |
missense |
probably damaging |
1.00 |
R9038:Scn9a
|
UTSW |
2 |
66,494,803 (GRCm38) |
missense |
probably damaging |
1.00 |
R9126:Scn9a
|
UTSW |
2 |
66,484,400 (GRCm38) |
missense |
probably damaging |
1.00 |
R9205:Scn9a
|
UTSW |
2 |
66,533,313 (GRCm38) |
missense |
probably damaging |
1.00 |
R9300:Scn9a
|
UTSW |
2 |
66,504,892 (GRCm38) |
missense |
probably benign |
0.39 |
R9373:Scn9a
|
UTSW |
2 |
66,483,917 (GRCm38) |
missense |
probably benign |
0.00 |
R9404:Scn9a
|
UTSW |
2 |
66,526,696 (GRCm38) |
missense |
probably benign |
0.02 |
R9443:Scn9a
|
UTSW |
2 |
66,565,209 (GRCm38) |
missense |
probably damaging |
1.00 |
R9590:Scn9a
|
UTSW |
2 |
66,483,984 (GRCm38) |
missense |
probably benign |
0.05 |
R9612:Scn9a
|
UTSW |
2 |
66,533,364 (GRCm38) |
missense |
probably damaging |
1.00 |
R9617:Scn9a
|
UTSW |
2 |
66,562,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R9717:Scn9a
|
UTSW |
2 |
66,526,658 (GRCm38) |
missense |
probably benign |
|
X0003:Scn9a
|
UTSW |
2 |
66,508,647 (GRCm38) |
missense |
probably benign |
0.02 |
X0062:Scn9a
|
UTSW |
2 |
66,568,077 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Scn9a
|
UTSW |
2 |
66,540,592 (GRCm38) |
missense |
probably benign |
0.00 |
Z1177:Scn9a
|
UTSW |
2 |
66,494,685 (GRCm38) |
missense |
possibly damaging |
0.68 |
|