Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930546C10Rik |
A |
T |
18: 68,950,137 (GRCm38) |
M2K |
unknown |
Het |
6430531B16Rik |
A |
T |
7: 139,976,052 (GRCm38) |
C225* |
probably null |
Het |
Ablim3 |
T |
C |
18: 61,821,994 (GRCm38) |
D308G |
probably damaging |
Het |
Adamts17 |
A |
T |
7: 66,968,849 (GRCm38) |
K370N |
probably benign |
Het |
Adcy4 |
T |
C |
14: 55,778,327 (GRCm38) |
Y435C |
probably damaging |
Het |
Adgb |
A |
T |
10: 10,377,949 (GRCm38) |
F1216I |
possibly damaging |
Het |
Akr1a1 |
G |
A |
4: 116,641,054 (GRCm38) |
T98I |
probably damaging |
Het |
Alyref2 |
G |
T |
1: 171,503,533 (GRCm38) |
|
probably benign |
Het |
Ank3 |
T |
A |
10: 69,822,249 (GRCm38) |
H168Q |
unknown |
Het |
Bnc1 |
A |
C |
7: 81,974,492 (GRCm38) |
L329R |
possibly damaging |
Het |
Btaf1 |
G |
A |
19: 36,958,382 (GRCm38) |
A191T |
probably benign |
Het |
Carmil3 |
T |
G |
14: 55,497,747 (GRCm38) |
|
probably null |
Het |
Cd200r1 |
C |
A |
16: 44,789,848 (GRCm38) |
D143E |
probably benign |
Het |
Cep112 |
A |
G |
11: 108,808,681 (GRCm38) |
H98R |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,069,323 (GRCm38) |
Q3346L |
probably damaging |
Het |
Cpne4 |
T |
A |
9: 104,872,740 (GRCm38) |
V81E |
possibly damaging |
Het |
Ctnnd2 |
T |
A |
15: 30,966,768 (GRCm38) |
M955K |
probably damaging |
Het |
Ctsj |
A |
T |
13: 61,000,559 (GRCm38) |
M307K |
possibly damaging |
Het |
Ddhd2 |
G |
T |
8: 25,754,290 (GRCm38) |
R103S |
possibly damaging |
Het |
Depdc5 |
A |
G |
5: 32,927,936 (GRCm38) |
T700A |
probably benign |
Het |
Dhx57 |
A |
C |
17: 80,267,577 (GRCm38) |
D657E |
possibly damaging |
Het |
Dmbt1 |
G |
A |
7: 131,112,236 (GRCm38) |
G1678S |
unknown |
Het |
Dnajb1 |
A |
G |
8: 83,610,303 (GRCm38) |
D234G |
probably benign |
Het |
Dsc2 |
C |
T |
18: 20,041,926 (GRCm38) |
V431M |
possibly damaging |
Het |
Evi5 |
C |
A |
5: 107,809,823 (GRCm38) |
|
probably null |
Het |
Exoc2 |
T |
C |
13: 30,906,663 (GRCm38) |
|
probably null |
Het |
Foxo3 |
T |
C |
10: 42,197,360 (GRCm38) |
D387G |
probably benign |
Het |
Gda |
A |
G |
19: 21,409,886 (GRCm38) |
I325T |
probably benign |
Het |
Gm960 |
G |
A |
19: 4,663,558 (GRCm38) |
R285* |
probably null |
Het |
Iqgap1 |
A |
G |
7: 80,726,042 (GRCm38) |
S1362P |
probably damaging |
Het |
Klf10 |
G |
T |
15: 38,296,949 (GRCm38) |
N282K |
possibly damaging |
Het |
Mettl13 |
A |
G |
1: 162,548,154 (GRCm38) |
Y35H |
probably damaging |
Het |
Mill2 |
A |
G |
7: 18,858,290 (GRCm38) |
T279A |
probably benign |
Het |
Ncaph2 |
G |
A |
15: 89,370,256 (GRCm38) |
W386* |
probably null |
Het |
Nploc4 |
A |
T |
11: 120,408,881 (GRCm38) |
S338T |
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,293,887 (GRCm38) |
S261G |
probably damaging |
Het |
Olfr1042 |
A |
G |
2: 86,159,530 (GRCm38) |
V280A |
possibly damaging |
Het |
Olfr1354 |
T |
A |
10: 78,916,843 (GRCm38) |
M1K |
probably null |
Het |
Olfr1388 |
T |
C |
11: 49,444,400 (GRCm38) |
F183S |
possibly damaging |
Het |
Palld |
A |
G |
8: 61,532,052 (GRCm38) |
F1060L |
unknown |
Het |
Pfas |
C |
G |
11: 69,003,774 (GRCm38) |
V22L |
probably benign |
Het |
Pygo2 |
T |
G |
3: 89,432,821 (GRCm38) |
F175L |
probably benign |
Het |
Rnf2 |
T |
C |
1: 151,471,380 (GRCm38) |
E316G |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,707,772 (GRCm38) |
M642K |
probably damaging |
Het |
Saa3 |
A |
G |
7: 46,714,923 (GRCm38) |
C60R |
unknown |
Het |
Scap |
A |
G |
9: 110,373,169 (GRCm38) |
T202A |
probably benign |
Het |
Slc6a19 |
A |
T |
13: 73,689,891 (GRCm38) |
V163E |
possibly damaging |
Het |
Smc5 |
G |
A |
19: 23,215,175 (GRCm38) |
H850Y |
possibly damaging |
Het |
Sqle |
G |
A |
15: 59,330,754 (GRCm38) |
R519Q |
probably benign |
Het |
Sulf1 |
T |
C |
1: 12,838,361 (GRCm38) |
Y533H |
probably benign |
Het |
Tex45 |
A |
G |
8: 3,487,079 (GRCm38) |
K475R |
probably benign |
Het |
Thbs2 |
A |
G |
17: 14,673,150 (GRCm38) |
S923P |
possibly damaging |
Het |
Themis |
A |
G |
10: 28,789,747 (GRCm38) |
D602G |
probably benign |
Het |
Tmem132c |
A |
G |
5: 127,563,926 (GRCm38) |
K1054E |
probably benign |
Het |
Tmem161b |
C |
A |
13: 84,222,418 (GRCm38) |
|
probably benign |
Het |
Tnrc6c |
T |
A |
11: 117,721,954 (GRCm38) |
C313S |
probably benign |
Het |
Tpm1 |
T |
C |
9: 67,028,167 (GRCm38) |
I284M |
probably benign |
Het |
Trpm4 |
A |
T |
7: 45,314,640 (GRCm38) |
L722H |
possibly damaging |
Het |
Trub2 |
T |
G |
2: 29,786,595 (GRCm38) |
Q41P |
probably benign |
Het |
Usp17le |
A |
C |
7: 104,768,307 (GRCm38) |
|
probably null |
Het |
Zfp398 |
G |
A |
6: 47,858,950 (GRCm38) |
V148I |
probably benign |
Het |
Zfp40 |
T |
C |
17: 23,177,007 (GRCm38) |
E202G |
probably damaging |
Het |
Zfp618 |
T |
A |
4: 63,095,385 (GRCm38) |
|
probably null |
Het |
Zfp667 |
T |
A |
7: 6,305,950 (GRCm38) |
I539N |
possibly damaging |
Het |
Zfp738 |
A |
T |
13: 67,670,250 (GRCm38) |
C541S |
probably 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 |
R6261:Scn9a
|
UTSW |
2 |
66,483,896 (GRCm38) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|