Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
A |
G |
11: 100,410,576 (GRCm39) |
F134S |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,257,262 (GRCm39) |
|
probably null |
Het |
Adam29 |
G |
T |
8: 56,325,463 (GRCm39) |
N330K |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,677,033 (GRCm39) |
S1933P |
probably benign |
Het |
Afap1l2 |
T |
C |
19: 56,902,824 (GRCm39) |
H785R |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,987,800 (GRCm39) |
L3028* |
probably null |
Het |
Ajuba |
T |
C |
14: 54,807,847 (GRCm39) |
T462A |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,534,016 (GRCm39) |
N289S |
possibly damaging |
Het |
Ankrd46 |
A |
T |
15: 36,486,001 (GRCm39) |
L84Q |
probably damaging |
Het |
Ankrd54 |
T |
G |
15: 78,940,270 (GRCm39) |
D163A |
probably damaging |
Het |
Arhgef28 |
A |
G |
13: 98,282,064 (GRCm39) |
L10P |
probably benign |
Het |
Atm |
A |
T |
9: 53,367,288 (GRCm39) |
|
probably null |
Het |
Azin1 |
G |
C |
15: 38,492,572 (GRCm39) |
F312L |
probably damaging |
Het |
C2cd4c |
A |
G |
10: 79,448,482 (GRCm39) |
S222P |
probably damaging |
Het |
Cdyl |
A |
G |
13: 36,000,147 (GRCm39) |
T143A |
probably benign |
Het |
Clhc1 |
G |
A |
11: 29,503,751 (GRCm39) |
V56I |
possibly damaging |
Het |
Cntn4 |
T |
C |
6: 106,486,471 (GRCm39) |
S300P |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,551,224 (GRCm39) |
Y2131H |
probably damaging |
Het |
Cyp3a41b |
A |
G |
5: 145,506,190 (GRCm39) |
S287P |
probably benign |
Het |
Dctn4 |
A |
G |
18: 60,689,401 (GRCm39) |
D424G |
probably benign |
Het |
Dnajb8 |
C |
T |
6: 88,199,940 (GRCm39) |
R159C |
possibly damaging |
Het |
Dop1b |
A |
G |
16: 93,546,847 (GRCm39) |
T284A |
probably benign |
Het |
E330034G19Rik |
A |
C |
14: 24,346,135 (GRCm39) |
|
probably null |
Het |
Ehhadh |
G |
A |
16: 21,581,373 (GRCm39) |
P540S |
possibly damaging |
Het |
Emsy |
T |
C |
7: 98,297,111 (GRCm39) |
E24G |
probably damaging |
Het |
F930015N05Rik |
A |
C |
11: 64,326,418 (GRCm39) |
L74W |
unknown |
Het |
Fat1 |
A |
G |
8: 45,406,390 (GRCm39) |
D1047G |
|
Het |
Galnt7 |
A |
G |
8: 58,005,600 (GRCm39) |
V211A |
possibly damaging |
Het |
Gdap2 |
T |
C |
3: 100,109,611 (GRCm39) |
C543R |
unknown |
Het |
Ghr |
A |
C |
15: 3,362,901 (GRCm39) |
D190E |
probably benign |
Het |
Glrx |
A |
G |
13: 75,995,346 (GRCm39) |
M89V |
probably benign |
Het |
Gm10323 |
A |
C |
13: 67,000,859 (GRCm39) |
Y91* |
noncoding transcript |
Het |
Gnb4 |
A |
T |
3: 32,644,184 (GRCm39) |
D153E |
possibly damaging |
Het |
Gnptab |
G |
T |
10: 88,276,254 (GRCm39) |
|
probably null |
Het |
Grip2 |
T |
C |
6: 91,762,665 (GRCm39) |
D193G |
possibly damaging |
Het |
Igsf3 |
T |
C |
3: 101,347,038 (GRCm39) |
W658R |
probably damaging |
Het |
Ip6k1 |
T |
A |
9: 107,923,115 (GRCm39) |
F416I |
probably benign |
Het |
Klhl1 |
T |
G |
14: 96,517,546 (GRCm39) |
T377P |
possibly damaging |
Het |
Lrrc38 |
G |
A |
4: 143,077,303 (GRCm39) |
G189R |
probably damaging |
Het |
Lrrfip1 |
T |
C |
1: 91,042,878 (GRCm39) |
S428P |
probably benign |
Het |
Megf10 |
A |
G |
18: 57,416,893 (GRCm39) |
D754G |
probably benign |
Het |
Mrgprx2 |
T |
A |
7: 48,132,527 (GRCm39) |
Y97F |
probably benign |
Het |
Msantd2 |
T |
G |
9: 37,400,684 (GRCm39) |
V22G |
probably damaging |
Het |
Myl6b |
T |
C |
10: 128,333,209 (GRCm39) |
K11R |
unknown |
Het |
Nab2 |
C |
A |
10: 127,498,645 (GRCm39) |
V475L |
probably benign |
Het |
Npas1 |
T |
C |
7: 16,189,890 (GRCm39) |
E552G |
probably damaging |
Het |
Pknox2 |
T |
C |
9: 36,821,040 (GRCm39) |
N274S |
possibly damaging |
Het |
Pmepa1 |
A |
T |
2: 173,069,700 (GRCm39) |
L247Q |
probably damaging |
Het |
Poll |
T |
C |
19: 45,542,047 (GRCm39) |
K420E |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,628,344 (GRCm39) |
V1283A |
probably benign |
Het |
Ppil4 |
A |
T |
10: 7,671,444 (GRCm39) |
Y36F |
probably benign |
Het |
Pramel20 |
T |
G |
4: 143,298,530 (GRCm39) |
Y158D |
probably benign |
Het |
Psd2 |
C |
T |
18: 36,113,478 (GRCm39) |
R317W |
probably damaging |
Het |
Pspc1 |
T |
A |
14: 57,015,616 (GRCm39) |
M1L |
probably benign |
Het |
Qrsl1 |
A |
T |
10: 43,758,080 (GRCm39) |
F338I |
possibly damaging |
Het |
Rcor3 |
A |
G |
1: 191,814,749 (GRCm39) |
Y77H |
unknown |
Het |
Sbno2 |
G |
A |
10: 79,905,845 (GRCm39) |
P157L |
probably benign |
Het |
Setd3 |
C |
G |
12: 108,073,612 (GRCm39) |
G555A |
possibly damaging |
Het |
Slc12a4 |
A |
T |
8: 106,678,601 (GRCm39) |
M245K |
probably benign |
Het |
Slc1a5 |
T |
A |
7: 16,515,902 (GRCm39) |
L26Q |
probably benign |
Het |
Slc38a3 |
T |
G |
9: 107,534,908 (GRCm39) |
M156L |
probably damaging |
Het |
Slc45a2 |
A |
T |
15: 11,001,233 (GRCm39) |
I111F |
probably benign |
Het |
Slc4a3 |
T |
A |
1: 75,528,810 (GRCm39) |
M491K |
probably benign |
Het |
Son |
A |
G |
16: 91,453,734 (GRCm39) |
D827G |
probably damaging |
Het |
Sppl2c |
A |
T |
11: 104,077,710 (GRCm39) |
H170L |
probably damaging |
Het |
St6gal2 |
T |
A |
17: 55,797,935 (GRCm39) |
|
probably null |
Het |
Taf4b |
T |
A |
18: 15,031,106 (GRCm39) |
L830H |
probably damaging |
Het |
Tex22 |
A |
G |
12: 113,038,696 (GRCm39) |
|
probably null |
Het |
Tiam2 |
C |
T |
17: 3,568,860 (GRCm39) |
R1669C |
probably damaging |
Het |
Tmprss15 |
T |
A |
16: 78,821,223 (GRCm39) |
N506I |
probably damaging |
Het |
Topors |
A |
T |
4: 40,260,686 (GRCm39) |
I866K |
unknown |
Het |
Trip12 |
G |
T |
1: 84,743,771 (GRCm39) |
T512K |
possibly damaging |
Het |
Ubr1 |
T |
A |
2: 120,791,585 (GRCm39) |
H133L |
probably damaging |
Het |
Wwtr1 |
T |
C |
3: 57,366,441 (GRCm39) |
D422G |
probably damaging |
Het |
Zfp689 |
A |
C |
7: 127,043,758 (GRCm39) |
C291G |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,576,877 (GRCm39) |
L68P |
possibly damaging |
Het |
Zswim5 |
G |
T |
4: 116,735,219 (GRCm39) |
R188L |
probably benign |
Het |
|
Other mutations in Scn10a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Scn10a
|
APN |
9 |
119,501,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Scn10a
|
APN |
9 |
119,451,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01467:Scn10a
|
APN |
9 |
119,487,478 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01472:Scn10a
|
APN |
9 |
119,446,829 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01481:Scn10a
|
APN |
9 |
119,438,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01539:Scn10a
|
APN |
9 |
119,467,764 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01580:Scn10a
|
APN |
9 |
119,456,225 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01676:Scn10a
|
APN |
9 |
119,501,231 (GRCm39) |
nonsense |
probably null |
|
IGL01681:Scn10a
|
APN |
9 |
119,523,143 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01748:Scn10a
|
APN |
9 |
119,456,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Scn10a
|
APN |
9 |
119,464,568 (GRCm39) |
nonsense |
probably null |
|
IGL01998:Scn10a
|
APN |
9 |
119,438,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02015:Scn10a
|
APN |
9 |
119,494,017 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02098:Scn10a
|
APN |
9 |
119,520,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02113:Scn10a
|
APN |
9 |
119,438,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Scn10a
|
APN |
9 |
119,501,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02262:Scn10a
|
APN |
9 |
119,487,499 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02317:Scn10a
|
APN |
9 |
119,467,621 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02428:Scn10a
|
APN |
9 |
119,520,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Scn10a
|
APN |
9 |
119,447,914 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02583:Scn10a
|
APN |
9 |
119,520,506 (GRCm39) |
splice site |
probably benign |
|
IGL02597:Scn10a
|
APN |
9 |
119,439,189 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02680:Scn10a
|
APN |
9 |
119,495,125 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Scn10a
|
APN |
9 |
119,445,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Scn10a
|
APN |
9 |
119,500,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02992:Scn10a
|
APN |
9 |
119,438,626 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03040:Scn10a
|
APN |
9 |
119,452,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03049:Scn10a
|
APN |
9 |
119,495,056 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03407:Scn10a
|
APN |
9 |
119,477,237 (GRCm39) |
missense |
probably damaging |
0.99 |
possum
|
UTSW |
9 |
119,467,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Scn10a
|
UTSW |
9 |
119,499,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0030:Scn10a
|
UTSW |
9 |
119,499,056 (GRCm39) |
missense |
probably benign |
0.01 |
R0328:Scn10a
|
UTSW |
9 |
119,523,168 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0494:Scn10a
|
UTSW |
9 |
119,453,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Scn10a
|
UTSW |
9 |
119,442,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R0548:Scn10a
|
UTSW |
9 |
119,494,994 (GRCm39) |
missense |
probably benign |
0.00 |
R0584:Scn10a
|
UTSW |
9 |
119,499,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Scn10a
|
UTSW |
9 |
119,495,129 (GRCm39) |
missense |
probably benign |
0.01 |
R0894:Scn10a
|
UTSW |
9 |
119,459,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1022:Scn10a
|
UTSW |
9 |
119,438,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Scn10a
|
UTSW |
9 |
119,438,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Scn10a
|
UTSW |
9 |
119,446,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Scn10a
|
UTSW |
9 |
119,520,544 (GRCm39) |
missense |
probably benign |
0.01 |
R1466:Scn10a
|
UTSW |
9 |
119,495,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Scn10a
|
UTSW |
9 |
119,495,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1573:Scn10a
|
UTSW |
9 |
119,442,692 (GRCm39) |
missense |
probably benign |
0.04 |
R1704:Scn10a
|
UTSW |
9 |
119,438,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1933:Scn10a
|
UTSW |
9 |
119,439,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Scn10a
|
UTSW |
9 |
119,520,520 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2013:Scn10a
|
UTSW |
9 |
119,442,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R2155:Scn10a
|
UTSW |
9 |
119,438,514 (GRCm39) |
missense |
probably benign |
0.02 |
R2196:Scn10a
|
UTSW |
9 |
119,438,070 (GRCm39) |
missense |
probably benign |
|
R2231:Scn10a
|
UTSW |
9 |
119,462,916 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2353:Scn10a
|
UTSW |
9 |
119,467,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Scn10a
|
UTSW |
9 |
119,456,268 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2895:Scn10a
|
UTSW |
9 |
119,490,467 (GRCm39) |
missense |
probably benign |
0.00 |
R2926:Scn10a
|
UTSW |
9 |
119,467,767 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3783:Scn10a
|
UTSW |
9 |
119,520,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3821:Scn10a
|
UTSW |
9 |
119,467,699 (GRCm39) |
missense |
probably benign |
|
R4003:Scn10a
|
UTSW |
9 |
119,438,034 (GRCm39) |
missense |
probably null |
0.00 |
R4208:Scn10a
|
UTSW |
9 |
119,445,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R4231:Scn10a
|
UTSW |
9 |
119,460,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R4626:Scn10a
|
UTSW |
9 |
119,460,571 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4702:Scn10a
|
UTSW |
9 |
119,462,857 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4713:Scn10a
|
UTSW |
9 |
119,438,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Scn10a
|
UTSW |
9 |
119,500,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Scn10a
|
UTSW |
9 |
119,451,976 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4822:Scn10a
|
UTSW |
9 |
119,467,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Scn10a
|
UTSW |
9 |
119,523,376 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4856:Scn10a
|
UTSW |
9 |
119,523,375 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4932:Scn10a
|
UTSW |
9 |
119,516,940 (GRCm39) |
splice site |
probably null |
|
R5015:Scn10a
|
UTSW |
9 |
119,451,987 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5193:Scn10a
|
UTSW |
9 |
119,438,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Scn10a
|
UTSW |
9 |
119,490,298 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5320:Scn10a
|
UTSW |
9 |
119,477,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Scn10a
|
UTSW |
9 |
119,438,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R5448:Scn10a
|
UTSW |
9 |
119,517,013 (GRCm39) |
missense |
probably benign |
0.25 |
R5457:Scn10a
|
UTSW |
9 |
119,523,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Scn10a
|
UTSW |
9 |
119,523,196 (GRCm39) |
missense |
probably benign |
0.01 |
R5680:Scn10a
|
UTSW |
9 |
119,453,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5762:Scn10a
|
UTSW |
9 |
119,464,507 (GRCm39) |
critical splice donor site |
probably null |
|
R5935:Scn10a
|
UTSW |
9 |
119,456,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R5956:Scn10a
|
UTSW |
9 |
119,460,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Scn10a
|
UTSW |
9 |
119,438,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6047:Scn10a
|
UTSW |
9 |
119,451,897 (GRCm39) |
missense |
probably benign |
0.20 |
R6132:Scn10a
|
UTSW |
9 |
119,442,761 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6156:Scn10a
|
UTSW |
9 |
119,464,649 (GRCm39) |
missense |
probably benign |
0.00 |
R6309:Scn10a
|
UTSW |
9 |
119,453,181 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6318:Scn10a
|
UTSW |
9 |
119,456,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Scn10a
|
UTSW |
9 |
119,490,386 (GRCm39) |
missense |
probably benign |
0.36 |
R6711:Scn10a
|
UTSW |
9 |
119,438,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Scn10a
|
UTSW |
9 |
119,500,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6877:Scn10a
|
UTSW |
9 |
119,438,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R6909:Scn10a
|
UTSW |
9 |
119,438,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Scn10a
|
UTSW |
9 |
119,442,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R7205:Scn10a
|
UTSW |
9 |
119,442,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R7254:Scn10a
|
UTSW |
9 |
119,447,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R7261:Scn10a
|
UTSW |
9 |
119,438,790 (GRCm39) |
missense |
probably damaging |
0.97 |
R7283:Scn10a
|
UTSW |
9 |
119,493,845 (GRCm39) |
critical splice donor site |
probably null |
|
R7453:Scn10a
|
UTSW |
9 |
119,467,618 (GRCm39) |
missense |
probably benign |
|
R7561:Scn10a
|
UTSW |
9 |
119,523,390 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R7590:Scn10a
|
UTSW |
9 |
119,495,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Scn10a
|
UTSW |
9 |
119,477,198 (GRCm39) |
nonsense |
probably null |
|
R7765:Scn10a
|
UTSW |
9 |
119,438,970 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7851:Scn10a
|
UTSW |
9 |
119,446,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7875:Scn10a
|
UTSW |
9 |
119,464,508 (GRCm39) |
critical splice donor site |
probably null |
|
R7975:Scn10a
|
UTSW |
9 |
119,501,286 (GRCm39) |
missense |
probably benign |
0.31 |
R8010:Scn10a
|
UTSW |
9 |
119,490,233 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8027:Scn10a
|
UTSW |
9 |
119,462,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R8249:Scn10a
|
UTSW |
9 |
119,446,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Scn10a
|
UTSW |
9 |
119,499,455 (GRCm39) |
missense |
probably benign |
0.04 |
R8323:Scn10a
|
UTSW |
9 |
119,438,462 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8539:Scn10a
|
UTSW |
9 |
119,467,840 (GRCm39) |
nonsense |
probably null |
|
R8679:Scn10a
|
UTSW |
9 |
119,501,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R8680:Scn10a
|
UTSW |
9 |
119,520,509 (GRCm39) |
critical splice donor site |
probably null |
|
R8844:Scn10a
|
UTSW |
9 |
119,446,791 (GRCm39) |
missense |
probably damaging |
0.98 |
R9011:Scn10a
|
UTSW |
9 |
119,459,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R9055:Scn10a
|
UTSW |
9 |
119,451,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R9206:Scn10a
|
UTSW |
9 |
119,445,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:Scn10a
|
UTSW |
9 |
119,487,504 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9622:Scn10a
|
UTSW |
9 |
119,438,046 (GRCm39) |
missense |
probably benign |
0.11 |
R9641:Scn10a
|
UTSW |
9 |
119,445,869 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9651:Scn10a
|
UTSW |
9 |
119,439,063 (GRCm39) |
missense |
probably benign |
0.17 |
X0058:Scn10a
|
UTSW |
9 |
119,438,430 (GRCm39) |
nonsense |
probably null |
|
Z1177:Scn10a
|
UTSW |
9 |
119,453,211 (GRCm39) |
critical splice acceptor site |
probably null |
|
|