Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap11 |
A |
T |
14: 78,760,029 (GRCm39) |
|
probably null |
Het |
Alpi |
T |
A |
1: 87,028,428 (GRCm39) |
Y154F |
possibly damaging |
Het |
Als2 |
A |
T |
1: 59,206,356 (GRCm39) |
F1635I |
probably damaging |
Het |
Anxa1 |
C |
T |
19: 20,361,213 (GRCm39) |
V60M |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,116,464 (GRCm39) |
Y937C |
probably damaging |
Het |
Brd4 |
C |
A |
17: 32,443,121 (GRCm39) |
E167* |
probably null |
Het |
Cacna1h |
G |
A |
17: 25,606,455 (GRCm39) |
T1048I |
probably benign |
Het |
Ccdc113 |
A |
G |
8: 96,283,820 (GRCm39) |
D298G |
probably benign |
Het |
Cfap100 |
T |
A |
6: 90,394,605 (GRCm39) |
N74I |
possibly damaging |
Het |
Chd8 |
A |
T |
14: 52,440,042 (GRCm39) |
H4Q |
possibly damaging |
Het |
Clcn1 |
A |
G |
6: 42,284,524 (GRCm39) |
T621A |
possibly damaging |
Het |
Clcn1 |
A |
G |
6: 42,290,172 (GRCm39) |
T843A |
possibly damaging |
Het |
Clcn3 |
C |
T |
8: 61,394,325 (GRCm39) |
R68Q |
probably damaging |
Het |
Dcaf13 |
T |
A |
15: 39,007,132 (GRCm39) |
N355K |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,132,401 (GRCm39) |
C1100* |
probably null |
Het |
Dync2h1 |
A |
T |
9: 7,168,331 (GRCm39) |
V428E |
probably damaging |
Het |
E230025N22Rik |
T |
C |
18: 36,819,839 (GRCm39) |
E317G |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Evc2 |
C |
A |
5: 37,535,619 (GRCm39) |
D431E |
probably damaging |
Het |
Gcm2 |
T |
G |
13: 41,263,373 (GRCm39) |
T20P |
probably damaging |
Het |
Gdf9 |
A |
G |
11: 53,327,524 (GRCm39) |
Y160C |
probably damaging |
Het |
Gm8220 |
A |
G |
14: 44,523,134 (GRCm39) |
|
probably benign |
Het |
Gpalpp1 |
A |
T |
14: 76,344,852 (GRCm39) |
S44T |
possibly damaging |
Het |
Grip2 |
T |
C |
6: 91,764,182 (GRCm39) |
Y134C |
probably damaging |
Het |
Hephl1 |
A |
G |
9: 14,985,397 (GRCm39) |
F753S |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,302,341 (GRCm39) |
T727A |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,865,729 (GRCm39) |
E4232G |
probably damaging |
Het |
Ifi207 |
A |
G |
1: 173,556,581 (GRCm39) |
L726P |
probably benign |
Het |
Itga11 |
T |
A |
9: 62,642,548 (GRCm39) |
|
probably null |
Het |
Jrkl |
A |
C |
9: 13,245,495 (GRCm39) |
Y55* |
probably null |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Kif18b |
A |
G |
11: 102,805,236 (GRCm39) |
V303A |
probably damaging |
Het |
Klhl29 |
A |
T |
12: 5,144,830 (GRCm39) |
C423* |
probably null |
Het |
Klhl29 |
T |
C |
12: 5,187,720 (GRCm39) |
S215G |
probably benign |
Het |
Lamp5 |
A |
G |
2: 135,902,929 (GRCm39) |
D216G |
possibly damaging |
Het |
Leo1 |
T |
A |
9: 75,352,752 (GRCm39) |
D98E |
probably benign |
Het |
Map3k3 |
T |
C |
11: 106,039,709 (GRCm39) |
V283A |
probably benign |
Het |
Med12l |
A |
G |
3: 59,142,508 (GRCm39) |
K902E |
probably damaging |
Het |
Mmp1b |
C |
A |
9: 7,386,316 (GRCm39) |
D202Y |
probably benign |
Het |
Muc21 |
A |
T |
17: 35,931,058 (GRCm39) |
|
probably benign |
Het |
Onecut3 |
A |
G |
10: 80,331,847 (GRCm39) |
I336V |
probably damaging |
Het |
Oprl1 |
C |
T |
2: 181,360,795 (GRCm39) |
R257C |
probably damaging |
Het |
Or10g9 |
T |
C |
9: 39,912,001 (GRCm39) |
Q174R |
probably benign |
Het |
Or10h1 |
G |
A |
17: 33,418,487 (GRCm39) |
G155D |
probably damaging |
Het |
Or4c11b |
C |
T |
2: 88,625,296 (GRCm39) |
T190I |
probably benign |
Het |
Or56b1 |
T |
A |
7: 104,284,909 (GRCm39) |
N9K |
possibly damaging |
Het |
Or56b1 |
T |
C |
7: 104,285,234 (GRCm39) |
S118P |
possibly damaging |
Het |
Or5p64 |
C |
T |
7: 107,854,970 (GRCm39) |
R125H |
possibly damaging |
Het |
Or6c69 |
G |
T |
10: 129,747,789 (GRCm39) |
D119E |
probably damaging |
Het |
Osbpl6 |
T |
C |
2: 76,386,298 (GRCm39) |
V207A |
probably benign |
Het |
Pde3a |
A |
T |
6: 141,433,237 (GRCm39) |
H756L |
probably damaging |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phyh |
A |
G |
2: 4,940,814 (GRCm39) |
D238G |
probably benign |
Het |
Pnliprp2 |
T |
A |
19: 58,750,030 (GRCm39) |
N92K |
probably benign |
Het |
Pole3 |
T |
C |
4: 62,442,263 (GRCm39) |
|
probably benign |
Het |
Ppm1d |
T |
C |
11: 85,230,498 (GRCm39) |
V372A |
probably benign |
Het |
Prpf40a |
A |
T |
2: 53,034,890 (GRCm39) |
I766N |
probably damaging |
Het |
Prr5 |
T |
A |
15: 84,583,925 (GRCm39) |
V175E |
probably damaging |
Het |
Prss59 |
A |
T |
6: 40,898,726 (GRCm39) |
L174* |
probably null |
Het |
Ptprq |
T |
A |
10: 107,478,804 (GRCm39) |
K1280* |
probably null |
Het |
Rbp2 |
T |
A |
9: 98,389,873 (GRCm39) |
V95E |
possibly damaging |
Het |
Rictor |
T |
C |
15: 6,798,790 (GRCm39) |
F346L |
possibly damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Setd5 |
T |
G |
6: 113,092,505 (GRCm39) |
V295G |
probably damaging |
Het |
Shcbp1 |
A |
T |
8: 4,786,176 (GRCm39) |
M642K |
probably damaging |
Het |
Slc13a3 |
C |
T |
2: 165,276,017 (GRCm39) |
G243E |
probably damaging |
Het |
Smg9 |
T |
C |
7: 24,121,732 (GRCm39) |
Y498H |
probably damaging |
Het |
Sox5 |
T |
C |
6: 143,987,039 (GRCm39) |
D175G |
probably damaging |
Het |
Stard7 |
A |
G |
2: 127,126,161 (GRCm39) |
D71G |
probably damaging |
Het |
Stxbp5 |
A |
T |
10: 9,774,975 (GRCm39) |
Y59* |
probably null |
Het |
Supt6 |
G |
A |
11: 78,121,891 (GRCm39) |
R254C |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,037,269 (GRCm39) |
T3817I |
probably benign |
Het |
Tas2r124 |
T |
A |
6: 132,732,039 (GRCm39) |
I116N |
probably damaging |
Het |
Trim9 |
T |
A |
12: 70,301,987 (GRCm39) |
E550D |
possibly damaging |
Het |
Vmn2r50 |
A |
G |
7: 9,774,253 (GRCm39) |
S548P |
probably damaging |
Het |
Zmynd8 |
C |
A |
2: 165,687,943 (GRCm39) |
E126* |
probably null |
Het |
Zswim9 |
A |
T |
7: 12,994,889 (GRCm39) |
S422R |
probably damaging |
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 |
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 |
R8221:Scn10a
|
UTSW |
9 |
119,446,829 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|