Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,006,889 (GRCm39) |
K435E |
probably damaging |
Het |
Acly |
T |
C |
11: 100,395,785 (GRCm39) |
T412A |
probably damaging |
Het |
Aldh3b2 |
T |
A |
19: 4,029,489 (GRCm39) |
D287E |
probably benign |
Het |
Asphd1 |
G |
A |
7: 126,547,974 (GRCm39) |
P110S |
|
Het |
Atg7 |
T |
C |
6: 114,654,993 (GRCm39) |
L142P |
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,239,277 (GRCm39) |
I796V |
|
Het |
Bbx |
A |
G |
16: 50,095,022 (GRCm39) |
V98A |
probably damaging |
Het |
Brca2 |
T |
C |
5: 150,480,410 (GRCm39) |
S2727P |
probably damaging |
Het |
Camk1 |
T |
A |
6: 113,318,850 (GRCm39) |
D21V |
possibly damaging |
Het |
Cdc5l |
A |
T |
17: 45,715,709 (GRCm39) |
D634E |
probably benign |
Het |
Cfap418 |
T |
C |
4: 10,893,304 (GRCm39) |
I141T |
possibly damaging |
Het |
Cyfip1 |
A |
T |
7: 55,528,853 (GRCm39) |
D275V |
possibly damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,328,162 (GRCm39) |
E477G |
probably damaging |
Het |
Cyp4f16 |
C |
T |
17: 32,769,246 (GRCm39) |
P379S |
probably damaging |
Het |
Dchs2 |
C |
T |
3: 83,263,766 (GRCm39) |
Q3345* |
probably null |
Het |
Dnaaf1 |
A |
G |
8: 120,315,001 (GRCm39) |
T270A |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,561,356 (GRCm39) |
V334A |
|
Het |
Dnhd1 |
T |
C |
7: 105,353,342 (GRCm39) |
F2832L |
probably benign |
Het |
Dock8 |
A |
G |
19: 25,098,545 (GRCm39) |
N623S |
probably null |
Het |
Eif4enif1 |
T |
C |
11: 3,165,714 (GRCm39) |
I97T |
probably benign |
Het |
Elmo1 |
C |
G |
13: 20,392,310 (GRCm39) |
P29A |
probably benign |
Het |
Erich6 |
G |
C |
3: 58,544,162 (GRCm39) |
P142A |
possibly damaging |
Het |
Fam135b |
T |
C |
15: 71,397,686 (GRCm39) |
R125G |
probably damaging |
Het |
Fcrla |
T |
A |
1: 170,749,808 (GRCm39) |
H83L |
probably damaging |
Het |
Flt3 |
C |
T |
5: 147,303,841 (GRCm39) |
E366K |
possibly damaging |
Het |
Gabbr2 |
C |
T |
4: 46,724,283 (GRCm39) |
|
probably null |
Het |
Gigyf1 |
T |
A |
5: 137,522,926 (GRCm39) |
L809* |
probably null |
Het |
Glg1 |
C |
T |
8: 111,899,133 (GRCm39) |
G711R |
probably damaging |
Het |
Gp1bb |
T |
C |
16: 18,439,527 (GRCm39) |
E189G |
probably benign |
Het |
H2-Q1 |
A |
T |
17: 35,542,532 (GRCm39) |
I326F |
probably benign |
Het |
Hoxb3 |
A |
T |
11: 96,235,420 (GRCm39) |
K116* |
probably null |
Het |
Kcnb1 |
T |
C |
2: 167,030,161 (GRCm39) |
Y128C |
probably damaging |
Het |
Kif5b |
G |
A |
18: 6,225,672 (GRCm39) |
R171C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,561,228 (GRCm39) |
Q18* |
probably null |
Het |
Lrp1b |
G |
A |
2: 40,779,354 (GRCm39) |
Q2677* |
probably null |
Het |
Map4k3 |
T |
A |
17: 80,958,538 (GRCm39) |
T145S |
probably damaging |
Het |
Mas1 |
T |
C |
17: 13,060,898 (GRCm39) |
E175G |
probably benign |
Het |
Metap2 |
T |
C |
10: 93,707,366 (GRCm39) |
T202A |
probably benign |
Het |
Mras |
A |
T |
9: 99,275,054 (GRCm39) |
M131K |
probably benign |
Het |
Mtor |
T |
C |
4: 148,568,169 (GRCm39) |
V1092A |
probably damaging |
Het |
Mug2 |
T |
C |
6: 122,028,751 (GRCm39) |
S582P |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,848,017 (GRCm39) |
N1085S |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,603,103 (GRCm39) |
T1149A |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,366,373 (GRCm39) |
S1239T |
probably benign |
Het |
Nkpd1 |
C |
A |
7: 19,257,867 (GRCm39) |
R549S |
probably benign |
Het |
Or10a3m |
T |
A |
7: 108,312,677 (GRCm39) |
M39K |
probably benign |
Het |
Or10p1 |
G |
A |
10: 129,444,084 (GRCm39) |
H89Y |
probably benign |
Het |
Or1j1 |
A |
G |
2: 36,702,621 (GRCm39) |
L161P |
probably damaging |
Het |
Or51i2 |
T |
A |
7: 103,689,522 (GRCm39) |
V173D |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,711,229 (GRCm39) |
N29D |
probably benign |
Het |
Pdzrn4 |
T |
C |
15: 92,294,949 (GRCm39) |
W52R |
probably benign |
Het |
Plekhb1 |
T |
C |
7: 100,304,588 (GRCm39) |
K39E |
probably damaging |
Het |
Pramel28 |
A |
G |
4: 143,692,348 (GRCm39) |
S218P |
probably benign |
Het |
Psmb4 |
C |
A |
3: 94,792,285 (GRCm39) |
E212D |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,205,348 (GRCm39) |
L69P |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,729,952 (GRCm39) |
R1082G |
probably benign |
Het |
Rorb |
T |
C |
19: 18,955,115 (GRCm39) |
Y167C |
probably damaging |
Het |
Sanbr |
T |
A |
11: 23,534,590 (GRCm39) |
K589I |
probably damaging |
Het |
Sbsn |
GGAAATATGGCAGACAAGTTTGGTCAGGGGGCCCACCATGCTTTTGGTCAGGGCAG |
GG |
7: 30,452,067 (GRCm39) |
|
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,248,170 (GRCm39) |
F1164L |
probably benign |
Het |
Serpinb2 |
A |
G |
1: 107,452,298 (GRCm39) |
N292S |
probably benign |
Het |
Sparcl1 |
C |
A |
5: 104,234,998 (GRCm39) |
V506L |
possibly damaging |
Het |
Stt3a |
A |
G |
9: 36,661,025 (GRCm39) |
V262A |
possibly damaging |
Het |
Syt17 |
C |
A |
7: 118,036,191 (GRCm39) |
M58I |
probably benign |
Het |
Tas2r134 |
A |
C |
2: 51,518,358 (GRCm39) |
N279T |
possibly damaging |
Het |
Tbc1d2 |
T |
C |
4: 46,609,065 (GRCm39) |
E724G |
probably damaging |
Het |
Teddm1b |
T |
A |
1: 153,750,620 (GRCm39) |
L143Q |
|
Het |
Tlk1 |
T |
A |
2: 70,617,281 (GRCm39) |
R66S |
probably damaging |
Het |
Tmem139 |
A |
T |
6: 42,240,176 (GRCm39) |
|
probably null |
Het |
Tom1l2 |
T |
C |
11: 60,151,942 (GRCm39) |
Y155C |
possibly damaging |
Het |
Trmt1l |
C |
A |
1: 151,304,710 (GRCm39) |
S28* |
probably null |
Het |
Ttf2 |
T |
C |
3: 100,859,918 (GRCm39) |
I679V |
probably benign |
Het |
Unc13b |
T |
G |
4: 43,172,513 (GRCm39) |
F1114V |
|
Het |
Vmn2r25 |
T |
A |
6: 123,816,579 (GRCm39) |
D334V |
probably damaging |
Het |
Vps13c |
T |
G |
9: 67,856,715 (GRCm39) |
Y2581D |
probably damaging |
Het |
Xkr5 |
A |
G |
8: 18,984,247 (GRCm39) |
S432P |
probably benign |
Het |
Zc2hc1b |
G |
A |
10: 13,043,677 (GRCm39) |
P73S |
possibly damaging |
Het |
Zfhx2 |
A |
C |
14: 55,303,483 (GRCm39) |
F1500L |
probably benign |
Het |
Zfp3 |
T |
G |
11: 70,662,739 (GRCm39) |
S233A |
possibly damaging |
Het |
Zmat5 |
T |
C |
11: 4,687,453 (GRCm39) |
W169R |
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 |
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 |
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 |
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 |
|
|