Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad10 |
A |
T |
5: 121,794,075 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
C |
19: 8,982,186 (GRCm39) |
S1157P |
probably damaging |
Het |
Akap12 |
T |
G |
10: 4,303,967 (GRCm39) |
V364G |
probably benign |
Het |
Ankrd17 |
A |
G |
5: 90,447,855 (GRCm39) |
S229P |
probably benign |
Het |
Apof |
A |
T |
10: 128,104,636 (GRCm39) |
Y5F |
probably benign |
Het |
Arhgap24 |
T |
A |
5: 102,989,174 (GRCm39) |
M94K |
probably benign |
Het |
Ash2l |
G |
T |
8: 26,312,798 (GRCm39) |
D479E |
probably damaging |
Het |
Atp8a2 |
A |
T |
14: 60,245,824 (GRCm39) |
C623S |
probably benign |
Het |
Bmper |
T |
A |
9: 23,395,238 (GRCm39) |
N656K |
probably benign |
Het |
Braf |
T |
C |
6: 39,604,772 (GRCm39) |
I619V |
possibly damaging |
Het |
Brwd1 |
T |
C |
16: 95,857,373 (GRCm39) |
R396G |
probably damaging |
Het |
Car7 |
A |
T |
8: 105,276,216 (GRCm39) |
T234S |
probably benign |
Het |
Catsper4 |
A |
T |
4: 133,945,552 (GRCm39) |
V169E |
probably damaging |
Het |
Cemip |
T |
G |
7: 83,647,784 (GRCm39) |
I99L |
probably damaging |
Het |
Chrna7 |
C |
A |
7: 62,754,738 (GRCm39) |
V290L |
probably damaging |
Het |
Clip1 |
A |
T |
5: 123,755,447 (GRCm39) |
D944E |
probably benign |
Het |
Cplane2 |
A |
G |
4: 140,947,153 (GRCm39) |
D178G |
probably damaging |
Het |
Cyp2c68 |
T |
C |
19: 39,677,581 (GRCm39) |
T470A |
probably benign |
Het |
Dmbx1 |
G |
T |
4: 115,780,908 (GRCm39) |
A31D |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,214,579 (GRCm39) |
F1115L |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,493,283 (GRCm39) |
I1897V |
probably benign |
Het |
Efcab3 |
A |
G |
11: 105,000,112 (GRCm39) |
I234V |
probably benign |
Het |
Eid2b |
T |
G |
7: 27,977,243 (GRCm39) |
L13R |
probably damaging |
Het |
Enam |
A |
G |
5: 88,649,679 (GRCm39) |
Y396C |
probably damaging |
Het |
Fam161a |
A |
T |
11: 22,971,006 (GRCm39) |
T395S |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,476,197 (GRCm39) |
R1748G |
probably benign |
Het |
Fdxacb1 |
C |
A |
9: 50,681,451 (GRCm39) |
T124K |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,513,794 (GRCm39) |
D1563V |
possibly damaging |
Het |
Gm20834 |
T |
C |
Y: 10,323,226 (GRCm39) |
H70R |
probably damaging |
Het |
Gucy2d |
T |
A |
7: 98,098,964 (GRCm39) |
M261K |
probably damaging |
Het |
Hcar2 |
T |
A |
5: 124,002,861 (GRCm39) |
Q214L |
probably benign |
Het |
Hdac11 |
C |
T |
6: 91,136,214 (GRCm39) |
H75Y |
probably damaging |
Het |
Hoxa2 |
C |
A |
6: 52,141,279 (GRCm39) |
A116S |
probably benign |
Het |
Ints2 |
A |
G |
11: 86,106,444 (GRCm39) |
C989R |
probably damaging |
Het |
Jpt1 |
T |
C |
11: 115,393,950 (GRCm39) |
E36G |
probably damaging |
Het |
Kdm5d |
G |
A |
Y: 914,044 (GRCm39) |
R327Q |
possibly damaging |
Het |
Klhl1 |
T |
C |
14: 96,584,304 (GRCm39) |
M309V |
probably benign |
Het |
Larp4 |
A |
G |
15: 99,889,659 (GRCm39) |
K193E |
probably benign |
Het |
Lmo3 |
C |
T |
6: 138,393,500 (GRCm39) |
C40Y |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,448,306 (GRCm39) |
V417A |
probably benign |
Het |
Med8 |
A |
G |
4: 118,268,176 (GRCm39) |
E34G |
probably damaging |
Het |
Mex3b |
G |
T |
7: 82,517,114 (GRCm39) |
A86S |
possibly damaging |
Het |
Muc6 |
T |
C |
7: 141,224,245 (GRCm39) |
T1646A |
unknown |
Het |
Myo15b |
A |
T |
11: 115,749,570 (GRCm39) |
E113D |
|
Het |
Myo7a |
T |
A |
7: 97,712,881 (GRCm39) |
H1698L |
probably benign |
Het |
Myocos |
T |
A |
1: 162,484,678 (GRCm39) |
M44L |
unknown |
Het |
Nalcn |
A |
G |
14: 123,551,499 (GRCm39) |
V1036A |
probably damaging |
Het |
Nfrkb |
C |
T |
9: 31,325,328 (GRCm39) |
Q924* |
probably null |
Het |
Nol6 |
A |
G |
4: 41,117,424 (GRCm39) |
L923P |
possibly damaging |
Het |
Nrxn3 |
T |
C |
12: 89,477,232 (GRCm39) |
Y472H |
probably damaging |
Het |
Nudcd1 |
A |
G |
15: 44,269,253 (GRCm39) |
Y136H |
possibly damaging |
Het |
Obox2 |
T |
C |
7: 15,131,241 (GRCm39) |
C116R |
probably damaging |
Het |
Onecut3 |
A |
T |
10: 80,331,310 (GRCm39) |
S157C |
unknown |
Het |
Or10ak11 |
A |
G |
4: 118,687,517 (GRCm39) |
V39A |
probably damaging |
Het |
Or11g27 |
T |
A |
14: 50,771,472 (GRCm39) |
V201D |
probably benign |
Het |
Or2d2b |
T |
A |
7: 106,705,982 (GRCm39) |
I29F |
probably benign |
Het |
Or4f15 |
T |
C |
2: 111,814,124 (GRCm39) |
I98M |
probably damaging |
Het |
Oscp1 |
C |
T |
4: 125,967,726 (GRCm39) |
R91* |
probably null |
Het |
Pclo |
A |
T |
5: 14,762,606 (GRCm39) |
D408V |
|
Het |
Pde8a |
T |
C |
7: 80,932,581 (GRCm39) |
V81A |
probably benign |
Het |
Pde8b |
T |
A |
13: 95,164,251 (GRCm39) |
D653V |
probably damaging |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pik3cg |
T |
C |
12: 32,245,647 (GRCm39) |
Y867C |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Psd4 |
A |
T |
2: 24,294,768 (GRCm39) |
D776V |
possibly damaging |
Het |
Ptprb |
A |
G |
10: 116,119,334 (GRCm39) |
E156G |
probably benign |
Het |
Rad54b |
A |
G |
4: 11,610,372 (GRCm39) |
Y663C |
probably damaging |
Het |
Ranbp3l |
T |
A |
15: 9,030,955 (GRCm39) |
V78D |
possibly damaging |
Het |
Rbm12 |
T |
C |
2: 155,940,138 (GRCm39) |
I45V |
unknown |
Het |
Sdcbp |
T |
C |
4: 6,393,089 (GRCm39) |
I242T |
possibly damaging |
Het |
Slc25a24 |
A |
G |
3: 109,066,751 (GRCm39) |
T302A |
probably damaging |
Het |
Slc45a3 |
G |
T |
1: 131,904,549 (GRCm39) |
|
probably benign |
Het |
Srpk1 |
T |
C |
17: 28,813,192 (GRCm39) |
I517M |
probably benign |
Het |
Tmx4 |
A |
G |
2: 134,481,581 (GRCm39) |
M114T |
probably benign |
Het |
Trhr |
T |
A |
15: 44,092,627 (GRCm39) |
V288D |
probably damaging |
Het |
Tspoap1 |
A |
T |
11: 87,652,351 (GRCm39) |
I42F |
probably benign |
Het |
Ttn |
A |
T |
2: 76,781,856 (GRCm39) |
D1063E |
unknown |
Het |
Tusc3 |
A |
G |
8: 39,538,635 (GRCm39) |
I225V |
probably benign |
Het |
Ugt2b38 |
A |
G |
5: 87,571,973 (GRCm39) |
S20P |
probably damaging |
Het |
Upf2 |
A |
G |
2: 6,032,219 (GRCm39) |
T922A |
unknown |
Het |
Usp38 |
C |
T |
8: 81,741,190 (GRCm39) |
|
probably benign |
Het |
Vmn1r216 |
A |
G |
13: 23,283,738 (GRCm39) |
I140M |
probably damaging |
Het |
Vmn2r115 |
T |
A |
17: 23,565,371 (GRCm39) |
N419K |
possibly damaging |
Het |
Vmn2r55 |
C |
T |
7: 12,404,755 (GRCm39) |
G216D |
probably benign |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wnt7b |
C |
A |
15: 85,421,615 (GRCm39) |
R349L |
possibly damaging |
Het |
Xbp1 |
T |
C |
11: 5,471,098 (GRCm39) |
V35A |
probably benign |
Het |
Zan |
A |
T |
5: 137,445,057 (GRCm39) |
M1734K |
unknown |
Het |
Zfhx4 |
A |
G |
3: 5,477,237 (GRCm39) |
E3284G |
probably damaging |
Het |
Zfp458 |
A |
G |
13: 67,404,978 (GRCm39) |
L487S |
possibly damaging |
Het |
Zfp687 |
C |
T |
3: 94,914,841 (GRCm39) |
R1220H |
probably damaging |
Het |
Zp1 |
A |
G |
19: 10,895,280 (GRCm39) |
L324P |
possibly damaging |
Het |
|
Other mutations in Scn9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00514:Scn9a
|
APN |
2 |
66,393,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00570:Scn9a
|
APN |
2 |
66,314,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00809:Scn9a
|
APN |
2 |
66,314,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00977:Scn9a
|
APN |
2 |
66,314,645 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01120:Scn9a
|
APN |
2 |
66,357,316 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01134:Scn9a
|
APN |
2 |
66,335,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01300:Scn9a
|
APN |
2 |
66,318,397 (GRCm39) |
nonsense |
probably null |
|
IGL01452:Scn9a
|
APN |
2 |
66,357,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01531:Scn9a
|
APN |
2 |
66,367,722 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01572:Scn9a
|
APN |
2 |
66,324,230 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01645:Scn9a
|
APN |
2 |
66,317,986 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01823:Scn9a
|
APN |
2 |
66,314,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01965:Scn9a
|
APN |
2 |
66,314,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02127:Scn9a
|
APN |
2 |
66,325,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02127:Scn9a
|
APN |
2 |
66,377,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Scn9a
|
APN |
2 |
66,323,447 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02183:Scn9a
|
APN |
2 |
66,314,955 (GRCm39) |
splice site |
probably benign |
|
IGL02640:Scn9a
|
APN |
2 |
66,366,440 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02685:Scn9a
|
APN |
2 |
66,367,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02798:Scn9a
|
APN |
2 |
66,370,903 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02832:Scn9a
|
APN |
2 |
66,398,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Scn9a
|
APN |
2 |
66,392,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03270:Scn9a
|
APN |
2 |
66,314,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03408:Scn9a
|
APN |
2 |
66,357,091 (GRCm39) |
missense |
probably benign |
0.00 |
BB007:Scn9a
|
UTSW |
2 |
66,335,193 (GRCm39) |
missense |
probably damaging |
0.99 |
BB017:Scn9a
|
UTSW |
2 |
66,335,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R0039:Scn9a
|
UTSW |
2 |
66,392,788 (GRCm39) |
missense |
probably damaging |
0.98 |
R0173:Scn9a
|
UTSW |
2 |
66,363,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Scn9a
|
UTSW |
2 |
66,398,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R0344:Scn9a
|
UTSW |
2 |
66,335,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R0421:Scn9a
|
UTSW |
2 |
66,373,621 (GRCm39) |
missense |
probably benign |
|
R0465:Scn9a
|
UTSW |
2 |
66,357,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Scn9a
|
UTSW |
2 |
66,314,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Scn9a
|
UTSW |
2 |
66,357,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R0627:Scn9a
|
UTSW |
2 |
66,367,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0644:Scn9a
|
UTSW |
2 |
66,363,405 (GRCm39) |
critical splice donor site |
probably null |
|
R0653:Scn9a
|
UTSW |
2 |
66,363,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Scn9a
|
UTSW |
2 |
66,313,843 (GRCm39) |
missense |
probably benign |
0.02 |
R0718:Scn9a
|
UTSW |
2 |
66,377,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Scn9a
|
UTSW |
2 |
66,366,468 (GRCm39) |
nonsense |
probably null |
|
R0890:Scn9a
|
UTSW |
2 |
66,314,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R1139:Scn9a
|
UTSW |
2 |
66,335,341 (GRCm39) |
missense |
probably benign |
0.02 |
R1385:Scn9a
|
UTSW |
2 |
66,393,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1398:Scn9a
|
UTSW |
2 |
66,314,930 (GRCm39) |
missense |
probably benign |
0.11 |
R1496:Scn9a
|
UTSW |
2 |
66,357,232 (GRCm39) |
missense |
probably benign |
|
R1511:Scn9a
|
UTSW |
2 |
66,357,157 (GRCm39) |
missense |
probably benign |
0.01 |
R1517:Scn9a
|
UTSW |
2 |
66,335,371 (GRCm39) |
splice site |
probably benign |
|
R1564:Scn9a
|
UTSW |
2 |
66,314,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Scn9a
|
UTSW |
2 |
66,318,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Scn9a
|
UTSW |
2 |
66,313,803 (GRCm39) |
missense |
probably benign |
0.00 |
R1695:Scn9a
|
UTSW |
2 |
66,335,220 (GRCm39) |
nonsense |
probably null |
|
R1709:Scn9a
|
UTSW |
2 |
66,313,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R1741:Scn9a
|
UTSW |
2 |
66,317,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R1755:Scn9a
|
UTSW |
2 |
66,332,060 (GRCm39) |
missense |
probably benign |
0.38 |
R1914:Scn9a
|
UTSW |
2 |
66,396,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Scn9a
|
UTSW |
2 |
66,314,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Scn9a
|
UTSW |
2 |
66,345,724 (GRCm39) |
missense |
probably damaging |
0.97 |
R2017:Scn9a
|
UTSW |
2 |
66,345,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R2092:Scn9a
|
UTSW |
2 |
66,363,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R2105:Scn9a
|
UTSW |
2 |
66,398,527 (GRCm39) |
missense |
probably benign |
0.25 |
R2114:Scn9a
|
UTSW |
2 |
66,314,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R2115:Scn9a
|
UTSW |
2 |
66,314,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Scn9a
|
UTSW |
2 |
66,356,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:Scn9a
|
UTSW |
2 |
66,366,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Scn9a
|
UTSW |
2 |
66,364,573 (GRCm39) |
missense |
probably damaging |
0.98 |
R2350:Scn9a
|
UTSW |
2 |
66,335,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R3694:Scn9a
|
UTSW |
2 |
66,392,749 (GRCm39) |
missense |
probably benign |
|
R3771:Scn9a
|
UTSW |
2 |
66,313,992 (GRCm39) |
missense |
probably benign |
0.26 |
R3772:Scn9a
|
UTSW |
2 |
66,313,992 (GRCm39) |
missense |
probably benign |
0.26 |
R3773:Scn9a
|
UTSW |
2 |
66,313,992 (GRCm39) |
missense |
probably benign |
0.26 |
R3922:Scn9a
|
UTSW |
2 |
66,357,217 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3926:Scn9a
|
UTSW |
2 |
66,357,217 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4258:Scn9a
|
UTSW |
2 |
66,395,398 (GRCm39) |
intron |
probably benign |
|
R4385:Scn9a
|
UTSW |
2 |
66,314,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R4415:Scn9a
|
UTSW |
2 |
66,357,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Scn9a
|
UTSW |
2 |
66,313,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4682:Scn9a
|
UTSW |
2 |
66,377,362 (GRCm39) |
missense |
probably benign |
|
R4783:Scn9a
|
UTSW |
2 |
66,370,967 (GRCm39) |
missense |
probably benign |
0.01 |
R4822:Scn9a
|
UTSW |
2 |
66,314,093 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4829:Scn9a
|
UTSW |
2 |
66,382,057 (GRCm39) |
missense |
probably benign |
|
R4908:Scn9a
|
UTSW |
2 |
66,357,087 (GRCm39) |
missense |
probably benign |
0.03 |
R4983:Scn9a
|
UTSW |
2 |
66,396,614 (GRCm39) |
missense |
probably benign |
0.02 |
R5047:Scn9a
|
UTSW |
2 |
66,392,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Scn9a
|
UTSW |
2 |
66,364,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R5140:Scn9a
|
UTSW |
2 |
66,395,511 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5398:Scn9a
|
UTSW |
2 |
66,318,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R5557:Scn9a
|
UTSW |
2 |
66,377,447 (GRCm39) |
missense |
probably damaging |
0.99 |
R5582:Scn9a
|
UTSW |
2 |
66,395,373 (GRCm39) |
intron |
probably benign |
|
R6108:Scn9a
|
UTSW |
2 |
66,314,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Scn9a
|
UTSW |
2 |
66,393,973 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6143:Scn9a
|
UTSW |
2 |
66,317,868 (GRCm39) |
missense |
probably benign |
0.00 |
R6261:Scn9a
|
UTSW |
2 |
66,314,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Scn9a
|
UTSW |
2 |
66,398,608 (GRCm39) |
start codon destroyed |
possibly damaging |
0.91 |
R6429:Scn9a
|
UTSW |
2 |
66,357,307 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6632:Scn9a
|
UTSW |
2 |
66,313,846 (GRCm39) |
missense |
probably benign |
0.23 |
R6681:Scn9a
|
UTSW |
2 |
66,393,686 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6830:Scn9a
|
UTSW |
2 |
66,398,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Scn9a
|
UTSW |
2 |
66,379,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Scn9a
|
UTSW |
2 |
66,364,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7243:Scn9a
|
UTSW |
2 |
66,370,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R7311:Scn9a
|
UTSW |
2 |
66,314,748 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7328:Scn9a
|
UTSW |
2 |
66,314,931 (GRCm39) |
missense |
probably benign |
|
R7386:Scn9a
|
UTSW |
2 |
66,370,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7438:Scn9a
|
UTSW |
2 |
66,377,531 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7485:Scn9a
|
UTSW |
2 |
66,364,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Scn9a
|
UTSW |
2 |
66,313,990 (GRCm39) |
missense |
probably benign |
|
R7617:Scn9a
|
UTSW |
2 |
66,370,893 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7642:Scn9a
|
UTSW |
2 |
66,366,580 (GRCm39) |
missense |
probably benign |
0.02 |
R7653:Scn9a
|
UTSW |
2 |
66,357,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Scn9a
|
UTSW |
2 |
66,314,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Scn9a
|
UTSW |
2 |
66,314,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R7864:Scn9a
|
UTSW |
2 |
66,314,904 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7890:Scn9a
|
UTSW |
2 |
66,373,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7930:Scn9a
|
UTSW |
2 |
66,335,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R7975:Scn9a
|
UTSW |
2 |
66,314,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Scn9a
|
UTSW |
2 |
66,345,774 (GRCm39) |
missense |
probably benign |
0.06 |
R8145:Scn9a
|
UTSW |
2 |
66,317,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8163:Scn9a
|
UTSW |
2 |
66,314,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R8165:Scn9a
|
UTSW |
2 |
66,370,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8342:Scn9a
|
UTSW |
2 |
66,366,626 (GRCm39) |
missense |
probably benign |
|
R8345:Scn9a
|
UTSW |
2 |
66,324,966 (GRCm39) |
missense |
probably damaging |
0.96 |
R8464:Scn9a
|
UTSW |
2 |
66,396,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R8467:Scn9a
|
UTSW |
2 |
66,332,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Scn9a
|
UTSW |
2 |
66,366,628 (GRCm39) |
missense |
probably benign |
0.00 |
R8810:Scn9a
|
UTSW |
2 |
66,332,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R8822:Scn9a
|
UTSW |
2 |
66,370,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R8829:Scn9a
|
UTSW |
2 |
66,313,961 (GRCm39) |
missense |
probably benign |
|
R9009:Scn9a
|
UTSW |
2 |
66,338,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R9038:Scn9a
|
UTSW |
2 |
66,325,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R9126:Scn9a
|
UTSW |
2 |
66,314,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R9205:Scn9a
|
UTSW |
2 |
66,363,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R9300:Scn9a
|
UTSW |
2 |
66,335,236 (GRCm39) |
missense |
probably benign |
0.39 |
R9373:Scn9a
|
UTSW |
2 |
66,314,261 (GRCm39) |
missense |
probably benign |
0.00 |
R9404:Scn9a
|
UTSW |
2 |
66,357,040 (GRCm39) |
missense |
probably benign |
0.02 |
R9443:Scn9a
|
UTSW |
2 |
66,395,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R9590:Scn9a
|
UTSW |
2 |
66,314,328 (GRCm39) |
missense |
probably benign |
0.05 |
R9612:Scn9a
|
UTSW |
2 |
66,363,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Scn9a
|
UTSW |
2 |
66,392,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R9717:Scn9a
|
UTSW |
2 |
66,357,002 (GRCm39) |
missense |
probably benign |
|
X0003:Scn9a
|
UTSW |
2 |
66,338,991 (GRCm39) |
missense |
probably benign |
0.02 |
X0062:Scn9a
|
UTSW |
2 |
66,398,421 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scn9a
|
UTSW |
2 |
66,370,936 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Scn9a
|
UTSW |
2 |
66,325,029 (GRCm39) |
missense |
possibly damaging |
0.68 |
|