Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat3 |
C |
T |
10: 80,442,234 (GRCm39) |
A24V |
probably benign |
Het |
Agbl1 |
A |
T |
7: 76,239,241 (GRCm39) |
E832D |
unknown |
Het |
Akap8l |
G |
A |
17: 32,554,545 (GRCm39) |
S347L |
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,804,379 (GRCm39) |
A868E |
probably damaging |
Het |
Ankrd49 |
A |
T |
9: 14,693,837 (GRCm39) |
L110* |
probably null |
Het |
Aoc3 |
A |
G |
11: 101,228,229 (GRCm39) |
T679A |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,592,018 (GRCm39) |
Y111H |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,402,659 (GRCm39) |
N777K |
probably damaging |
Het |
Atp4b |
A |
T |
8: 13,436,732 (GRCm39) |
M260K |
probably benign |
Het |
Bcl2l15 |
A |
T |
3: 103,740,729 (GRCm39) |
D65V |
probably damaging |
Het |
Bicdl1 |
G |
T |
5: 115,801,845 (GRCm39) |
S340* |
probably null |
Het |
Ccdc15 |
T |
C |
9: 37,226,574 (GRCm39) |
R467G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,102,084 (GRCm39) |
M327K |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,873,138 (GRCm39) |
T406A |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,468,232 (GRCm39) |
V55D |
probably damaging |
Het |
Cdcp3 |
C |
A |
7: 130,830,562 (GRCm39) |
P332Q |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,008 (GRCm39) |
F140L |
probably benign |
Het |
Copb1 |
A |
C |
7: 113,844,720 (GRCm39) |
I213S |
possibly damaging |
Het |
Cps1 |
G |
A |
1: 67,179,016 (GRCm39) |
G76D |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,567,627 (GRCm39) |
W159R |
probably damaging |
Het |
Cul4a |
C |
T |
8: 13,190,279 (GRCm39) |
T572M |
possibly damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,796,050 (GRCm39) |
Y109* |
probably null |
Het |
Dcc |
A |
G |
18: 71,553,317 (GRCm39) |
Y780H |
probably benign |
Het |
Dctn1 |
C |
T |
6: 83,166,887 (GRCm39) |
A283V |
possibly damaging |
Het |
Dio1 |
T |
C |
4: 107,154,874 (GRCm39) |
D134G |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,198,390 (GRCm39) |
D1514E |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,227,907 (GRCm39) |
L338Q |
probably damaging |
Het |
Dlgap2 |
A |
T |
8: 14,879,952 (GRCm39) |
K767N |
probably damaging |
Het |
Dst |
A |
T |
1: 34,313,270 (GRCm39) |
I4346F |
probably benign |
Het |
Dzip1l |
T |
C |
9: 99,543,065 (GRCm39) |
F507L |
probably benign |
Het |
Erich2 |
A |
T |
2: 70,362,109 (GRCm39) |
D300V |
probably damaging |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fam131a |
C |
T |
16: 20,520,444 (GRCm39) |
A299V |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,247,143 (GRCm39) |
|
probably null |
Het |
Fbn2 |
T |
C |
18: 58,204,912 (GRCm39) |
D1177G |
possibly damaging |
Het |
Fbxl6 |
T |
C |
15: 76,422,113 (GRCm39) |
|
probably null |
Het |
Frem3 |
A |
T |
8: 81,339,965 (GRCm39) |
I753F |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,288,744 (GRCm39) |
S234P |
probably damaging |
Het |
Gtse1 |
T |
A |
15: 85,752,901 (GRCm39) |
S339T |
probably benign |
Het |
Hdgfl3 |
T |
C |
7: 81,550,106 (GRCm39) |
N76S |
probably benign |
Het |
Herc6 |
A |
G |
6: 57,558,089 (GRCm39) |
E23G |
probably benign |
Het |
Hid1 |
T |
A |
11: 115,245,545 (GRCm39) |
H420L |
probably damaging |
Het |
Igsf21 |
G |
A |
4: 139,755,049 (GRCm39) |
T440I |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,468,451 (GRCm39) |
H676L |
unknown |
Het |
Il18r1 |
A |
G |
1: 40,520,140 (GRCm39) |
E177G |
probably benign |
Het |
Iqch |
A |
G |
9: 63,415,599 (GRCm39) |
Y558H |
possibly damaging |
Het |
Kif11 |
A |
T |
19: 37,399,072 (GRCm39) |
N752I |
possibly damaging |
Het |
Kntc1 |
T |
A |
5: 123,925,019 (GRCm39) |
C1111S |
possibly damaging |
Het |
Krtap9-5 |
A |
G |
11: 99,839,800 (GRCm39) |
K167R |
unknown |
Het |
Lgalsl2 |
C |
T |
7: 5,362,440 (GRCm39) |
R24C |
probably benign |
Het |
Lipe |
G |
T |
7: 25,080,036 (GRCm39) |
T704K |
probably benign |
Het |
Lrrc32 |
A |
T |
7: 98,147,414 (GRCm39) |
I65F |
possibly damaging |
Het |
Mogs |
C |
T |
6: 83,093,188 (GRCm39) |
H179Y |
probably damaging |
Het |
Mtnr1b |
A |
T |
9: 15,774,590 (GRCm39) |
Y156* |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,537,590 (GRCm39) |
H42R |
probably benign |
Het |
Mx2 |
T |
A |
16: 97,346,918 (GRCm39) |
D128E |
probably benign |
Het |
Myof |
A |
T |
19: 37,939,939 (GRCm39) |
L829* |
probably null |
Het |
Naip6 |
T |
C |
13: 100,420,359 (GRCm39) |
K1304E |
probably benign |
Het |
Neo1 |
A |
C |
9: 58,791,826 (GRCm39) |
S1307R |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,359,779 (GRCm39) |
D1475E |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,875 (GRCm39) |
F371I |
probably damaging |
Het |
Nrip1 |
A |
T |
16: 76,088,338 (GRCm39) |
M1073K |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,567,863 (GRCm39) |
N195D |
probably damaging |
Het |
Or13a18 |
T |
A |
7: 140,190,091 (GRCm39) |
I4K |
probably benign |
Het |
Or1j18 |
T |
A |
2: 36,624,650 (GRCm39) |
F106I |
probably benign |
Het |
Or5ac24 |
A |
T |
16: 59,165,687 (GRCm39) |
C126S |
probably damaging |
Het |
Or5b99 |
C |
T |
19: 12,976,922 (GRCm39) |
H191Y |
probably benign |
Het |
Or5p64 |
C |
A |
7: 107,855,045 (GRCm39) |
C100F |
probably damaging |
Het |
Pax7 |
T |
C |
4: 139,511,880 (GRCm39) |
K232E |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,310,689 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
C |
A |
11: 8,915,148 (GRCm39) |
V131L |
|
Het |
Ppp2r5a |
A |
G |
1: 191,128,532 (GRCm39) |
S28P |
probably benign |
Het |
Prl8a1 |
A |
G |
13: 27,758,068 (GRCm39) |
S214P |
probably damaging |
Het |
Prmt2 |
A |
T |
10: 76,056,838 (GRCm39) |
C228* |
probably null |
Het |
Prpf8 |
C |
T |
11: 75,399,738 (GRCm39) |
R2266* |
probably null |
Het |
Rabl6 |
A |
G |
2: 25,474,153 (GRCm39) |
S648P |
unknown |
Het |
Ralgapa1 |
T |
C |
12: 55,759,457 (GRCm39) |
K1022R |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,285,275 (GRCm39) |
D591E |
probably benign |
Het |
Rprd1a |
A |
G |
18: 24,639,889 (GRCm39) |
|
probably null |
Het |
Rsu1 |
T |
C |
2: 13,221,686 (GRCm39) |
R165G |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,842,491 (GRCm39) |
E334G |
probably benign |
Het |
Sez6 |
A |
G |
11: 77,864,711 (GRCm39) |
D557G |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,427,501 (GRCm39) |
|
probably null |
Het |
Slc17a3 |
T |
A |
13: 24,039,832 (GRCm39) |
M290K |
|
Het |
Snd1 |
T |
A |
6: 28,531,449 (GRCm39) |
V330E |
probably benign |
Het |
Tceanc2 |
T |
C |
4: 107,022,852 (GRCm39) |
K45R |
probably damaging |
Het |
Tg |
A |
T |
15: 66,568,437 (GRCm39) |
I1375F |
probably benign |
Het |
Tmem116 |
T |
A |
5: 121,633,124 (GRCm39) |
I357K |
|
Het |
Tmem39a |
G |
T |
16: 38,408,658 (GRCm39) |
R407L |
possibly damaging |
Het |
Tmem74 |
A |
T |
15: 43,730,761 (GRCm39) |
M94K |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,398,751 (GRCm39) |
C226Y |
probably damaging |
Het |
Trbv21 |
T |
C |
6: 41,179,861 (GRCm39) |
I59T |
not run |
Het |
Trim11 |
A |
G |
11: 58,869,463 (GRCm39) |
D133G |
probably benign |
Het |
Uaca |
G |
A |
9: 60,753,282 (GRCm39) |
V76I |
probably damaging |
Het |
Ugt2a3 |
A |
G |
5: 87,475,539 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
G |
T |
17: 20,249,737 (GRCm39) |
H845N |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,045,101 (GRCm39) |
Y279H |
probably damaging |
Het |
Zbtb46 |
A |
G |
2: 181,065,512 (GRCm39) |
S213P |
probably benign |
Het |
Zdhhc13 |
C |
A |
7: 48,461,103 (GRCm39) |
Y346* |
probably null |
Het |
Zfp280b |
A |
T |
10: 75,875,075 (GRCm39) |
H318L |
probably 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 |
R7483:Scn9a
|
UTSW |
2 |
66,363,692 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|