Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
Acaca |
T |
G |
11: 84,142,105 (GRCm39) |
H637Q |
probably benign |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Akap6 |
C |
A |
12: 52,984,000 (GRCm39) |
A848E |
probably damaging |
Het |
Cxxc4 |
A |
G |
3: 133,946,420 (GRCm39) |
I334V |
probably null |
Het |
Cyp2b13 |
T |
A |
7: 25,781,125 (GRCm39) |
I179N |
probably damaging |
Het |
Cyp2d40 |
C |
A |
15: 82,645,102 (GRCm39) |
A183S |
unknown |
Het |
Cyp2g1 |
A |
G |
7: 26,509,256 (GRCm39) |
N110S |
probably benign |
Het |
F5 |
A |
T |
1: 164,019,548 (GRCm39) |
R674S |
possibly damaging |
Het |
Fnip2 |
G |
T |
3: 79,419,810 (GRCm39) |
Y155* |
probably null |
Het |
Fut9 |
G |
T |
4: 25,620,446 (GRCm39) |
Q123K |
probably benign |
Het |
Gda |
A |
G |
19: 21,394,429 (GRCm39) |
S143P |
probably damaging |
Het |
Gpr162 |
T |
C |
6: 124,835,820 (GRCm39) |
|
probably null |
Het |
Hsf2bp |
A |
G |
17: 32,206,378 (GRCm39) |
L251S |
probably damaging |
Het |
Hsh2d |
A |
T |
8: 72,947,375 (GRCm39) |
D24V |
probably damaging |
Het |
Htr1f |
T |
A |
16: 64,746,501 (GRCm39) |
T264S |
probably benign |
Het |
Med12l |
G |
A |
3: 58,949,696 (GRCm39) |
E151K |
possibly damaging |
Het |
Mgat3 |
C |
A |
15: 80,096,377 (GRCm39) |
N401K |
probably benign |
Het |
Mmp27 |
T |
G |
9: 7,573,298 (GRCm39) |
M130R |
probably benign |
Het |
Mroh2b |
T |
A |
15: 4,944,634 (GRCm39) |
S412T |
probably benign |
Het |
Mrps9 |
A |
G |
1: 42,942,557 (GRCm39) |
I338M |
probably damaging |
Het |
Mtmr4 |
C |
T |
11: 87,494,893 (GRCm39) |
T395M |
probably damaging |
Het |
Nlrp9b |
A |
G |
7: 19,757,112 (GRCm39) |
I116M |
probably benign |
Het |
Nqo1 |
T |
C |
8: 108,115,587 (GRCm39) |
D230G |
probably benign |
Het |
Pcnx2 |
C |
T |
8: 126,589,889 (GRCm39) |
V795I |
probably benign |
Het |
Pde8a |
G |
A |
7: 80,968,826 (GRCm39) |
R449Q |
possibly damaging |
Het |
Sema3e |
A |
G |
5: 14,302,784 (GRCm39) |
R770G |
probably damaging |
Het |
Smr2 |
T |
C |
5: 88,256,378 (GRCm39) |
S19P |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,220,849 (GRCm39) |
S2529P |
probably benign |
Het |
Uspl1 |
T |
A |
5: 149,141,103 (GRCm39) |
F367L |
probably damaging |
Het |
Vps41 |
A |
G |
13: 19,050,320 (GRCm39) |
S838G |
probably benign |
Het |
Ythdf2 |
A |
T |
4: 131,932,789 (GRCm39) |
F124I |
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 |
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 |
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 |
|