Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb6 |
A |
G |
1: 75,154,347 (GRCm39) |
F311S |
probably benign |
Het |
Adamts7 |
C |
A |
9: 90,055,826 (GRCm39) |
T193N |
possibly damaging |
Het |
Akr1b7 |
A |
G |
6: 34,397,457 (GRCm39) |
N273S |
probably damaging |
Het |
Asz1 |
G |
A |
6: 18,077,252 (GRCm39) |
T151M |
probably damaging |
Het |
Atosb |
A |
G |
4: 43,036,533 (GRCm39) |
L66P |
probably damaging |
Het |
Atrnl1 |
T |
A |
19: 57,703,119 (GRCm39) |
Y1046N |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,564,022 (GRCm39) |
S902P |
probably damaging |
Het |
Casp3 |
T |
A |
8: 47,087,368 (GRCm39) |
I105K |
probably benign |
Het |
Ccdc146 |
C |
T |
5: 21,506,450 (GRCm39) |
V664I |
probably benign |
Het |
Cfap61 |
G |
A |
2: 145,805,451 (GRCm39) |
C267Y |
possibly damaging |
Het |
Dgkz |
A |
T |
2: 91,764,399 (GRCm39) |
|
probably null |
Het |
Dnah11 |
G |
T |
12: 118,104,505 (GRCm39) |
|
probably null |
Het |
Duox1 |
C |
A |
2: 122,156,616 (GRCm39) |
Y514* |
probably null |
Het |
Epha7 |
C |
T |
4: 28,871,937 (GRCm39) |
S422L |
probably benign |
Het |
Fan1 |
A |
T |
7: 64,003,979 (GRCm39) |
|
probably null |
Het |
Fgfrl1 |
A |
T |
5: 108,853,211 (GRCm39) |
K278M |
probably damaging |
Het |
Fign |
T |
C |
2: 63,809,063 (GRCm39) |
I736V |
possibly damaging |
Het |
Galns |
A |
G |
8: 123,318,184 (GRCm39) |
F410S |
probably benign |
Het |
Hspbp1 |
C |
A |
7: 4,663,821 (GRCm39) |
K341N |
possibly damaging |
Het |
Idh3b |
A |
T |
2: 130,122,900 (GRCm39) |
S296R |
probably damaging |
Het |
Ifi44 |
A |
G |
3: 151,438,045 (GRCm39) |
F414S |
probably damaging |
Het |
Kdm3a |
T |
A |
6: 71,577,731 (GRCm39) |
M690L |
probably benign |
Het |
Ldaf1 |
A |
G |
7: 119,704,011 (GRCm39) |
K19E |
probably damaging |
Het |
Lrrc49 |
C |
T |
9: 60,510,005 (GRCm39) |
G488S |
probably null |
Het |
Mcc |
T |
C |
18: 44,624,294 (GRCm39) |
N417S |
possibly damaging |
Het |
Melk |
T |
A |
4: 44,325,571 (GRCm39) |
|
probably null |
Het |
Mtcl1 |
T |
C |
17: 66,650,300 (GRCm39) |
R1722G |
probably damaging |
Het |
Or4a79 |
A |
G |
2: 89,551,642 (GRCm39) |
V271A |
probably benign |
Het |
Or51f23c-ps1 |
A |
G |
7: 102,431,132 (GRCm39) |
I150V |
probably benign |
Het |
Or5b119 |
G |
A |
19: 13,456,956 (GRCm39) |
T202I |
possibly damaging |
Het |
Or8d2 |
T |
A |
9: 38,759,806 (GRCm39) |
V132D |
possibly damaging |
Het |
Pdzrn3 |
T |
C |
6: 101,128,713 (GRCm39) |
E651G |
probably damaging |
Het |
Pop5 |
A |
G |
5: 115,375,931 (GRCm39) |
|
probably benign |
Het |
Prox1 |
T |
A |
1: 189,885,642 (GRCm39) |
M602L |
probably benign |
Het |
Prpf39 |
G |
A |
12: 65,100,220 (GRCm39) |
A298T |
probably benign |
Het |
Scg2 |
T |
C |
1: 79,413,898 (GRCm39) |
E275G |
probably benign |
Het |
Slc16a4 |
A |
T |
3: 107,210,443 (GRCm39) |
Y371F |
probably damaging |
Het |
Slc4a1ap |
T |
A |
5: 31,693,533 (GRCm39) |
M489K |
possibly damaging |
Het |
Spata13 |
A |
G |
14: 60,929,956 (GRCm39) |
N505D |
possibly damaging |
Het |
Tas2r129 |
A |
G |
6: 132,928,156 (GRCm39) |
N31S |
probably damaging |
Het |
Tnn |
A |
T |
1: 159,915,984 (GRCm39) |
Y1508* |
probably null |
Het |
Trim23 |
T |
C |
13: 104,328,541 (GRCm39) |
V354A |
probably benign |
Het |
Tsc1 |
A |
T |
2: 28,548,748 (GRCm39) |
T18S |
probably benign |
Het |
Txlnb |
A |
G |
10: 17,691,146 (GRCm39) |
K232R |
probably damaging |
Het |
Vmn1r53 |
C |
T |
6: 90,201,104 (GRCm39) |
M73I |
probably benign |
Het |
Vmn1r67 |
G |
A |
7: 10,181,290 (GRCm39) |
V185M |
possibly damaging |
Het |
Vmn2r14 |
A |
G |
5: 109,369,276 (GRCm39) |
I99T |
probably benign |
Het |
Zfp318 |
T |
G |
17: 46,710,935 (GRCm39) |
V886G |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,941,797 (GRCm39) |
N324S |
probably benign |
Het |
Zfp819 |
T |
C |
7: 43,266,357 (GRCm39) |
V280A |
probably benign |
Het |
|
Other mutations in Scn11a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Scn11a
|
APN |
9 |
119,599,572 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00272:Scn11a
|
APN |
9 |
119,645,669 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00332:Scn11a
|
APN |
9 |
119,598,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00533:Scn11a
|
APN |
9 |
119,603,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00972:Scn11a
|
APN |
9 |
119,623,004 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01338:Scn11a
|
APN |
9 |
119,613,227 (GRCm39) |
splice site |
probably benign |
|
IGL01534:Scn11a
|
APN |
9 |
119,609,888 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01838:Scn11a
|
APN |
9 |
119,587,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01991:Scn11a
|
APN |
9 |
119,648,970 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02057:Scn11a
|
APN |
9 |
119,594,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02290:Scn11a
|
APN |
9 |
119,603,508 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02454:Scn11a
|
APN |
9 |
119,587,610 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02517:Scn11a
|
APN |
9 |
119,621,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Scn11a
|
APN |
9 |
119,633,555 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Scn11a
|
APN |
9 |
119,634,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Scn11a
|
APN |
9 |
119,619,029 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03171:Scn11a
|
APN |
9 |
119,648,913 (GRCm39) |
missense |
probably benign |
0.00 |
Kleinie
|
UTSW |
9 |
119,632,569 (GRCm39) |
missense |
probably benign |
0.16 |
H8441:Scn11a
|
UTSW |
9 |
119,636,976 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4449001:Scn11a
|
UTSW |
9 |
119,599,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Scn11a
|
UTSW |
9 |
119,648,928 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Scn11a
|
UTSW |
9 |
119,619,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Scn11a
|
UTSW |
9 |
119,640,226 (GRCm39) |
missense |
probably benign |
0.41 |
R0828:Scn11a
|
UTSW |
9 |
119,584,073 (GRCm39) |
missense |
probably benign |
0.00 |
R0893:Scn11a
|
UTSW |
9 |
119,632,396 (GRCm39) |
splice site |
probably null |
|
R0932:Scn11a
|
UTSW |
9 |
119,636,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Scn11a
|
UTSW |
9 |
119,624,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R1161:Scn11a
|
UTSW |
9 |
119,584,123 (GRCm39) |
nonsense |
probably null |
|
R1162:Scn11a
|
UTSW |
9 |
119,634,710 (GRCm39) |
splice site |
probably benign |
|
R1310:Scn11a
|
UTSW |
9 |
119,584,123 (GRCm39) |
nonsense |
probably null |
|
R1589:Scn11a
|
UTSW |
9 |
119,598,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Scn11a
|
UTSW |
9 |
119,633,478 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1781:Scn11a
|
UTSW |
9 |
119,584,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R1812:Scn11a
|
UTSW |
9 |
119,609,931 (GRCm39) |
nonsense |
probably null |
|
R1901:Scn11a
|
UTSW |
9 |
119,608,102 (GRCm39) |
nonsense |
probably null |
|
R1978:Scn11a
|
UTSW |
9 |
119,609,861 (GRCm39) |
nonsense |
probably null |
|
R1985:Scn11a
|
UTSW |
9 |
119,583,744 (GRCm39) |
missense |
probably benign |
0.19 |
R2022:Scn11a
|
UTSW |
9 |
119,640,274 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2072:Scn11a
|
UTSW |
9 |
119,640,274 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2098:Scn11a
|
UTSW |
9 |
119,621,560 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2163:Scn11a
|
UTSW |
9 |
119,584,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R2250:Scn11a
|
UTSW |
9 |
119,587,668 (GRCm39) |
missense |
probably benign |
0.01 |
R2373:Scn11a
|
UTSW |
9 |
119,642,252 (GRCm39) |
missense |
probably benign |
0.43 |
R2508:Scn11a
|
UTSW |
9 |
119,594,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R3757:Scn11a
|
UTSW |
9 |
119,632,569 (GRCm39) |
missense |
probably benign |
0.16 |
R3767:Scn11a
|
UTSW |
9 |
119,613,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3770:Scn11a
|
UTSW |
9 |
119,613,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R4089:Scn11a
|
UTSW |
9 |
119,624,719 (GRCm39) |
splice site |
probably null |
|
R4092:Scn11a
|
UTSW |
9 |
119,619,036 (GRCm39) |
missense |
probably benign |
0.03 |
R4247:Scn11a
|
UTSW |
9 |
119,636,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R4279:Scn11a
|
UTSW |
9 |
119,583,428 (GRCm39) |
missense |
probably benign |
0.25 |
R4299:Scn11a
|
UTSW |
9 |
119,594,572 (GRCm39) |
missense |
probably damaging |
0.97 |
R4403:Scn11a
|
UTSW |
9 |
119,624,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R4468:Scn11a
|
UTSW |
9 |
119,584,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Scn11a
|
UTSW |
9 |
119,584,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Scn11a
|
UTSW |
9 |
119,644,269 (GRCm39) |
splice site |
probably null |
|
R4739:Scn11a
|
UTSW |
9 |
119,583,627 (GRCm39) |
missense |
probably benign |
0.39 |
R4809:Scn11a
|
UTSW |
9 |
119,648,936 (GRCm39) |
missense |
probably benign |
0.00 |
R4954:Scn11a
|
UTSW |
9 |
119,587,725 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5012:Scn11a
|
UTSW |
9 |
119,609,944 (GRCm39) |
missense |
probably benign |
0.31 |
R5044:Scn11a
|
UTSW |
9 |
119,648,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R5222:Scn11a
|
UTSW |
9 |
119,644,268 (GRCm39) |
splice site |
probably null |
|
R5224:Scn11a
|
UTSW |
9 |
119,583,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Scn11a
|
UTSW |
9 |
119,598,974 (GRCm39) |
missense |
probably damaging |
0.97 |
R5555:Scn11a
|
UTSW |
9 |
119,584,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5711:Scn11a
|
UTSW |
9 |
119,618,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Scn11a
|
UTSW |
9 |
119,640,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Scn11a
|
UTSW |
9 |
119,613,082 (GRCm39) |
missense |
probably benign |
|
R6057:Scn11a
|
UTSW |
9 |
119,594,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Scn11a
|
UTSW |
9 |
119,624,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Scn11a
|
UTSW |
9 |
119,583,933 (GRCm39) |
missense |
probably benign |
0.00 |
R6892:Scn11a
|
UTSW |
9 |
119,636,035 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6908:Scn11a
|
UTSW |
9 |
119,621,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Scn11a
|
UTSW |
9 |
119,594,580 (GRCm39) |
missense |
probably benign |
0.04 |
R7112:Scn11a
|
UTSW |
9 |
119,583,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Scn11a
|
UTSW |
9 |
119,588,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Scn11a
|
UTSW |
9 |
119,648,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R7265:Scn11a
|
UTSW |
9 |
119,644,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7302:Scn11a
|
UTSW |
9 |
119,636,017 (GRCm39) |
missense |
probably benign |
0.03 |
R7391:Scn11a
|
UTSW |
9 |
119,624,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Scn11a
|
UTSW |
9 |
119,587,692 (GRCm39) |
missense |
probably benign |
0.01 |
R7479:Scn11a
|
UTSW |
9 |
119,588,941 (GRCm39) |
missense |
probably benign |
0.38 |
R7768:Scn11a
|
UTSW |
9 |
119,644,338 (GRCm39) |
missense |
probably benign |
0.13 |
R7785:Scn11a
|
UTSW |
9 |
119,645,622 (GRCm39) |
missense |
probably benign |
0.00 |
R7794:Scn11a
|
UTSW |
9 |
119,594,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R7818:Scn11a
|
UTSW |
9 |
119,613,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R7884:Scn11a
|
UTSW |
9 |
119,633,617 (GRCm39) |
missense |
probably benign |
0.01 |
R7988:Scn11a
|
UTSW |
9 |
119,594,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R8049:Scn11a
|
UTSW |
9 |
119,584,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8127:Scn11a
|
UTSW |
9 |
119,633,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Scn11a
|
UTSW |
9 |
119,632,548 (GRCm39) |
missense |
probably benign |
|
R8344:Scn11a
|
UTSW |
9 |
119,611,036 (GRCm39) |
missense |
probably benign |
0.00 |
R8346:Scn11a
|
UTSW |
9 |
119,608,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Scn11a
|
UTSW |
9 |
119,618,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R8819:Scn11a
|
UTSW |
9 |
119,645,586 (GRCm39) |
missense |
probably benign |
0.19 |
R8820:Scn11a
|
UTSW |
9 |
119,645,586 (GRCm39) |
missense |
probably benign |
0.19 |
R8837:Scn11a
|
UTSW |
9 |
119,621,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Scn11a
|
UTSW |
9 |
119,623,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Scn11a
|
UTSW |
9 |
119,603,363 (GRCm39) |
nonsense |
probably null |
|
R8975:Scn11a
|
UTSW |
9 |
119,587,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:Scn11a
|
UTSW |
9 |
119,588,989 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9222:Scn11a
|
UTSW |
9 |
119,611,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R9355:Scn11a
|
UTSW |
9 |
119,584,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Scn11a
|
UTSW |
9 |
119,624,774 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9712:Scn11a
|
UTSW |
9 |
119,619,076 (GRCm39) |
nonsense |
probably null |
|
R9766:Scn11a
|
UTSW |
9 |
119,584,181 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Scn11a
|
UTSW |
9 |
119,584,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn11a
|
UTSW |
9 |
119,648,886 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn11a
|
UTSW |
9 |
119,584,064 (GRCm39) |
missense |
possibly damaging |
0.94 |
|