Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
T |
C |
9: 57,165,928 (GRCm39) |
T149A |
probably benign |
Het |
4932414N04Rik |
A |
C |
2: 68,561,474 (GRCm39) |
Q267P |
possibly damaging |
Het |
Actr5 |
T |
C |
2: 158,478,617 (GRCm39) |
V489A |
probably benign |
Het |
Adam26b |
T |
C |
8: 43,972,895 (GRCm39) |
|
probably benign |
Het |
Aff4 |
A |
G |
11: 53,290,567 (GRCm39) |
N509S |
probably benign |
Het |
Arhgap22 |
C |
T |
14: 33,085,229 (GRCm39) |
|
probably benign |
Het |
Arhgap9 |
C |
A |
10: 127,165,476 (GRCm39) |
H628Q |
probably damaging |
Het |
Asap1 |
A |
T |
15: 64,001,123 (GRCm39) |
I486N |
probably damaging |
Het |
Asb15 |
A |
T |
6: 24,558,787 (GRCm39) |
|
probably benign |
Het |
Avil |
A |
G |
10: 126,842,431 (GRCm39) |
D70G |
probably damaging |
Het |
Cct6b |
T |
C |
11: 82,645,780 (GRCm39) |
|
probably benign |
Het |
Cep63 |
A |
T |
9: 102,464,180 (GRCm39) |
I717K |
probably damaging |
Het |
Chd4 |
G |
T |
6: 125,085,730 (GRCm39) |
A875S |
probably damaging |
Het |
Col4a4 |
A |
T |
1: 82,471,237 (GRCm39) |
M706K |
unknown |
Het |
Cr1l |
T |
C |
1: 194,806,019 (GRCm39) |
T155A |
probably benign |
Het |
Ctnna3 |
A |
G |
10: 63,339,844 (GRCm39) |
N10S |
probably benign |
Het |
Cubn |
A |
G |
2: 13,450,843 (GRCm39) |
V854A |
probably damaging |
Het |
Dgkh |
T |
C |
14: 78,823,091 (GRCm39) |
T845A |
possibly damaging |
Het |
F10 |
G |
A |
8: 13,098,252 (GRCm39) |
A152T |
probably damaging |
Het |
Gabrg3 |
C |
A |
7: 56,632,439 (GRCm39) |
E170* |
probably null |
Het |
Heatr5a |
A |
G |
12: 51,968,149 (GRCm39) |
V829A |
probably benign |
Het |
Icam4 |
T |
C |
9: 20,941,770 (GRCm39) |
Y257H |
possibly damaging |
Het |
Jph1 |
A |
G |
1: 17,074,675 (GRCm39) |
S448P |
probably benign |
Het |
Kansl1l |
G |
A |
1: 66,812,604 (GRCm39) |
L125F |
probably damaging |
Het |
Kifc1 |
A |
T |
17: 34,100,467 (GRCm39) |
C46* |
probably null |
Het |
Lce3b |
A |
G |
3: 92,841,193 (GRCm39) |
D96G |
unknown |
Het |
Mab21l1 |
A |
T |
3: 55,690,505 (GRCm39) |
I31F |
possibly damaging |
Het |
Mctp2 |
A |
G |
7: 71,909,089 (GRCm39) |
Y75H |
possibly damaging |
Het |
Mesp2 |
A |
G |
7: 79,461,274 (GRCm39) |
I200V |
probably benign |
Het |
Msr1 |
T |
C |
8: 40,085,870 (GRCm39) |
|
probably benign |
Het |
Mtfr2 |
C |
T |
10: 20,224,084 (GRCm39) |
T6I |
probably benign |
Het |
Myo5b |
T |
C |
18: 74,828,438 (GRCm39) |
|
probably benign |
Het |
Myoc |
T |
A |
1: 162,467,029 (GRCm39) |
I66N |
probably benign |
Het |
Or10d1b |
T |
C |
9: 39,613,937 (GRCm39) |
I43V |
probably damaging |
Het |
Or4a70 |
A |
T |
2: 89,324,171 (GRCm39) |
Y162N |
probably damaging |
Het |
Or51k1 |
A |
C |
7: 103,661,609 (GRCm39) |
L100W |
probably damaging |
Het |
Or52n20 |
T |
C |
7: 104,320,136 (GRCm39) |
C76R |
probably damaging |
Het |
Or52n2b |
A |
G |
7: 104,565,859 (GRCm39) |
C215R |
probably damaging |
Het |
Or7a39 |
T |
C |
10: 78,715,759 (GRCm39) |
L251S |
probably damaging |
Het |
Per2 |
T |
C |
1: 91,378,450 (GRCm39) |
D33G |
possibly damaging |
Het |
Pknox1 |
A |
G |
17: 31,821,793 (GRCm39) |
I295V |
possibly damaging |
Het |
Rgs11 |
G |
A |
17: 26,426,605 (GRCm39) |
V279I |
probably benign |
Het |
Rhot2 |
A |
G |
17: 26,063,270 (GRCm39) |
S19P |
probably damaging |
Het |
Rps6kb1 |
C |
A |
11: 86,426,236 (GRCm39) |
|
probably null |
Het |
Serpinb1b |
C |
T |
13: 33,275,648 (GRCm39) |
T194I |
probably benign |
Het |
Smarcad1 |
T |
A |
6: 65,029,790 (GRCm39) |
|
probably benign |
Het |
Stxbp4 |
A |
G |
11: 90,428,759 (GRCm39) |
S449P |
probably benign |
Het |
Thrb |
A |
C |
14: 18,026,721 (GRCm38) |
I275L |
probably benign |
Het |
Tjp1 |
T |
A |
7: 64,979,431 (GRCm39) |
K365* |
probably null |
Het |
Tjp1 |
T |
A |
7: 64,979,430 (GRCm39) |
K365I |
possibly damaging |
Het |
Tm4sf4 |
C |
A |
3: 57,333,939 (GRCm39) |
C75* |
probably null |
Het |
Tmem131 |
T |
C |
1: 36,864,560 (GRCm39) |
T558A |
probably benign |
Het |
Txndc16 |
T |
C |
14: 45,399,730 (GRCm39) |
T408A |
probably benign |
Het |
Ube2j1 |
T |
C |
4: 33,038,206 (GRCm39) |
L38P |
possibly damaging |
Het |
Urb2 |
T |
C |
8: 124,757,425 (GRCm39) |
I1044T |
probably benign |
Het |
|
Other mutations in Htt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Htt
|
APN |
5 |
34,956,752 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00233:Htt
|
APN |
5 |
35,053,370 (GRCm39) |
splice site |
probably null |
|
IGL00559:Htt
|
APN |
5 |
35,006,448 (GRCm39) |
splice site |
probably benign |
|
IGL00765:Htt
|
APN |
5 |
35,034,769 (GRCm39) |
splice site |
probably benign |
|
IGL00950:Htt
|
APN |
5 |
35,048,785 (GRCm39) |
missense |
probably benign |
|
IGL00953:Htt
|
APN |
5 |
34,976,021 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00957:Htt
|
APN |
5 |
34,964,068 (GRCm39) |
missense |
probably benign |
|
IGL01314:Htt
|
APN |
5 |
35,036,200 (GRCm39) |
missense |
probably benign |
|
IGL01412:Htt
|
APN |
5 |
35,055,916 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01510:Htt
|
APN |
5 |
35,064,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01617:Htt
|
APN |
5 |
35,034,099 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01893:Htt
|
APN |
5 |
35,034,174 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01914:Htt
|
APN |
5 |
34,987,053 (GRCm39) |
missense |
probably benign |
|
IGL01994:Htt
|
APN |
5 |
34,989,948 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02102:Htt
|
APN |
5 |
35,048,825 (GRCm39) |
splice site |
probably benign |
|
IGL02381:Htt
|
APN |
5 |
34,987,104 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02529:Htt
|
APN |
5 |
34,976,387 (GRCm39) |
splice site |
probably benign |
|
IGL02678:Htt
|
APN |
5 |
35,057,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02731:Htt
|
APN |
5 |
34,961,137 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02931:Htt
|
APN |
5 |
35,034,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03167:Htt
|
APN |
5 |
34,976,330 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03343:Htt
|
APN |
5 |
34,983,385 (GRCm39) |
missense |
probably benign |
|
IGL03344:Htt
|
APN |
5 |
35,037,172 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03344:Htt
|
APN |
5 |
35,064,810 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03366:Htt
|
APN |
5 |
35,064,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03410:Htt
|
APN |
5 |
34,956,789 (GRCm39) |
missense |
probably damaging |
0.99 |
Chalk
|
UTSW |
5 |
35,064,430 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02796:Htt
|
UTSW |
5 |
35,034,826 (GRCm39) |
missense |
probably benign |
0.43 |
PIT4377001:Htt
|
UTSW |
5 |
35,033,309 (GRCm39) |
missense |
probably benign |
0.10 |
R0013:Htt
|
UTSW |
5 |
34,977,448 (GRCm39) |
missense |
probably benign |
0.25 |
R0049:Htt
|
UTSW |
5 |
35,066,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R0049:Htt
|
UTSW |
5 |
35,066,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R0056:Htt
|
UTSW |
5 |
34,983,422 (GRCm39) |
splice site |
probably benign |
|
R0207:Htt
|
UTSW |
5 |
35,054,252 (GRCm39) |
missense |
probably benign |
0.11 |
R0329:Htt
|
UTSW |
5 |
34,974,478 (GRCm39) |
splice site |
probably benign |
|
R0494:Htt
|
UTSW |
5 |
34,979,188 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0548:Htt
|
UTSW |
5 |
35,028,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Htt
|
UTSW |
5 |
35,003,347 (GRCm39) |
missense |
probably benign |
0.08 |
R0799:Htt
|
UTSW |
5 |
34,975,097 (GRCm39) |
missense |
probably benign |
0.00 |
R0947:Htt
|
UTSW |
5 |
35,056,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1053:Htt
|
UTSW |
5 |
35,008,561 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1147:Htt
|
UTSW |
5 |
35,008,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R1147:Htt
|
UTSW |
5 |
35,008,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R1478:Htt
|
UTSW |
5 |
34,961,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R1573:Htt
|
UTSW |
5 |
35,021,718 (GRCm39) |
splice site |
probably benign |
|
R1677:Htt
|
UTSW |
5 |
34,985,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Htt
|
UTSW |
5 |
35,064,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Htt
|
UTSW |
5 |
34,961,084 (GRCm39) |
missense |
probably benign |
0.01 |
R1833:Htt
|
UTSW |
5 |
35,063,092 (GRCm39) |
splice site |
probably benign |
|
R1837:Htt
|
UTSW |
5 |
34,976,367 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Htt
|
UTSW |
5 |
35,006,288 (GRCm39) |
missense |
probably damaging |
0.98 |
R1875:Htt
|
UTSW |
5 |
34,951,456 (GRCm39) |
missense |
probably benign |
0.05 |
R1899:Htt
|
UTSW |
5 |
35,064,429 (GRCm39) |
missense |
probably benign |
0.01 |
R2013:Htt
|
UTSW |
5 |
35,010,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2064:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2067:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2068:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2131:Htt
|
UTSW |
5 |
35,034,453 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2162:Htt
|
UTSW |
5 |
34,979,062 (GRCm39) |
missense |
probably benign |
0.44 |
R2169:Htt
|
UTSW |
5 |
35,034,819 (GRCm39) |
missense |
probably benign |
0.08 |
R2345:Htt
|
UTSW |
5 |
34,983,348 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2433:Htt
|
UTSW |
5 |
35,064,885 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3027:Htt
|
UTSW |
5 |
34,977,439 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3123:Htt
|
UTSW |
5 |
34,961,875 (GRCm39) |
missense |
probably benign |
|
R3125:Htt
|
UTSW |
5 |
34,961,875 (GRCm39) |
missense |
probably benign |
|
R3717:Htt
|
UTSW |
5 |
34,968,866 (GRCm39) |
splice site |
probably benign |
|
R3758:Htt
|
UTSW |
5 |
35,053,314 (GRCm39) |
missense |
probably damaging |
0.97 |
R3805:Htt
|
UTSW |
5 |
35,034,548 (GRCm39) |
splice site |
probably null |
|
R3833:Htt
|
UTSW |
5 |
34,979,062 (GRCm39) |
missense |
probably benign |
0.44 |
R4066:Htt
|
UTSW |
5 |
35,036,191 (GRCm39) |
missense |
probably benign |
|
R4272:Htt
|
UTSW |
5 |
35,006,413 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4625:Htt
|
UTSW |
5 |
34,987,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R4634:Htt
|
UTSW |
5 |
35,033,292 (GRCm39) |
missense |
probably benign |
0.06 |
R4655:Htt
|
UTSW |
5 |
35,063,476 (GRCm39) |
missense |
probably benign |
0.06 |
R4679:Htt
|
UTSW |
5 |
34,977,424 (GRCm39) |
missense |
probably benign |
|
R4684:Htt
|
UTSW |
5 |
35,010,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Htt
|
UTSW |
5 |
34,982,184 (GRCm39) |
missense |
probably benign |
0.01 |
R4833:Htt
|
UTSW |
5 |
35,009,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R4973:Htt
|
UTSW |
5 |
34,970,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R5095:Htt
|
UTSW |
5 |
34,981,739 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5132:Htt
|
UTSW |
5 |
35,063,023 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5351:Htt
|
UTSW |
5 |
34,961,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R5361:Htt
|
UTSW |
5 |
35,064,928 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5399:Htt
|
UTSW |
5 |
35,034,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R5462:Htt
|
UTSW |
5 |
35,042,851 (GRCm39) |
nonsense |
probably null |
|
R5552:Htt
|
UTSW |
5 |
34,979,118 (GRCm39) |
missense |
probably benign |
|
R5566:Htt
|
UTSW |
5 |
35,006,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Htt
|
UTSW |
5 |
35,062,741 (GRCm39) |
missense |
probably damaging |
0.96 |
R5617:Htt
|
UTSW |
5 |
35,028,150 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5835:Htt
|
UTSW |
5 |
34,970,534 (GRCm39) |
missense |
probably benign |
0.16 |
R5891:Htt
|
UTSW |
5 |
35,028,167 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6158:Htt
|
UTSW |
5 |
35,064,430 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6159:Htt
|
UTSW |
5 |
34,962,020 (GRCm39) |
missense |
probably benign |
0.08 |
R6169:Htt
|
UTSW |
5 |
35,064,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Htt
|
UTSW |
5 |
35,003,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Htt
|
UTSW |
5 |
35,009,431 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6280:Htt
|
UTSW |
5 |
35,028,103 (GRCm39) |
missense |
probably benign |
0.00 |
R6294:Htt
|
UTSW |
5 |
34,979,170 (GRCm39) |
missense |
probably benign |
|
R6331:Htt
|
UTSW |
5 |
35,053,231 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6448:Htt
|
UTSW |
5 |
35,033,336 (GRCm39) |
missense |
probably benign |
0.05 |
R6474:Htt
|
UTSW |
5 |
34,982,239 (GRCm39) |
missense |
probably benign |
0.06 |
R6592:Htt
|
UTSW |
5 |
35,034,388 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6818:Htt
|
UTSW |
5 |
34,940,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R6830:Htt
|
UTSW |
5 |
34,991,670 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6920:Htt
|
UTSW |
5 |
35,034,444 (GRCm39) |
missense |
probably null |
1.00 |
R6962:Htt
|
UTSW |
5 |
35,057,115 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7057:Htt
|
UTSW |
5 |
34,979,067 (GRCm39) |
missense |
probably null |
0.05 |
R7144:Htt
|
UTSW |
5 |
35,003,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Htt
|
UTSW |
5 |
35,010,238 (GRCm39) |
missense |
probably benign |
0.42 |
R7329:Htt
|
UTSW |
5 |
34,987,099 (GRCm39) |
missense |
probably benign |
0.03 |
R7378:Htt
|
UTSW |
5 |
34,961,143 (GRCm39) |
missense |
probably benign |
0.04 |
R7418:Htt
|
UTSW |
5 |
34,947,697 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7495:Htt
|
UTSW |
5 |
34,968,821 (GRCm39) |
missense |
probably benign |
0.00 |
R7554:Htt
|
UTSW |
5 |
35,022,084 (GRCm39) |
missense |
probably damaging |
0.97 |
R7575:Htt
|
UTSW |
5 |
35,062,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Htt
|
UTSW |
5 |
35,009,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Htt
|
UTSW |
5 |
35,040,336 (GRCm39) |
missense |
probably benign |
0.03 |
R7850:Htt
|
UTSW |
5 |
35,009,631 (GRCm39) |
splice site |
probably null |
|
R7870:Htt
|
UTSW |
5 |
35,055,891 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7871:Htt
|
UTSW |
5 |
35,021,993 (GRCm39) |
missense |
probably benign |
0.00 |
R7879:Htt
|
UTSW |
5 |
34,981,252 (GRCm39) |
missense |
probably benign |
|
R7992:Htt
|
UTSW |
5 |
34,987,225 (GRCm39) |
critical splice donor site |
probably null |
|
R8058:Htt
|
UTSW |
5 |
34,977,444 (GRCm39) |
missense |
probably benign |
|
R8168:Htt
|
UTSW |
5 |
35,040,300 (GRCm39) |
missense |
probably benign |
0.00 |
R8188:Htt
|
UTSW |
5 |
34,919,287 (GRCm39) |
missense |
probably benign |
0.03 |
R8262:Htt
|
UTSW |
5 |
35,053,304 (GRCm39) |
missense |
probably benign |
|
R8343:Htt
|
UTSW |
5 |
35,063,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Htt
|
UTSW |
5 |
35,034,499 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8769:Htt
|
UTSW |
5 |
34,977,633 (GRCm39) |
missense |
probably benign |
0.05 |
R8808:Htt
|
UTSW |
5 |
35,046,791 (GRCm39) |
missense |
probably benign |
0.10 |
R8825:Htt
|
UTSW |
5 |
34,983,304 (GRCm39) |
missense |
probably benign |
0.24 |
R8843:Htt
|
UTSW |
5 |
35,046,809 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8856:Htt
|
UTSW |
5 |
35,060,675 (GRCm39) |
missense |
probably benign |
0.44 |
R8882:Htt
|
UTSW |
5 |
34,979,061 (GRCm39) |
missense |
probably benign |
|
R8898:Htt
|
UTSW |
5 |
34,976,376 (GRCm39) |
missense |
probably benign |
0.01 |
R8964:Htt
|
UTSW |
5 |
35,062,720 (GRCm39) |
missense |
probably benign |
0.09 |
R8987:Htt
|
UTSW |
5 |
34,977,368 (GRCm39) |
missense |
probably benign |
0.18 |
R8991:Htt
|
UTSW |
5 |
35,063,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Htt
|
UTSW |
5 |
34,975,095 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9019:Htt
|
UTSW |
5 |
35,023,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R9057:Htt
|
UTSW |
5 |
35,009,454 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9157:Htt
|
UTSW |
5 |
34,987,171 (GRCm39) |
missense |
probably null |
0.89 |
R9205:Htt
|
UTSW |
5 |
34,976,367 (GRCm39) |
missense |
probably benign |
0.00 |
R9223:Htt
|
UTSW |
5 |
35,062,692 (GRCm39) |
missense |
probably benign |
0.01 |
R9243:Htt
|
UTSW |
5 |
35,056,276 (GRCm39) |
splice site |
probably benign |
|
R9329:Htt
|
UTSW |
5 |
34,989,957 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9355:Htt
|
UTSW |
5 |
35,053,247 (GRCm39) |
missense |
probably benign |
|
R9402:Htt
|
UTSW |
5 |
35,006,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9446:Htt
|
UTSW |
5 |
34,919,272 (GRCm39) |
missense |
probably benign |
|
R9716:Htt
|
UTSW |
5 |
35,012,019 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Htt
|
UTSW |
5 |
35,009,575 (GRCm39) |
missense |
probably null |
0.87 |
|