Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
A2ml1 |
A |
T |
6: 128,529,271 (GRCm39) |
M957K |
probably benign |
Het |
Adam7 |
C |
A |
14: 68,742,610 (GRCm39) |
V668F |
probably benign |
Het |
Adcy7 |
T |
G |
8: 89,038,902 (GRCm39) |
L306R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano7 |
T |
C |
1: 93,318,035 (GRCm39) |
V249A |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,098,351 (GRCm39) |
|
probably null |
Het |
Asah2 |
A |
T |
19: 32,002,274 (GRCm39) |
V290E |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Atxn2l |
T |
A |
7: 126,095,038 (GRCm39) |
K421N |
probably damaging |
Het |
Cars2 |
T |
C |
8: 11,597,747 (GRCm39) |
I110V |
probably damaging |
Het |
Ccdc74a |
A |
G |
16: 17,467,890 (GRCm39) |
N249S |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,928,082 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
C |
T |
15: 82,574,289 (GRCm39) |
|
noncoding transcript |
Het |
Cyp3a25 |
A |
G |
5: 145,923,779 (GRCm39) |
|
probably benign |
Het |
Dis3l |
G |
T |
9: 64,246,855 (GRCm39) |
Q67K |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,993,086 (GRCm39) |
V2936A |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,366,416 (GRCm39) |
R2710C |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Dvl3 |
G |
A |
16: 20,345,101 (GRCm39) |
S361N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,881,181 (GRCm39) |
V1085A |
probably benign |
Het |
Eif3b |
T |
C |
5: 140,412,208 (GRCm39) |
Y226H |
probably damaging |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ercc1 |
A |
G |
7: 19,088,295 (GRCm39) |
*37W |
probably null |
Het |
Evi2a |
G |
A |
11: 79,418,593 (GRCm39) |
Q6* |
probably null |
Het |
Faah |
C |
T |
4: 115,855,770 (GRCm39) |
V552M |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,477,369 (GRCm39) |
N2138K |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,479,741 (GRCm39) |
V2929E |
probably damaging |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
A |
T |
16: 12,578,979 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Hspg2 |
A |
T |
4: 137,286,678 (GRCm39) |
T3666S |
possibly damaging |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Iqgap1 |
G |
A |
7: 80,373,727 (GRCm39) |
Q1421* |
probably null |
Het |
Itga3 |
T |
A |
11: 94,944,902 (GRCm39) |
Q802L |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Lztr1 |
T |
C |
16: 17,327,534 (GRCm39) |
V79A |
probably damaging |
Het |
Mast4 |
C |
T |
13: 102,895,601 (GRCm39) |
E736K |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Myof |
A |
G |
19: 37,904,194 (GRCm39) |
V2A |
possibly damaging |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,555,882 (GRCm39) |
T1683M |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,993,578 (GRCm39) |
|
probably benign |
Het |
Nebl |
A |
T |
2: 17,401,932 (GRCm39) |
M427K |
probably benign |
Het |
Ngdn |
T |
C |
14: 55,259,564 (GRCm39) |
V205A |
possibly damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,043,277 (GRCm39) |
F20L |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or2w3 |
G |
T |
11: 58,556,808 (GRCm39) |
C141F |
probably damaging |
Het |
Or5m9 |
A |
G |
2: 85,877,299 (GRCm39) |
T158A |
probably damaging |
Het |
Or6c205 |
T |
A |
10: 129,087,001 (GRCm39) |
Y199* |
probably null |
Het |
Park7 |
T |
C |
4: 150,989,732 (GRCm39) |
N76S |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,271,559 (GRCm39) |
I2998T |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppard |
A |
G |
17: 28,518,663 (GRCm39) |
H388R |
probably damaging |
Het |
Psma1 |
A |
G |
7: 113,869,001 (GRCm39) |
S142P |
possibly damaging |
Het |
Pth2r |
T |
C |
1: 65,382,721 (GRCm39) |
I158T |
probably damaging |
Het |
Rbl2 |
C |
A |
8: 91,833,367 (GRCm39) |
P714Q |
probably damaging |
Het |
Rexo2 |
A |
T |
9: 48,385,813 (GRCm39) |
S104T |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,609,363 (GRCm39) |
|
probably benign |
Het |
Spmip10 |
C |
T |
18: 56,721,535 (GRCm39) |
Q25* |
probably null |
Het |
Sun2 |
A |
G |
15: 79,622,852 (GRCm39) |
L109P |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,477,368 (GRCm39) |
T116A |
probably benign |
Het |
Terb1 |
A |
T |
8: 105,195,380 (GRCm39) |
M587K |
possibly damaging |
Het |
Tmcc1 |
C |
T |
6: 116,020,019 (GRCm39) |
V118M |
probably benign |
Het |
Tnfsf11 |
T |
A |
14: 78,516,362 (GRCm39) |
N202I |
probably damaging |
Het |
Togaram2 |
T |
C |
17: 72,023,360 (GRCm39) |
S759P |
probably benign |
Het |
Ttc7b |
G |
A |
12: 100,291,948 (GRCm39) |
A208V |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,338 (GRCm39) |
|
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,905,118 (GRCm39) |
|
probably null |
Het |
Zfyve26 |
T |
C |
12: 79,330,806 (GRCm39) |
|
probably null |
Het |
Zfyve28 |
T |
C |
5: 34,391,681 (GRCm39) |
M157V |
probably null |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
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 |
IGL02707:Htt
|
APN |
5 |
34,987,225 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|