Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310039H08Rik |
T |
C |
17: 47,083,872 (GRCm39) |
V45A |
probably benign |
Het |
4921509C19Rik |
A |
G |
2: 151,313,791 (GRCm39) |
I629T |
unknown |
Het |
4933402N03Rik |
T |
C |
7: 130,740,413 (GRCm39) |
R268G |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,384,193 (GRCm39) |
R3882* |
probably null |
Het |
Adamts3 |
T |
G |
5: 89,850,866 (GRCm39) |
T558P |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,767,304 (GRCm39) |
N214S |
probably benign |
Het |
Arhgef4 |
A |
T |
1: 34,850,866 (GRCm39) |
|
probably null |
Het |
Boc |
C |
T |
16: 44,320,743 (GRCm39) |
A306T |
probably benign |
Het |
Capn10 |
T |
C |
1: 92,871,503 (GRCm39) |
F367S |
probably damaging |
Het |
Ccdc6 |
T |
C |
10: 70,025,086 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
G |
T |
2: 64,929,372 (GRCm39) |
S688R |
possibly damaging |
Het |
Cpxm2 |
G |
T |
7: 131,650,767 (GRCm39) |
P631Q |
possibly damaging |
Het |
Cyp2c68 |
A |
G |
19: 39,687,779 (GRCm39) |
V406A |
possibly damaging |
Het |
Cyp4a30b |
T |
A |
4: 115,312,200 (GRCm39) |
Y118N |
probably damaging |
Het |
Dgki |
A |
T |
6: 37,276,781 (GRCm39) |
|
probably benign |
Het |
Disp2 |
A |
G |
2: 118,623,237 (GRCm39) |
N1323S |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,326,138 (GRCm39) |
Y42* |
probably null |
Het |
Eps8l1 |
C |
A |
7: 4,476,944 (GRCm39) |
P471Q |
probably damaging |
Het |
Fam20a |
A |
C |
11: 109,612,513 (GRCm39) |
L10R |
unknown |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,446 (GRCm39) |
I151K |
probably damaging |
Het |
Gga1 |
C |
A |
15: 78,769,509 (GRCm39) |
P161T |
probably damaging |
Het |
Gm9923 |
T |
A |
10: 72,145,306 (GRCm39) |
Y52* |
probably null |
Het |
Gucy2g |
A |
G |
19: 55,194,688 (GRCm39) |
F910L |
probably damaging |
Het |
H2-T5 |
A |
T |
17: 36,476,750 (GRCm39) |
H241Q |
possibly damaging |
Het |
Helz |
T |
C |
11: 107,539,971 (GRCm39) |
V315A |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,716,629 (GRCm39) |
Y301C |
probably damaging |
Het |
Iah1 |
T |
C |
12: 21,366,434 (GRCm39) |
M1T |
probably null |
Het |
Ik |
T |
C |
18: 36,885,467 (GRCm39) |
S287P |
probably damaging |
Het |
Itga1 |
T |
A |
13: 115,185,906 (GRCm39) |
D32V |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Klk14 |
A |
G |
7: 43,341,392 (GRCm39) |
I15V |
probably benign |
Het |
Kng2 |
T |
C |
16: 22,806,391 (GRCm39) |
I603V |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,080,773 (GRCm39) |
I1267T |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 40,812,316 (GRCm39) |
L2430V |
probably benign |
Het |
Lrrn3 |
T |
G |
12: 41,504,243 (GRCm39) |
K25Q |
possibly damaging |
Het |
Lta4h |
T |
A |
10: 93,304,678 (GRCm39) |
N233K |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,989,023 (GRCm39) |
I53T |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,666,430 (GRCm39) |
F123L |
probably damaging |
Het |
Myh4 |
G |
C |
11: 67,136,637 (GRCm39) |
D472H |
probably damaging |
Het |
Nipa2 |
A |
T |
7: 55,585,574 (GRCm39) |
N121K |
probably benign |
Het |
Nostrin |
C |
T |
2: 69,014,268 (GRCm39) |
T408M |
probably benign |
Het |
Oosp2 |
C |
T |
19: 11,627,017 (GRCm39) |
R102H |
probably damaging |
Het |
Or1j18 |
A |
G |
2: 36,624,686 (GRCm39) |
M118V |
probably damaging |
Het |
Or4k15b |
T |
C |
14: 50,272,287 (GRCm39) |
D191G |
probably damaging |
Het |
Osgin2 |
T |
A |
4: 16,001,946 (GRCm39) |
I202L |
probably benign |
Het |
Pbld2 |
C |
A |
10: 62,893,476 (GRCm39) |
R271S |
probably damaging |
Het |
Pex6 |
C |
T |
17: 47,023,027 (GRCm39) |
T201I |
probably benign |
Het |
Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
Pllp |
T |
A |
8: 95,403,906 (GRCm39) |
D47V |
possibly damaging |
Het |
Plxna2 |
A |
G |
1: 194,444,902 (GRCm39) |
S765G |
probably benign |
Het |
Prkca |
A |
T |
11: 107,852,434 (GRCm39) |
Y100N |
probably damaging |
Het |
Prkg1 |
T |
A |
19: 31,641,579 (GRCm39) |
K35* |
probably null |
Het |
Psmc2 |
A |
G |
5: 22,008,263 (GRCm39) |
D389G |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,951 (GRCm39) |
T2387A |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,005,192 (GRCm39) |
N914S |
probably damaging |
Het |
Ruvbl1 |
C |
A |
6: 88,468,581 (GRCm39) |
T367K |
probably benign |
Het |
Scube2 |
C |
T |
7: 109,409,920 (GRCm39) |
R525H |
probably damaging |
Het |
Sec14l4 |
T |
C |
11: 3,985,200 (GRCm39) |
|
probably null |
Het |
Secisbp2l |
T |
C |
2: 125,587,862 (GRCm39) |
D751G |
probably damaging |
Het |
Setd3 |
T |
C |
12: 108,074,949 (GRCm39) |
D402G |
probably benign |
Het |
Slc15a2 |
T |
A |
16: 36,578,211 (GRCm39) |
K359N |
probably damaging |
Het |
Slc25a21 |
A |
G |
12: 57,243,721 (GRCm39) |
S2P |
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,908,332 (GRCm39) |
H70Q |
probably benign |
Het |
Spef2 |
T |
C |
15: 9,647,576 (GRCm39) |
I944V |
probably benign |
Het |
Spg11 |
A |
G |
2: 121,895,557 (GRCm39) |
F1887S |
probably damaging |
Het |
Sptbn4 |
A |
T |
7: 27,066,160 (GRCm39) |
D649E |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,063,844 (GRCm39) |
E879G |
probably damaging |
Het |
Stx5a |
C |
A |
19: 8,720,725 (GRCm39) |
R121S |
probably damaging |
Het |
Tbcd |
T |
C |
11: 121,384,597 (GRCm39) |
L26P |
probably damaging |
Het |
Tecpr1 |
T |
C |
5: 144,144,255 (GRCm39) |
D649G |
probably benign |
Het |
Tfam |
A |
G |
10: 71,073,677 (GRCm39) |
S32P |
probably benign |
Het |
Tmt1b |
G |
T |
10: 128,796,571 (GRCm39) |
C79* |
probably null |
Het |
Trmt44 |
C |
T |
5: 35,715,387 (GRCm39) |
R642H |
probably benign |
Het |
Trpm3 |
G |
A |
19: 22,965,145 (GRCm39) |
A1547T |
probably benign |
Het |
Ttll6 |
T |
C |
11: 96,044,003 (GRCm39) |
V519A |
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,217,088 (GRCm39) |
F1107L |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,794,919 (GRCm39) |
V677E |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,643,307 (GRCm39) |
L605* |
probably null |
Het |
Utrn |
T |
C |
10: 12,620,984 (GRCm39) |
D229G |
probably damaging |
Het |
Uty |
A |
T |
Y: 1,176,502 (GRCm39) |
L178* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,650,791 (GRCm39) |
D168V |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,646,324 (GRCm39) |
V1476A |
probably damaging |
Het |
Vps13b |
C |
A |
15: 35,879,967 (GRCm39) |
T3014K |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,841,487 (GRCm39) |
H2506Y |
probably benign |
Het |
Vps37c |
T |
C |
19: 10,690,132 (GRCm39) |
V198A |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,259,290 (GRCm39) |
Y1621H |
probably benign |
Het |
Zfp251 |
T |
C |
15: 76,738,607 (GRCm39) |
D162G |
possibly damaging |
Het |
Zfp292 |
T |
C |
4: 34,807,078 (GRCm39) |
T1994A |
probably benign |
Het |
Zfp791 |
A |
G |
8: 85,837,559 (GRCm39) |
Y102H |
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 |
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 |
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 |
|
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 |
|