Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,884,067 (GRCm39) |
F597S |
probably benign |
Het |
Aasdh |
C |
A |
5: 77,036,501 (GRCm39) |
E347* |
probably null |
Het |
Abca16 |
G |
T |
7: 120,126,309 (GRCm39) |
C1155F |
probably damaging |
Het |
Adam26a |
T |
C |
8: 44,021,918 (GRCm39) |
D524G |
probably damaging |
Het |
Adamts20 |
G |
C |
15: 94,277,656 (GRCm39) |
H269D |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,100,145 (GRCm39) |
|
probably null |
Het |
Akt3 |
T |
C |
1: 176,877,693 (GRCm39) |
I358M |
possibly damaging |
Het |
Aldh9a1 |
G |
T |
1: 167,189,376 (GRCm39) |
A375S |
probably damaging |
Het |
Alg2 |
A |
G |
4: 47,473,974 (GRCm39) |
S105P |
probably benign |
Het |
Amph |
A |
G |
13: 19,288,515 (GRCm39) |
T335A |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,756,050 (GRCm39) |
V1056M |
probably damaging |
Het |
Apoh |
A |
G |
11: 108,298,204 (GRCm39) |
D168G |
probably benign |
Het |
Arfgef3 |
C |
T |
10: 18,465,454 (GRCm39) |
A2130T |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,230,897 (GRCm39) |
D218G |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,699,894 (GRCm39) |
P1906S |
probably damaging |
Het |
Atp11b |
T |
G |
3: 35,861,157 (GRCm39) |
|
probably null |
Het |
B4galnt2 |
A |
G |
11: 95,759,255 (GRCm39) |
V343A |
probably damaging |
Het |
Barhl1 |
T |
C |
2: 28,799,785 (GRCm39) |
Y280C |
probably damaging |
Het |
Bcar1 |
A |
T |
8: 112,447,669 (GRCm39) |
Y103N |
probably damaging |
Het |
Bid |
A |
G |
6: 120,872,707 (GRCm39) |
I150T |
probably benign |
Het |
Ccdc171 |
T |
C |
4: 83,467,876 (GRCm39) |
S74P |
probably damaging |
Het |
Ccni |
A |
T |
5: 93,336,113 (GRCm39) |
|
probably null |
Het |
Cct8l1 |
A |
G |
5: 25,721,891 (GRCm39) |
E202G |
probably benign |
Het |
Cd200r3 |
A |
G |
16: 44,774,622 (GRCm39) |
K212E |
probably benign |
Het |
Cdh19 |
A |
G |
1: 110,817,694 (GRCm39) |
S683P |
probably damaging |
Het |
Ces2b |
A |
T |
8: 105,559,413 (GRCm39) |
H93L |
probably benign |
Het |
Cimip2b |
T |
A |
4: 43,427,514 (GRCm39) |
Q270L |
possibly damaging |
Het |
Clec4a1 |
G |
A |
6: 122,907,654 (GRCm39) |
C114Y |
probably damaging |
Het |
Dcc |
G |
T |
18: 71,675,320 (GRCm39) |
S636* |
probably null |
Het |
Dcdc2c |
T |
C |
12: 28,580,472 (GRCm39) |
D187G |
possibly damaging |
Het |
Dgkb |
G |
T |
12: 38,164,657 (GRCm39) |
E150* |
probably null |
Het |
Dhx30 |
A |
G |
9: 109,915,029 (GRCm39) |
L884P |
probably damaging |
Het |
Dmwd |
T |
G |
7: 18,815,228 (GRCm39) |
|
probably null |
Het |
Dnm2 |
G |
A |
9: 21,392,633 (GRCm39) |
S447N |
probably benign |
Het |
Elk4 |
G |
A |
1: 131,945,419 (GRCm39) |
G99D |
probably damaging |
Het |
Entpd1 |
A |
T |
19: 40,727,965 (GRCm39) |
|
probably benign |
Het |
Fam114a1 |
T |
A |
5: 65,137,070 (GRCm39) |
D4E |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,241,681 (GRCm39) |
D754G |
probably damaging |
Het |
Fhip2a |
T |
C |
19: 57,367,069 (GRCm39) |
V204A |
probably benign |
Het |
Foxred2 |
T |
C |
15: 77,840,035 (GRCm39) |
N85S |
probably damaging |
Het |
Fut9 |
A |
G |
4: 25,799,591 (GRCm39) |
|
probably benign |
Het |
Gm1818 |
G |
A |
12: 48,606,607 (GRCm39) |
|
noncoding transcript |
Het |
Gm4894 |
C |
A |
9: 49,190,000 (GRCm39) |
Q92K |
unknown |
Het |
Gpx2 |
T |
C |
12: 76,839,574 (GRCm39) |
I141M |
probably benign |
Het |
Gusb |
T |
C |
5: 130,024,326 (GRCm39) |
T476A |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,667 (GRCm39) |
T180I |
possibly damaging |
Het |
Itgbl1 |
T |
C |
14: 124,210,780 (GRCm39) |
Y493H |
probably benign |
Het |
Klhdc9 |
G |
T |
1: 171,187,951 (GRCm39) |
C93* |
probably null |
Het |
Ldaf1 |
T |
C |
7: 119,715,535 (GRCm39) |
S120P |
probably damaging |
Het |
Lpar3 |
A |
G |
3: 145,990,506 (GRCm39) |
K275E |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,692,897 (GRCm39) |
|
probably null |
Het |
Lrrc63 |
C |
T |
14: 75,322,389 (GRCm39) |
G572S |
probably damaging |
Het |
Mapk11 |
A |
T |
15: 89,030,685 (GRCm39) |
D98E |
probably benign |
Het |
Mgat4f |
T |
A |
1: 134,317,714 (GRCm39) |
M162K |
probably benign |
Het |
Net1 |
G |
A |
13: 3,934,905 (GRCm39) |
R374W |
probably damaging |
Het |
Nlrp4g |
T |
A |
9: 124,354,005 (GRCm38) |
|
noncoding transcript |
Het |
Nrap |
T |
A |
19: 56,335,652 (GRCm39) |
Y923F |
probably damaging |
Het |
Or13a20 |
T |
A |
7: 140,232,534 (GRCm39) |
M214K |
probably benign |
Het |
Or4c108 |
T |
A |
2: 88,803,834 (GRCm39) |
I134F |
probably damaging |
Het |
Or6c215 |
A |
T |
10: 129,637,932 (GRCm39) |
V154E |
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,677,335 (GRCm39) |
V964A |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,262,498 (GRCm39) |
I731V |
probably benign |
Het |
Polq |
T |
A |
16: 36,848,274 (GRCm39) |
S294T |
probably benign |
Het |
Pomgnt2 |
T |
C |
9: 121,811,620 (GRCm39) |
D387G |
probably benign |
Het |
Pramel25 |
T |
C |
4: 143,520,407 (GRCm39) |
V53A |
possibly damaging |
Het |
Prmt2 |
G |
A |
10: 76,056,842 (GRCm39) |
T227I |
probably damaging |
Het |
Psmd1 |
T |
A |
1: 86,010,947 (GRCm39) |
F341I |
probably damaging |
Het |
Ptpn23 |
T |
C |
9: 110,221,806 (GRCm39) |
M127V |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,017,238 (GRCm39) |
F483L |
probably damaging |
Het |
Rab35 |
A |
C |
5: 115,778,147 (GRCm39) |
I38L |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,548,143 (GRCm39) |
T486A |
probably damaging |
Het |
Rgl3 |
A |
T |
9: 21,899,004 (GRCm39) |
C68* |
probably null |
Het |
Rilpl1 |
T |
C |
5: 124,653,594 (GRCm39) |
E189G |
possibly damaging |
Het |
Rnf217 |
T |
C |
10: 31,393,520 (GRCm39) |
I354V |
probably benign |
Het |
Rspo3 |
T |
C |
10: 29,382,524 (GRCm39) |
D50G |
probably damaging |
Het |
Sbno1 |
A |
G |
5: 124,512,672 (GRCm39) |
S1366P |
possibly damaging |
Het |
Sema3c |
A |
G |
5: 17,899,684 (GRCm39) |
D392G |
probably benign |
Het |
Serpinb9e |
A |
T |
13: 33,436,935 (GRCm39) |
Y85F |
probably benign |
Het |
Shprh |
C |
T |
10: 11,032,863 (GRCm39) |
T283I |
probably benign |
Het |
Sipa1l1 |
T |
C |
12: 82,388,103 (GRCm39) |
S110P |
probably benign |
Het |
Slc16a12 |
T |
A |
19: 34,652,643 (GRCm39) |
I168F |
probably damaging |
Het |
Slc23a3 |
A |
G |
1: 75,109,268 (GRCm39) |
S221P |
probably damaging |
Het |
Slc35b3 |
A |
T |
13: 39,116,887 (GRCm39) |
I366K |
possibly damaging |
Het |
Slc44a5 |
T |
C |
3: 153,949,252 (GRCm39) |
|
probably null |
Het |
Slc5a12 |
A |
T |
2: 110,450,753 (GRCm39) |
D316V |
probably damaging |
Het |
Ssr3 |
A |
G |
3: 65,299,874 (GRCm39) |
S29P |
probably damaging |
Het |
Taf2 |
G |
A |
15: 54,890,619 (GRCm39) |
Q1055* |
probably null |
Het |
Them6 |
A |
T |
15: 74,593,367 (GRCm39) |
D75V |
probably damaging |
Het |
Tom1l2 |
A |
G |
11: 60,149,744 (GRCm39) |
S239P |
probably damaging |
Het |
Tspear |
A |
G |
10: 77,710,877 (GRCm39) |
T500A |
probably damaging |
Het |
Tubgcp6 |
G |
A |
15: 88,985,752 (GRCm39) |
A1487V |
probably damaging |
Het |
Uba7 |
G |
A |
9: 107,856,190 (GRCm39) |
V522I |
possibly damaging |
Het |
Virma |
C |
A |
4: 11,521,147 (GRCm39) |
C901* |
probably null |
Het |
Vmn1r172 |
A |
T |
7: 23,359,312 (GRCm39) |
I66F |
possibly damaging |
Het |
Vmn2r82 |
A |
T |
10: 79,215,010 (GRCm39) |
Y331F |
probably benign |
Het |
Wdr55 |
G |
A |
18: 36,895,451 (GRCm39) |
V143I |
probably benign |
Het |
Zbtb49 |
A |
T |
5: 38,371,307 (GRCm39) |
D191E |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,307,071 (GRCm39) |
H99R |
probably damaging |
Het |
Zfp1005 |
C |
T |
2: 150,110,680 (GRCm39) |
H457Y |
unknown |
Het |
Zfp560 |
C |
T |
9: 20,259,263 (GRCm39) |
C533Y |
probably damaging |
Het |
Zfp646 |
C |
T |
7: 127,478,354 (GRCm39) |
A177V |
probably benign |
Het |
Zfp653 |
C |
T |
9: 21,967,074 (GRCm39) |
E604K |
probably damaging |
Het |
|
Other mutations in Dnah17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Dnah17
|
APN |
11 |
117,979,040 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00531:Dnah17
|
APN |
11 |
117,933,999 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00764:Dnah17
|
APN |
11 |
117,987,311 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00795:Dnah17
|
APN |
11 |
117,984,460 (GRCm39) |
missense |
probably benign |
0.35 |
IGL00823:Dnah17
|
APN |
11 |
117,937,987 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01145:Dnah17
|
APN |
11 |
117,937,999 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01433:Dnah17
|
APN |
11 |
117,940,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01454:Dnah17
|
APN |
11 |
117,949,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01545:Dnah17
|
APN |
11 |
118,010,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Dnah17
|
APN |
11 |
117,989,438 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01557:Dnah17
|
APN |
11 |
117,964,512 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01632:Dnah17
|
APN |
11 |
117,924,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01636:Dnah17
|
APN |
11 |
117,931,882 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01672:Dnah17
|
APN |
11 |
117,932,986 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01822:Dnah17
|
APN |
11 |
117,972,819 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01869:Dnah17
|
APN |
11 |
117,943,502 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01916:Dnah17
|
APN |
11 |
118,016,114 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02131:Dnah17
|
APN |
11 |
117,963,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02154:Dnah17
|
APN |
11 |
118,015,087 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02220:Dnah17
|
APN |
11 |
117,963,793 (GRCm39) |
nonsense |
probably null |
|
IGL02454:Dnah17
|
APN |
11 |
117,971,593 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02458:Dnah17
|
APN |
11 |
117,927,176 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02588:Dnah17
|
APN |
11 |
117,916,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02865:Dnah17
|
APN |
11 |
117,964,374 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02881:Dnah17
|
APN |
11 |
117,932,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02952:Dnah17
|
APN |
11 |
117,979,094 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03382:Dnah17
|
APN |
11 |
117,972,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Dnah17
|
APN |
11 |
117,985,805 (GRCm39) |
missense |
probably damaging |
1.00 |
ergos
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
watt
|
UTSW |
11 |
117,971,592 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4280001:Dnah17
|
UTSW |
11 |
117,989,408 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0004:Dnah17
|
UTSW |
11 |
117,950,918 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0112:Dnah17
|
UTSW |
11 |
117,965,260 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0116:Dnah17
|
UTSW |
11 |
117,949,132 (GRCm39) |
missense |
probably benign |
0.01 |
R0157:Dnah17
|
UTSW |
11 |
118,017,997 (GRCm39) |
missense |
probably benign |
|
R0320:Dnah17
|
UTSW |
11 |
117,943,500 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0362:Dnah17
|
UTSW |
11 |
117,989,365 (GRCm39) |
missense |
probably benign |
0.10 |
R0382:Dnah17
|
UTSW |
11 |
118,019,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Dnah17
|
UTSW |
11 |
117,958,373 (GRCm39) |
missense |
probably benign |
|
R0400:Dnah17
|
UTSW |
11 |
117,972,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Dnah17
|
UTSW |
11 |
117,930,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Dnah17
|
UTSW |
11 |
117,937,950 (GRCm39) |
missense |
probably benign |
|
R0533:Dnah17
|
UTSW |
11 |
118,001,363 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0562:Dnah17
|
UTSW |
11 |
117,963,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R0564:Dnah17
|
UTSW |
11 |
117,973,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R0604:Dnah17
|
UTSW |
11 |
118,012,297 (GRCm39) |
missense |
probably benign |
0.00 |
R0608:Dnah17
|
UTSW |
11 |
117,981,575 (GRCm39) |
nonsense |
probably null |
|
R0614:Dnah17
|
UTSW |
11 |
117,961,394 (GRCm39) |
splice site |
probably benign |
|
R0632:Dnah17
|
UTSW |
11 |
117,958,508 (GRCm39) |
splice site |
probably benign |
|
R0831:Dnah17
|
UTSW |
11 |
117,951,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R0838:Dnah17
|
UTSW |
11 |
117,950,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0879:Dnah17
|
UTSW |
11 |
117,947,661 (GRCm39) |
splice site |
probably benign |
|
R1061:Dnah17
|
UTSW |
11 |
117,943,514 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1190:Dnah17
|
UTSW |
11 |
117,933,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1293:Dnah17
|
UTSW |
11 |
118,017,963 (GRCm39) |
critical splice donor site |
probably null |
|
R1297:Dnah17
|
UTSW |
11 |
118,012,192 (GRCm39) |
splice site |
probably benign |
|
R1332:Dnah17
|
UTSW |
11 |
117,934,041 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1336:Dnah17
|
UTSW |
11 |
117,934,041 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1364:Dnah17
|
UTSW |
11 |
118,016,432 (GRCm39) |
splice site |
probably benign |
|
R1418:Dnah17
|
UTSW |
11 |
117,964,849 (GRCm39) |
missense |
probably damaging |
0.98 |
R1432:Dnah17
|
UTSW |
11 |
117,914,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Dnah17
|
UTSW |
11 |
118,005,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1500:Dnah17
|
UTSW |
11 |
117,991,879 (GRCm39) |
missense |
probably benign |
|
R1506:Dnah17
|
UTSW |
11 |
118,016,213 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1512:Dnah17
|
UTSW |
11 |
117,985,841 (GRCm39) |
missense |
probably benign |
|
R1567:Dnah17
|
UTSW |
11 |
118,016,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Dnah17
|
UTSW |
11 |
117,994,324 (GRCm39) |
splice site |
probably benign |
|
R1665:Dnah17
|
UTSW |
11 |
118,012,321 (GRCm39) |
splice site |
probably benign |
|
R1703:Dnah17
|
UTSW |
11 |
117,917,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Dnah17
|
UTSW |
11 |
117,923,424 (GRCm39) |
missense |
probably benign |
0.00 |
R1727:Dnah17
|
UTSW |
11 |
117,987,362 (GRCm39) |
nonsense |
probably null |
|
R1727:Dnah17
|
UTSW |
11 |
117,961,315 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Dnah17
|
UTSW |
11 |
117,960,345 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1784:Dnah17
|
UTSW |
11 |
117,960,345 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1852:Dnah17
|
UTSW |
11 |
118,012,742 (GRCm39) |
missense |
probably damaging |
0.97 |
R1869:Dnah17
|
UTSW |
11 |
117,938,015 (GRCm39) |
nonsense |
probably null |
|
R1886:Dnah17
|
UTSW |
11 |
117,998,987 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1893:Dnah17
|
UTSW |
11 |
117,957,794 (GRCm39) |
missense |
probably benign |
0.00 |
R1954:Dnah17
|
UTSW |
11 |
117,915,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Dnah17
|
UTSW |
11 |
117,995,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1971:Dnah17
|
UTSW |
11 |
117,995,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1975:Dnah17
|
UTSW |
11 |
117,987,362 (GRCm39) |
nonsense |
probably null |
|
R1977:Dnah17
|
UTSW |
11 |
118,003,417 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2055:Dnah17
|
UTSW |
11 |
117,958,357 (GRCm39) |
missense |
probably benign |
0.00 |
R2115:Dnah17
|
UTSW |
11 |
118,010,628 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Dnah17
|
UTSW |
11 |
117,924,573 (GRCm39) |
missense |
probably damaging |
0.98 |
R2200:Dnah17
|
UTSW |
11 |
117,993,235 (GRCm39) |
splice site |
probably benign |
|
R2277:Dnah17
|
UTSW |
11 |
117,987,387 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2279:Dnah17
|
UTSW |
11 |
117,987,387 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2400:Dnah17
|
UTSW |
11 |
118,017,210 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2402:Dnah17
|
UTSW |
11 |
118,016,800 (GRCm39) |
missense |
probably benign |
0.10 |
R2497:Dnah17
|
UTSW |
11 |
117,977,850 (GRCm39) |
splice site |
probably null |
|
R2923:Dnah17
|
UTSW |
11 |
117,984,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R3121:Dnah17
|
UTSW |
11 |
117,931,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Dnah17
|
UTSW |
11 |
117,985,680 (GRCm39) |
missense |
probably benign |
0.08 |
R3237:Dnah17
|
UTSW |
11 |
117,985,680 (GRCm39) |
missense |
probably benign |
0.08 |
R3498:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3499:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3746:Dnah17
|
UTSW |
11 |
117,973,742 (GRCm39) |
missense |
probably benign |
0.00 |
R3749:Dnah17
|
UTSW |
11 |
117,973,742 (GRCm39) |
missense |
probably benign |
0.00 |
R3762:Dnah17
|
UTSW |
11 |
117,995,352 (GRCm39) |
missense |
probably benign |
0.00 |
R3826:Dnah17
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
R3828:Dnah17
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
R3829:Dnah17
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
R3877:Dnah17
|
UTSW |
11 |
117,915,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Dnah17
|
UTSW |
11 |
117,985,634 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3900:Dnah17
|
UTSW |
11 |
117,985,634 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3911:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3913:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3930:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3931:Dnah17
|
UTSW |
11 |
117,971,675 (GRCm39) |
splice site |
probably benign |
|
R3969:Dnah17
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
R3970:Dnah17
|
UTSW |
11 |
117,931,984 (GRCm39) |
splice site |
probably benign |
|
R4056:Dnah17
|
UTSW |
11 |
117,961,364 (GRCm39) |
missense |
probably benign |
0.05 |
R4113:Dnah17
|
UTSW |
11 |
118,003,420 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4295:Dnah17
|
UTSW |
11 |
118,009,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R4324:Dnah17
|
UTSW |
11 |
117,985,039 (GRCm39) |
missense |
probably benign |
0.01 |
R4412:Dnah17
|
UTSW |
11 |
117,964,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4413:Dnah17
|
UTSW |
11 |
117,915,994 (GRCm39) |
missense |
probably benign |
0.00 |
R4422:Dnah17
|
UTSW |
11 |
117,972,799 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4552:Dnah17
|
UTSW |
11 |
117,943,769 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4669:Dnah17
|
UTSW |
11 |
117,965,119 (GRCm39) |
missense |
probably benign |
0.02 |
R4677:Dnah17
|
UTSW |
11 |
118,010,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dnah17
|
UTSW |
11 |
117,964,474 (GRCm39) |
missense |
probably benign |
0.02 |
R4832:Dnah17
|
UTSW |
11 |
117,917,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R4868:Dnah17
|
UTSW |
11 |
117,999,038 (GRCm39) |
missense |
probably benign |
0.03 |
R4897:Dnah17
|
UTSW |
11 |
117,969,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Dnah17
|
UTSW |
11 |
117,918,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Dnah17
|
UTSW |
11 |
117,965,124 (GRCm39) |
missense |
probably benign |
0.44 |
R5008:Dnah17
|
UTSW |
11 |
118,001,403 (GRCm39) |
missense |
probably benign |
0.01 |
R5016:Dnah17
|
UTSW |
11 |
117,971,592 (GRCm39) |
missense |
probably damaging |
0.96 |
R5027:Dnah17
|
UTSW |
11 |
117,993,365 (GRCm39) |
missense |
probably benign |
0.01 |
R5133:Dnah17
|
UTSW |
11 |
118,007,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5140:Dnah17
|
UTSW |
11 |
117,977,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R5146:Dnah17
|
UTSW |
11 |
118,005,005 (GRCm39) |
missense |
probably damaging |
0.99 |
R5151:Dnah17
|
UTSW |
11 |
117,918,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Dnah17
|
UTSW |
11 |
117,973,800 (GRCm39) |
nonsense |
probably null |
|
R5192:Dnah17
|
UTSW |
11 |
117,925,185 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5315:Dnah17
|
UTSW |
11 |
118,018,109 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5317:Dnah17
|
UTSW |
11 |
118,018,109 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5335:Dnah17
|
UTSW |
11 |
118,003,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R5379:Dnah17
|
UTSW |
11 |
118,008,029 (GRCm39) |
intron |
probably benign |
|
R5396:Dnah17
|
UTSW |
11 |
118,018,108 (GRCm39) |
missense |
probably benign |
|
R5418:Dnah17
|
UTSW |
11 |
117,985,810 (GRCm39) |
missense |
probably benign |
0.04 |
R5534:Dnah17
|
UTSW |
11 |
117,943,596 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5539:Dnah17
|
UTSW |
11 |
117,964,486 (GRCm39) |
missense |
probably benign |
0.03 |
R5594:Dnah17
|
UTSW |
11 |
117,934,055 (GRCm39) |
splice site |
probably null |
|
R5634:Dnah17
|
UTSW |
11 |
117,943,752 (GRCm39) |
splice site |
probably null |
|
R5696:Dnah17
|
UTSW |
11 |
117,991,882 (GRCm39) |
missense |
probably benign |
0.44 |
R5802:Dnah17
|
UTSW |
11 |
117,927,272 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5826:Dnah17
|
UTSW |
11 |
117,925,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R5873:Dnah17
|
UTSW |
11 |
117,947,723 (GRCm39) |
missense |
probably benign |
0.01 |
R5898:Dnah17
|
UTSW |
11 |
118,005,039 (GRCm39) |
missense |
probably benign |
0.00 |
R5934:Dnah17
|
UTSW |
11 |
117,931,928 (GRCm39) |
missense |
probably benign |
|
R6030:Dnah17
|
UTSW |
11 |
117,916,375 (GRCm39) |
missense |
probably benign |
0.32 |
R6030:Dnah17
|
UTSW |
11 |
117,916,375 (GRCm39) |
missense |
probably benign |
0.32 |
R6038:Dnah17
|
UTSW |
11 |
117,946,715 (GRCm39) |
missense |
probably benign |
0.00 |
R6038:Dnah17
|
UTSW |
11 |
117,946,715 (GRCm39) |
missense |
probably benign |
0.00 |
R6113:Dnah17
|
UTSW |
11 |
118,017,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6117:Dnah17
|
UTSW |
11 |
118,010,397 (GRCm39) |
missense |
probably benign |
0.00 |
R6137:Dnah17
|
UTSW |
11 |
117,916,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6173:Dnah17
|
UTSW |
11 |
117,930,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Dnah17
|
UTSW |
11 |
118,017,149 (GRCm39) |
nonsense |
probably null |
|
R6258:Dnah17
|
UTSW |
11 |
118,017,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Dnah17
|
UTSW |
11 |
118,017,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Dnah17
|
UTSW |
11 |
118,017,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Dnah17
|
UTSW |
11 |
118,017,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Dnah17
|
UTSW |
11 |
118,017,149 (GRCm39) |
nonsense |
probably null |
|
R6278:Dnah17
|
UTSW |
11 |
118,017,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R6298:Dnah17
|
UTSW |
11 |
117,998,987 (GRCm39) |
missense |
probably benign |
0.00 |
R6300:Dnah17
|
UTSW |
11 |
117,925,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Dnah17
|
UTSW |
11 |
118,019,981 (GRCm39) |
missense |
probably benign |
0.09 |
R6363:Dnah17
|
UTSW |
11 |
118,001,331 (GRCm39) |
missense |
probably benign |
|
R6381:Dnah17
|
UTSW |
11 |
118,020,011 (GRCm39) |
missense |
probably benign |
0.08 |
R6418:Dnah17
|
UTSW |
11 |
118,020,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R6660:Dnah17
|
UTSW |
11 |
117,991,014 (GRCm39) |
missense |
probably benign |
|
R6803:Dnah17
|
UTSW |
11 |
118,016,198 (GRCm39) |
missense |
probably benign |
0.00 |
R6820:Dnah17
|
UTSW |
11 |
117,959,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R6885:Dnah17
|
UTSW |
11 |
117,981,598 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6921:Dnah17
|
UTSW |
11 |
117,932,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R6932:Dnah17
|
UTSW |
11 |
117,950,905 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6954:Dnah17
|
UTSW |
11 |
117,957,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:Dnah17
|
UTSW |
11 |
117,916,528 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7007:Dnah17
|
UTSW |
11 |
118,009,697 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7048:Dnah17
|
UTSW |
11 |
117,936,944 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7056:Dnah17
|
UTSW |
11 |
118,016,212 (GRCm39) |
missense |
probably benign |
|
R7131:Dnah17
|
UTSW |
11 |
117,970,484 (GRCm39) |
missense |
probably benign |
0.14 |
R7143:Dnah17
|
UTSW |
11 |
117,976,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7146:Dnah17
|
UTSW |
11 |
117,972,936 (GRCm39) |
missense |
probably damaging |
0.98 |
R7147:Dnah17
|
UTSW |
11 |
117,985,755 (GRCm39) |
missense |
probably benign |
0.31 |
R7172:Dnah17
|
UTSW |
11 |
117,931,957 (GRCm39) |
nonsense |
probably null |
|
R7183:Dnah17
|
UTSW |
11 |
118,020,014 (GRCm39) |
missense |
probably benign |
|
R7297:Dnah17
|
UTSW |
11 |
117,994,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R7297:Dnah17
|
UTSW |
11 |
117,946,556 (GRCm39) |
critical splice donor site |
probably null |
|
R7367:Dnah17
|
UTSW |
11 |
118,006,022 (GRCm39) |
missense |
probably benign |
|
R7398:Dnah17
|
UTSW |
11 |
117,971,550 (GRCm39) |
missense |
probably damaging |
0.96 |
R7426:Dnah17
|
UTSW |
11 |
117,981,543 (GRCm39) |
missense |
probably null |
0.79 |
R7524:Dnah17
|
UTSW |
11 |
118,012,307 (GRCm39) |
missense |
probably benign |
0.03 |
R7529:Dnah17
|
UTSW |
11 |
117,940,692 (GRCm39) |
critical splice donor site |
probably null |
|
R7615:Dnah17
|
UTSW |
11 |
118,001,373 (GRCm39) |
nonsense |
probably null |
|
R7681:Dnah17
|
UTSW |
11 |
117,916,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R7702:Dnah17
|
UTSW |
11 |
118,012,304 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7702:Dnah17
|
UTSW |
11 |
117,916,466 (GRCm39) |
missense |
probably benign |
0.00 |
R7713:Dnah17
|
UTSW |
11 |
117,915,997 (GRCm39) |
missense |
probably benign |
0.02 |
R7809:Dnah17
|
UTSW |
11 |
117,995,462 (GRCm39) |
missense |
probably benign |
0.09 |
R7842:Dnah17
|
UTSW |
11 |
117,970,508 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7935:Dnah17
|
UTSW |
11 |
118,018,048 (GRCm39) |
missense |
probably benign |
0.20 |
R7951:Dnah17
|
UTSW |
11 |
118,009,592 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8070:Dnah17
|
UTSW |
11 |
117,915,497 (GRCm39) |
missense |
probably damaging |
0.97 |
R8098:Dnah17
|
UTSW |
11 |
117,941,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8101:Dnah17
|
UTSW |
11 |
118,016,744 (GRCm39) |
missense |
probably benign |
|
R8177:Dnah17
|
UTSW |
11 |
118,019,753 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8343:Dnah17
|
UTSW |
11 |
118,005,021 (GRCm39) |
missense |
probably benign |
|
R8350:Dnah17
|
UTSW |
11 |
117,977,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R8393:Dnah17
|
UTSW |
11 |
117,947,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8401:Dnah17
|
UTSW |
11 |
117,915,485 (GRCm39) |
missense |
probably damaging |
0.96 |
R8418:Dnah17
|
UTSW |
11 |
117,994,284 (GRCm39) |
missense |
probably benign |
0.01 |
R8450:Dnah17
|
UTSW |
11 |
117,977,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R8546:Dnah17
|
UTSW |
11 |
118,015,101 (GRCm39) |
missense |
probably benign |
0.00 |
R8697:Dnah17
|
UTSW |
11 |
117,976,985 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8710:Dnah17
|
UTSW |
11 |
117,932,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Dnah17
|
UTSW |
11 |
117,979,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Dnah17
|
UTSW |
11 |
117,961,283 (GRCm39) |
nonsense |
probably null |
|
R8797:Dnah17
|
UTSW |
11 |
117,992,201 (GRCm39) |
missense |
probably benign |
0.00 |
R8953:Dnah17
|
UTSW |
11 |
118,016,238 (GRCm39) |
splice site |
probably benign |
|
R8965:Dnah17
|
UTSW |
11 |
117,915,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Dnah17
|
UTSW |
11 |
117,917,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R9090:Dnah17
|
UTSW |
11 |
117,931,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R9128:Dnah17
|
UTSW |
11 |
117,937,004 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9134:Dnah17
|
UTSW |
11 |
117,978,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Dnah17
|
UTSW |
11 |
118,016,503 (GRCm39) |
missense |
probably benign |
0.02 |
R9251:Dnah17
|
UTSW |
11 |
118,012,618 (GRCm39) |
missense |
probably benign |
0.03 |
R9271:Dnah17
|
UTSW |
11 |
117,931,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Dnah17
|
UTSW |
11 |
118,012,212 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9367:Dnah17
|
UTSW |
11 |
117,987,464 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9381:Dnah17
|
UTSW |
11 |
117,914,219 (GRCm39) |
missense |
probably benign |
|
R9405:Dnah17
|
UTSW |
11 |
118,009,737 (GRCm39) |
missense |
probably benign |
|
R9449:Dnah17
|
UTSW |
11 |
117,987,452 (GRCm39) |
missense |
probably benign |
0.07 |
R9517:Dnah17
|
UTSW |
11 |
117,915,440 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9588:Dnah17
|
UTSW |
11 |
118,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
R9629:Dnah17
|
UTSW |
11 |
117,979,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R9654:Dnah17
|
UTSW |
11 |
117,927,156 (GRCm39) |
critical splice donor site |
probably null |
|
R9655:Dnah17
|
UTSW |
11 |
117,971,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9662:Dnah17
|
UTSW |
11 |
117,925,166 (GRCm39) |
missense |
probably damaging |
0.97 |
R9686:Dnah17
|
UTSW |
11 |
117,979,048 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9689:Dnah17
|
UTSW |
11 |
117,963,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R9706:Dnah17
|
UTSW |
11 |
118,017,026 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Dnah17
|
UTSW |
11 |
117,973,751 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah17
|
UTSW |
11 |
118,017,992 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dnah17
|
UTSW |
11 |
117,977,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah17
|
UTSW |
11 |
117,969,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Dnah17
|
UTSW |
11 |
118,017,968 (GRCm39) |
nonsense |
probably null |
|
|