Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406C07Rik |
A |
T |
9: 15,202,066 (GRCm39) |
V152E |
probably damaging |
Het |
Abca5 |
T |
G |
11: 110,167,331 (GRCm39) |
E1495A |
probably damaging |
Het |
Abcc12 |
G |
A |
8: 87,261,627 (GRCm39) |
S668F |
probably benign |
Het |
Adgrl4 |
A |
T |
3: 151,223,247 (GRCm39) |
T608S |
probably benign |
Het |
Angel2 |
G |
A |
1: 190,673,187 (GRCm39) |
D255N |
probably benign |
Het |
Apob |
T |
A |
12: 8,039,113 (GRCm39) |
|
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,715,603 (GRCm39) |
R1349S |
probably damaging |
Het |
Atp2b2 |
C |
T |
6: 113,770,656 (GRCm39) |
V418I |
probably damaging |
Het |
Birc6 |
C |
A |
17: 74,930,741 (GRCm39) |
|
probably benign |
Het |
Capn13 |
T |
A |
17: 73,658,519 (GRCm39) |
Y183F |
probably damaging |
Het |
Cngb1 |
A |
G |
8: 95,987,266 (GRCm39) |
S352P |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,741,273 (GRCm39) |
S720P |
probably damaging |
Het |
Cpa4 |
C |
T |
6: 30,579,657 (GRCm39) |
R155W |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,908,914 (GRCm39) |
I1176V |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,252,520 (GRCm39) |
I1734N |
possibly damaging |
Het |
Dnajb7 |
A |
G |
15: 81,291,555 (GRCm39) |
Y261H |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,579,392 (GRCm39) |
|
probably benign |
Het |
Dyrk3 |
A |
T |
1: 131,057,576 (GRCm39) |
V199E |
probably damaging |
Het |
F2r |
G |
T |
13: 95,740,994 (GRCm39) |
C180* |
probably null |
Het |
F5 |
A |
G |
1: 164,012,483 (GRCm39) |
S466G |
probably benign |
Het |
Fbn2 |
A |
T |
18: 58,235,445 (GRCm39) |
C677* |
probably null |
Het |
Fbxo41 |
A |
G |
6: 85,454,890 (GRCm39) |
S673P |
probably damaging |
Het |
Fhad1 |
G |
T |
4: 141,667,406 (GRCm39) |
H639N |
probably benign |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Foxa2 |
A |
G |
2: 147,885,481 (GRCm39) |
S270P |
probably damaging |
Het |
Fxyd7 |
C |
T |
7: 30,746,793 (GRCm39) |
|
probably null |
Het |
Gm5225 |
A |
G |
17: 24,243,032 (GRCm39) |
D67G |
probably benign |
Het |
Grik3 |
G |
A |
4: 125,564,349 (GRCm39) |
E444K |
probably benign |
Het |
Gsdma2 |
A |
G |
11: 98,540,009 (GRCm39) |
K44E |
probably damaging |
Het |
Haus1 |
T |
A |
18: 77,849,770 (GRCm39) |
K130* |
probably null |
Het |
Heg1 |
A |
G |
16: 33,556,028 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
A |
G |
11: 4,362,206 (GRCm39) |
|
probably benign |
Het |
Hsd17b3 |
G |
A |
13: 64,206,403 (GRCm39) |
R300C |
possibly damaging |
Het |
Irf5 |
T |
C |
6: 29,536,108 (GRCm39) |
F374S |
probably damaging |
Het |
Itch |
A |
G |
2: 155,059,903 (GRCm39) |
|
probably benign |
Het |
Jade2 |
A |
T |
11: 51,722,136 (GRCm39) |
L139Q |
probably damaging |
Het |
Kif5c |
G |
A |
2: 49,642,251 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
C |
17: 68,083,918 (GRCm39) |
Y1387H |
probably benign |
Het |
Larp4b |
A |
G |
13: 9,220,724 (GRCm39) |
R658G |
probably damaging |
Het |
Mcph1 |
C |
T |
8: 18,838,264 (GRCm39) |
L729F |
probably benign |
Het |
Me1 |
A |
T |
9: 86,536,720 (GRCm39) |
N118K |
probably benign |
Het |
Med13 |
A |
G |
11: 86,210,723 (GRCm39) |
L473S |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,635,921 (GRCm39) |
Y359N |
probably damaging |
Het |
Morc2b |
A |
G |
17: 33,356,015 (GRCm39) |
S586P |
probably damaging |
Het |
Mthfr |
A |
G |
4: 148,135,980 (GRCm39) |
D310G |
probably benign |
Het |
Mtmr7 |
A |
T |
8: 41,034,447 (GRCm39) |
|
probably benign |
Het |
Mtus1 |
A |
G |
8: 41,451,514 (GRCm39) |
|
probably benign |
Het |
Mus81 |
G |
T |
19: 5,536,552 (GRCm39) |
A138D |
probably damaging |
Het |
Myom2 |
A |
T |
8: 15,167,633 (GRCm39) |
I1073F |
probably damaging |
Het |
Nhsl1 |
A |
T |
10: 18,400,990 (GRCm39) |
K739* |
probably null |
Het |
Nlrp4d |
T |
A |
7: 10,108,818 (GRCm39) |
K762N |
probably benign |
Het |
Nrap |
T |
C |
19: 56,343,978 (GRCm39) |
Y724C |
probably damaging |
Het |
Ogn |
A |
T |
13: 49,774,514 (GRCm39) |
Y219F |
possibly damaging |
Het |
Or6c212 |
T |
A |
10: 129,558,846 (GRCm39) |
D189V |
probably damaging |
Het |
Or8b56 |
T |
C |
9: 38,739,860 (GRCm39) |
L291P |
probably damaging |
Het |
Or8g30 |
A |
T |
9: 39,230,160 (GRCm39) |
I250N |
probably damaging |
Het |
Padi2 |
T |
C |
4: 140,653,550 (GRCm39) |
V180A |
probably benign |
Het |
Papss2 |
C |
T |
19: 32,615,768 (GRCm39) |
R167* |
probably null |
Het |
Pcbp2 |
T |
C |
15: 102,382,670 (GRCm39) |
|
probably benign |
Het |
Per1 |
T |
A |
11: 68,992,706 (GRCm39) |
|
probably benign |
Het |
Pik3ca |
T |
C |
3: 32,514,094 (GRCm39) |
I860T |
probably damaging |
Het |
Pkdrej |
G |
A |
15: 85,701,746 (GRCm39) |
Q1397* |
probably null |
Het |
Plce1 |
T |
C |
19: 38,710,265 (GRCm39) |
V1133A |
probably benign |
Het |
Pnma8a |
T |
G |
7: 16,694,625 (GRCm39) |
V160G |
probably damaging |
Het |
Prss12 |
T |
C |
3: 123,276,423 (GRCm39) |
C351R |
probably damaging |
Het |
Qprt |
A |
T |
7: 126,708,269 (GRCm39) |
L54Q |
probably damaging |
Het |
Raf1 |
C |
T |
6: 115,603,344 (GRCm39) |
S165N |
probably damaging |
Het |
Rere |
A |
G |
4: 150,701,433 (GRCm39) |
N1271S |
probably benign |
Het |
Rnasel |
T |
A |
1: 153,630,258 (GRCm39) |
L258H |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,724,807 (GRCm39) |
D2502G |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,633,510 (GRCm39) |
S2081L |
probably damaging |
Het |
Sc5d |
G |
T |
9: 42,171,155 (GRCm39) |
Y11* |
probably null |
Het |
Slc25a29 |
A |
C |
12: 108,793,017 (GRCm39) |
L187R |
possibly damaging |
Het |
Slc2a7 |
G |
A |
4: 150,252,721 (GRCm39) |
V454M |
probably benign |
Het |
Slco1b2 |
A |
T |
6: 141,615,114 (GRCm39) |
T340S |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,976,172 (GRCm39) |
N153S |
possibly damaging |
Het |
Snx1 |
C |
A |
9: 65,995,821 (GRCm39) |
E516* |
probably null |
Het |
Sptlc2 |
T |
C |
12: 87,403,454 (GRCm39) |
D115G |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,464,736 (GRCm39) |
N67S |
probably damaging |
Het |
Styxl2 |
A |
C |
1: 165,927,270 (GRCm39) |
S781A |
probably benign |
Het |
Swap70 |
G |
A |
7: 109,872,489 (GRCm39) |
R368H |
probably benign |
Het |
Tcaf3 |
T |
C |
6: 42,568,284 (GRCm39) |
K691E |
probably benign |
Het |
Tmco4 |
T |
C |
4: 138,781,231 (GRCm39) |
F465S |
probably damaging |
Het |
Tmem245 |
A |
G |
4: 56,926,213 (GRCm39) |
S290P |
probably benign |
Het |
Top2a |
T |
C |
11: 98,894,416 (GRCm39) |
T972A |
probably benign |
Het |
Tpr |
T |
A |
1: 150,285,898 (GRCm39) |
S527R |
probably damaging |
Het |
Traf2 |
T |
C |
2: 25,409,621 (GRCm39) |
D443G |
probably damaging |
Het |
Trim40 |
A |
T |
17: 37,194,039 (GRCm39) |
|
probably null |
Het |
Trim42 |
A |
T |
9: 97,245,456 (GRCm39) |
I448N |
possibly damaging |
Het |
Ttll9 |
G |
A |
2: 152,825,054 (GRCm39) |
V78M |
probably damaging |
Het |
Vav1 |
C |
T |
17: 57,603,039 (GRCm39) |
L88F |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,423,301 (GRCm39) |
D207G |
probably damaging |
Het |
Wdsub1 |
A |
G |
2: 59,707,009 (GRCm39) |
|
probably null |
Het |
Zfp799 |
A |
G |
17: 33,040,009 (GRCm39) |
W85R |
possibly damaging |
Het |
Zfp839 |
A |
T |
12: 110,825,203 (GRCm39) |
|
probably benign |
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 |
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 |
R4937:Dnah17
|
UTSW |
11 |
117,932,980 (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 |
|
|