Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500009L16Rik |
G |
A |
10: 83,595,502 (GRCm39) |
|
probably benign |
Het |
1700048O20Rik |
A |
T |
9: 121,769,769 (GRCm39) |
|
noncoding transcript |
Het |
AA986860 |
A |
G |
1: 130,671,562 (GRCm39) |
R595G |
probably damaging |
Het |
Acrbp |
C |
A |
6: 125,031,759 (GRCm39) |
F353L |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,251,452 (GRCm39) |
Q445L |
probably benign |
Het |
Adgrg5 |
A |
G |
8: 95,660,136 (GRCm39) |
D26G |
possibly damaging |
Het |
Atad2b |
A |
T |
12: 4,995,035 (GRCm39) |
|
probably benign |
Het |
Atg2a |
G |
T |
19: 6,306,631 (GRCm39) |
G1439C |
probably damaging |
Het |
Atg2a |
G |
T |
19: 6,306,632 (GRCm39) |
G1439V |
probably benign |
Het |
B3galt1 |
G |
A |
2: 67,948,932 (GRCm39) |
V216I |
probably benign |
Het |
Bmerb1 |
T |
C |
16: 13,913,803 (GRCm39) |
*113R |
probably null |
Het |
C2cd2 |
A |
G |
16: 97,660,788 (GRCm39) |
|
probably benign |
Het |
Cacna2d1 |
G |
A |
5: 16,564,025 (GRCm39) |
V884M |
probably damaging |
Het |
Cers5 |
C |
A |
15: 99,643,795 (GRCm39) |
C22F |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,924,307 (GRCm39) |
C14F |
probably benign |
Het |
Cntn3 |
G |
T |
6: 102,180,927 (GRCm39) |
P756Q |
probably damaging |
Het |
Col4a1 |
T |
C |
8: 11,286,423 (GRCm39) |
|
probably benign |
Het |
Col5a3 |
A |
G |
9: 20,693,777 (GRCm39) |
|
probably null |
Het |
Cox5b |
G |
A |
1: 36,731,636 (GRCm39) |
|
probably null |
Het |
Cwc27 |
C |
A |
13: 104,947,724 (GRCm39) |
|
probably null |
Het |
Cyp27b1 |
A |
C |
10: 126,886,026 (GRCm39) |
M260L |
probably benign |
Het |
Ddx19b |
A |
T |
8: 111,735,310 (GRCm39) |
N465K |
probably benign |
Het |
Depdc1b |
T |
C |
13: 108,510,382 (GRCm39) |
V298A |
probably benign |
Het |
Dnaaf1 |
A |
G |
8: 120,317,405 (GRCm39) |
I311M |
possibly damaging |
Het |
Dus4l |
G |
A |
12: 31,691,656 (GRCm39) |
T184I |
possibly damaging |
Het |
Dzip3 |
T |
C |
16: 48,768,076 (GRCm39) |
K453E |
possibly damaging |
Het |
Fhod3 |
C |
T |
18: 24,842,673 (GRCm39) |
T3M |
probably damaging |
Het |
Galnt10 |
T |
C |
11: 57,672,048 (GRCm39) |
L446P |
probably damaging |
Het |
Gfod1 |
T |
A |
13: 43,354,012 (GRCm39) |
D321V |
possibly damaging |
Het |
Glt8d2 |
C |
A |
10: 82,497,987 (GRCm39) |
|
probably benign |
Het |
Gm11115 |
A |
G |
5: 88,301,948 (GRCm39) |
M4T |
unknown |
Het |
Gm11568 |
G |
A |
11: 99,749,209 (GRCm39) |
C138Y |
unknown |
Het |
Gm57859 |
C |
T |
11: 113,580,021 (GRCm39) |
T472I |
possibly damaging |
Het |
Gm9742 |
A |
G |
13: 8,085,052 (GRCm39) |
|
noncoding transcript |
Het |
Gnrhr |
G |
T |
5: 86,345,434 (GRCm39) |
T84N |
probably damaging |
Het |
Gpr176 |
C |
A |
2: 118,110,204 (GRCm39) |
G352W |
probably damaging |
Het |
Habp2 |
T |
C |
19: 56,304,864 (GRCm39) |
|
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Inpp5j |
C |
G |
11: 3,449,738 (GRCm39) |
W681C |
probably damaging |
Het |
Insl6 |
A |
G |
19: 29,298,968 (GRCm39) |
M148T |
probably benign |
Het |
Itgb1 |
T |
G |
8: 129,452,648 (GRCm39) |
M771R |
possibly damaging |
Het |
Kank1 |
G |
T |
19: 25,403,357 (GRCm39) |
|
probably benign |
Het |
Kcnd3 |
T |
C |
3: 105,366,942 (GRCm39) |
Y271H |
probably damaging |
Het |
Kcnq4 |
C |
A |
4: 120,573,798 (GRCm39) |
R221L |
probably damaging |
Het |
Klk1b26 |
G |
A |
7: 43,665,772 (GRCm39) |
V195I |
probably benign |
Het |
Lactb |
A |
C |
9: 66,878,145 (GRCm39) |
V228G |
possibly damaging |
Het |
Ldb3 |
T |
C |
14: 34,258,541 (GRCm39) |
D649G |
probably damaging |
Het |
Lilra6 |
T |
A |
7: 3,916,138 (GRCm39) |
R240S |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,338,145 (GRCm39) |
Y1212H |
probably damaging |
Het |
Mapk8ip1 |
A |
T |
2: 92,216,321 (GRCm39) |
|
probably null |
Het |
Mctp1 |
C |
T |
13: 76,975,846 (GRCm39) |
L483F |
probably damaging |
Het |
Mmp16 |
T |
C |
4: 18,115,878 (GRCm39) |
|
probably benign |
Het |
Mphosph9 |
A |
T |
5: 124,445,033 (GRCm39) |
L360* |
probably null |
Het |
Myh4 |
A |
G |
11: 67,143,123 (GRCm39) |
E1017G |
probably damaging |
Het |
Nell1 |
A |
T |
7: 49,879,928 (GRCm39) |
M307L |
probably benign |
Het |
Or10al3 |
C |
T |
17: 38,012,188 (GRCm39) |
A209V |
probably benign |
Het |
Or10d1 |
A |
C |
9: 39,484,139 (GRCm39) |
C139G |
probably damaging |
Het |
Or5m11 |
A |
G |
2: 85,781,587 (GRCm39) |
Y60C |
probably damaging |
Het |
Or8k35 |
A |
G |
2: 86,424,752 (GRCm39) |
V140A |
probably benign |
Het |
Phc2 |
A |
G |
4: 128,617,100 (GRCm39) |
|
probably benign |
Het |
Pp2d1 |
C |
A |
17: 53,814,999 (GRCm39) |
C575F |
probably benign |
Het |
Ptpra |
T |
A |
2: 130,381,605 (GRCm39) |
N364K |
probably damaging |
Het |
R3hcc1l |
A |
G |
19: 42,550,995 (GRCm39) |
|
probably benign |
Het |
Rims1 |
A |
G |
1: 22,507,263 (GRCm39) |
|
probably benign |
Het |
Shank3 |
G |
A |
15: 89,427,442 (GRCm39) |
|
probably benign |
Het |
Sit1 |
T |
A |
4: 43,482,991 (GRCm39) |
Q86L |
possibly damaging |
Het |
Skint4 |
C |
A |
4: 111,975,136 (GRCm39) |
|
probably benign |
Het |
Skint8 |
G |
T |
4: 111,796,020 (GRCm39) |
|
probably benign |
Het |
Smim13 |
T |
C |
13: 41,426,186 (GRCm39) |
I74T |
probably benign |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Speg |
A |
G |
1: 75,361,676 (GRCm39) |
E230G |
possibly damaging |
Het |
Spmap2l |
A |
G |
5: 77,185,204 (GRCm39) |
|
probably benign |
Het |
Srpra |
A |
G |
9: 35,127,291 (GRCm39) |
T614A |
possibly damaging |
Het |
Synpo2 |
T |
C |
3: 122,907,981 (GRCm39) |
D445G |
probably damaging |
Het |
Tas2r102 |
A |
T |
6: 132,739,328 (GRCm39) |
I79F |
probably damaging |
Het |
Tmc4 |
A |
G |
7: 3,670,609 (GRCm39) |
L494P |
probably damaging |
Het |
Togaram1 |
G |
T |
12: 65,053,805 (GRCm39) |
V1412F |
probably damaging |
Het |
Topors |
T |
C |
4: 40,261,952 (GRCm39) |
D444G |
probably damaging |
Het |
Trappc8 |
T |
A |
18: 20,978,658 (GRCm39) |
I813F |
possibly damaging |
Het |
Trim26 |
T |
C |
17: 37,163,598 (GRCm39) |
|
probably benign |
Het |
Unc13a |
T |
C |
8: 72,097,557 (GRCm39) |
D1171G |
probably damaging |
Het |
Usp7 |
A |
G |
16: 8,517,126 (GRCm39) |
V245A |
probably damaging |
Het |
Vmn1r38 |
T |
A |
6: 66,753,979 (GRCm39) |
T46S |
probably benign |
Het |
Vmn2r76 |
T |
C |
7: 85,874,959 (GRCm39) |
T673A |
probably damaging |
Het |
Zcchc14 |
T |
A |
8: 122,355,388 (GRCm39) |
|
probably benign |
Het |
Zfp451 |
T |
A |
1: 33,809,991 (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 |
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 |
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 |
|
|