Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
G |
5: 88,112,335 (GRCm39) |
|
probably benign |
Het |
4930562C15Rik |
A |
C |
16: 4,653,835 (GRCm39) |
Q128P |
unknown |
Het |
Abcc3 |
T |
A |
11: 94,258,426 (GRCm39) |
K473M |
probably benign |
Het |
Acacb |
TGGGG |
TGGG |
5: 114,347,828 (GRCm39) |
|
probably null |
Het |
Adgrg7 |
C |
A |
16: 56,588,281 (GRCm39) |
A199S |
probably damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Ap2b1 |
T |
A |
11: 83,215,587 (GRCm39) |
|
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,331 (GRCm39) |
S54P |
probably damaging |
Het |
Atp13a2 |
T |
A |
4: 140,732,327 (GRCm39) |
M864K |
probably damaging |
Het |
B3gnt3 |
G |
A |
8: 72,145,971 (GRCm39) |
T186M |
probably damaging |
Het |
Cars1 |
C |
A |
7: 143,146,211 (GRCm39) |
R71M |
probably damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccdc157 |
A |
T |
11: 4,100,004 (GRCm39) |
V116E |
probably damaging |
Het |
Ccdc85a |
G |
A |
11: 28,384,151 (GRCm39) |
T408I |
probably benign |
Het |
Celf1 |
G |
T |
2: 90,840,791 (GRCm39) |
G353W |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,916,168 (GRCm39) |
I602F |
possibly damaging |
Het |
Cenpb |
C |
T |
2: 131,021,226 (GRCm39) |
V191M |
probably damaging |
Het |
Cenpn |
G |
A |
8: 117,661,536 (GRCm39) |
|
probably null |
Het |
Cfap65 |
A |
C |
1: 74,946,850 (GRCm39) |
C1287G |
probably damaging |
Het |
Cmya5 |
G |
A |
13: 93,205,891 (GRCm39) |
T3326I |
probably damaging |
Het |
Cnn3 |
A |
T |
3: 121,245,584 (GRCm39) |
E100V |
probably damaging |
Het |
Col4a4 |
G |
A |
1: 82,475,581 (GRCm39) |
R583C |
unknown |
Het |
Commd7 |
A |
C |
2: 153,463,586 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,320,899 (GRCm39) |
T304A |
probably benign |
Het |
Cyp4a14 |
A |
T |
4: 115,348,588 (GRCm39) |
S325R |
probably damaging |
Het |
Dclk2 |
T |
C |
3: 86,827,353 (GRCm39) |
N42S |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,576,946 (GRCm39) |
Q134L |
probably damaging |
Het |
Dnaaf3 |
T |
A |
7: 4,526,800 (GRCm39) |
I426L |
probably benign |
Het |
Dock6 |
A |
G |
9: 21,757,814 (GRCm39) |
S97P |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,473,854 (GRCm39) |
S976T |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,377,222 (GRCm39) |
M29K |
probably null |
Het |
Eif3i |
A |
T |
4: 129,490,719 (GRCm39) |
H18Q |
probably benign |
Het |
Epm2a |
A |
G |
10: 11,219,426 (GRCm39) |
E71G |
probably benign |
Het |
Eps15l1 |
A |
T |
8: 73,140,712 (GRCm39) |
V260D |
probably benign |
Het |
Faf1 |
A |
G |
4: 109,568,042 (GRCm39) |
N34S |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,158,015 (GRCm39) |
|
probably null |
Het |
Fbxw10 |
T |
A |
11: 62,750,683 (GRCm39) |
I422N |
probably damaging |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,899 (GRCm39) |
P1842S |
probably damaging |
Het |
Fkbp15 |
C |
A |
4: 62,246,136 (GRCm39) |
G431W |
probably damaging |
Het |
Flnb |
A |
C |
14: 7,873,376 (GRCm38) |
D224A |
probably benign |
Het |
Flnc |
G |
A |
6: 29,443,675 (GRCm39) |
V566M |
probably damaging |
Het |
Gli3 |
T |
A |
13: 15,900,134 (GRCm39) |
S1174T |
possibly damaging |
Het |
Glmn |
A |
T |
5: 107,726,321 (GRCm39) |
V93E |
probably damaging |
Het |
Glrx2 |
T |
C |
1: 143,620,842 (GRCm39) |
S74P |
possibly damaging |
Het |
Gm5422 |
G |
A |
10: 31,124,929 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
T |
C |
7: 33,905,339 (GRCm39) |
K362E |
probably damaging |
Het |
Gtpbp2 |
T |
C |
17: 46,472,128 (GRCm39) |
M21T |
probably benign |
Het |
Gxylt1 |
A |
G |
15: 93,142,851 (GRCm39) |
*405R |
probably null |
Het |
Heyl |
T |
C |
4: 123,139,876 (GRCm39) |
V145A |
probably damaging |
Het |
Hhipl1 |
A |
C |
12: 108,277,949 (GRCm39) |
E92D |
probably damaging |
Het |
Ifi207 |
A |
G |
1: 173,557,337 (GRCm39) |
F467S |
possibly damaging |
Het |
Ift70b |
G |
T |
2: 75,767,129 (GRCm39) |
H541Q |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,941,095 (GRCm39) |
I462N |
probably benign |
Het |
Inpp5b |
A |
T |
4: 124,678,961 (GRCm39) |
|
probably benign |
Het |
Kansl2 |
A |
G |
15: 98,427,278 (GRCm39) |
I201T |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,200,961 (GRCm39) |
V465A |
probably damaging |
Het |
Kcnu1 |
T |
A |
8: 26,341,928 (GRCm39) |
I91N |
probably damaging |
Het |
Kif5c |
T |
A |
2: 49,648,817 (GRCm39) |
|
probably benign |
Het |
Klrc3 |
T |
A |
6: 129,618,501 (GRCm39) |
Y94F |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,284,113 (GRCm39) |
T489S |
probably benign |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Magi1 |
T |
C |
6: 93,674,255 (GRCm39) |
E951G |
probably damaging |
Het |
Mcm7 |
T |
C |
5: 138,167,364 (GRCm39) |
Q86R |
probably damaging |
Het |
Med12l |
G |
T |
3: 59,172,703 (GRCm39) |
|
probably null |
Het |
Morc2a |
A |
G |
11: 3,629,787 (GRCm39) |
E402G |
possibly damaging |
Het |
Mphosph8 |
T |
C |
14: 56,916,161 (GRCm39) |
C486R |
probably benign |
Het |
Mpo |
A |
G |
11: 87,688,187 (GRCm39) |
D282G |
possibly damaging |
Het |
Mtcl1 |
G |
T |
17: 66,650,618 (GRCm39) |
H1616N |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,698,115 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,702 (GRCm39) |
E777G |
probably damaging |
Het |
Nid1 |
A |
G |
13: 13,684,071 (GRCm39) |
H1186R |
probably benign |
Het |
Nppb |
T |
A |
4: 148,070,454 (GRCm39) |
S8T |
probably benign |
Het |
Nrp1 |
A |
T |
8: 129,224,997 (GRCm39) |
E782D |
probably damaging |
Het |
Ntrk3 |
G |
A |
7: 78,127,683 (GRCm39) |
|
probably benign |
Het |
Or1ak2 |
A |
G |
2: 36,827,704 (GRCm39) |
N191S |
probably benign |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,605 (GRCm39) |
V134A |
possibly damaging |
Het |
Or5b99 |
T |
A |
19: 12,976,402 (GRCm39) |
D17E |
probably benign |
Het |
Or6f1 |
C |
T |
7: 85,970,687 (GRCm39) |
V158M |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,416,558 (GRCm39) |
I546K |
probably damaging |
Het |
Pard6g |
T |
C |
18: 80,160,523 (GRCm39) |
V212A |
probably damaging |
Het |
Pate6 |
T |
G |
9: 35,701,039 (GRCm39) |
|
probably benign |
Het |
Pdlim4 |
A |
G |
11: 53,954,563 (GRCm39) |
L48S |
possibly damaging |
Het |
Phactr3 |
T |
C |
2: 177,925,759 (GRCm39) |
F345L |
probably benign |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Prcp |
T |
A |
7: 92,550,488 (GRCm39) |
V95D |
probably benign |
Het |
Rfwd3 |
A |
T |
8: 112,024,034 (GRCm39) |
V96E |
probably benign |
Het |
Ror1 |
A |
G |
4: 100,267,222 (GRCm39) |
N308D |
probably benign |
Het |
Sdccag8 |
C |
A |
1: 176,783,455 (GRCm39) |
Q655K |
probably damaging |
Het |
Senp1 |
T |
A |
15: 97,973,848 (GRCm39) |
T132S |
probably benign |
Het |
Skap1 |
T |
C |
11: 96,355,559 (GRCm39) |
I10T |
possibly damaging |
Het |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Smad2 |
T |
A |
18: 76,421,155 (GRCm39) |
C161* |
probably null |
Het |
Spata31d1a |
G |
T |
13: 59,848,857 (GRCm39) |
D1090E |
probably damaging |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,724 (GRCm39) |
T1775A |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Terf1 |
A |
G |
1: 15,875,909 (GRCm39) |
E3G |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tnfrsf26 |
C |
T |
7: 143,171,577 (GRCm39) |
|
probably null |
Het |
Tor1aip1 |
A |
C |
1: 155,883,308 (GRCm39) |
M180R |
probably damaging |
Het |
Trabd2b |
A |
T |
4: 114,467,205 (GRCm39) |
Q478L |
probably benign |
Het |
Trim41 |
C |
A |
11: 48,698,419 (GRCm39) |
G516W |
probably damaging |
Het |
Ttc39a |
A |
G |
4: 109,299,903 (GRCm39) |
Y464C |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,138,896 (GRCm39) |
S92G |
probably damaging |
Het |
Unc5d |
A |
C |
8: 29,365,557 (GRCm39) |
S143A |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,414,556 (GRCm39) |
H2833L |
possibly damaging |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Wdr17 |
T |
G |
8: 55,125,541 (GRCm39) |
K446N |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,338,392 (GRCm39) |
Q211L |
possibly damaging |
Het |
Xkr7 |
G |
A |
2: 152,894,816 (GRCm39) |
R256Q |
probably benign |
Het |
Zfp236 |
T |
C |
18: 82,639,429 (GRCm39) |
M1225V |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,350,803 (GRCm39) |
|
probably benign |
Het |
Zfp280d |
T |
C |
9: 72,215,287 (GRCm39) |
F133L |
probably damaging |
Het |
Zfp747l1 |
T |
C |
7: 126,986,107 (GRCm39) |
D8G |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,594,951 (GRCm39) |
H479R |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,912,350 (GRCm39) |
N284S |
possibly damaging |
Het |
Zfyve26 |
T |
A |
12: 79,315,208 (GRCm39) |
I1423F |
possibly 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 |
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 |
|
|