Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
T |
A |
10: 28,857,575 (GRCm39) |
Q194L |
probably damaging |
Het |
Acsf2 |
T |
A |
11: 94,449,699 (GRCm39) |
K574* |
probably null |
Het |
Adam22 |
T |
C |
5: 8,171,108 (GRCm39) |
E614G |
probably damaging |
Het |
Ap4e1 |
T |
C |
2: 126,889,083 (GRCm39) |
|
probably null |
Het |
Arid3c |
T |
A |
4: 41,724,744 (GRCm39) |
I364F |
probably damaging |
Het |
Bcan |
T |
A |
3: 87,900,401 (GRCm39) |
S611C |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,909,966 (GRCm39) |
V1453A |
probably benign |
Het |
Carnmt1 |
T |
C |
19: 18,680,734 (GRCm39) |
L336P |
probably damaging |
Het |
Ccdc146 |
C |
A |
5: 21,604,719 (GRCm39) |
D40Y |
probably benign |
Het |
Ccdc83 |
C |
T |
7: 89,873,285 (GRCm39) |
V357I |
probably damaging |
Het |
Cdh22 |
A |
T |
2: 164,985,767 (GRCm39) |
|
probably null |
Het |
Cdk5rap2 |
A |
C |
4: 70,184,915 (GRCm39) |
S1178R |
probably benign |
Het |
Cdkl3 |
T |
C |
11: 51,923,322 (GRCm39) |
V45A |
probably benign |
Het |
Chd7 |
A |
G |
4: 8,785,532 (GRCm39) |
D612G |
probably damaging |
Het |
Chst11 |
T |
C |
10: 83,027,004 (GRCm39) |
Y144H |
probably damaging |
Het |
Cops6 |
A |
T |
5: 138,159,403 (GRCm39) |
N10I |
probably benign |
Het |
Cyfip1 |
G |
T |
7: 55,549,705 (GRCm39) |
R624L |
probably null |
Het |
Cyp27a1 |
A |
G |
1: 74,775,846 (GRCm39) |
N344D |
probably damaging |
Het |
Des |
T |
G |
1: 75,340,137 (GRCm39) |
M348R |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,238,165 (GRCm39) |
D109V |
probably damaging |
Het |
Disp3 |
C |
T |
4: 148,356,059 (GRCm39) |
R267Q |
possibly damaging |
Het |
Dnah3 |
T |
A |
7: 119,574,352 (GRCm39) |
I2136F |
probably benign |
Het |
Dnajb14 |
G |
A |
3: 137,591,141 (GRCm39) |
G31S |
probably benign |
Het |
Dop1a |
T |
G |
9: 86,376,471 (GRCm39) |
V235G |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,831,200 (GRCm39) |
R571S |
probably benign |
Het |
Emsy |
T |
G |
7: 98,275,830 (GRCm39) |
K352N |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,238,047 (GRCm39) |
N814S |
probably damaging |
Het |
Fgfbp1 |
T |
A |
5: 44,136,672 (GRCm39) |
M207L |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,212 (GRCm39) |
E469G |
probably damaging |
Het |
Garem2 |
T |
G |
5: 30,321,972 (GRCm39) |
L777R |
probably damaging |
Het |
Garin5b |
T |
A |
7: 4,761,186 (GRCm39) |
T509S |
probably benign |
Het |
Hkdc1 |
T |
C |
10: 62,253,677 (GRCm39) |
T35A |
probably benign |
Het |
Hps6 |
C |
T |
19: 45,994,121 (GRCm39) |
A686V |
possibly damaging |
Het |
Irs1 |
T |
C |
1: 82,266,180 (GRCm39) |
S679G |
probably benign |
Het |
Ism1 |
T |
A |
2: 139,599,293 (GRCm39) |
I415N |
probably damaging |
Het |
Kdm1b |
TCATTGTCC |
TCATTGTCCATTGTCC |
13: 47,217,564 (GRCm39) |
|
probably null |
Het |
Kpna1 |
G |
A |
16: 35,851,591 (GRCm39) |
A392T |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,488,290 (GRCm39) |
R119* |
probably null |
Het |
Lrrc37 |
T |
C |
11: 103,505,033 (GRCm39) |
T2312A |
possibly damaging |
Het |
Mocs1 |
A |
T |
17: 49,756,137 (GRCm39) |
K198M |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Msh5 |
A |
G |
17: 35,263,366 (GRCm39) |
I154T |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,217,423 (GRCm39) |
T2417S |
possibly damaging |
Het |
Ncbp2 |
T |
C |
16: 31,775,769 (GRCm39) |
Y138H |
probably damaging |
Het |
Ndufv1 |
C |
A |
19: 4,058,347 (GRCm39) |
R359L |
probably benign |
Het |
Neu3 |
G |
C |
7: 99,462,650 (GRCm39) |
R358G |
probably benign |
Het |
Ntrk3 |
A |
C |
7: 78,166,471 (GRCm39) |
|
probably null |
Het |
Or1n1 |
G |
A |
2: 36,749,637 (GRCm39) |
S241F |
probably damaging |
Het |
Or8b12i |
T |
A |
9: 20,082,705 (GRCm39) |
H54L |
possibly damaging |
Het |
Or8j3 |
A |
G |
2: 86,028,161 (GRCm39) |
F312L |
probably benign |
Het |
Pik3c2b |
T |
C |
1: 133,031,166 (GRCm39) |
S1491P |
probably benign |
Het |
Plb1 |
G |
T |
5: 32,450,586 (GRCm39) |
D376Y |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,651,956 (GRCm39) |
K378N |
probably damaging |
Het |
Plekhm1 |
C |
T |
11: 103,277,948 (GRCm39) |
E383K |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,931,776 (GRCm39) |
|
probably null |
Het |
Prkdc |
A |
G |
16: 15,472,681 (GRCm39) |
|
probably null |
Het |
Prpf8 |
T |
A |
11: 75,386,189 (GRCm39) |
V946E |
probably damaging |
Het |
Psma5-ps |
A |
G |
10: 85,149,595 (GRCm39) |
|
noncoding transcript |
Het |
Ptprh |
C |
A |
7: 4,606,132 (GRCm39) |
|
probably benign |
Het |
Rngtt |
T |
A |
4: 33,500,302 (GRCm39) |
C565* |
probably null |
Het |
Sacs |
A |
G |
14: 61,442,109 (GRCm39) |
H1385R |
probably benign |
Het |
Sec24a |
A |
G |
11: 51,607,277 (GRCm39) |
S656P |
possibly damaging |
Het |
Serpinb13 |
A |
T |
1: 106,926,756 (GRCm39) |
I251L |
possibly damaging |
Het |
Shc1 |
G |
A |
3: 89,330,849 (GRCm39) |
G91S |
probably damaging |
Het |
Sin3b |
T |
A |
8: 73,460,047 (GRCm39) |
N211K |
probably benign |
Het |
Slc22a2 |
A |
T |
17: 12,805,692 (GRCm39) |
M148L |
probably benign |
Het |
Slc3a1 |
G |
A |
17: 85,371,220 (GRCm39) |
V591I |
probably benign |
Het |
Slc47a2 |
A |
T |
11: 61,219,352 (GRCm39) |
|
probably null |
Het |
Spag17 |
C |
T |
3: 100,014,113 (GRCm39) |
P2129S |
probably damaging |
Het |
Specc1l |
C |
T |
10: 75,081,438 (GRCm39) |
S278F |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,234,942 (GRCm39) |
D1628V |
probably damaging |
Het |
Themis3 |
C |
T |
17: 66,862,699 (GRCm39) |
V420I |
possibly damaging |
Het |
Ttc39d |
A |
G |
17: 80,524,675 (GRCm39) |
K445E |
probably damaging |
Het |
U2surp |
T |
C |
9: 95,373,473 (GRCm39) |
E232G |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,873,317 (GRCm39) |
F458L |
probably damaging |
Het |
Usp7 |
T |
C |
16: 8,516,333 (GRCm39) |
S649G |
probably benign |
Het |
Vmn1r10 |
A |
G |
6: 57,091,088 (GRCm39) |
T227A |
probably damaging |
Het |
Zcchc12 |
C |
T |
X: 35,462,118 (GRCm39) |
T345M |
possibly damaging |
Het |
Zfp444 |
T |
C |
7: 6,192,554 (GRCm39) |
C191R |
probably damaging |
Het |
Zfp729b |
A |
T |
13: 67,740,352 (GRCm39) |
C648S |
probably damaging |
Het |
Zfp799 |
A |
G |
17: 33,040,777 (GRCm39) |
Y58H |
probably damaging |
Het |
Zfp938 |
C |
T |
10: 82,061,381 (GRCm39) |
G413D |
probably damaging |
Het |
|
Other mutations in Dnah9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00696:Dnah9
|
APN |
11 |
65,732,064 (GRCm39) |
splice site |
probably benign |
|
IGL00805:Dnah9
|
APN |
11 |
65,772,521 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00826:Dnah9
|
APN |
11 |
65,880,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01108:Dnah9
|
APN |
11 |
65,740,806 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01152:Dnah9
|
APN |
11 |
65,962,882 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01353:Dnah9
|
APN |
11 |
65,971,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01364:Dnah9
|
APN |
11 |
66,046,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01479:Dnah9
|
APN |
11 |
65,846,543 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01537:Dnah9
|
APN |
11 |
65,838,506 (GRCm39) |
missense |
probably benign |
|
IGL01565:Dnah9
|
APN |
11 |
65,924,655 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01597:Dnah9
|
APN |
11 |
66,009,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Dnah9
|
APN |
11 |
65,722,441 (GRCm39) |
nonsense |
probably null |
|
IGL01625:Dnah9
|
APN |
11 |
65,935,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01803:Dnah9
|
APN |
11 |
66,009,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01819:Dnah9
|
APN |
11 |
65,998,952 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01896:Dnah9
|
APN |
11 |
66,021,492 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01922:Dnah9
|
APN |
11 |
65,965,860 (GRCm39) |
splice site |
probably benign |
|
IGL01923:Dnah9
|
APN |
11 |
66,016,061 (GRCm39) |
splice site |
probably benign |
|
IGL02059:Dnah9
|
APN |
11 |
65,963,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Dnah9
|
APN |
11 |
65,951,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Dnah9
|
APN |
11 |
66,008,318 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02146:Dnah9
|
APN |
11 |
65,818,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02264:Dnah9
|
APN |
11 |
65,971,314 (GRCm39) |
splice site |
probably benign |
|
IGL02325:Dnah9
|
APN |
11 |
65,725,043 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02426:Dnah9
|
APN |
11 |
66,015,979 (GRCm39) |
missense |
probably benign |
|
IGL02440:Dnah9
|
APN |
11 |
65,846,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02471:Dnah9
|
APN |
11 |
65,838,444 (GRCm39) |
nonsense |
probably null |
|
IGL02496:Dnah9
|
APN |
11 |
65,920,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02672:Dnah9
|
APN |
11 |
65,818,427 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02718:Dnah9
|
APN |
11 |
65,777,466 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02832:Dnah9
|
APN |
11 |
65,931,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Dnah9
|
APN |
11 |
65,928,570 (GRCm39) |
splice site |
probably benign |
|
IGL02859:Dnah9
|
APN |
11 |
65,772,445 (GRCm39) |
splice site |
probably benign |
|
IGL02864:Dnah9
|
APN |
11 |
65,951,829 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Dnah9
|
APN |
11 |
66,009,793 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02987:Dnah9
|
APN |
11 |
65,732,099 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02987:Dnah9
|
APN |
11 |
65,746,098 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03160:Dnah9
|
APN |
11 |
65,998,880 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03171:Dnah9
|
APN |
11 |
65,872,067 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03180:Dnah9
|
APN |
11 |
65,777,465 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03388:Dnah9
|
APN |
11 |
65,838,368 (GRCm39) |
missense |
probably damaging |
1.00 |
anarchy
|
UTSW |
11 |
65,846,074 (GRCm39) |
missense |
probably damaging |
0.99 |
sacco
|
UTSW |
11 |
66,058,905 (GRCm39) |
missense |
possibly damaging |
0.82 |
Tweed
|
UTSW |
11 |
65,962,898 (GRCm39) |
missense |
probably damaging |
0.99 |
vanzetti
|
UTSW |
11 |
65,746,198 (GRCm39) |
nonsense |
probably null |
|
IGL02837:Dnah9
|
UTSW |
11 |
65,765,022 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Dnah9
|
UTSW |
11 |
65,895,839 (GRCm39) |
missense |
probably benign |
0.44 |
R0021:Dnah9
|
UTSW |
11 |
65,860,805 (GRCm39) |
missense |
probably benign |
0.36 |
R0021:Dnah9
|
UTSW |
11 |
65,860,805 (GRCm39) |
missense |
probably benign |
0.36 |
R0025:Dnah9
|
UTSW |
11 |
65,860,781 (GRCm39) |
splice site |
probably benign |
|
R0025:Dnah9
|
UTSW |
11 |
65,860,781 (GRCm39) |
splice site |
probably benign |
|
R0070:Dnah9
|
UTSW |
11 |
66,050,866 (GRCm39) |
missense |
probably benign |
0.10 |
R0164:Dnah9
|
UTSW |
11 |
65,809,630 (GRCm39) |
nonsense |
probably null |
|
R0164:Dnah9
|
UTSW |
11 |
65,809,630 (GRCm39) |
nonsense |
probably null |
|
R0180:Dnah9
|
UTSW |
11 |
66,038,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0195:Dnah9
|
UTSW |
11 |
65,786,731 (GRCm39) |
missense |
probably benign |
0.30 |
R0230:Dnah9
|
UTSW |
11 |
65,746,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Dnah9
|
UTSW |
11 |
65,802,678 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0279:Dnah9
|
UTSW |
11 |
65,802,615 (GRCm39) |
critical splice donor site |
probably null |
|
R0288:Dnah9
|
UTSW |
11 |
65,915,960 (GRCm39) |
critical splice donor site |
probably null |
|
R0309:Dnah9
|
UTSW |
11 |
65,917,798 (GRCm39) |
splice site |
probably benign |
|
R0356:Dnah9
|
UTSW |
11 |
66,021,388 (GRCm39) |
critical splice donor site |
probably null |
|
R0403:Dnah9
|
UTSW |
11 |
65,975,615 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0413:Dnah9
|
UTSW |
11 |
65,998,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Dnah9
|
UTSW |
11 |
65,809,539 (GRCm39) |
splice site |
probably benign |
|
R0496:Dnah9
|
UTSW |
11 |
65,965,961 (GRCm39) |
missense |
probably null |
1.00 |
R0557:Dnah9
|
UTSW |
11 |
65,975,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0584:Dnah9
|
UTSW |
11 |
65,881,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R0598:Dnah9
|
UTSW |
11 |
66,009,703 (GRCm39) |
missense |
probably benign |
0.02 |
R0599:Dnah9
|
UTSW |
11 |
65,856,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Dnah9
|
UTSW |
11 |
65,732,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Dnah9
|
UTSW |
11 |
65,976,284 (GRCm39) |
missense |
probably benign |
0.01 |
R0715:Dnah9
|
UTSW |
11 |
65,972,074 (GRCm39) |
splice site |
probably benign |
|
R0726:Dnah9
|
UTSW |
11 |
65,856,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Dnah9
|
UTSW |
11 |
65,998,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Dnah9
|
UTSW |
11 |
66,046,356 (GRCm39) |
missense |
probably benign |
0.30 |
R0792:Dnah9
|
UTSW |
11 |
65,786,827 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0829:Dnah9
|
UTSW |
11 |
65,896,002 (GRCm39) |
missense |
probably benign |
0.00 |
R0973:Dnah9
|
UTSW |
11 |
65,896,663 (GRCm39) |
splice site |
probably null |
|
R0974:Dnah9
|
UTSW |
11 |
65,896,663 (GRCm39) |
splice site |
probably null |
|
R1055:Dnah9
|
UTSW |
11 |
66,050,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R1081:Dnah9
|
UTSW |
11 |
65,975,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R1184:Dnah9
|
UTSW |
11 |
65,975,438 (GRCm39) |
critical splice donor site |
probably null |
|
R1225:Dnah9
|
UTSW |
11 |
65,761,886 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1304:Dnah9
|
UTSW |
11 |
65,818,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R1417:Dnah9
|
UTSW |
11 |
65,846,573 (GRCm39) |
missense |
probably damaging |
0.96 |
R1439:Dnah9
|
UTSW |
11 |
65,764,958 (GRCm39) |
missense |
probably benign |
0.22 |
R1447:Dnah9
|
UTSW |
11 |
65,999,308 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1450:Dnah9
|
UTSW |
11 |
65,818,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Dnah9
|
UTSW |
11 |
65,818,648 (GRCm39) |
missense |
probably benign |
0.11 |
R1470:Dnah9
|
UTSW |
11 |
65,818,648 (GRCm39) |
missense |
probably benign |
0.11 |
R1486:Dnah9
|
UTSW |
11 |
65,725,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Dnah9
|
UTSW |
11 |
65,772,587 (GRCm39) |
missense |
probably damaging |
0.96 |
R1570:Dnah9
|
UTSW |
11 |
66,003,156 (GRCm39) |
missense |
probably benign |
|
R1617:Dnah9
|
UTSW |
11 |
65,786,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Dnah9
|
UTSW |
11 |
65,928,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1626:Dnah9
|
UTSW |
11 |
65,976,093 (GRCm39) |
missense |
probably benign |
0.05 |
R1671:Dnah9
|
UTSW |
11 |
65,818,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R1694:Dnah9
|
UTSW |
11 |
65,845,650 (GRCm39) |
nonsense |
probably null |
|
R1701:Dnah9
|
UTSW |
11 |
65,802,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Dnah9
|
UTSW |
11 |
65,976,021 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1708:Dnah9
|
UTSW |
11 |
65,805,980 (GRCm39) |
missense |
probably benign |
0.11 |
R1718:Dnah9
|
UTSW |
11 |
66,058,905 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1729:Dnah9
|
UTSW |
11 |
65,975,846 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1760:Dnah9
|
UTSW |
11 |
65,872,048 (GRCm39) |
missense |
probably benign |
0.31 |
R1784:Dnah9
|
UTSW |
11 |
65,975,846 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1793:Dnah9
|
UTSW |
11 |
66,010,420 (GRCm39) |
critical splice donor site |
probably null |
|
R1801:Dnah9
|
UTSW |
11 |
65,846,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R1827:Dnah9
|
UTSW |
11 |
65,740,887 (GRCm39) |
missense |
probably damaging |
0.97 |
R1836:Dnah9
|
UTSW |
11 |
66,009,667 (GRCm39) |
missense |
probably benign |
0.10 |
R1840:Dnah9
|
UTSW |
11 |
65,725,024 (GRCm39) |
nonsense |
probably null |
|
R1847:Dnah9
|
UTSW |
11 |
65,725,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Dnah9
|
UTSW |
11 |
65,928,316 (GRCm39) |
missense |
probably benign |
0.16 |
R1929:Dnah9
|
UTSW |
11 |
65,867,224 (GRCm39) |
missense |
probably benign |
0.05 |
R1969:Dnah9
|
UTSW |
11 |
65,739,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Dnah9
|
UTSW |
11 |
65,739,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Dnah9
|
UTSW |
11 |
65,846,164 (GRCm39) |
missense |
probably benign |
0.11 |
R2049:Dnah9
|
UTSW |
11 |
65,935,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Dnah9
|
UTSW |
11 |
66,036,261 (GRCm39) |
missense |
probably benign |
0.31 |
R2104:Dnah9
|
UTSW |
11 |
65,951,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Dnah9
|
UTSW |
11 |
65,928,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R2160:Dnah9
|
UTSW |
11 |
66,008,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Dnah9
|
UTSW |
11 |
65,963,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Dnah9
|
UTSW |
11 |
65,750,325 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2272:Dnah9
|
UTSW |
11 |
66,003,188 (GRCm39) |
missense |
probably benign |
0.37 |
R2396:Dnah9
|
UTSW |
11 |
65,975,984 (GRCm39) |
missense |
probably benign |
0.01 |
R2398:Dnah9
|
UTSW |
11 |
65,806,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R2418:Dnah9
|
UTSW |
11 |
65,986,241 (GRCm39) |
nonsense |
probably null |
|
R2419:Dnah9
|
UTSW |
11 |
65,986,241 (GRCm39) |
nonsense |
probably null |
|
R2510:Dnah9
|
UTSW |
11 |
65,895,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Dnah9
|
UTSW |
11 |
65,924,751 (GRCm39) |
missense |
probably benign |
0.00 |
R2875:Dnah9
|
UTSW |
11 |
66,059,287 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2979:Dnah9
|
UTSW |
11 |
66,008,414 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3236:Dnah9
|
UTSW |
11 |
65,845,815 (GRCm39) |
missense |
probably benign |
0.11 |
R3237:Dnah9
|
UTSW |
11 |
65,845,815 (GRCm39) |
missense |
probably benign |
0.11 |
R3433:Dnah9
|
UTSW |
11 |
65,965,938 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3737:Dnah9
|
UTSW |
11 |
66,047,734 (GRCm39) |
nonsense |
probably null |
|
R3820:Dnah9
|
UTSW |
11 |
65,741,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3821:Dnah9
|
UTSW |
11 |
65,741,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3822:Dnah9
|
UTSW |
11 |
65,741,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3861:Dnah9
|
UTSW |
11 |
65,943,820 (GRCm39) |
splice site |
probably benign |
|
R3918:Dnah9
|
UTSW |
11 |
65,761,800 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4011:Dnah9
|
UTSW |
11 |
65,725,290 (GRCm39) |
missense |
probably damaging |
0.98 |
R4044:Dnah9
|
UTSW |
11 |
66,024,461 (GRCm39) |
missense |
probably benign |
0.03 |
R4072:Dnah9
|
UTSW |
11 |
65,975,730 (GRCm39) |
missense |
probably benign |
0.00 |
R4076:Dnah9
|
UTSW |
11 |
65,975,730 (GRCm39) |
missense |
probably benign |
0.00 |
R4097:Dnah9
|
UTSW |
11 |
65,881,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4409:Dnah9
|
UTSW |
11 |
65,976,303 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4410:Dnah9
|
UTSW |
11 |
65,976,303 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4417:Dnah9
|
UTSW |
11 |
65,872,040 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4420:Dnah9
|
UTSW |
11 |
66,009,575 (GRCm39) |
missense |
probably benign |
0.00 |
R4434:Dnah9
|
UTSW |
11 |
65,998,901 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4451:Dnah9
|
UTSW |
11 |
65,772,467 (GRCm39) |
missense |
probably benign |
0.07 |
R4452:Dnah9
|
UTSW |
11 |
65,917,908 (GRCm39) |
missense |
probably damaging |
0.96 |
R4454:Dnah9
|
UTSW |
11 |
66,038,215 (GRCm39) |
missense |
probably damaging |
0.96 |
R4551:Dnah9
|
UTSW |
11 |
65,732,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4552:Dnah9
|
UTSW |
11 |
65,732,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Dnah9
|
UTSW |
11 |
65,931,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Dnah9
|
UTSW |
11 |
66,058,978 (GRCm39) |
missense |
probably benign |
|
R4655:Dnah9
|
UTSW |
11 |
65,846,558 (GRCm39) |
missense |
probably benign |
0.00 |
R4667:Dnah9
|
UTSW |
11 |
66,046,357 (GRCm39) |
missense |
probably benign |
|
R4718:Dnah9
|
UTSW |
11 |
65,976,299 (GRCm39) |
missense |
probably benign |
|
R4720:Dnah9
|
UTSW |
11 |
65,967,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R4734:Dnah9
|
UTSW |
11 |
65,724,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Dnah9
|
UTSW |
11 |
65,724,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Dnah9
|
UTSW |
11 |
65,818,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Dnah9
|
UTSW |
11 |
65,764,950 (GRCm39) |
nonsense |
probably null |
|
R4963:Dnah9
|
UTSW |
11 |
65,975,437 (GRCm39) |
splice site |
probably null |
|
R5074:Dnah9
|
UTSW |
11 |
65,740,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Dnah9
|
UTSW |
11 |
65,975,492 (GRCm39) |
missense |
probably damaging |
0.99 |
R5262:Dnah9
|
UTSW |
11 |
66,003,159 (GRCm39) |
missense |
probably benign |
0.34 |
R5364:Dnah9
|
UTSW |
11 |
65,772,522 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5370:Dnah9
|
UTSW |
11 |
65,920,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Dnah9
|
UTSW |
11 |
65,920,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Dnah9
|
UTSW |
11 |
65,986,140 (GRCm39) |
nonsense |
probably null |
|
R5541:Dnah9
|
UTSW |
11 |
66,036,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Dnah9
|
UTSW |
11 |
65,772,566 (GRCm39) |
missense |
probably benign |
0.00 |
R5576:Dnah9
|
UTSW |
11 |
65,724,922 (GRCm39) |
splice site |
probably null |
|
R5648:Dnah9
|
UTSW |
11 |
65,818,581 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Dnah9
|
UTSW |
11 |
65,740,806 (GRCm39) |
missense |
probably damaging |
0.99 |
R5713:Dnah9
|
UTSW |
11 |
65,916,049 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5763:Dnah9
|
UTSW |
11 |
65,846,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Dnah9
|
UTSW |
11 |
66,017,427 (GRCm39) |
missense |
probably benign |
0.01 |
R5831:Dnah9
|
UTSW |
11 |
65,998,947 (GRCm39) |
missense |
probably benign |
0.00 |
R5847:Dnah9
|
UTSW |
11 |
65,986,066 (GRCm39) |
frame shift |
probably null |
|
R5870:Dnah9
|
UTSW |
11 |
65,976,036 (GRCm39) |
missense |
probably benign |
0.01 |
R5902:Dnah9
|
UTSW |
11 |
65,916,013 (GRCm39) |
missense |
probably benign |
0.08 |
R5918:Dnah9
|
UTSW |
11 |
65,725,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Dnah9
|
UTSW |
11 |
65,725,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Dnah9
|
UTSW |
11 |
66,036,223 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6065:Dnah9
|
UTSW |
11 |
65,746,164 (GRCm39) |
missense |
probably benign |
0.05 |
R6086:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
R6086:Dnah9
|
UTSW |
11 |
65,880,741 (GRCm39) |
missense |
probably damaging |
0.99 |
R6102:Dnah9
|
UTSW |
11 |
65,881,342 (GRCm39) |
missense |
probably damaging |
0.97 |
R6120:Dnah9
|
UTSW |
11 |
66,038,225 (GRCm39) |
missense |
probably benign |
|
R6154:Dnah9
|
UTSW |
11 |
65,746,164 (GRCm39) |
missense |
probably benign |
0.00 |
R6262:Dnah9
|
UTSW |
11 |
65,772,631 (GRCm39) |
splice site |
probably null |
|
R6265:Dnah9
|
UTSW |
11 |
66,058,920 (GRCm39) |
missense |
probably benign |
0.04 |
R6290:Dnah9
|
UTSW |
11 |
65,732,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:Dnah9
|
UTSW |
11 |
65,928,519 (GRCm39) |
missense |
probably damaging |
0.97 |
R6357:Dnah9
|
UTSW |
11 |
65,765,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R6534:Dnah9
|
UTSW |
11 |
65,846,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R6574:Dnah9
|
UTSW |
11 |
66,059,107 (GRCm39) |
missense |
probably benign |
0.37 |
R6582:Dnah9
|
UTSW |
11 |
65,951,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Dnah9
|
UTSW |
11 |
65,846,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R6800:Dnah9
|
UTSW |
11 |
65,963,565 (GRCm39) |
critical splice donor site |
probably null |
|
R6812:Dnah9
|
UTSW |
11 |
65,872,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R6931:Dnah9
|
UTSW |
11 |
66,008,452 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6944:Dnah9
|
UTSW |
11 |
65,975,975 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6958:Dnah9
|
UTSW |
11 |
65,967,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R6977:Dnah9
|
UTSW |
11 |
65,998,735 (GRCm39) |
missense |
probably benign |
0.37 |
R7021:Dnah9
|
UTSW |
11 |
65,872,057 (GRCm39) |
missense |
probably benign |
|
R7161:Dnah9
|
UTSW |
11 |
65,746,198 (GRCm39) |
nonsense |
probably null |
|
R7175:Dnah9
|
UTSW |
11 |
66,024,463 (GRCm39) |
missense |
probably benign |
0.03 |
R7199:Dnah9
|
UTSW |
11 |
66,009,770 (GRCm39) |
missense |
probably benign |
0.04 |
R7231:Dnah9
|
UTSW |
11 |
65,856,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R7284:Dnah9
|
UTSW |
11 |
65,881,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7314:Dnah9
|
UTSW |
11 |
65,880,677 (GRCm39) |
missense |
probably benign |
0.00 |
R7350:Dnah9
|
UTSW |
11 |
65,971,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7420:Dnah9
|
UTSW |
11 |
66,008,233 (GRCm39) |
critical splice donor site |
probably null |
|
R7427:Dnah9
|
UTSW |
11 |
65,846,045 (GRCm39) |
missense |
probably benign |
|
R7477:Dnah9
|
UTSW |
11 |
65,883,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R7515:Dnah9
|
UTSW |
11 |
65,732,240 (GRCm39) |
missense |
probably benign |
0.01 |
R7521:Dnah9
|
UTSW |
11 |
65,880,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R7573:Dnah9
|
UTSW |
11 |
66,016,041 (GRCm39) |
missense |
probably benign |
0.43 |
R7659:Dnah9
|
UTSW |
11 |
65,880,606 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:Dnah9
|
UTSW |
11 |
66,009,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R7749:Dnah9
|
UTSW |
11 |
65,802,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Dnah9
|
UTSW |
11 |
65,740,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Dnah9
|
UTSW |
11 |
65,896,631 (GRCm39) |
nonsense |
probably null |
|
R7814:Dnah9
|
UTSW |
11 |
65,896,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Dnah9
|
UTSW |
11 |
65,916,037 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7890:Dnah9
|
UTSW |
11 |
65,962,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R7976:Dnah9
|
UTSW |
11 |
65,732,227 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8121:Dnah9
|
UTSW |
11 |
65,908,201 (GRCm39) |
missense |
probably benign |
0.02 |
R8232:Dnah9
|
UTSW |
11 |
65,746,149 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8311:Dnah9
|
UTSW |
11 |
65,880,644 (GRCm39) |
missense |
probably benign |
0.00 |
R8326:Dnah9
|
UTSW |
11 |
66,008,452 (GRCm39) |
missense |
probably benign |
0.01 |
R8338:Dnah9
|
UTSW |
11 |
65,732,067 (GRCm39) |
critical splice donor site |
probably null |
|
R8356:Dnah9
|
UTSW |
11 |
66,047,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8456:Dnah9
|
UTSW |
11 |
66,047,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8468:Dnah9
|
UTSW |
11 |
65,722,556 (GRCm39) |
missense |
probably benign |
0.00 |
R8721:Dnah9
|
UTSW |
11 |
65,986,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R8747:Dnah9
|
UTSW |
11 |
65,818,816 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8798:Dnah9
|
UTSW |
11 |
65,796,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R8806:Dnah9
|
UTSW |
11 |
65,750,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Dnah9
|
UTSW |
11 |
65,740,742 (GRCm39) |
missense |
probably benign |
0.13 |
R8837:Dnah9
|
UTSW |
11 |
65,746,060 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8886:Dnah9
|
UTSW |
11 |
65,943,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Dnah9
|
UTSW |
11 |
65,746,210 (GRCm39) |
missense |
probably benign |
0.01 |
R8921:Dnah9
|
UTSW |
11 |
65,802,747 (GRCm39) |
missense |
probably benign |
|
R8933:Dnah9
|
UTSW |
11 |
65,746,078 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8949:Dnah9
|
UTSW |
11 |
66,059,226 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8967:Dnah9
|
UTSW |
11 |
66,015,938 (GRCm39) |
critical splice donor site |
probably null |
|
R8979:Dnah9
|
UTSW |
11 |
65,895,978 (GRCm39) |
missense |
probably benign |
|
R8991:Dnah9
|
UTSW |
11 |
65,777,506 (GRCm39) |
missense |
probably damaging |
0.96 |
R9016:Dnah9
|
UTSW |
11 |
65,998,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R9025:Dnah9
|
UTSW |
11 |
65,896,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Dnah9
|
UTSW |
11 |
65,845,680 (GRCm39) |
missense |
|
|
R9047:Dnah9
|
UTSW |
11 |
65,962,925 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9076:Dnah9
|
UTSW |
11 |
66,008,464 (GRCm39) |
missense |
probably benign |
0.21 |
R9113:Dnah9
|
UTSW |
11 |
65,880,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9152:Dnah9
|
UTSW |
11 |
66,021,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9187:Dnah9
|
UTSW |
11 |
65,895,972 (GRCm39) |
missense |
probably benign |
|
R9198:Dnah9
|
UTSW |
11 |
65,846,570 (GRCm39) |
missense |
probably benign |
0.02 |
R9203:Dnah9
|
UTSW |
11 |
65,746,113 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9234:Dnah9
|
UTSW |
11 |
65,924,751 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9245:Dnah9
|
UTSW |
11 |
65,786,731 (GRCm39) |
missense |
probably benign |
0.30 |
R9265:Dnah9
|
UTSW |
11 |
65,732,081 (GRCm39) |
missense |
probably benign |
0.01 |
R9307:Dnah9
|
UTSW |
11 |
65,976,300 (GRCm39) |
missense |
probably benign |
0.14 |
R9336:Dnah9
|
UTSW |
11 |
65,761,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R9386:Dnah9
|
UTSW |
11 |
65,838,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Dnah9
|
UTSW |
11 |
65,739,199 (GRCm39) |
missense |
probably damaging |
0.99 |
R9508:Dnah9
|
UTSW |
11 |
65,725,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9524:Dnah9
|
UTSW |
11 |
65,976,309 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9577:Dnah9
|
UTSW |
11 |
65,867,347 (GRCm39) |
missense |
probably benign |
0.00 |
R9583:Dnah9
|
UTSW |
11 |
65,856,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9587:Dnah9
|
UTSW |
11 |
65,999,217 (GRCm39) |
missense |
probably null |
0.92 |
R9612:Dnah9
|
UTSW |
11 |
65,818,475 (GRCm39) |
missense |
probably benign |
0.00 |
R9748:Dnah9
|
UTSW |
11 |
65,976,290 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9749:Dnah9
|
UTSW |
11 |
65,986,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R9759:Dnah9
|
UTSW |
11 |
65,965,944 (GRCm39) |
missense |
probably null |
0.93 |
R9784:Dnah9
|
UTSW |
11 |
65,975,960 (GRCm39) |
missense |
probably damaging |
0.99 |
V3553:Dnah9
|
UTSW |
11 |
65,860,902 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Dnah9
|
UTSW |
11 |
65,976,305 (GRCm39) |
missense |
probably benign |
0.07 |
X0028:Dnah9
|
UTSW |
11 |
65,881,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah9
|
UTSW |
11 |
65,860,910 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah9
|
UTSW |
11 |
65,818,679 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah9
|
UTSW |
11 |
65,786,798 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah9
|
UTSW |
11 |
65,963,661 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah9
|
UTSW |
11 |
65,928,300 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah9
|
UTSW |
11 |
66,017,476 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1186:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1187:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1187:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1188:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1188:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1189:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1189:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1190:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1190:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1191:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1191:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
Z1192:Dnah9
|
UTSW |
11 |
66,038,207 (GRCm39) |
missense |
probably benign |
|
Z1192:Dnah9
|
UTSW |
11 |
65,976,000 (GRCm39) |
missense |
probably benign |
|
|