Other mutations in this stock |
Total: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
G |
5: 64,055,806 (GRCm39) |
Y181D |
probably benign |
Het |
1700029H14Rik |
A |
G |
8: 13,604,715 (GRCm39) |
V196A |
possibly damaging |
Het |
2410004B18Rik |
A |
G |
3: 145,643,833 (GRCm39) |
D7G |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,776,252 (GRCm39) |
V249A |
probably damaging |
Het |
Acat2 |
A |
T |
17: 13,162,908 (GRCm39) |
D313E |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,604,823 (GRCm39) |
T325A |
probably benign |
Het |
Adamdec1 |
C |
T |
14: 68,819,407 (GRCm39) |
|
probably null |
Het |
Adat2 |
A |
G |
10: 13,429,037 (GRCm39) |
T10A |
probably benign |
Het |
Aff4 |
T |
A |
11: 53,288,685 (GRCm39) |
S400R |
possibly damaging |
Het |
Agbl2 |
C |
T |
2: 90,621,825 (GRCm39) |
P104L |
possibly damaging |
Het |
Alox12 |
G |
T |
11: 70,133,542 (GRCm39) |
T594K |
possibly damaging |
Het |
Als2 |
C |
A |
1: 59,254,546 (GRCm39) |
K270N |
probably benign |
Het |
Ankhd1 |
T |
A |
18: 36,767,787 (GRCm39) |
C1235S |
probably damaging |
Het |
Ankrd24 |
T |
A |
10: 81,470,778 (GRCm39) |
I69N |
probably damaging |
Het |
Aox4 |
G |
A |
1: 58,252,235 (GRCm39) |
V37I |
probably benign |
Het |
Arfgap3 |
A |
G |
15: 83,214,714 (GRCm39) |
|
probably benign |
Het |
Arhgef4 |
T |
A |
1: 34,846,080 (GRCm39) |
|
probably null |
Het |
Asic1 |
C |
T |
15: 99,596,498 (GRCm39) |
|
probably benign |
Het |
Atp8b5 |
A |
G |
4: 43,366,057 (GRCm39) |
N776S |
probably benign |
Het |
Bbs7 |
A |
G |
3: 36,659,883 (GRCm39) |
I184T |
probably benign |
Het |
Bbs9 |
A |
T |
9: 22,425,297 (GRCm39) |
H117L |
probably damaging |
Het |
Bnip2 |
T |
C |
9: 69,902,787 (GRCm39) |
W10R |
probably damaging |
Het |
Brd4 |
G |
T |
17: 32,443,097 (GRCm39) |
Q175K |
probably benign |
Het |
Bysl |
A |
T |
17: 47,917,821 (GRCm39) |
V124E |
possibly damaging |
Het |
Cadm3 |
A |
G |
1: 173,174,140 (GRCm39) |
|
probably benign |
Het |
Cc2d2a |
T |
C |
5: 43,853,980 (GRCm39) |
|
probably benign |
Het |
Ccdc134 |
G |
T |
15: 82,025,147 (GRCm39) |
E215D |
probably damaging |
Het |
Celsr3 |
G |
T |
9: 108,720,923 (GRCm39) |
|
probably benign |
Het |
Cntn5 |
T |
A |
9: 9,781,780 (GRCm39) |
D428V |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,547,821 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
G |
T |
17: 34,281,520 (GRCm39) |
|
probably benign |
Het |
Cyp4f13 |
G |
A |
17: 33,143,943 (GRCm39) |
|
probably benign |
Het |
Dffb |
T |
A |
4: 154,049,835 (GRCm39) |
K343* |
probably null |
Het |
Dolk |
A |
T |
2: 30,176,031 (GRCm39) |
C5S |
probably benign |
Het |
Dynlt2b |
A |
G |
16: 32,245,705 (GRCm39) |
D118G |
probably damaging |
Het |
Ebf1 |
A |
T |
11: 44,759,915 (GRCm39) |
|
probably benign |
Het |
Elac1 |
A |
G |
18: 73,875,434 (GRCm39) |
L199P |
probably damaging |
Het |
Elmod1 |
A |
C |
9: 53,842,831 (GRCm39) |
|
probably benign |
Het |
Ep400 |
A |
C |
5: 110,872,273 (GRCm39) |
|
probably benign |
Het |
F10 |
A |
T |
8: 13,098,196 (GRCm39) |
N133I |
probably damaging |
Het |
Fasn |
A |
G |
11: 120,706,141 (GRCm39) |
Y1068H |
probably benign |
Het |
Fbxo24 |
T |
C |
5: 137,622,819 (GRCm39) |
E12G |
probably damaging |
Het |
Fer |
G |
T |
17: 64,385,941 (GRCm39) |
L304F |
probably benign |
Het |
Filip1 |
A |
C |
9: 79,726,285 (GRCm39) |
L778R |
probably damaging |
Het |
Fli1 |
A |
T |
9: 32,335,277 (GRCm39) |
I385N |
probably benign |
Het |
Fpgs |
A |
T |
2: 32,582,506 (GRCm39) |
L89* |
probably null |
Het |
Gab2 |
T |
G |
7: 96,948,448 (GRCm39) |
I346R |
probably damaging |
Het |
Gm10764 |
G |
A |
10: 87,126,841 (GRCm39) |
G83R |
unknown |
Het |
Gpr83 |
G |
T |
9: 14,776,138 (GRCm39) |
C153F |
possibly damaging |
Het |
Gtf3c3 |
A |
G |
1: 54,442,695 (GRCm39) |
L783P |
possibly damaging |
Het |
Gys2 |
A |
G |
6: 142,418,394 (GRCm39) |
|
probably benign |
Het |
Heatr9 |
C |
T |
11: 83,404,164 (GRCm39) |
V378I |
possibly damaging |
Het |
Helz |
A |
T |
11: 107,528,740 (GRCm39) |
Y920F |
possibly damaging |
Het |
Inpp5f |
A |
T |
7: 128,296,907 (GRCm39) |
Q459L |
probably damaging |
Het |
Ints12 |
T |
C |
3: 132,814,806 (GRCm39) |
S338P |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,944,827 (GRCm39) |
T925A |
probably benign |
Het |
Kif1a |
C |
T |
1: 92,969,815 (GRCm39) |
V1051I |
probably damaging |
Het |
Kif7 |
T |
A |
7: 79,349,308 (GRCm39) |
H1119L |
possibly damaging |
Het |
Kmt2d |
C |
T |
15: 98,748,018 (GRCm39) |
|
probably benign |
Het |
Krt90 |
C |
T |
15: 101,471,110 (GRCm39) |
G51S |
possibly damaging |
Het |
Krtap31-2 |
A |
T |
11: 99,827,572 (GRCm39) |
I135F |
possibly damaging |
Het |
Lrp2 |
T |
C |
2: 69,258,974 (GRCm39) |
E4572G |
probably benign |
Het |
Mapk8ip1 |
T |
C |
2: 92,216,289 (GRCm39) |
E493G |
probably damaging |
Het |
Matk |
T |
G |
10: 81,094,326 (GRCm39) |
L28V |
probably benign |
Het |
Mcc |
T |
A |
18: 44,892,366 (GRCm39) |
T83S |
probably benign |
Het |
Mtch1 |
A |
T |
17: 29,559,080 (GRCm39) |
M204K |
possibly damaging |
Het |
Muc4 |
T |
G |
16: 32,586,120 (GRCm39) |
C2622G |
possibly damaging |
Het |
Myo5a |
G |
A |
9: 75,093,405 (GRCm39) |
|
probably null |
Het |
Myoz3 |
T |
C |
18: 60,712,023 (GRCm39) |
Y185C |
probably damaging |
Het |
Nnmt |
A |
G |
9: 48,503,438 (GRCm39) |
V196A |
probably benign |
Het |
Nr2f2 |
G |
C |
7: 70,009,923 (GRCm39) |
P52R |
probably damaging |
Het |
Nup214 |
T |
A |
2: 31,888,069 (GRCm39) |
|
probably benign |
Het |
Or2aj4 |
T |
G |
16: 19,385,044 (GRCm39) |
E196D |
probably damaging |
Het |
Or2y13 |
T |
C |
11: 49,414,739 (GRCm39) |
L63P |
probably damaging |
Het |
Or4c126 |
T |
A |
2: 89,824,150 (GRCm39) |
F138I |
probably benign |
Het |
Pank3 |
T |
C |
11: 35,672,543 (GRCm39) |
|
probably benign |
Het |
Parm1 |
A |
T |
5: 91,742,153 (GRCm39) |
N174Y |
possibly damaging |
Het |
Pcgf2 |
A |
T |
11: 97,583,244 (GRCm39) |
|
probably null |
Het |
Pclo |
A |
T |
5: 14,825,434 (GRCm39) |
K4661M |
unknown |
Het |
Pcsk7 |
A |
C |
9: 45,827,357 (GRCm39) |
S375R |
probably damaging |
Het |
Pdzrn4 |
G |
T |
15: 92,668,200 (GRCm39) |
S784I |
possibly damaging |
Het |
Pex6 |
T |
A |
17: 47,034,663 (GRCm39) |
|
probably null |
Het |
Pi4ka |
C |
T |
16: 17,115,499 (GRCm39) |
V1384M |
probably benign |
Het |
Polr3f |
T |
A |
2: 144,378,195 (GRCm39) |
|
probably benign |
Het |
Ppp2r3d |
A |
T |
9: 101,089,483 (GRCm39) |
V280E |
probably damaging |
Het |
Prdm14 |
C |
T |
1: 13,192,672 (GRCm39) |
G356R |
probably damaging |
Het |
Prepl |
A |
G |
17: 85,372,466 (GRCm39) |
|
probably null |
Het |
Primpol |
T |
C |
8: 47,052,849 (GRCm39) |
D154G |
probably damaging |
Het |
Ptchd4 |
A |
C |
17: 42,814,307 (GRCm39) |
H736P |
probably damaging |
Het |
Rab11fip1 |
A |
G |
8: 27,642,253 (GRCm39) |
S849P |
probably damaging |
Het |
Rap1gap |
T |
A |
4: 137,446,662 (GRCm39) |
D405E |
probably damaging |
Het |
Rbm26 |
T |
C |
14: 105,369,374 (GRCm39) |
T686A |
probably benign |
Het |
Resf1 |
T |
C |
6: 149,227,739 (GRCm39) |
Y262H |
probably damaging |
Het |
Rint1 |
A |
G |
5: 24,021,930 (GRCm39) |
|
probably benign |
Het |
Rnasek |
G |
T |
11: 70,129,266 (GRCm39) |
Y62* |
probably null |
Het |
Rnf17 |
T |
G |
14: 56,719,541 (GRCm39) |
N930K |
possibly damaging |
Het |
Sap130 |
A |
G |
18: 31,813,734 (GRCm39) |
|
probably benign |
Het |
Sectm1b |
T |
A |
11: 120,946,611 (GRCm39) |
I95F |
probably damaging |
Het |
Sema4f |
A |
T |
6: 82,916,447 (GRCm39) |
I53N |
possibly damaging |
Het |
Shld1 |
T |
C |
2: 132,592,559 (GRCm39) |
V202A |
probably benign |
Het |
Siglec1 |
T |
C |
2: 130,927,396 (GRCm39) |
T137A |
probably damaging |
Het |
Six5 |
A |
C |
7: 18,830,947 (GRCm39) |
|
probably null |
Het |
Slc22a30 |
A |
T |
19: 8,322,721 (GRCm39) |
I345N |
probably benign |
Het |
Slc25a27 |
A |
T |
17: 43,954,518 (GRCm39) |
M316K |
probably benign |
Het |
Slc2a8 |
A |
T |
2: 32,870,116 (GRCm39) |
|
probably benign |
Het |
Snx1 |
G |
A |
9: 66,008,608 (GRCm39) |
|
probably benign |
Het |
Spag17 |
A |
G |
3: 99,992,684 (GRCm39) |
T1727A |
probably benign |
Het |
Spata20 |
T |
C |
11: 94,372,472 (GRCm39) |
D633G |
probably benign |
Het |
Spock1 |
C |
T |
13: 57,583,922 (GRCm39) |
|
probably null |
Het |
Sra1 |
A |
T |
18: 36,808,759 (GRCm39) |
Y291* |
probably null |
Het |
Sspo |
C |
A |
6: 48,470,120 (GRCm39) |
P4520T |
probably damaging |
Het |
Stat4 |
A |
G |
1: 52,051,016 (GRCm39) |
N25S |
probably benign |
Het |
Tbx18 |
A |
T |
9: 87,597,569 (GRCm39) |
|
probably benign |
Het |
Tep1 |
T |
A |
14: 51,084,444 (GRCm39) |
I187F |
probably damaging |
Het |
Tfap2b |
A |
T |
1: 19,304,347 (GRCm39) |
I368F |
probably damaging |
Het |
Tmtc1 |
A |
T |
6: 148,148,335 (GRCm39) |
L711Q |
probably damaging |
Het |
Tmx3 |
T |
A |
18: 90,556,613 (GRCm39) |
|
probably benign |
Het |
Tnc |
G |
T |
4: 63,888,657 (GRCm39) |
T1803K |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Tpgs1 |
C |
T |
10: 79,511,700 (GRCm39) |
P281S |
probably benign |
Het |
Trim45 |
A |
G |
3: 100,837,160 (GRCm39) |
R499G |
probably benign |
Het |
Tulp3 |
A |
T |
6: 128,302,921 (GRCm39) |
Y299* |
probably null |
Het |
Ube4a |
A |
T |
9: 44,857,476 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
G |
2: 69,781,749 (GRCm39) |
S642R |
probably damaging |
Het |
Vcpip1 |
A |
T |
1: 9,817,431 (GRCm39) |
Y317* |
probably null |
Het |
Vmn1r115 |
G |
A |
7: 20,578,327 (GRCm39) |
T195I |
probably benign |
Het |
Vmn1r226 |
G |
A |
17: 20,907,839 (GRCm39) |
V24I |
probably benign |
Het |
Wdr41 |
C |
T |
13: 95,153,914 (GRCm39) |
A321V |
probably damaging |
Het |
Wfdc5 |
T |
C |
2: 164,020,755 (GRCm39) |
N44D |
probably benign |
Het |
Wnt7b |
C |
A |
15: 85,443,103 (GRCm39) |
|
probably null |
Het |
Zfp108 |
T |
C |
7: 23,961,208 (GRCm39) |
S600P |
possibly damaging |
Het |
Zfp267 |
A |
G |
3: 36,219,303 (GRCm39) |
H442R |
possibly damaging |
Het |
Zfp385b |
A |
G |
2: 77,246,072 (GRCm39) |
|
probably null |
Het |
Zfp395 |
T |
C |
14: 65,623,929 (GRCm39) |
S133P |
probably benign |
Het |
Zfp407 |
T |
A |
18: 84,576,836 (GRCm39) |
M1426L |
probably damaging |
Het |
Zfp641 |
T |
G |
15: 98,187,008 (GRCm39) |
N191T |
possibly damaging |
Het |
Zfp687 |
T |
C |
3: 94,918,864 (GRCm39) |
S303G |
probably damaging |
Het |
Zfp759 |
T |
A |
13: 67,286,877 (GRCm39) |
F143I |
possibly damaging |
Het |
Zgrf1 |
G |
C |
3: 127,409,095 (GRCm39) |
E1690Q |
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 |
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 |
R2271:Dnah9
|
UTSW |
11 |
66,003,188 (GRCm39) |
missense |
probably benign |
0.37 |
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 |
|
|