Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,884,144 (GRCm39) |
H571Q |
probably damaging |
Het |
Abcf2 |
T |
A |
5: 24,773,774 (GRCm39) |
M372L |
probably benign |
Het |
Acaca |
A |
C |
11: 84,206,795 (GRCm39) |
T1552P |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,229,219 (GRCm39) |
D1682G |
probably damaging |
Het |
Acvr1b |
T |
C |
15: 101,091,906 (GRCm39) |
V62A |
probably benign |
Het |
Aimp1 |
C |
T |
3: 132,379,825 (GRCm39) |
V97M |
probably benign |
Het |
Aldh1l1 |
C |
T |
6: 90,554,813 (GRCm39) |
T557I |
possibly damaging |
Het |
Alpk1 |
T |
C |
3: 127,471,447 (GRCm39) |
T1012A |
probably damaging |
Het |
Amot |
G |
A |
X: 144,233,585 (GRCm39) |
|
probably benign |
Het |
Arap1 |
T |
A |
7: 101,037,829 (GRCm39) |
H477Q |
probably benign |
Het |
Arhgap18 |
T |
A |
10: 26,736,732 (GRCm39) |
|
probably benign |
Het |
Arhgef10l |
C |
T |
4: 140,242,684 (GRCm39) |
V862M |
probably damaging |
Het |
Arl4d |
A |
G |
11: 101,557,554 (GRCm39) |
I27V |
probably benign |
Het |
Asb18 |
G |
A |
1: 89,942,277 (GRCm39) |
P8L |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,977,616 (GRCm39) |
H2682R |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,385,079 (GRCm39) |
V241E |
probably benign |
Het |
Atf7ip |
G |
T |
6: 136,586,217 (GRCm39) |
|
probably benign |
Het |
AY358078 |
T |
G |
14: 52,042,051 (GRCm39) |
M142R |
unknown |
Het |
C3 |
T |
A |
17: 57,526,592 (GRCm39) |
K796N |
possibly damaging |
Het |
Ceacam16 |
T |
C |
7: 19,590,041 (GRCm39) |
T301A |
probably damaging |
Het |
Ceacam5 |
T |
G |
7: 17,481,320 (GRCm39) |
Y356D |
probably benign |
Het |
Cep192 |
C |
T |
18: 67,984,838 (GRCm39) |
A1616V |
possibly damaging |
Het |
Cfap91 |
T |
A |
16: 38,141,781 (GRCm39) |
N384Y |
possibly damaging |
Het |
Cherp |
A |
T |
8: 73,216,994 (GRCm39) |
H645Q |
probably benign |
Het |
CK137956 |
T |
C |
4: 127,845,242 (GRCm39) |
D167G |
probably benign |
Het |
Clcn1 |
T |
A |
6: 42,275,860 (GRCm39) |
|
probably null |
Het |
Cntn1 |
C |
T |
15: 92,189,552 (GRCm39) |
T625I |
possibly damaging |
Het |
Cpn2 |
T |
A |
16: 30,078,142 (GRCm39) |
N520Y |
probably damaging |
Het |
Crocc |
G |
A |
4: 140,746,620 (GRCm39) |
R1762W |
probably damaging |
Het |
Cts3 |
C |
A |
13: 61,715,967 (GRCm39) |
V100F |
probably benign |
Het |
Ddx56 |
A |
T |
11: 6,216,934 (GRCm39) |
V87D |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,700,456 (GRCm39) |
|
probably null |
Het |
Dst |
T |
A |
1: 34,191,552 (GRCm39) |
Y291* |
probably null |
Het |
Eif4g3 |
T |
C |
4: 137,898,442 (GRCm39) |
I1071T |
probably damaging |
Het |
Fblim1 |
T |
C |
4: 141,322,549 (GRCm39) |
Q78R |
probably damaging |
Het |
Fcamr |
C |
T |
1: 130,739,284 (GRCm39) |
P195S |
probably benign |
Het |
Fcho1 |
G |
A |
8: 72,161,666 (GRCm39) |
Q835* |
probably null |
Het |
Frem3 |
A |
G |
8: 81,339,741 (GRCm39) |
N678S |
probably benign |
Het |
Frk |
G |
A |
10: 34,483,878 (GRCm39) |
R413H |
probably benign |
Het |
Gm10619 |
C |
A |
7: 73,459,758 (GRCm39) |
|
noncoding transcript |
Het |
Gm12185 |
G |
A |
11: 48,806,583 (GRCm39) |
R203* |
probably null |
Het |
Gm12886 |
A |
G |
4: 121,280,174 (GRCm39) |
V34A |
probably benign |
Het |
Gna12 |
A |
T |
5: 140,746,707 (GRCm39) |
I246N |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,507,867 (GRCm39) |
M201T |
probably benign |
Het |
Gpsm2 |
T |
G |
3: 108,608,225 (GRCm39) |
D220A |
probably benign |
Het |
Grip2 |
C |
G |
6: 91,760,623 (GRCm39) |
V325L |
probably benign |
Het |
Grk5 |
C |
A |
19: 61,065,200 (GRCm39) |
A288D |
probably damaging |
Het |
Herpud2 |
G |
A |
9: 25,021,953 (GRCm39) |
A231V |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,624,834 (GRCm39) |
S1024G |
probably benign |
Het |
Hp1bp3 |
A |
G |
4: 137,957,820 (GRCm39) |
D295G |
probably damaging |
Het |
Igsf21 |
T |
C |
4: 139,761,703 (GRCm39) |
H325R |
probably damaging |
Het |
Ing2 |
T |
A |
8: 48,122,364 (GRCm39) |
L61F |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,138,590 (GRCm39) |
|
probably benign |
Het |
Kcnn3 |
T |
A |
3: 89,516,712 (GRCm39) |
C374S |
probably benign |
Het |
Klk1b22 |
A |
G |
7: 43,765,775 (GRCm39) |
|
probably benign |
Het |
Larp1 |
T |
C |
11: 57,940,764 (GRCm39) |
M630T |
possibly damaging |
Het |
Lhx5 |
T |
A |
5: 120,572,725 (GRCm39) |
C115S |
probably damaging |
Het |
Lmcd1 |
C |
A |
6: 112,305,712 (GRCm39) |
T271K |
probably benign |
Het |
Lpar1 |
G |
A |
4: 58,486,798 (GRCm39) |
R158* |
probably null |
Het |
Lyst |
T |
A |
13: 13,821,668 (GRCm39) |
C1347* |
probably null |
Het |
Map3k8 |
G |
A |
18: 4,332,389 (GRCm39) |
Q441* |
probably null |
Het |
Mboat1 |
T |
C |
13: 30,403,633 (GRCm39) |
V144A |
probably damaging |
Het |
Mcur1 |
C |
T |
13: 43,713,491 (GRCm39) |
G38S |
unknown |
Het |
Med13 |
T |
A |
11: 86,220,177 (GRCm39) |
M276L |
probably benign |
Het |
Mefv |
A |
G |
16: 3,526,528 (GRCm39) |
S699P |
possibly damaging |
Het |
Mfsd4a |
C |
A |
1: 131,987,077 (GRCm39) |
A62S |
probably damaging |
Het |
Mmp27 |
A |
G |
9: 7,571,459 (GRCm39) |
M1V |
probably null |
Het |
Myo1c |
C |
T |
11: 75,548,415 (GRCm39) |
T58I |
probably damaging |
Het |
Myom3 |
A |
T |
4: 135,538,066 (GRCm39) |
D1316V |
probably benign |
Het |
Naa25 |
T |
A |
5: 121,555,478 (GRCm39) |
C235S |
possibly damaging |
Het |
Naa25 |
C |
A |
5: 121,558,656 (GRCm39) |
R333S |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,539,233 (GRCm39) |
T2056I |
probably benign |
Het |
Nol4 |
A |
G |
18: 22,902,878 (GRCm39) |
Y378H |
probably damaging |
Het |
Npat |
G |
A |
9: 53,463,589 (GRCm39) |
R124Q |
probably damaging |
Het |
Npr3 |
T |
A |
15: 11,848,665 (GRCm39) |
E434V |
probably benign |
Het |
Nptx2 |
A |
G |
5: 144,485,130 (GRCm39) |
T208A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,968,606 (GRCm39) |
V2798M |
probably damaging |
Het |
Odad4 |
C |
A |
11: 100,460,679 (GRCm39) |
|
probably null |
Het |
Or10j7 |
A |
T |
1: 173,011,976 (GRCm39) |
H8Q |
probably benign |
Het |
Or52r1 |
A |
G |
7: 102,537,250 (GRCm39) |
Y37H |
probably benign |
Het |
Or5b122 |
C |
T |
19: 13,562,779 (GRCm39) |
T37I |
probably benign |
Het |
Padi1 |
G |
A |
4: 140,541,967 (GRCm39) |
P652S |
probably damaging |
Het |
Pcdh1 |
G |
T |
18: 38,331,938 (GRCm39) |
P355Q |
probably damaging |
Het |
Pck2 |
G |
A |
14: 55,781,422 (GRCm39) |
R189H |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,432,114 (GRCm39) |
K1500N |
possibly damaging |
Het |
Phc3 |
A |
T |
3: 31,002,865 (GRCm39) |
S218T |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,239,355 (GRCm39) |
M510L |
possibly damaging |
Het |
Polr1g |
T |
C |
7: 19,091,904 (GRCm39) |
T68A |
possibly damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,754,717 (GRCm39) |
Y177N |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,361 (GRCm39) |
D195E |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,088,827 (GRCm39) |
V463A |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,836,281 (GRCm39) |
R574Q |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,756,314 (GRCm39) |
T14S |
possibly damaging |
Het |
Rbm11 |
A |
T |
16: 75,397,685 (GRCm39) |
K205M |
probably damaging |
Het |
Rfx1 |
T |
A |
8: 84,793,050 (GRCm39) |
|
probably benign |
Het |
Rnasel |
C |
A |
1: 153,630,169 (GRCm39) |
H228Q |
probably damaging |
Het |
Sap130 |
T |
A |
18: 31,831,640 (GRCm39) |
I710K |
probably benign |
Het |
Slc27a4 |
C |
A |
2: 29,695,733 (GRCm39) |
D89E |
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,779 (GRCm39) |
V309A |
probably benign |
Het |
Syt7 |
T |
G |
19: 10,421,354 (GRCm39) |
Y420D |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,515,859 (GRCm39) |
|
probably null |
Het |
Tbc1d10b |
A |
G |
7: 126,802,930 (GRCm39) |
S333P |
possibly damaging |
Het |
Tenm2 |
G |
A |
11: 35,914,209 (GRCm39) |
P2442S |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 49,127,579 (GRCm39) |
C33Y |
probably damaging |
Het |
Timmdc1 |
A |
G |
16: 38,319,419 (GRCm39) |
L245P |
possibly damaging |
Het |
Tlr5 |
T |
C |
1: 182,800,012 (GRCm39) |
F5L |
probably benign |
Het |
Ttll4 |
T |
A |
1: 74,726,999 (GRCm39) |
F784L |
possibly damaging |
Het |
Tulp4 |
A |
G |
17: 6,189,387 (GRCm39) |
T70A |
possibly damaging |
Het |
Txndc17 |
T |
A |
11: 72,099,571 (GRCm39) |
N81K |
probably benign |
Het |
Ubr3 |
C |
T |
2: 69,830,895 (GRCm39) |
|
probably benign |
Het |
Uri1 |
A |
C |
7: 37,681,116 (GRCm39) |
V96G |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,150,246 (GRCm39) |
I482N |
probably damaging |
Het |
Vmn1r229 |
A |
G |
17: 21,034,974 (GRCm39) |
N73S |
possibly damaging |
Het |
Vwa7 |
G |
T |
17: 35,243,388 (GRCm39) |
G689* |
probably null |
Het |
Zfp114 |
T |
A |
7: 23,877,164 (GRCm39) |
|
probably null |
Het |
Zfp618 |
A |
G |
4: 63,051,474 (GRCm39) |
S659G |
probably damaging |
Het |
Zfp872 |
A |
G |
9: 22,111,349 (GRCm39) |
K275R |
probably damaging |
Het |
Zzef1 |
C |
T |
11: 72,777,535 (GRCm39) |
P1789S |
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 |
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 |
|
|