Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
G |
A |
12: 84,662,156 (GRCm39) |
S30F |
probably benign |
Het |
Abtb1 |
T |
C |
6: 88,813,601 (GRCm39) |
D379G |
possibly damaging |
Het |
Adgre1 |
A |
G |
17: 57,748,350 (GRCm39) |
I517V |
probably benign |
Het |
Ajm1 |
C |
T |
2: 25,468,000 (GRCm39) |
G637D |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Angpt4 |
G |
A |
2: 151,780,909 (GRCm39) |
V386M |
probably damaging |
Het |
Asic1 |
A |
G |
15: 99,594,535 (GRCm39) |
H360R |
probably null |
Het |
Asxl1 |
G |
A |
2: 153,243,526 (GRCm39) |
A1359T |
probably benign |
Het |
Atp8a2 |
C |
T |
14: 60,258,207 (GRCm39) |
|
probably null |
Het |
Bltp3a |
T |
C |
17: 28,109,045 (GRCm39) |
F1088S |
possibly damaging |
Het |
C1qtnf2 |
T |
A |
11: 43,382,114 (GRCm39) |
F279I |
probably damaging |
Het |
Car8 |
A |
T |
4: 8,221,671 (GRCm39) |
L100* |
probably null |
Het |
Cd52 |
T |
C |
4: 133,822,295 (GRCm39) |
M1V |
probably null |
Het |
Celf5 |
T |
C |
10: 81,303,053 (GRCm39) |
I163V |
possibly damaging |
Het |
Cep250 |
A |
T |
2: 155,834,107 (GRCm39) |
T2010S |
possibly damaging |
Het |
Cfap65 |
C |
T |
1: 74,958,107 (GRCm39) |
V934M |
probably damaging |
Het |
Colec11 |
A |
T |
12: 28,644,858 (GRCm39) |
I212N |
probably damaging |
Het |
Cpa3 |
C |
T |
3: 20,277,391 (GRCm39) |
|
probably null |
Het |
Ctnnd1 |
G |
T |
2: 84,445,553 (GRCm39) |
H495N |
probably damaging |
Het |
Cyb5a |
T |
C |
18: 84,869,686 (GRCm39) |
V28A |
probably benign |
Het |
Ddo |
A |
T |
10: 40,523,625 (GRCm39) |
Q205L |
probably benign |
Het |
E2f1 |
A |
T |
2: 154,402,849 (GRCm39) |
V306E |
probably benign |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Eef1d |
A |
C |
15: 75,773,024 (GRCm39) |
F25C |
probably damaging |
Het |
Ehd3 |
A |
T |
17: 74,137,354 (GRCm39) |
I508F |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,831,975 (GRCm39) |
I232F |
probably benign |
Het |
Enc1 |
T |
A |
13: 97,382,991 (GRCm39) |
D500E |
probably benign |
Het |
Enc1 |
C |
A |
13: 97,382,993 (GRCm39) |
T501K |
possibly damaging |
Het |
Fam83f |
C |
T |
15: 80,574,283 (GRCm39) |
R213W |
possibly damaging |
Het |
Fbxo31 |
A |
T |
8: 122,287,177 (GRCm39) |
L158* |
probably null |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,797 (GRCm39) |
P1808S |
probably damaging |
Het |
Foxi3 |
C |
A |
6: 70,937,794 (GRCm39) |
T342N |
possibly damaging |
Het |
Gpr179 |
T |
A |
11: 97,227,382 (GRCm39) |
D1591V |
possibly damaging |
Het |
Gpsm2 |
A |
G |
3: 108,609,166 (GRCm39) |
V151A |
probably damaging |
Het |
Grk2 |
T |
G |
19: 4,337,968 (GRCm39) |
I513L |
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,486,346 (GRCm39) |
E135G |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,296,138 (GRCm39) |
K578* |
probably null |
Het |
Hycc1 |
T |
G |
5: 24,191,149 (GRCm39) |
T173P |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,198,171 (GRCm39) |
N1533S |
probably benign |
Het |
Kif3c |
A |
G |
12: 3,417,299 (GRCm39) |
N440S |
probably benign |
Het |
Klhdc2 |
T |
C |
12: 69,347,071 (GRCm39) |
|
probably null |
Het |
Kmo |
G |
T |
1: 175,465,461 (GRCm39) |
V72L |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,651,315 (GRCm39) |
I56T |
possibly damaging |
Het |
Krt72 |
T |
C |
15: 101,689,987 (GRCm39) |
|
probably null |
Het |
Krt78 |
T |
A |
15: 101,859,300 (GRCm39) |
Q299L |
probably damaging |
Het |
Loxhd1 |
C |
T |
18: 77,493,603 (GRCm39) |
R1521C |
probably damaging |
Het |
Loxhd1 |
G |
A |
18: 77,513,335 (GRCm39) |
E1774K |
possibly damaging |
Het |
Ly6g6f |
T |
C |
17: 35,302,478 (GRCm39) |
S20G |
probably benign |
Het |
Mecr |
T |
A |
4: 131,592,382 (GRCm39) |
M282K |
probably damaging |
Het |
Mfsd14a |
G |
T |
3: 116,428,596 (GRCm39) |
A353D |
probably damaging |
Het |
Mroh9 |
A |
T |
1: 162,873,279 (GRCm39) |
N564K |
probably damaging |
Het |
Mrs2 |
T |
A |
13: 25,181,111 (GRCm39) |
T237S |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,398,377 (GRCm39) |
L534S |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,115,183 (GRCm39) |
I1906T |
probably benign |
Het |
Myh4 |
T |
A |
11: 67,151,150 (GRCm39) |
V1935D |
probably benign |
Het |
Myo18a |
T |
C |
11: 77,720,170 (GRCm39) |
I684T |
possibly damaging |
Het |
Myo7b |
C |
T |
18: 32,119,728 (GRCm39) |
R788H |
possibly damaging |
Het |
Nbea |
A |
T |
3: 55,551,129 (GRCm39) |
D2678E |
possibly damaging |
Het |
Ndufs3 |
A |
C |
2: 90,729,050 (GRCm39) |
Y145* |
probably null |
Het |
Nrros |
A |
G |
16: 31,962,329 (GRCm39) |
F563L |
probably damaging |
Het |
Ntn4 |
T |
C |
10: 93,581,633 (GRCm39) |
V602A |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,920,163 (GRCm39) |
R6736L |
possibly damaging |
Het |
Odr4 |
T |
C |
1: 150,251,305 (GRCm39) |
N283S |
probably benign |
Het |
Or13c7d |
T |
A |
4: 43,770,495 (GRCm39) |
D172V |
possibly damaging |
Het |
Or2ag16 |
T |
C |
7: 106,351,756 (GRCm39) |
I280V |
probably benign |
Het |
Or7g22 |
C |
A |
9: 19,049,213 (GRCm39) |
T308K |
probably benign |
Het |
Or8d1 |
T |
A |
9: 38,766,820 (GRCm39) |
V154D |
probably benign |
Het |
Or8g54 |
C |
T |
9: 39,707,301 (GRCm39) |
P210L |
possibly damaging |
Het |
Or8g55 |
A |
G |
9: 39,785,267 (GRCm39) |
E232G |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,738,576 (GRCm39) |
F751L |
possibly damaging |
Het |
Plekhh2 |
A |
G |
17: 84,906,561 (GRCm39) |
|
probably null |
Het |
Postn |
A |
G |
3: 54,281,177 (GRCm39) |
H434R |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,539,114 (GRCm39) |
D118G |
possibly damaging |
Het |
Ralyl |
G |
T |
3: 14,208,493 (GRCm39) |
G211V |
possibly damaging |
Het |
Rbak |
T |
A |
5: 143,159,202 (GRCm39) |
E617V |
probably damaging |
Het |
Rbms3 |
A |
T |
9: 116,548,401 (GRCm39) |
W80R |
probably damaging |
Het |
Retnlg |
A |
T |
16: 48,694,610 (GRCm39) |
Y86F |
probably benign |
Het |
Rtel1 |
T |
A |
2: 180,993,896 (GRCm39) |
S643T |
probably benign |
Het |
Semp2l2a |
A |
T |
8: 13,886,816 (GRCm39) |
L425* |
probably null |
Het |
Serpina11 |
A |
T |
12: 103,950,954 (GRCm39) |
F256I |
probably damaging |
Het |
Setd2 |
A |
T |
9: 110,446,884 (GRCm39) |
|
probably null |
Het |
Setd2 |
A |
T |
9: 110,379,413 (GRCm39) |
Y1076F |
probably benign |
Het |
Sgsm1 |
T |
C |
5: 113,421,483 (GRCm39) |
T248A |
possibly damaging |
Het |
Slc6a21 |
T |
C |
7: 44,930,179 (GRCm39) |
Y193H |
probably damaging |
Het |
Slfn9 |
T |
C |
11: 82,872,781 (GRCm39) |
K652E |
probably benign |
Het |
Stt3b |
A |
T |
9: 115,077,675 (GRCm39) |
Y692* |
probably null |
Het |
Sval3 |
A |
G |
6: 41,945,096 (GRCm39) |
Q8R |
probably benign |
Het |
Synm |
T |
A |
7: 67,383,748 (GRCm39) |
I1305F |
possibly damaging |
Het |
Tdrd1 |
T |
C |
19: 56,826,215 (GRCm39) |
F169L |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,295,493 (GRCm39) |
D334V |
probably damaging |
Het |
Tle2 |
G |
A |
10: 81,425,331 (GRCm39) |
|
probably null |
Het |
Tmem243 |
A |
G |
5: 9,166,489 (GRCm39) |
I30V |
probably benign |
Het |
Treml2 |
T |
C |
17: 48,616,530 (GRCm39) |
*330R |
probably null |
Het |
Trpm6 |
A |
G |
19: 18,804,931 (GRCm39) |
D961G |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,155,907 (GRCm39) |
V2244A |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,109,005 (GRCm39) |
V2148F |
probably damaging |
Het |
Ush2a |
A |
C |
1: 188,643,024 (GRCm39) |
T4129P |
probably benign |
Het |
Vgll2 |
G |
A |
10: 51,901,324 (GRCm39) |
V85I |
probably damaging |
Het |
Vmn1r16 |
T |
C |
6: 57,300,256 (GRCm39) |
Y122C |
probably benign |
Het |
Vmn1r22 |
A |
T |
6: 57,877,134 (GRCm39) |
I91N |
probably damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,213,011 (GRCm39) |
Y465* |
probably null |
Het |
Wdr64 |
A |
T |
1: 175,544,897 (GRCm39) |
E110V |
probably damaging |
Het |
Wfdc6a |
A |
T |
2: 164,422,231 (GRCm39) |
C123S |
probably damaging |
Het |
Xrcc1 |
A |
G |
7: 24,247,252 (GRCm39) |
Y30C |
probably damaging |
Het |
Zdhhc7 |
T |
C |
8: 120,812,157 (GRCm39) |
K155R |
probably benign |
Het |
Zfp560 |
A |
G |
9: 20,263,226 (GRCm39) |
F50S |
possibly damaging |
Het |
Zfp616 |
C |
T |
11: 73,976,671 (GRCm39) |
T980I |
probably damaging |
Het |
Zfp808 |
C |
T |
13: 62,319,670 (GRCm39) |
P300S |
probably damaging |
Het |
Zfp979 |
G |
A |
4: 147,697,740 (GRCm39) |
T323I |
probably damaging |
Het |
|
Other mutations in Dnah1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Dnah1
|
APN |
14 |
31,009,830 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00227:Dnah1
|
APN |
14 |
31,008,853 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00491:Dnah1
|
APN |
14 |
30,983,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00787:Dnah1
|
APN |
14 |
31,022,020 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00809:Dnah1
|
APN |
14 |
31,022,766 (GRCm39) |
nonsense |
probably null |
|
IGL00911:Dnah1
|
APN |
14 |
31,026,391 (GRCm39) |
splice site |
probably null |
|
IGL00949:Dnah1
|
APN |
14 |
31,029,047 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00976:Dnah1
|
APN |
14 |
31,000,095 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01484:Dnah1
|
APN |
14 |
31,021,897 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01629:Dnah1
|
APN |
14 |
31,014,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Dnah1
|
APN |
14 |
30,985,335 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01893:Dnah1
|
APN |
14 |
30,988,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Dnah1
|
APN |
14 |
31,032,872 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01938:Dnah1
|
APN |
14 |
31,005,844 (GRCm39) |
missense |
probably benign |
|
IGL02032:Dnah1
|
APN |
14 |
30,996,326 (GRCm39) |
missense |
probably benign |
|
IGL02052:Dnah1
|
APN |
14 |
30,990,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02097:Dnah1
|
APN |
14 |
31,026,958 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02127:Dnah1
|
APN |
14 |
31,026,885 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02143:Dnah1
|
APN |
14 |
31,005,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Dnah1
|
APN |
14 |
31,022,924 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02442:Dnah1
|
APN |
14 |
31,009,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02525:Dnah1
|
APN |
14 |
31,027,790 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02558:Dnah1
|
APN |
14 |
30,996,336 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02633:Dnah1
|
APN |
14 |
31,006,772 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02720:Dnah1
|
APN |
14 |
30,984,177 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02728:Dnah1
|
APN |
14 |
31,005,955 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02738:Dnah1
|
APN |
14 |
31,014,597 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02863:Dnah1
|
APN |
14 |
31,017,250 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02944:Dnah1
|
APN |
14 |
31,022,828 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03110:Dnah1
|
APN |
14 |
30,988,674 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03201:Dnah1
|
APN |
14 |
31,022,906 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03215:Dnah1
|
APN |
14 |
30,996,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03230:Dnah1
|
APN |
14 |
30,992,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Dnah1
|
APN |
14 |
30,991,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Dnah1
|
APN |
14 |
31,008,545 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03299:Dnah1
|
APN |
14 |
31,037,079 (GRCm39) |
nonsense |
probably null |
|
IGL03301:Dnah1
|
APN |
14 |
31,014,649 (GRCm39) |
missense |
probably damaging |
1.00 |
ergonomic
|
UTSW |
14 |
31,022,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
Faraday
|
UTSW |
14 |
31,032,839 (GRCm39) |
missense |
probably null |
0.05 |
K3955:Dnah1
|
UTSW |
14 |
30,988,416 (GRCm39) |
missense |
probably benign |
|
PIT1430001:Dnah1
|
UTSW |
14 |
30,984,537 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Dnah1
|
UTSW |
14 |
31,006,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0043:Dnah1
|
UTSW |
14 |
30,996,362 (GRCm39) |
missense |
probably damaging |
0.97 |
R0092:Dnah1
|
UTSW |
14 |
30,993,566 (GRCm39) |
missense |
probably benign |
0.00 |
R0100:Dnah1
|
UTSW |
14 |
30,984,109 (GRCm39) |
critical splice donor site |
probably null |
|
R0100:Dnah1
|
UTSW |
14 |
30,984,109 (GRCm39) |
critical splice donor site |
probably null |
|
R0101:Dnah1
|
UTSW |
14 |
31,005,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Dnah1
|
UTSW |
14 |
30,989,831 (GRCm39) |
splice site |
probably benign |
|
R0279:Dnah1
|
UTSW |
14 |
31,024,332 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0299:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Dnah1
|
UTSW |
14 |
31,000,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0739:Dnah1
|
UTSW |
14 |
30,987,872 (GRCm39) |
nonsense |
probably null |
|
R0789:Dnah1
|
UTSW |
14 |
31,026,548 (GRCm39) |
missense |
probably benign |
|
R0826:Dnah1
|
UTSW |
14 |
31,025,864 (GRCm39) |
missense |
probably benign |
0.02 |
R1102:Dnah1
|
UTSW |
14 |
31,018,414 (GRCm39) |
nonsense |
probably null |
|
R1116:Dnah1
|
UTSW |
14 |
31,029,824 (GRCm39) |
missense |
probably benign |
0.13 |
R1229:Dnah1
|
UTSW |
14 |
31,032,808 (GRCm39) |
missense |
probably benign |
0.11 |
R1447:Dnah1
|
UTSW |
14 |
31,028,855 (GRCm39) |
missense |
probably benign |
0.06 |
R1449:Dnah1
|
UTSW |
14 |
30,985,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Dnah1
|
UTSW |
14 |
30,990,738 (GRCm39) |
splice site |
probably benign |
|
R1482:Dnah1
|
UTSW |
14 |
31,016,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R1500:Dnah1
|
UTSW |
14 |
31,038,715 (GRCm39) |
missense |
probably benign |
|
R1512:Dnah1
|
UTSW |
14 |
31,014,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1591:Dnah1
|
UTSW |
14 |
30,994,289 (GRCm39) |
missense |
probably benign |
0.01 |
R1598:Dnah1
|
UTSW |
14 |
31,023,219 (GRCm39) |
missense |
probably benign |
0.07 |
R1644:Dnah1
|
UTSW |
14 |
31,024,249 (GRCm39) |
splice site |
probably benign |
|
R1672:Dnah1
|
UTSW |
14 |
30,998,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Dnah1
|
UTSW |
14 |
31,001,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Dnah1
|
UTSW |
14 |
31,032,839 (GRCm39) |
missense |
probably null |
0.05 |
R1902:Dnah1
|
UTSW |
14 |
31,041,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R1903:Dnah1
|
UTSW |
14 |
31,041,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R1905:Dnah1
|
UTSW |
14 |
30,986,587 (GRCm39) |
missense |
probably benign |
0.06 |
R1908:Dnah1
|
UTSW |
14 |
30,984,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Dnah1
|
UTSW |
14 |
30,987,348 (GRCm39) |
nonsense |
probably null |
|
R1973:Dnah1
|
UTSW |
14 |
30,987,348 (GRCm39) |
nonsense |
probably null |
|
R2004:Dnah1
|
UTSW |
14 |
31,023,813 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2051:Dnah1
|
UTSW |
14 |
31,001,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Dnah1
|
UTSW |
14 |
30,993,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2188:Dnah1
|
UTSW |
14 |
31,001,121 (GRCm39) |
missense |
probably damaging |
0.98 |
R2240:Dnah1
|
UTSW |
14 |
31,021,931 (GRCm39) |
missense |
probably benign |
0.00 |
R2862:Dnah1
|
UTSW |
14 |
31,006,719 (GRCm39) |
missense |
probably benign |
0.21 |
R2894:Dnah1
|
UTSW |
14 |
31,020,718 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3120:Dnah1
|
UTSW |
14 |
30,988,779 (GRCm39) |
nonsense |
probably null |
|
R3410:Dnah1
|
UTSW |
14 |
30,991,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3411:Dnah1
|
UTSW |
14 |
30,991,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3435:Dnah1
|
UTSW |
14 |
31,038,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R3615:Dnah1
|
UTSW |
14 |
31,037,105 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3616:Dnah1
|
UTSW |
14 |
31,037,105 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3741:Dnah1
|
UTSW |
14 |
30,987,424 (GRCm39) |
splice site |
probably benign |
|
R3805:Dnah1
|
UTSW |
14 |
31,016,720 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3894:Dnah1
|
UTSW |
14 |
31,028,985 (GRCm39) |
missense |
probably benign |
|
R4007:Dnah1
|
UTSW |
14 |
31,025,741 (GRCm39) |
splice site |
probably benign |
|
R4201:Dnah1
|
UTSW |
14 |
30,984,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4232:Dnah1
|
UTSW |
14 |
31,026,873 (GRCm39) |
missense |
probably benign |
|
R4372:Dnah1
|
UTSW |
14 |
31,026,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R4391:Dnah1
|
UTSW |
14 |
31,016,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Dnah1
|
UTSW |
14 |
31,006,718 (GRCm39) |
missense |
probably benign |
0.00 |
R4526:Dnah1
|
UTSW |
14 |
31,007,955 (GRCm39) |
missense |
probably benign |
0.05 |
R4650:Dnah1
|
UTSW |
14 |
31,006,844 (GRCm39) |
splice site |
probably null |
|
R4723:Dnah1
|
UTSW |
14 |
30,994,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Dnah1
|
UTSW |
14 |
31,041,902 (GRCm39) |
missense |
probably benign |
|
R4783:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Dnah1
|
UTSW |
14 |
30,986,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Dnah1
|
UTSW |
14 |
31,022,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4897:Dnah1
|
UTSW |
14 |
30,989,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Dnah1
|
UTSW |
14 |
31,017,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Dnah1
|
UTSW |
14 |
31,008,855 (GRCm39) |
missense |
probably null |
1.00 |
R5070:Dnah1
|
UTSW |
14 |
31,004,375 (GRCm39) |
missense |
probably benign |
0.05 |
R5128:Dnah1
|
UTSW |
14 |
31,018,152 (GRCm39) |
splice site |
probably null |
|
R5409:Dnah1
|
UTSW |
14 |
30,985,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Dnah1
|
UTSW |
14 |
31,038,704 (GRCm39) |
missense |
probably benign |
|
R5481:Dnah1
|
UTSW |
14 |
31,030,828 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5550:Dnah1
|
UTSW |
14 |
31,038,665 (GRCm39) |
missense |
probably benign |
0.00 |
R5555:Dnah1
|
UTSW |
14 |
31,012,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R5566:Dnah1
|
UTSW |
14 |
30,996,323 (GRCm39) |
missense |
probably benign |
0.35 |
R5623:Dnah1
|
UTSW |
14 |
31,007,980 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5701:Dnah1
|
UTSW |
14 |
30,996,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Dnah1
|
UTSW |
14 |
31,032,863 (GRCm39) |
missense |
probably benign |
0.00 |
R5823:Dnah1
|
UTSW |
14 |
30,988,375 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6030:Dnah1
|
UTSW |
14 |
30,989,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Dnah1
|
UTSW |
14 |
30,989,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Dnah1
|
UTSW |
14 |
30,991,382 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6139:Dnah1
|
UTSW |
14 |
31,007,984 (GRCm39) |
missense |
probably benign |
0.02 |
R6145:Dnah1
|
UTSW |
14 |
31,022,927 (GRCm39) |
missense |
probably benign |
0.07 |
R6306:Dnah1
|
UTSW |
14 |
31,026,544 (GRCm39) |
missense |
probably damaging |
0.97 |
R6376:Dnah1
|
UTSW |
14 |
30,997,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Dnah1
|
UTSW |
14 |
31,022,765 (GRCm39) |
missense |
probably benign |
0.08 |
R6549:Dnah1
|
UTSW |
14 |
30,991,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6748:Dnah1
|
UTSW |
14 |
31,021,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R6826:Dnah1
|
UTSW |
14 |
31,008,247 (GRCm39) |
missense |
probably benign |
0.00 |
R6870:Dnah1
|
UTSW |
14 |
30,993,018 (GRCm39) |
nonsense |
probably null |
|
R6932:Dnah1
|
UTSW |
14 |
31,009,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6944:Dnah1
|
UTSW |
14 |
30,990,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Dnah1
|
UTSW |
14 |
30,986,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Dnah1
|
UTSW |
14 |
31,019,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Dnah1
|
UTSW |
14 |
31,008,033 (GRCm39) |
missense |
probably benign |
|
R7136:Dnah1
|
UTSW |
14 |
31,020,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Dnah1
|
UTSW |
14 |
30,996,339 (GRCm39) |
missense |
probably benign |
|
R7241:Dnah1
|
UTSW |
14 |
30,986,896 (GRCm39) |
missense |
probably benign |
0.00 |
R7260:Dnah1
|
UTSW |
14 |
30,991,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7264:Dnah1
|
UTSW |
14 |
30,991,851 (GRCm39) |
missense |
probably benign |
|
R7291:Dnah1
|
UTSW |
14 |
31,020,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Dnah1
|
UTSW |
14 |
31,009,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7300:Dnah1
|
UTSW |
14 |
30,991,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7319:Dnah1
|
UTSW |
14 |
31,018,551 (GRCm39) |
missense |
probably benign |
0.02 |
R7323:Dnah1
|
UTSW |
14 |
31,020,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Dnah1
|
UTSW |
14 |
31,022,748 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7472:Dnah1
|
UTSW |
14 |
30,983,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Dnah1
|
UTSW |
14 |
31,037,079 (GRCm39) |
nonsense |
probably null |
|
R7526:Dnah1
|
UTSW |
14 |
31,009,833 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7560:Dnah1
|
UTSW |
14 |
31,026,940 (GRCm39) |
missense |
probably benign |
|
R7574:Dnah1
|
UTSW |
14 |
31,041,865 (GRCm39) |
missense |
probably benign |
0.00 |
R7617:Dnah1
|
UTSW |
14 |
31,006,739 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7620:Dnah1
|
UTSW |
14 |
31,025,863 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7692:Dnah1
|
UTSW |
14 |
31,014,295 (GRCm39) |
missense |
probably benign |
0.00 |
R7702:Dnah1
|
UTSW |
14 |
31,032,866 (GRCm39) |
missense |
probably benign |
|
R7786:Dnah1
|
UTSW |
14 |
30,984,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7984:Dnah1
|
UTSW |
14 |
30,989,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Dnah1
|
UTSW |
14 |
31,020,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Dnah1
|
UTSW |
14 |
30,986,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8032:Dnah1
|
UTSW |
14 |
30,993,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R8099:Dnah1
|
UTSW |
14 |
31,024,321 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Dnah1
|
UTSW |
14 |
31,019,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Dnah1
|
UTSW |
14 |
31,015,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Dnah1
|
UTSW |
14 |
31,017,531 (GRCm39) |
missense |
probably benign |
0.00 |
R8345:Dnah1
|
UTSW |
14 |
30,986,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Dnah1
|
UTSW |
14 |
31,015,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Dnah1
|
UTSW |
14 |
31,005,159 (GRCm39) |
missense |
probably benign |
|
R8356:Dnah1
|
UTSW |
14 |
30,994,972 (GRCm39) |
missense |
probably benign |
0.00 |
R8376:Dnah1
|
UTSW |
14 |
31,023,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Dnah1
|
UTSW |
14 |
31,015,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8461:Dnah1
|
UTSW |
14 |
31,027,915 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Dnah1
|
UTSW |
14 |
31,023,805 (GRCm39) |
missense |
probably benign |
0.16 |
R8544:Dnah1
|
UTSW |
14 |
30,990,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Dnah1
|
UTSW |
14 |
30,989,767 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8716:Dnah1
|
UTSW |
14 |
30,989,941 (GRCm39) |
critical splice donor site |
probably benign |
|
R8750:Dnah1
|
UTSW |
14 |
31,026,924 (GRCm39) |
missense |
probably benign |
0.30 |
R8790:Dnah1
|
UTSW |
14 |
31,018,232 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8808:Dnah1
|
UTSW |
14 |
31,008,771 (GRCm39) |
missense |
probably benign |
|
R8821:Dnah1
|
UTSW |
14 |
31,018,455 (GRCm39) |
missense |
probably benign |
|
R8887:Dnah1
|
UTSW |
14 |
31,032,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8948:Dnah1
|
UTSW |
14 |
31,012,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Dnah1
|
UTSW |
14 |
31,012,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Dnah1
|
UTSW |
14 |
31,007,950 (GRCm39) |
missense |
probably benign |
|
R8987:Dnah1
|
UTSW |
14 |
31,033,704 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8998:Dnah1
|
UTSW |
14 |
31,018,235 (GRCm39) |
missense |
probably benign |
0.12 |
R8999:Dnah1
|
UTSW |
14 |
31,018,235 (GRCm39) |
missense |
probably benign |
0.12 |
R9015:Dnah1
|
UTSW |
14 |
30,986,316 (GRCm39) |
missense |
probably damaging |
0.96 |
R9031:Dnah1
|
UTSW |
14 |
31,001,128 (GRCm39) |
missense |
probably benign |
|
R9088:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably benign |
0.04 |
R9096:Dnah1
|
UTSW |
14 |
30,983,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R9117:Dnah1
|
UTSW |
14 |
31,033,581 (GRCm39) |
splice site |
probably benign |
|
R9157:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R9296:Dnah1
|
UTSW |
14 |
30,996,011 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9313:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R9325:Dnah1
|
UTSW |
14 |
30,998,160 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9352:Dnah1
|
UTSW |
14 |
31,038,620 (GRCm39) |
missense |
probably benign |
0.00 |
R9411:Dnah1
|
UTSW |
14 |
31,018,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R9429:Dnah1
|
UTSW |
14 |
30,997,499 (GRCm39) |
nonsense |
probably null |
|
R9452:Dnah1
|
UTSW |
14 |
31,018,448 (GRCm39) |
missense |
probably benign |
0.35 |
R9562:Dnah1
|
UTSW |
14 |
30,986,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Dnah1
|
UTSW |
14 |
30,986,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Dnah1
|
UTSW |
14 |
31,026,400 (GRCm39) |
missense |
probably null |
0.20 |
R9621:Dnah1
|
UTSW |
14 |
31,016,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9677:Dnah1
|
UTSW |
14 |
31,029,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Dnah1
|
UTSW |
14 |
30,987,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9758:Dnah1
|
UTSW |
14 |
30,985,395 (GRCm39) |
missense |
probably damaging |
0.98 |
RF006:Dnah1
|
UTSW |
14 |
31,029,832 (GRCm39) |
missense |
probably benign |
0.08 |
Z1088:Dnah1
|
UTSW |
14 |
31,026,768 (GRCm39) |
missense |
probably benign |
0.17 |
|