Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
C |
A |
11: 109,847,924 (GRCm39) |
L852F |
possibly damaging |
Het |
Abcc6 |
T |
C |
7: 45,669,558 (GRCm39) |
|
probably null |
Het |
Alg11 |
T |
G |
8: 22,555,584 (GRCm39) |
C240G |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,141,783 (GRCm39) |
I1190V |
probably damaging |
Het |
Apc2 |
T |
G |
10: 80,150,678 (GRCm39) |
S1911A |
probably benign |
Het |
Arfgef3 |
T |
C |
10: 18,528,511 (GRCm39) |
D292G |
possibly damaging |
Het |
Arhgef4 |
C |
A |
1: 34,763,340 (GRCm39) |
S865R |
probably benign |
Het |
Ass1 |
T |
A |
2: 31,383,160 (GRCm39) |
Y190* |
probably null |
Het |
B4galnt3 |
A |
T |
6: 120,187,051 (GRCm39) |
|
probably null |
Het |
Btnl10 |
C |
A |
11: 58,811,367 (GRCm39) |
P230Q |
possibly damaging |
Het |
C3 |
A |
G |
17: 57,516,489 (GRCm39) |
Y1348H |
probably damaging |
Het |
Ccdc198 |
G |
T |
14: 49,464,032 (GRCm39) |
D292E |
probably damaging |
Het |
Cebpz |
A |
T |
17: 79,242,336 (GRCm39) |
Y439* |
probably null |
Het |
Cic |
C |
A |
7: 24,986,265 (GRCm39) |
T1229K |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,144,744 (GRCm39) |
S524P |
probably damaging |
Het |
Col6a3 |
A |
C |
1: 90,739,421 (GRCm39) |
I269R |
probably damaging |
Het |
Dbh |
C |
T |
2: 27,071,506 (GRCm39) |
T533I |
possibly damaging |
Het |
Dcaf17 |
A |
T |
2: 70,890,713 (GRCm39) |
R83* |
probably null |
Het |
Dennd2b |
G |
A |
7: 109,124,533 (GRCm39) |
Q686* |
probably null |
Het |
Dnah7a |
A |
T |
1: 53,670,721 (GRCm39) |
D510E |
probably benign |
Het |
Dock6 |
A |
G |
9: 21,752,925 (GRCm39) |
F296S |
probably damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,177,455 (GRCm39) |
S341P |
probably damaging |
Het |
Epb41l1 |
G |
T |
2: 156,352,737 (GRCm39) |
G461V |
possibly damaging |
Het |
Epg5 |
T |
A |
18: 78,002,247 (GRCm39) |
D555E |
probably benign |
Het |
Fes |
T |
C |
7: 80,036,609 (GRCm39) |
R113G |
probably damaging |
Het |
Garre1 |
T |
A |
7: 33,957,461 (GRCm39) |
I59L |
probably benign |
Het |
Gm10684 |
A |
G |
9: 45,021,511 (GRCm39) |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,806,231 (GRCm39) |
E320G |
probably benign |
Het |
Gm14412 |
G |
T |
2: 177,007,269 (GRCm39) |
H209N |
probably damaging |
Het |
Gm14412 |
A |
C |
2: 177,007,630 (GRCm39) |
S88R |
probably benign |
Het |
Grhl1 |
T |
A |
12: 24,658,555 (GRCm39) |
L400Q |
probably damaging |
Het |
Havcr1 |
T |
A |
11: 46,664,511 (GRCm39) |
Y216* |
probably null |
Het |
Hephl1 |
A |
C |
9: 14,985,420 (GRCm39) |
Y745* |
probably null |
Het |
Hmcn2 |
T |
G |
2: 31,301,922 (GRCm39) |
|
probably null |
Het |
Hs3st6 |
A |
G |
17: 24,977,110 (GRCm39) |
K197E |
possibly damaging |
Het |
Ifi214 |
C |
T |
1: 173,357,077 (GRCm39) |
V9I |
probably benign |
Het |
Jakmip2 |
T |
C |
18: 43,700,209 (GRCm39) |
T450A |
probably benign |
Het |
Lrp4 |
T |
A |
2: 91,328,753 (GRCm39) |
V1551D |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,351,634 (GRCm39) |
H1634Q |
possibly damaging |
Het |
Mcpt8 |
T |
A |
14: 56,321,291 (GRCm39) |
I58F |
probably benign |
Het |
Mga |
T |
A |
2: 119,757,075 (GRCm39) |
H1018Q |
possibly damaging |
Het |
Myo10 |
T |
A |
15: 25,801,308 (GRCm39) |
V1499E |
probably damaging |
Het |
Myom2 |
G |
T |
8: 15,131,023 (GRCm39) |
D320Y |
probably damaging |
Het |
Or11g7 |
T |
A |
14: 50,691,295 (GRCm39) |
M262K |
probably damaging |
Het |
Or13a27 |
T |
C |
7: 139,925,378 (GRCm39) |
I175V |
probably benign |
Het |
Or2r11 |
C |
T |
6: 42,437,360 (GRCm39) |
V198M |
probably benign |
Het |
Or2t26 |
A |
C |
11: 49,039,101 (GRCm39) |
N6H |
possibly damaging |
Het |
Or4c115 |
G |
A |
2: 88,927,888 (GRCm39) |
P128S |
probably damaging |
Het |
Or5d47 |
A |
T |
2: 87,804,403 (GRCm39) |
V202D |
possibly damaging |
Het |
Pabpc4 |
G |
T |
4: 123,182,861 (GRCm39) |
R166L |
possibly damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,489,015 (GRCm39) |
E231G |
possibly damaging |
Het |
Pomgnt2 |
A |
T |
9: 121,811,257 (GRCm39) |
I508N |
possibly damaging |
Het |
Ppp2r5e |
C |
G |
12: 75,516,341 (GRCm39) |
A239P |
probably damaging |
Het |
Prdm15 |
G |
T |
16: 97,638,885 (GRCm39) |
D58E |
probably benign |
Het |
Rgl2 |
A |
G |
17: 34,151,122 (GRCm39) |
T117A |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,418,943 (GRCm39) |
I723T |
probably damaging |
Het |
Serpina3g |
A |
G |
12: 104,207,536 (GRCm39) |
E233G |
probably damaging |
Het |
Skint6 |
T |
A |
4: 112,749,187 (GRCm39) |
S798C |
probably benign |
Het |
Slc35f1 |
T |
C |
10: 52,898,000 (GRCm39) |
L137P |
possibly damaging |
Het |
Slc6a20a |
T |
C |
9: 123,485,373 (GRCm39) |
N246S |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,369,534 (GRCm39) |
L663S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,173 (GRCm39) |
|
probably null |
Het |
Slit2 |
A |
G |
5: 48,439,330 (GRCm39) |
T41A |
probably damaging |
Het |
Smc2 |
T |
C |
4: 52,450,863 (GRCm39) |
I227T |
probably damaging |
Het |
Smg1 |
A |
G |
7: 117,753,422 (GRCm39) |
|
probably benign |
Het |
Ssu2 |
A |
T |
6: 112,361,388 (GRCm39) |
L23M |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,141,053 (GRCm39) |
|
probably null |
Het |
Tekt1 |
T |
C |
11: 72,242,761 (GRCm39) |
T249A |
probably benign |
Het |
Tfr2 |
T |
C |
5: 137,569,954 (GRCm39) |
V120A |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,605,846 (GRCm39) |
P529L |
probably damaging |
Het |
Tll1 |
C |
T |
8: 64,478,141 (GRCm39) |
D871N |
probably damaging |
Het |
Tlr11 |
A |
C |
14: 50,598,664 (GRCm39) |
I217L |
probably benign |
Het |
Tmem87b |
T |
A |
2: 128,673,479 (GRCm39) |
V241D |
probably damaging |
Het |
Tshz2 |
T |
A |
2: 169,727,465 (GRCm39) |
I218N |
possibly damaging |
Het |
Vmn1r18 |
A |
T |
6: 57,367,026 (GRCm39) |
I176N |
possibly damaging |
Het |
Vmn2r68 |
T |
A |
7: 84,883,260 (GRCm39) |
H164L |
probably benign |
Het |
Vmn2r74 |
T |
C |
7: 85,601,650 (GRCm39) |
T663A |
probably benign |
Het |
Vmn2r8 |
T |
C |
5: 108,945,436 (GRCm39) |
T724A |
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,206,954 (GRCm39) |
V289A |
possibly damaging |
Het |
Zfp62 |
T |
A |
11: 49,107,047 (GRCm39) |
D379E |
probably damaging |
Het |
Zfp78 |
C |
T |
7: 6,381,897 (GRCm39) |
P316S |
probably damaging |
Het |
Zfyve27 |
T |
G |
19: 42,159,987 (GRCm39) |
M1R |
probably null |
Het |
Zkscan8 |
G |
A |
13: 21,709,325 (GRCm39) |
P191L |
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 |
R1796:Dnah1
|
UTSW |
14 |
30,983,050 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|