Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
G |
A |
18: 70,602,553 (GRCm39) |
Q87* |
probably null |
Het |
Abca13 |
G |
A |
11: 9,248,076 (GRCm39) |
E2608K |
probably benign |
Het |
Acad9 |
T |
C |
3: 36,139,564 (GRCm39) |
V388A |
probably damaging |
Het |
Acp3 |
T |
C |
9: 104,197,201 (GRCm39) |
E146G |
probably damaging |
Het |
Adamts18 |
A |
G |
8: 114,501,585 (GRCm39) |
I346T |
possibly damaging |
Het |
Adcy8 |
T |
A |
15: 64,588,015 (GRCm39) |
D894V |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,559,449 (GRCm39) |
|
probably benign |
Het |
Arg2 |
A |
G |
12: 79,194,386 (GRCm39) |
D70G |
probably damaging |
Het |
Cap1 |
A |
T |
4: 122,761,492 (GRCm39) |
L130Q |
probably damaging |
Het |
Carmil1 |
T |
A |
13: 24,266,003 (GRCm39) |
N253I |
probably damaging |
Het |
Caskin2 |
A |
G |
11: 115,693,253 (GRCm39) |
|
probably benign |
Het |
Cd69 |
C |
T |
6: 129,247,025 (GRCm39) |
S64N |
probably benign |
Het |
Cd96 |
T |
C |
16: 45,858,942 (GRCm39) |
|
probably benign |
Het |
Celf6 |
C |
A |
9: 59,510,161 (GRCm39) |
T86K |
probably benign |
Het |
Ces1c |
A |
T |
8: 93,833,345 (GRCm39) |
|
probably benign |
Het |
Ces1c |
A |
T |
8: 93,834,238 (GRCm39) |
L351M |
probably benign |
Het |
Cnih3 |
T |
A |
1: 181,282,309 (GRCm39) |
|
probably benign |
Het |
Col15a1 |
A |
T |
4: 47,262,950 (GRCm39) |
D534V |
probably damaging |
Het |
Cry1 |
A |
G |
10: 84,969,104 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
C |
15: 47,710,527 (GRCm39) |
T1687A |
probably benign |
Het |
Def8 |
G |
A |
8: 124,183,234 (GRCm39) |
A278T |
probably damaging |
Het |
Defb13 |
T |
C |
8: 22,436,877 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,934,483 (GRCm39) |
F1489L |
possibly damaging |
Het |
Elmo3 |
T |
C |
8: 106,036,400 (GRCm39) |
L668S |
probably damaging |
Het |
Elp2 |
T |
C |
18: 24,767,466 (GRCm39) |
I716T |
probably benign |
Het |
Fshr |
C |
G |
17: 89,316,713 (GRCm39) |
S169T |
probably benign |
Het |
Gm6327 |
T |
C |
16: 12,579,061 (GRCm39) |
|
noncoding transcript |
Het |
Gm839 |
A |
T |
6: 89,189,362 (GRCm39) |
|
noncoding transcript |
Het |
Gng5 |
T |
A |
3: 146,209,048 (GRCm39) |
C39S |
probably damaging |
Het |
Gpr55 |
C |
T |
1: 85,869,146 (GRCm39) |
W145* |
probably null |
Het |
Hdlbp |
A |
C |
1: 93,349,059 (GRCm39) |
|
probably benign |
Het |
Man2a2 |
G |
T |
7: 80,017,153 (GRCm39) |
N305K |
probably damaging |
Het |
Me2 |
A |
G |
18: 73,903,744 (GRCm39) |
S575P |
probably benign |
Het |
Mier3 |
T |
C |
13: 111,851,572 (GRCm39) |
V490A |
probably damaging |
Het |
Mpdz |
T |
C |
4: 81,210,768 (GRCm39) |
T1693A |
probably benign |
Het |
Mss51 |
T |
A |
14: 20,534,756 (GRCm39) |
Q338L |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,569,013 (GRCm39) |
|
probably benign |
Het |
Mug2 |
T |
A |
6: 122,013,022 (GRCm39) |
H311Q |
probably benign |
Het |
Neto1 |
G |
A |
18: 86,479,445 (GRCm39) |
R211Q |
probably benign |
Het |
Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
Nisch |
A |
G |
14: 30,893,881 (GRCm39) |
Y1231H |
probably damaging |
Het |
Obox3 |
T |
A |
7: 15,360,252 (GRCm39) |
|
probably null |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or1e34 |
C |
T |
11: 73,778,656 (GRCm39) |
V181I |
probably benign |
Het |
Pcdh15 |
T |
C |
10: 74,006,407 (GRCm39) |
F95S |
probably damaging |
Het |
Pcsk6 |
T |
C |
7: 65,688,791 (GRCm39) |
V820A |
probably benign |
Het |
Pde5a |
A |
G |
3: 122,542,107 (GRCm39) |
N199S |
probably damaging |
Het |
Pdgfrb |
T |
A |
18: 61,201,924 (GRCm39) |
V496E |
probably benign |
Het |
Per3 |
A |
G |
4: 151,109,005 (GRCm39) |
|
probably benign |
Het |
Pip4k2b |
A |
T |
11: 97,613,762 (GRCm39) |
|
probably benign |
Het |
Podn |
G |
T |
4: 107,878,791 (GRCm39) |
L359I |
probably damaging |
Het |
Rad21 |
A |
T |
15: 51,828,426 (GRCm39) |
D547E |
probably benign |
Het |
Rere |
T |
G |
4: 150,699,779 (GRCm39) |
|
probably benign |
Het |
Serpina1d |
A |
T |
12: 103,732,016 (GRCm39) |
L281Q |
probably damaging |
Het |
Serpina9 |
T |
C |
12: 103,967,729 (GRCm39) |
N222S |
probably benign |
Het |
Sh3bgrl2 |
A |
G |
9: 83,459,612 (GRCm39) |
K57E |
probably damaging |
Het |
Sh3bgrl3 |
A |
T |
4: 133,855,347 (GRCm39) |
I33N |
probably damaging |
Het |
Sik3 |
T |
C |
9: 46,120,038 (GRCm39) |
M659T |
possibly damaging |
Het |
Sppl3 |
T |
A |
5: 115,227,053 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
C |
A |
7: 130,223,605 (GRCm39) |
Q116K |
probably damaging |
Het |
Tecta |
T |
C |
9: 42,263,359 (GRCm39) |
D1409G |
probably damaging |
Het |
Tnpo3 |
A |
G |
6: 29,568,921 (GRCm39) |
V477A |
possibly damaging |
Het |
Trim7 |
G |
T |
11: 48,740,539 (GRCm39) |
R212L |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,809,957 (GRCm39) |
C1118S |
probably benign |
Het |
Ugcg |
G |
C |
4: 59,217,036 (GRCm39) |
V187L |
possibly damaging |
Het |
Vmn1r27 |
A |
G |
6: 58,192,704 (GRCm39) |
F100S |
possibly damaging |
Het |
Zbtb18 |
A |
G |
1: 177,275,723 (GRCm39) |
E361G |
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,712,677 (GRCm39) |
V199A |
probably benign |
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 |
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 |
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 |
|