Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf3 |
T |
C |
8: 123,508,284 (GRCm39) |
V260A |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,251,505 (GRCm39) |
D6204G |
probably damaging |
Het |
Ago3 |
T |
A |
4: 126,270,721 (GRCm39) |
K258* |
probably null |
Het |
Aspm |
T |
G |
1: 139,392,011 (GRCm39) |
Y787* |
probably null |
Het |
Atp8b5 |
A |
C |
4: 43,291,714 (GRCm39) |
D29A |
probably benign |
Het |
Bdh2 |
A |
T |
3: 135,001,013 (GRCm39) |
I128F |
probably damaging |
Het |
Bmper |
T |
A |
9: 23,136,126 (GRCm39) |
M69K |
probably benign |
Het |
Ccdc7a |
C |
T |
8: 129,525,245 (GRCm39) |
M1415I |
probably benign |
Het |
Ccpg1 |
G |
A |
9: 72,913,001 (GRCm39) |
R179H |
probably damaging |
Het |
Cdc23 |
G |
A |
18: 34,767,150 (GRCm39) |
T564I |
probably benign |
Het |
Cemip |
T |
A |
7: 83,591,373 (GRCm39) |
|
probably null |
Het |
Cfap65 |
C |
T |
1: 74,967,203 (GRCm39) |
G249R |
probably benign |
Het |
Clec2m |
T |
A |
6: 129,302,593 (GRCm39) |
N145Y |
probably damaging |
Het |
Cpsf1 |
T |
A |
15: 76,485,690 (GRCm39) |
T435S |
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,504,477 (GRCm39) |
T879A |
possibly damaging |
Het |
Diaph3 |
G |
A |
14: 87,066,529 (GRCm39) |
Q955* |
probably null |
Het |
Disp2 |
G |
A |
2: 118,641,284 (GRCm39) |
V298M |
unknown |
Het |
Dnmt3a |
T |
C |
12: 3,885,234 (GRCm39) |
S13P |
unknown |
Het |
Eci3 |
G |
A |
13: 35,132,164 (GRCm39) |
T228I |
probably damaging |
Het |
Ecm2 |
T |
C |
13: 49,674,276 (GRCm39) |
L232P |
probably benign |
Het |
Ednra |
G |
A |
8: 78,415,813 (GRCm39) |
R145C |
probably damaging |
Het |
Faap100 |
G |
T |
11: 120,267,856 (GRCm39) |
H306N |
possibly damaging |
Het |
Fam8a1 |
T |
A |
13: 46,827,054 (GRCm39) |
I275K |
probably damaging |
Het |
Fat3 |
C |
A |
9: 15,910,570 (GRCm39) |
V1811L |
probably benign |
Het |
Fbn2 |
C |
T |
18: 58,191,503 (GRCm39) |
C1540Y |
probably damaging |
Het |
Fcgbpl1 |
G |
A |
7: 27,854,785 (GRCm39) |
V1804M |
probably damaging |
Het |
Ffar3 |
A |
G |
7: 30,554,789 (GRCm39) |
L177P |
probably damaging |
Het |
Fmnl1 |
A |
G |
11: 103,077,440 (GRCm39) |
T267A |
possibly damaging |
Het |
Fsip1 |
T |
C |
2: 118,070,952 (GRCm39) |
E246G |
probably damaging |
Het |
Gemin4 |
A |
G |
11: 76,101,605 (GRCm39) |
L1052P |
probably damaging |
Het |
Gp2 |
C |
T |
7: 119,042,010 (GRCm39) |
C505Y |
probably benign |
Het |
Grm5 |
A |
T |
7: 87,723,746 (GRCm39) |
I679F |
probably damaging |
Het |
Hapln1 |
A |
T |
13: 89,732,902 (GRCm39) |
D21V |
probably benign |
Het |
Jak2 |
T |
C |
19: 29,262,270 (GRCm39) |
S364P |
probably damaging |
Het |
Kansl3 |
A |
G |
1: 36,387,897 (GRCm39) |
|
probably null |
Het |
Kntc1 |
T |
C |
5: 123,924,993 (GRCm39) |
L1102S |
probably benign |
Het |
Mbd3l2 |
A |
G |
9: 18,355,779 (GRCm39) |
I35V |
probably benign |
Het |
Mdfic |
G |
T |
6: 15,799,653 (GRCm39) |
C260F |
probably damaging |
Het |
Mroh2b |
T |
C |
15: 4,973,808 (GRCm39) |
S1109P |
probably benign |
Het |
Myocd |
A |
T |
11: 65,077,958 (GRCm39) |
C612* |
probably null |
Het |
Or4b13 |
A |
T |
2: 90,082,561 (GRCm39) |
M257K |
possibly damaging |
Het |
Or4c102 |
A |
G |
2: 88,422,435 (GRCm39) |
M96V |
probably benign |
Het |
Or4f17-ps1 |
T |
A |
2: 111,357,864 (GRCm39) |
C86* |
probably null |
Het |
Or52h7 |
T |
A |
7: 104,213,431 (GRCm39) |
M1K |
probably null |
Het |
Or5w22 |
A |
T |
2: 87,362,691 (GRCm39) |
T105S |
probably benign |
Het |
Or8k21 |
A |
T |
2: 86,145,451 (GRCm39) |
Y60N |
probably damaging |
Het |
Pard3 |
C |
T |
8: 128,050,549 (GRCm39) |
R204W |
probably damaging |
Het |
Per1 |
T |
A |
11: 68,998,382 (GRCm39) |
N1031K |
possibly damaging |
Het |
Plekhh3 |
A |
G |
11: 101,055,105 (GRCm39) |
S583P |
unknown |
Het |
Pramel12 |
C |
T |
4: 143,143,438 (GRCm39) |
T68I |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,270,118 (GRCm39) |
C1268S |
possibly damaging |
Het |
Prpf6 |
T |
C |
2: 181,291,951 (GRCm39) |
I756T |
probably benign |
Het |
Pum2 |
T |
C |
12: 8,759,454 (GRCm39) |
V98A |
probably damaging |
Het |
Rad50 |
A |
T |
11: 53,574,968 (GRCm39) |
S652T |
probably benign |
Het |
Rfng |
G |
T |
11: 120,674,901 (GRCm39) |
P30T |
unknown |
Het |
Rfx7 |
T |
C |
9: 72,524,973 (GRCm39) |
I721T |
probably benign |
Het |
Rpf1 |
G |
T |
3: 146,213,431 (GRCm39) |
T240K |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,483,270 (GRCm39) |
N4189S |
probably benign |
Het |
Samd15 |
G |
C |
12: 87,248,212 (GRCm39) |
R299T |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,329,335 (GRCm39) |
M765T |
possibly damaging |
Het |
Scn9a |
G |
A |
2: 66,324,966 (GRCm39) |
S1396L |
probably damaging |
Het |
Sec24a |
C |
T |
11: 51,634,605 (GRCm39) |
R107Q |
probably benign |
Het |
Sema4b |
T |
A |
7: 79,870,567 (GRCm39) |
V505E |
probably damaging |
Het |
Siglec1 |
T |
A |
2: 130,920,498 (GRCm39) |
T769S |
possibly damaging |
Het |
Sit1 |
T |
C |
4: 43,483,168 (GRCm39) |
E69G |
possibly damaging |
Het |
Slc12a8 |
C |
A |
16: 33,371,321 (GRCm39) |
D121E |
probably benign |
Het |
Slc30a10 |
A |
T |
1: 185,187,664 (GRCm39) |
Q135L |
probably benign |
Het |
Suox |
A |
G |
10: 128,507,200 (GRCm39) |
V276A |
probably benign |
Het |
Tbc1d9b |
A |
G |
11: 50,040,659 (GRCm39) |
D392G |
probably damaging |
Het |
Tmed5 |
A |
G |
5: 108,273,823 (GRCm39) |
W139R |
probably damaging |
Het |
Tnks1bp1 |
C |
T |
2: 84,893,226 (GRCm39) |
T389I |
possibly damaging |
Het |
Vmn1r65 |
A |
T |
7: 6,011,256 (GRCm39) |
I326K |
probably benign |
Het |
Vmn2r43 |
A |
G |
7: 8,256,601 (GRCm39) |
S421P |
possibly damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,076,968 (GRCm39) |
N399K |
possibly damaging |
Het |
Vmn2r90 |
T |
A |
17: 17,933,127 (GRCm39) |
L229* |
probably null |
Het |
Vwf |
A |
T |
6: 125,656,265 (GRCm39) |
D2610V |
|
Het |
Zfp646 |
C |
T |
7: 127,483,082 (GRCm39) |
S1753L |
probably benign |
Het |
Zfy2 |
C |
A |
Y: 2,107,096 (GRCm39) |
V513F |
possibly damaging |
Het |
Zranb2 |
A |
T |
3: 157,251,731 (GRCm39) |
I317F |
unknown |
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 |
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 |
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 |
|