Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,099,313 (GRCm39) |
D20G |
probably damaging |
Het |
2310061N02Rik |
T |
A |
16: 88,504,786 (GRCm39) |
S4C |
unknown |
Het |
Abca3 |
A |
T |
17: 24,595,666 (GRCm39) |
N340Y |
probably benign |
Het |
Abcc1 |
A |
G |
16: 14,240,981 (GRCm39) |
I513V |
possibly damaging |
Het |
Acacb |
C |
T |
5: 114,373,536 (GRCm39) |
T1855M |
probably damaging |
Het |
Ace |
A |
G |
11: 105,876,920 (GRCm39) |
|
probably benign |
Het |
Acss2 |
T |
A |
2: 155,400,550 (GRCm39) |
Y530N |
probably damaging |
Het |
Adarb1 |
C |
A |
10: 77,153,065 (GRCm39) |
|
probably benign |
Het |
Afm |
T |
A |
5: 90,674,283 (GRCm39) |
M265K |
probably benign |
Het |
Agl |
A |
G |
3: 116,582,000 (GRCm39) |
F293S |
probably benign |
Het |
Aox1 |
G |
A |
1: 58,348,150 (GRCm39) |
A623T |
probably benign |
Het |
Arhgap31 |
C |
A |
16: 38,424,065 (GRCm39) |
S667I |
probably benign |
Het |
Bco1 |
A |
G |
8: 117,844,176 (GRCm39) |
T297A |
probably benign |
Het |
Bmp1 |
T |
C |
14: 70,746,271 (GRCm39) |
S123G |
possibly damaging |
Het |
Caps2 |
G |
A |
10: 112,031,623 (GRCm39) |
D283N |
possibly damaging |
Het |
Ccdc57 |
A |
C |
11: 120,752,045 (GRCm39) |
S845R |
probably benign |
Het |
Cd209f |
A |
G |
8: 4,154,491 (GRCm39) |
S119P |
probably damaging |
Het |
Chrna6 |
A |
G |
8: 27,897,242 (GRCm39) |
S212P |
probably benign |
Het |
Col10a1 |
G |
C |
10: 34,271,011 (GRCm39) |
A328P |
probably damaging |
Het |
Col4a2 |
A |
G |
8: 11,452,997 (GRCm39) |
E188G |
probably benign |
Het |
Creb1 |
C |
T |
1: 64,590,109 (GRCm39) |
Q32* |
probably null |
Het |
Cttnbp2 |
C |
T |
6: 18,501,965 (GRCm39) |
V16M |
probably damaging |
Het |
D430041D05Rik |
A |
G |
2: 103,998,446 (GRCm39) |
S1102P |
probably damaging |
Het |
Ddx31 |
C |
T |
2: 28,782,465 (GRCm39) |
H603Y |
probably damaging |
Het |
Ddx52 |
G |
A |
11: 83,850,323 (GRCm39) |
C568Y |
probably benign |
Het |
Dgki |
C |
A |
6: 37,011,636 (GRCm39) |
|
probably benign |
Het |
Dmrt1 |
A |
T |
19: 25,487,063 (GRCm39) |
Q123L |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,409,270 (GRCm39) |
M3563L |
probably benign |
Het |
Dscaml1 |
T |
G |
9: 45,594,930 (GRCm39) |
S678A |
probably benign |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Ece1 |
A |
G |
4: 137,685,439 (GRCm39) |
N643S |
probably damaging |
Het |
Eno1b |
A |
G |
18: 48,180,530 (GRCm39) |
Y236C |
probably damaging |
Het |
Esco1 |
T |
C |
18: 10,594,350 (GRCm39) |
E312G |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,434,429 (GRCm39) |
V276E |
probably damaging |
Het |
Fam161b |
A |
G |
12: 84,395,552 (GRCm39) |
|
probably benign |
Het |
Fem1c |
C |
T |
18: 46,638,349 (GRCm39) |
G551D |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,429,718 (GRCm39) |
I155T |
possibly damaging |
Het |
Gbp7 |
A |
G |
3: 142,240,441 (GRCm39) |
Y53C |
probably damaging |
Het |
Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
Gm10030 |
C |
T |
9: 110,833,947 (GRCm39) |
|
noncoding transcript |
Het |
Gm3443 |
T |
A |
19: 21,533,043 (GRCm39) |
H2Q |
unknown |
Het |
Gm5800 |
T |
C |
14: 51,953,549 (GRCm39) |
E22G |
possibly damaging |
Het |
Gsdma2 |
G |
T |
11: 98,539,905 (GRCm39) |
R9L |
probably damaging |
Het |
Gvin3 |
A |
T |
7: 106,202,983 (GRCm39) |
V87D |
possibly damaging |
Het |
Ica1l |
A |
G |
1: 60,067,395 (GRCm39) |
|
probably benign |
Het |
Ice1 |
G |
A |
13: 70,763,457 (GRCm39) |
T167I |
probably damaging |
Het |
Ifi204 |
T |
A |
1: 173,575,172 (GRCm39) |
R618S |
unknown |
Het |
Itga2 |
C |
A |
13: 114,993,262 (GRCm39) |
K784N |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,993,263 (GRCm39) |
K784M |
probably damaging |
Het |
Kif3b |
A |
G |
2: 153,159,405 (GRCm39) |
E402G |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,297,224 (GRCm39) |
I3246V |
probably benign |
Het |
Lrrn3 |
G |
T |
12: 41,503,517 (GRCm39) |
L267I |
probably damaging |
Het |
Map1s |
A |
G |
8: 71,369,055 (GRCm39) |
Y868C |
probably damaging |
Het |
Mcm5 |
A |
G |
8: 75,845,901 (GRCm39) |
T370A |
possibly damaging |
Het |
Nat8f7 |
T |
C |
6: 85,684,793 (GRCm39) |
S16G |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,555,883 (GRCm39) |
T1683A |
probably damaging |
Het |
Nbeal2 |
T |
C |
9: 110,456,197 (GRCm39) |
N2417S |
probably damaging |
Het |
Neb |
T |
C |
2: 52,126,907 (GRCm39) |
N3605S |
probably damaging |
Het |
Net1 |
A |
T |
13: 3,962,941 (GRCm39) |
|
probably benign |
Het |
Nsd1 |
A |
G |
13: 55,461,164 (GRCm39) |
T2464A |
possibly damaging |
Het |
Nt5e |
T |
A |
9: 88,252,240 (GRCm39) |
I534N |
probably damaging |
Het |
Nudt12 |
T |
A |
17: 59,318,071 (GRCm39) |
H58L |
probably damaging |
Het |
Ocrl |
T |
A |
X: 47,050,993 (GRCm39) |
I74N |
probably damaging |
Het |
Or1a1 |
A |
G |
11: 74,086,479 (GRCm39) |
H50R |
probably benign |
Het |
Or2ag13 |
A |
G |
7: 106,473,348 (GRCm39) |
Y35H |
probably damaging |
Het |
Or5ae2 |
A |
G |
7: 84,505,690 (GRCm39) |
T38A |
probably damaging |
Het |
Or9k2b |
A |
G |
10: 130,016,701 (GRCm39) |
I16T |
probably benign |
Het |
Pef1 |
C |
A |
4: 130,014,966 (GRCm39) |
C10* |
probably null |
Het |
Phf21b |
A |
G |
15: 84,681,547 (GRCm39) |
Y256H |
probably damaging |
Het |
Phox2a |
G |
T |
7: 101,470,152 (GRCm39) |
|
probably null |
Het |
Pi16 |
A |
G |
17: 29,546,419 (GRCm39) |
E399G |
possibly damaging |
Het |
Pipox |
A |
T |
11: 77,772,949 (GRCm39) |
Y321N |
probably damaging |
Het |
Plin4 |
A |
G |
17: 56,410,522 (GRCm39) |
S1170P |
probably damaging |
Het |
Pnma2 |
C |
T |
14: 67,154,662 (GRCm39) |
S362L |
possibly damaging |
Het |
Ppp1r9a |
T |
C |
6: 5,113,710 (GRCm39) |
I738T |
probably damaging |
Het |
Prkcsh |
A |
T |
9: 21,919,634 (GRCm39) |
K188M |
probably damaging |
Het |
Rcc1l |
A |
T |
5: 134,192,498 (GRCm39) |
Y309N |
probably damaging |
Het |
Ripk1 |
A |
G |
13: 34,199,196 (GRCm39) |
T123A |
probably benign |
Het |
Robo4 |
A |
G |
9: 37,324,355 (GRCm39) |
D961G |
probably benign |
Het |
Rps27a |
A |
G |
11: 29,496,299 (GRCm39) |
Y105H |
probably benign |
Het |
Scaper |
A |
G |
9: 55,724,018 (GRCm39) |
Y641H |
possibly damaging |
Het |
Scn1a |
C |
A |
2: 66,154,960 (GRCm39) |
Q666H |
probably benign |
Het |
Scn1a |
T |
A |
2: 66,154,961 (GRCm39) |
Q666L |
probably benign |
Het |
Sdhaf4 |
T |
C |
1: 24,042,234 (GRCm39) |
|
probably null |
Het |
Sec14l3 |
A |
G |
11: 4,016,510 (GRCm39) |
|
probably benign |
Het |
Selp |
C |
A |
1: 163,955,729 (GRCm39) |
|
probably null |
Het |
Sim1 |
A |
G |
10: 50,785,924 (GRCm39) |
D259G |
probably damaging |
Het |
Sptan1 |
T |
A |
2: 29,882,013 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
A |
7: 27,066,071 (GRCm39) |
E679V |
probably null |
Het |
Sytl3 |
G |
A |
17: 6,995,726 (GRCm39) |
E169K |
probably benign |
Het |
Taar1 |
T |
C |
10: 23,797,087 (GRCm39) |
C262R |
probably benign |
Het |
Taf7l2 |
T |
C |
10: 115,948,570 (GRCm39) |
R319G |
probably benign |
Het |
Tbc1d32 |
A |
G |
10: 55,893,700 (GRCm39) |
I1291T |
probably benign |
Het |
Tet1 |
G |
A |
10: 62,649,444 (GRCm39) |
P89S |
probably damaging |
Het |
Tgfbrap1 |
C |
A |
1: 43,110,795 (GRCm39) |
G7W |
probably damaging |
Het |
Thada |
A |
G |
17: 84,533,432 (GRCm39) |
V1673A |
possibly damaging |
Het |
Thbs4 |
A |
G |
13: 92,897,989 (GRCm39) |
V610A |
probably benign |
Het |
Tmem163 |
A |
G |
1: 127,605,246 (GRCm39) |
S41P |
probably benign |
Het |
Tmem65 |
A |
T |
15: 58,658,962 (GRCm39) |
H200Q |
probably damaging |
Het |
Trgc3 |
A |
G |
13: 19,447,535 (GRCm39) |
T163A |
possibly damaging |
Het |
Trim62 |
T |
C |
4: 128,803,018 (GRCm39) |
V356A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,562,502 (GRCm39) |
D28781G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,593,604 (GRCm39) |
V20679I |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,962,749 (GRCm39) |
Y339* |
probably null |
Het |
Unc80 |
A |
T |
1: 66,678,407 (GRCm39) |
T2063S |
possibly damaging |
Het |
Vav3 |
A |
G |
3: 109,413,742 (GRCm39) |
T227A |
probably benign |
Het |
Vmn2r118 |
A |
T |
17: 55,899,456 (GRCm39) |
I816N |
probably damaging |
Het |
Vmn2r26 |
T |
A |
6: 124,038,369 (GRCm39) |
M648K |
possibly damaging |
Het |
Vmn2r88 |
T |
G |
14: 51,650,487 (GRCm39) |
|
probably benign |
Het |
Vwa3a |
A |
G |
7: 120,389,359 (GRCm39) |
T66A |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,341,484 (GRCm39) |
Y1242N |
probably damaging |
Het |
Ywhag |
G |
A |
5: 135,940,384 (GRCm39) |
T70M |
probably damaging |
Het |
Zfp248 |
T |
C |
6: 118,405,931 (GRCm39) |
T452A |
probably damaging |
Het |
Zfp988 |
A |
T |
4: 147,417,344 (GRCm39) |
I593F |
probably damaging |
Het |
|
Other mutations in Dnah7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Dnah7b
|
APN |
1 |
46,181,309 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00796:Dnah7b
|
APN |
1 |
46,250,497 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00825:Dnah7b
|
APN |
1 |
46,263,811 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00910:Dnah7b
|
APN |
1 |
46,105,889 (GRCm39) |
unclassified |
probably benign |
|
IGL00950:Dnah7b
|
APN |
1 |
46,253,482 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01142:Dnah7b
|
APN |
1 |
46,234,538 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01350:Dnah7b
|
APN |
1 |
46,120,592 (GRCm39) |
splice site |
probably benign |
|
IGL01392:Dnah7b
|
APN |
1 |
46,165,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01403:Dnah7b
|
APN |
1 |
46,155,460 (GRCm39) |
splice site |
probably benign |
|
IGL01460:Dnah7b
|
APN |
1 |
46,178,864 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01576:Dnah7b
|
APN |
1 |
46,307,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01693:Dnah7b
|
APN |
1 |
46,397,307 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01838:Dnah7b
|
APN |
1 |
46,397,297 (GRCm39) |
nonsense |
probably null |
|
IGL01906:Dnah7b
|
APN |
1 |
46,214,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01960:Dnah7b
|
APN |
1 |
46,163,497 (GRCm39) |
splice site |
probably benign |
|
IGL01989:Dnah7b
|
APN |
1 |
46,328,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02127:Dnah7b
|
APN |
1 |
46,179,035 (GRCm39) |
missense |
probably benign |
|
IGL02213:Dnah7b
|
APN |
1 |
46,272,752 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02267:Dnah7b
|
APN |
1 |
46,266,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02349:Dnah7b
|
APN |
1 |
46,138,663 (GRCm39) |
nonsense |
probably null |
|
IGL02381:Dnah7b
|
APN |
1 |
46,316,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02473:Dnah7b
|
APN |
1 |
46,273,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02484:Dnah7b
|
APN |
1 |
46,234,478 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Dnah7b
|
APN |
1 |
46,162,937 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02655:Dnah7b
|
APN |
1 |
46,155,461 (GRCm39) |
splice site |
probably benign |
|
IGL02704:Dnah7b
|
APN |
1 |
46,181,293 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02719:Dnah7b
|
APN |
1 |
46,138,768 (GRCm39) |
splice site |
probably benign |
|
IGL02745:Dnah7b
|
APN |
1 |
46,234,189 (GRCm39) |
splice site |
probably benign |
|
IGL02818:Dnah7b
|
APN |
1 |
46,329,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Dnah7b
|
APN |
1 |
46,158,458 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03285:Dnah7b
|
APN |
1 |
46,221,535 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03354:Dnah7b
|
APN |
1 |
46,124,849 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Dnah7b
|
APN |
1 |
46,158,464 (GRCm39) |
missense |
probably benign |
0.18 |
BB001:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
BB011:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4305001:Dnah7b
|
UTSW |
1 |
46,412,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Dnah7b
|
UTSW |
1 |
46,252,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0145:Dnah7b
|
UTSW |
1 |
46,262,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Dnah7b
|
UTSW |
1 |
46,258,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Dnah7b
|
UTSW |
1 |
46,162,937 (GRCm39) |
missense |
probably benign |
0.26 |
R0313:Dnah7b
|
UTSW |
1 |
46,246,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Dnah7b
|
UTSW |
1 |
46,173,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Dnah7b
|
UTSW |
1 |
46,280,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Dnah7b
|
UTSW |
1 |
46,316,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R0363:Dnah7b
|
UTSW |
1 |
46,275,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R0379:Dnah7b
|
UTSW |
1 |
46,179,336 (GRCm39) |
missense |
probably benign |
0.00 |
R0502:Dnah7b
|
UTSW |
1 |
46,258,704 (GRCm39) |
missense |
probably damaging |
0.96 |
R0602:Dnah7b
|
UTSW |
1 |
46,364,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Dnah7b
|
UTSW |
1 |
46,280,152 (GRCm39) |
missense |
probably benign |
0.02 |
R0664:Dnah7b
|
UTSW |
1 |
46,364,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0882:Dnah7b
|
UTSW |
1 |
46,379,292 (GRCm39) |
missense |
probably benign |
0.00 |
R0931:Dnah7b
|
UTSW |
1 |
46,138,772 (GRCm39) |
splice site |
probably benign |
|
R1035:Dnah7b
|
UTSW |
1 |
46,163,608 (GRCm39) |
missense |
probably benign |
|
R1147:Dnah7b
|
UTSW |
1 |
46,379,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Dnah7b
|
UTSW |
1 |
46,379,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1166:Dnah7b
|
UTSW |
1 |
46,364,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Dnah7b
|
UTSW |
1 |
46,379,280 (GRCm39) |
missense |
probably benign |
0.00 |
R1318:Dnah7b
|
UTSW |
1 |
46,138,669 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1334:Dnah7b
|
UTSW |
1 |
46,361,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R1429:Dnah7b
|
UTSW |
1 |
46,328,816 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1440:Dnah7b
|
UTSW |
1 |
46,117,753 (GRCm39) |
splice site |
probably benign |
|
R1484:Dnah7b
|
UTSW |
1 |
46,176,703 (GRCm39) |
missense |
probably benign |
0.00 |
R1529:Dnah7b
|
UTSW |
1 |
46,216,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Dnah7b
|
UTSW |
1 |
46,105,957 (GRCm39) |
missense |
unknown |
|
R1607:Dnah7b
|
UTSW |
1 |
46,329,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Dnah7b
|
UTSW |
1 |
46,392,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Dnah7b
|
UTSW |
1 |
46,214,550 (GRCm39) |
nonsense |
probably null |
|
R1681:Dnah7b
|
UTSW |
1 |
46,363,872 (GRCm39) |
nonsense |
probably null |
|
R1716:Dnah7b
|
UTSW |
1 |
46,230,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Dnah7b
|
UTSW |
1 |
46,361,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R1838:Dnah7b
|
UTSW |
1 |
46,316,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Dnah7b
|
UTSW |
1 |
46,155,337 (GRCm39) |
missense |
probably benign |
0.04 |
R1898:Dnah7b
|
UTSW |
1 |
46,275,874 (GRCm39) |
missense |
probably benign |
0.02 |
R1962:Dnah7b
|
UTSW |
1 |
46,281,263 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2001:Dnah7b
|
UTSW |
1 |
46,181,247 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2049:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Dnah7b
|
UTSW |
1 |
46,281,481 (GRCm39) |
nonsense |
probably null |
|
R2083:Dnah7b
|
UTSW |
1 |
46,280,227 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2140:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Dnah7b
|
UTSW |
1 |
46,137,152 (GRCm39) |
splice site |
probably benign |
|
R2172:Dnah7b
|
UTSW |
1 |
46,163,672 (GRCm39) |
missense |
probably benign |
0.12 |
R2239:Dnah7b
|
UTSW |
1 |
46,240,344 (GRCm39) |
splice site |
probably benign |
|
R2247:Dnah7b
|
UTSW |
1 |
46,316,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Dnah7b
|
UTSW |
1 |
46,273,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Dnah7b
|
UTSW |
1 |
46,402,114 (GRCm39) |
missense |
probably benign |
0.31 |
R2509:Dnah7b
|
UTSW |
1 |
46,234,447 (GRCm39) |
missense |
probably damaging |
0.96 |
R2895:Dnah7b
|
UTSW |
1 |
46,178,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R2965:Dnah7b
|
UTSW |
1 |
46,246,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R3013:Dnah7b
|
UTSW |
1 |
46,227,847 (GRCm39) |
critical splice donor site |
probably null |
|
R3022:Dnah7b
|
UTSW |
1 |
46,221,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R3056:Dnah7b
|
UTSW |
1 |
46,307,869 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3107:Dnah7b
|
UTSW |
1 |
46,392,033 (GRCm39) |
missense |
probably benign |
0.00 |
R3735:Dnah7b
|
UTSW |
1 |
46,339,035 (GRCm39) |
missense |
probably benign |
0.05 |
R3898:Dnah7b
|
UTSW |
1 |
46,282,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Dnah7b
|
UTSW |
1 |
46,176,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Dnah7b
|
UTSW |
1 |
46,272,871 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4041:Dnah7b
|
UTSW |
1 |
46,120,655 (GRCm39) |
missense |
probably benign |
|
R4172:Dnah7b
|
UTSW |
1 |
46,266,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4210:Dnah7b
|
UTSW |
1 |
46,176,578 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4306:Dnah7b
|
UTSW |
1 |
46,260,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R4391:Dnah7b
|
UTSW |
1 |
46,376,754 (GRCm39) |
splice site |
probably null |
|
R4414:Dnah7b
|
UTSW |
1 |
46,165,840 (GRCm39) |
missense |
probably benign |
0.00 |
R4495:Dnah7b
|
UTSW |
1 |
46,124,792 (GRCm39) |
missense |
probably benign |
0.00 |
R4660:Dnah7b
|
UTSW |
1 |
46,328,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R4670:Dnah7b
|
UTSW |
1 |
46,117,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4675:Dnah7b
|
UTSW |
1 |
46,256,317 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4685:Dnah7b
|
UTSW |
1 |
46,250,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4727:Dnah7b
|
UTSW |
1 |
46,246,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Dnah7b
|
UTSW |
1 |
46,106,115 (GRCm39) |
missense |
unknown |
|
R4780:Dnah7b
|
UTSW |
1 |
46,392,174 (GRCm39) |
missense |
probably benign |
|
R4828:Dnah7b
|
UTSW |
1 |
46,167,272 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4859:Dnah7b
|
UTSW |
1 |
46,395,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Dnah7b
|
UTSW |
1 |
46,234,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Dnah7b
|
UTSW |
1 |
46,120,604 (GRCm39) |
missense |
probably benign |
0.21 |
R4881:Dnah7b
|
UTSW |
1 |
46,240,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Dnah7b
|
UTSW |
1 |
46,329,935 (GRCm39) |
missense |
probably benign |
0.04 |
R4960:Dnah7b
|
UTSW |
1 |
46,272,886 (GRCm39) |
missense |
probably benign |
|
R5000:Dnah7b
|
UTSW |
1 |
46,138,663 (GRCm39) |
nonsense |
probably null |
|
R5005:Dnah7b
|
UTSW |
1 |
46,281,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Dnah7b
|
UTSW |
1 |
46,226,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R5080:Dnah7b
|
UTSW |
1 |
46,221,540 (GRCm39) |
nonsense |
probably null |
|
R5174:Dnah7b
|
UTSW |
1 |
46,282,509 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5178:Dnah7b
|
UTSW |
1 |
46,397,376 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5244:Dnah7b
|
UTSW |
1 |
46,273,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Dnah7b
|
UTSW |
1 |
46,412,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R5350:Dnah7b
|
UTSW |
1 |
46,272,849 (GRCm39) |
missense |
probably benign |
0.16 |
R5380:Dnah7b
|
UTSW |
1 |
46,256,351 (GRCm39) |
missense |
probably benign |
0.18 |
R5387:Dnah7b
|
UTSW |
1 |
46,227,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Dnah7b
|
UTSW |
1 |
46,397,431 (GRCm39) |
missense |
probably benign |
0.01 |
R5426:Dnah7b
|
UTSW |
1 |
46,281,366 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5451:Dnah7b
|
UTSW |
1 |
46,281,179 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5459:Dnah7b
|
UTSW |
1 |
46,148,472 (GRCm39) |
missense |
probably null |
|
R5479:Dnah7b
|
UTSW |
1 |
46,262,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Dnah7b
|
UTSW |
1 |
46,281,359 (GRCm39) |
missense |
probably benign |
0.06 |
R5637:Dnah7b
|
UTSW |
1 |
46,395,674 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5641:Dnah7b
|
UTSW |
1 |
46,307,924 (GRCm39) |
splice site |
probably null |
|
R5659:Dnah7b
|
UTSW |
1 |
46,392,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Dnah7b
|
UTSW |
1 |
46,273,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5759:Dnah7b
|
UTSW |
1 |
46,316,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R5821:Dnah7b
|
UTSW |
1 |
46,181,292 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5874:Dnah7b
|
UTSW |
1 |
46,230,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Dnah7b
|
UTSW |
1 |
46,376,753 (GRCm39) |
critical splice donor site |
probably null |
|
R5918:Dnah7b
|
UTSW |
1 |
46,260,803 (GRCm39) |
missense |
probably benign |
|
R5941:Dnah7b
|
UTSW |
1 |
46,226,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Dnah7b
|
UTSW |
1 |
46,402,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5987:Dnah7b
|
UTSW |
1 |
46,158,558 (GRCm39) |
splice site |
probably null |
|
R6041:Dnah7b
|
UTSW |
1 |
46,328,805 (GRCm39) |
missense |
probably benign |
0.04 |
R6043:Dnah7b
|
UTSW |
1 |
46,178,949 (GRCm39) |
missense |
probably benign |
|
R6049:Dnah7b
|
UTSW |
1 |
46,124,762 (GRCm39) |
missense |
probably benign |
|
R6131:Dnah7b
|
UTSW |
1 |
46,292,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6168:Dnah7b
|
UTSW |
1 |
46,329,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Dnah7b
|
UTSW |
1 |
46,243,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R6219:Dnah7b
|
UTSW |
1 |
46,272,745 (GRCm39) |
missense |
probably benign |
0.03 |
R6226:Dnah7b
|
UTSW |
1 |
46,165,828 (GRCm39) |
missense |
probably benign |
0.01 |
R6233:Dnah7b
|
UTSW |
1 |
46,243,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Dnah7b
|
UTSW |
1 |
46,265,048 (GRCm39) |
missense |
probably benign |
|
R6273:Dnah7b
|
UTSW |
1 |
46,281,476 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6279:Dnah7b
|
UTSW |
1 |
46,365,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Dnah7b
|
UTSW |
1 |
46,365,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6330:Dnah7b
|
UTSW |
1 |
46,379,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Dnah7b
|
UTSW |
1 |
46,281,364 (GRCm39) |
nonsense |
probably null |
|
R6494:Dnah7b
|
UTSW |
1 |
46,138,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Dnah7b
|
UTSW |
1 |
46,263,902 (GRCm39) |
missense |
probably benign |
0.12 |
R6800:Dnah7b
|
UTSW |
1 |
46,379,377 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6838:Dnah7b
|
UTSW |
1 |
46,230,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6937:Dnah7b
|
UTSW |
1 |
46,234,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Dnah7b
|
UTSW |
1 |
46,158,428 (GRCm39) |
missense |
probably benign |
0.12 |
R6969:Dnah7b
|
UTSW |
1 |
46,397,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Dnah7b
|
UTSW |
1 |
46,234,299 (GRCm39) |
critical splice donor site |
probably null |
|
R7040:Dnah7b
|
UTSW |
1 |
46,275,969 (GRCm39) |
missense |
probably benign |
0.01 |
R7117:Dnah7b
|
UTSW |
1 |
46,391,973 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7135:Dnah7b
|
UTSW |
1 |
46,178,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R7153:Dnah7b
|
UTSW |
1 |
46,165,964 (GRCm39) |
missense |
probably benign |
0.05 |
R7189:Dnah7b
|
UTSW |
1 |
46,281,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Dnah7b
|
UTSW |
1 |
46,179,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R7243:Dnah7b
|
UTSW |
1 |
46,122,914 (GRCm39) |
missense |
probably benign |
|
R7244:Dnah7b
|
UTSW |
1 |
46,316,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R7248:Dnah7b
|
UTSW |
1 |
46,181,245 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7318:Dnah7b
|
UTSW |
1 |
46,234,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Dnah7b
|
UTSW |
1 |
46,342,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Dnah7b
|
UTSW |
1 |
46,214,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Dnah7b
|
UTSW |
1 |
46,329,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Dnah7b
|
UTSW |
1 |
46,364,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Dnah7b
|
UTSW |
1 |
46,395,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dnah7b
|
UTSW |
1 |
46,163,506 (GRCm39) |
missense |
probably benign |
0.06 |
R7547:Dnah7b
|
UTSW |
1 |
46,253,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7620:Dnah7b
|
UTSW |
1 |
46,307,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7670:Dnah7b
|
UTSW |
1 |
46,148,462 (GRCm39) |
missense |
probably benign |
|
R7676:Dnah7b
|
UTSW |
1 |
46,273,324 (GRCm39) |
nonsense |
probably null |
|
R7731:Dnah7b
|
UTSW |
1 |
46,178,905 (GRCm39) |
missense |
probably benign |
0.00 |
R7760:Dnah7b
|
UTSW |
1 |
46,240,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Dnah7b
|
UTSW |
1 |
46,176,634 (GRCm39) |
missense |
probably benign |
|
R7807:Dnah7b
|
UTSW |
1 |
46,253,527 (GRCm39) |
missense |
probably benign |
|
R7895:Dnah7b
|
UTSW |
1 |
46,289,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Dnah7b
|
UTSW |
1 |
46,178,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
R7944:Dnah7b
|
UTSW |
1 |
46,266,163 (GRCm39) |
missense |
probably benign |
|
R7946:Dnah7b
|
UTSW |
1 |
46,272,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Dnah7b
|
UTSW |
1 |
46,282,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Dnah7b
|
UTSW |
1 |
46,282,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Dnah7b
|
UTSW |
1 |
46,263,866 (GRCm39) |
nonsense |
probably null |
|
R8094:Dnah7b
|
UTSW |
1 |
46,165,964 (GRCm39) |
missense |
probably benign |
0.01 |
R8137:Dnah7b
|
UTSW |
1 |
46,272,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R8167:Dnah7b
|
UTSW |
1 |
46,292,671 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8268:Dnah7b
|
UTSW |
1 |
46,395,736 (GRCm39) |
missense |
probably benign |
0.43 |
R8309:Dnah7b
|
UTSW |
1 |
46,179,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8313:Dnah7b
|
UTSW |
1 |
46,214,456 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8410:Dnah7b
|
UTSW |
1 |
46,395,819 (GRCm39) |
critical splice donor site |
probably null |
|
R8438:Dnah7b
|
UTSW |
1 |
46,227,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R8446:Dnah7b
|
UTSW |
1 |
46,329,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8471:Dnah7b
|
UTSW |
1 |
46,138,650 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8551:Dnah7b
|
UTSW |
1 |
46,155,360 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8711:Dnah7b
|
UTSW |
1 |
46,214,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Dnah7b
|
UTSW |
1 |
46,221,624 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8765:Dnah7b
|
UTSW |
1 |
46,392,159 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8797:Dnah7b
|
UTSW |
1 |
46,162,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Dnah7b
|
UTSW |
1 |
46,273,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8830:Dnah7b
|
UTSW |
1 |
46,230,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8861:Dnah7b
|
UTSW |
1 |
46,280,236 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8905:Dnah7b
|
UTSW |
1 |
46,292,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R9009:Dnah7b
|
UTSW |
1 |
46,262,232 (GRCm39) |
missense |
probably benign |
0.00 |
R9058:Dnah7b
|
UTSW |
1 |
46,282,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R9130:Dnah7b
|
UTSW |
1 |
46,173,674 (GRCm39) |
missense |
probably benign |
0.01 |
R9131:Dnah7b
|
UTSW |
1 |
46,266,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9181:Dnah7b
|
UTSW |
1 |
46,181,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R9182:Dnah7b
|
UTSW |
1 |
46,330,038 (GRCm39) |
missense |
probably benign |
0.06 |
R9223:Dnah7b
|
UTSW |
1 |
46,361,420 (GRCm39) |
missense |
probably benign |
0.12 |
R9391:Dnah7b
|
UTSW |
1 |
46,272,914 (GRCm39) |
nonsense |
probably null |
|
R9392:Dnah7b
|
UTSW |
1 |
46,162,898 (GRCm39) |
nonsense |
probably null |
|
R9456:Dnah7b
|
UTSW |
1 |
46,165,953 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9498:Dnah7b
|
UTSW |
1 |
46,253,564 (GRCm39) |
missense |
probably benign |
0.27 |
R9553:Dnah7b
|
UTSW |
1 |
46,264,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R9598:Dnah7b
|
UTSW |
1 |
46,292,621 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9653:Dnah7b
|
UTSW |
1 |
46,252,544 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9781:Dnah7b
|
UTSW |
1 |
46,376,754 (GRCm39) |
splice site |
probably null |
|
RF020:Dnah7b
|
UTSW |
1 |
46,412,421 (GRCm39) |
missense |
possibly damaging |
0.84 |
V8831:Dnah7b
|
UTSW |
1 |
46,412,458 (GRCm39) |
nonsense |
probably null |
|
X0023:Dnah7b
|
UTSW |
1 |
46,342,737 (GRCm39) |
missense |
probably benign |
0.04 |
|