Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,056,633 (GRCm39) |
H122L |
probably damaging |
Het |
9330182O14Rik |
G |
A |
15: 40,011,932 (GRCm39) |
M90I |
unknown |
Het |
9330182O14Rik |
G |
A |
15: 40,011,933 (GRCm39) |
D91N |
unknown |
Het |
Abca13 |
T |
A |
11: 9,240,722 (GRCm39) |
S862T |
probably damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adgb |
C |
A |
10: 10,226,004 (GRCm39) |
A1405S |
probably benign |
Het |
Adpgk |
T |
A |
9: 59,204,832 (GRCm39) |
V86E |
probably damaging |
Het |
Agfg2 |
G |
C |
5: 137,666,020 (GRCm39) |
P80A |
probably damaging |
Het |
Akap11 |
G |
A |
14: 78,736,304 (GRCm39) |
Q1829* |
probably null |
Het |
Aldh1l1 |
G |
A |
6: 90,536,281 (GRCm39) |
R62Q |
probably benign |
Het |
Amd1 |
G |
T |
10: 40,166,183 (GRCm39) |
D265E |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,259,253 (GRCm39) |
Q106L |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,800,159 (GRCm39) |
N1289K |
probably benign |
Het |
Arhgef12 |
T |
C |
9: 42,897,880 (GRCm39) |
S874G |
probably damaging |
Het |
Ccdc166 |
T |
C |
15: 75,853,945 (GRCm39) |
Q45R |
possibly damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Cdk14 |
A |
G |
5: 4,938,975 (GRCm39) |
S388P |
possibly damaging |
Het |
Chgb |
A |
T |
2: 132,635,453 (GRCm39) |
Q465L |
possibly damaging |
Het |
Commd9 |
T |
A |
2: 101,729,220 (GRCm39) |
W109R |
probably damaging |
Het |
Cspg4b |
G |
A |
13: 113,505,587 (GRCm39) |
V2239I |
probably benign |
Het |
Cyp2b9 |
T |
C |
7: 25,887,080 (GRCm39) |
V163A |
probably benign |
Het |
Dcpp2 |
T |
A |
17: 24,118,287 (GRCm39) |
H27Q |
possibly damaging |
Het |
Ddn |
T |
A |
15: 98,704,347 (GRCm39) |
E315V |
possibly damaging |
Het |
Defb29 |
C |
A |
2: 152,380,868 (GRCm39) |
C47F |
probably damaging |
Het |
Dock4 |
A |
T |
12: 40,795,744 (GRCm39) |
I854F |
probably damaging |
Het |
Dsg4 |
T |
C |
18: 20,591,541 (GRCm39) |
Y427H |
probably damaging |
Het |
E130114P18Rik |
C |
T |
4: 97,578,907 (GRCm39) |
A23T |
unknown |
Het |
Flacc1 |
T |
A |
1: 58,706,045 (GRCm39) |
K275* |
probably null |
Het |
Gemin5 |
A |
G |
11: 58,016,113 (GRCm39) |
S1297P |
probably benign |
Het |
Gm10309 |
A |
C |
17: 86,806,161 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
T |
A |
17: 79,148,663 (GRCm39) |
S155R |
possibly damaging |
Het |
Grin2b |
C |
A |
6: 135,709,366 (GRCm39) |
Q1393H |
probably damaging |
Het |
Heatr5b |
C |
T |
17: 79,081,142 (GRCm39) |
C1370Y |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,226,556 (GRCm39) |
T177I |
possibly damaging |
Het |
Ildr1 |
A |
T |
16: 36,529,981 (GRCm39) |
I123F |
probably damaging |
Het |
Kalrn |
A |
T |
16: 34,083,023 (GRCm39) |
V644D |
probably damaging |
Het |
Kifap3 |
A |
G |
1: 163,607,440 (GRCm39) |
M1V |
probably null |
Het |
Klhl11 |
A |
G |
11: 100,354,942 (GRCm39) |
L293P |
probably damaging |
Het |
Klrc3 |
G |
A |
6: 129,618,513 (GRCm39) |
S98L |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,511,586 (GRCm39) |
H127Q |
unknown |
Het |
Med12l |
G |
A |
3: 59,156,143 (GRCm39) |
M1220I |
probably damaging |
Het |
Ms4a7 |
C |
T |
19: 11,303,166 (GRCm39) |
|
probably null |
Het |
Mybpc2 |
A |
G |
7: 44,159,253 (GRCm39) |
V599A |
probably benign |
Het |
Naalad2 |
T |
C |
9: 18,258,815 (GRCm39) |
N487D |
probably benign |
Het |
Nat8f7 |
T |
G |
6: 85,684,805 (GRCm39) |
S12R |
probably benign |
Het |
Nefm |
T |
A |
14: 68,357,515 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
T |
C |
7: 23,117,626 (GRCm39) |
V450A |
probably damaging |
Het |
Nps |
G |
A |
7: 134,870,376 (GRCm39) |
|
probably null |
Het |
Or13c7d |
A |
G |
4: 43,770,168 (GRCm39) |
I281T |
probably benign |
Het |
Or2ag16 |
C |
A |
7: 106,351,773 (GRCm39) |
S274I |
probably benign |
Het |
Or4a74 |
T |
C |
2: 89,440,083 (GRCm39) |
Y121C |
probably damaging |
Het |
Or4b13 |
T |
A |
2: 90,082,955 (GRCm39) |
K126* |
probably null |
Het |
Or5e1 |
T |
C |
7: 108,354,924 (GRCm39) |
L287P |
possibly damaging |
Het |
Or5h24 |
G |
T |
16: 58,918,665 (GRCm39) |
P230Q |
possibly damaging |
Het |
Or5p67 |
T |
C |
7: 107,922,017 (GRCm39) |
N289D |
probably damaging |
Het |
Oxct2a |
C |
A |
4: 123,216,506 (GRCm39) |
G292W |
possibly damaging |
Het |
Pramel32 |
T |
A |
4: 88,547,647 (GRCm39) |
|
probably benign |
Het |
Prr27 |
T |
C |
5: 87,998,744 (GRCm39) |
|
probably benign |
Het |
Ptx3 |
T |
C |
3: 66,128,143 (GRCm39) |
M68T |
probably damaging |
Het |
Rufy1 |
A |
G |
11: 50,312,561 (GRCm39) |
L131S |
probably damaging |
Het |
Septin7 |
T |
A |
9: 25,197,986 (GRCm39) |
I100N |
possibly damaging |
Het |
Sgms2 |
T |
C |
3: 131,135,446 (GRCm39) |
I143V |
probably benign |
Het |
Slc25a34 |
A |
G |
4: 141,350,877 (GRCm39) |
V44A |
probably damaging |
Het |
Slc28a3 |
T |
A |
13: 58,710,968 (GRCm39) |
D518V |
probably damaging |
Het |
Slc6a7 |
C |
T |
18: 61,136,308 (GRCm39) |
|
probably null |
Het |
Slco4a1 |
C |
A |
2: 180,113,028 (GRCm39) |
A420D |
possibly damaging |
Het |
Smap1 |
T |
C |
1: 23,888,471 (GRCm39) |
T180A |
probably benign |
Het |
Specc1l |
T |
C |
10: 75,103,384 (GRCm39) |
S920P |
probably benign |
Het |
Tgtp2 |
A |
G |
11: 48,950,083 (GRCm39) |
M163T |
probably benign |
Het |
Tiam1 |
G |
T |
16: 89,662,280 (GRCm39) |
Q613K |
possibly damaging |
Het |
Vsig10l |
T |
A |
7: 43,114,247 (GRCm39) |
S190T |
probably damaging |
Het |
Vwa3b |
A |
G |
1: 37,154,752 (GRCm39) |
Y512C |
probably damaging |
Het |
Wdfy3 |
T |
A |
5: 102,067,312 (GRCm39) |
N1207Y |
probably damaging |
Het |
Wdr17 |
C |
T |
8: 55,134,434 (GRCm39) |
G349R |
probably damaging |
Het |
Wdr70 |
A |
G |
15: 7,951,586 (GRCm39) |
L417S |
possibly damaging |
Het |
Wdr81 |
A |
C |
11: 75,341,722 (GRCm39) |
S1182A |
possibly damaging |
Het |
Zfp458 |
A |
T |
13: 67,405,256 (GRCm39) |
C391* |
probably null |
Het |
Zfp638 |
A |
G |
6: 83,953,396 (GRCm39) |
E1167G |
probably damaging |
Het |
Zfp763 |
T |
A |
17: 33,238,569 (GRCm39) |
D192V |
probably benign |
Het |
Zfp853 |
T |
G |
5: 143,274,624 (GRCm39) |
Q332P |
unknown |
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 |
R1834:Dnah7b
|
UTSW |
1 |
46,272,919 (GRCm39) |
missense |
possibly damaging |
0.90 |
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 |
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 |
|