Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 138,065,370 (GRCm38) |
N107D |
probably benign |
Het |
4833413E03Rik |
A |
C |
17: 31,558,764 (GRCm38) |
|
noncoding transcript |
Het |
4931429L15Rik |
G |
T |
9: 46,308,846 (GRCm38) |
H129Q |
possibly damaging |
Het |
A730018C14Rik |
A |
G |
12: 112,415,635 (GRCm38) |
|
noncoding transcript |
Het |
Abcc6 |
T |
A |
7: 45,996,691 (GRCm38) |
K791N |
probably benign |
Het |
Adcy4 |
T |
G |
14: 55,775,036 (GRCm38) |
Q550P |
probably benign |
Het |
Add3 |
C |
A |
19: 53,234,792 (GRCm38) |
A325E |
possibly damaging |
Het |
Agbl4 |
T |
A |
4: 111,657,331 (GRCm38) |
I513N |
possibly damaging |
Het |
Agfg1 |
C |
A |
1: 82,886,387 (GRCm38) |
T392K |
probably damaging |
Het |
Akna |
C |
A |
4: 63,379,254 (GRCm38) |
M854I |
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,763,757 (GRCm38) |
N194S |
probably benign |
Het |
Anks1b |
A |
G |
10: 89,873,732 (GRCm38) |
K21E |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,609,172 (GRCm38) |
F154L |
probably benign |
Het |
Apbb2 |
T |
A |
5: 66,362,817 (GRCm38) |
N477I |
probably damaging |
Het |
Apobec3 |
T |
C |
15: 79,899,024 (GRCm38) |
C101R |
possibly damaging |
Het |
Arnt |
G |
T |
3: 95,488,385 (GRCm38) |
V410F |
probably damaging |
Het |
Arsg |
G |
A |
11: 109,534,013 (GRCm38) |
R270H |
possibly damaging |
Het |
B3gnt7 |
T |
A |
1: 86,305,270 (GRCm38) |
D79E |
probably damaging |
Het |
BC067074 |
A |
G |
13: 113,317,858 (GRCm38) |
Y146C |
probably damaging |
Het |
Cd44 |
G |
T |
2: 102,861,565 (GRCm38) |
A126D |
probably damaging |
Het |
Cd69 |
A |
G |
6: 129,271,355 (GRCm38) |
I56T |
probably damaging |
Het |
Cep120 |
G |
A |
18: 53,724,536 (GRCm38) |
P286S |
probably benign |
Het |
Ces2a |
T |
C |
8: 104,737,208 (GRCm38) |
F184S |
probably damaging |
Het |
Chrng |
A |
G |
1: 87,207,524 (GRCm38) |
N185S |
probably damaging |
Het |
Cldn6 |
A |
T |
17: 23,681,247 (GRCm38) |
M62L |
probably benign |
Het |
Cntn6 |
T |
A |
6: 104,845,784 (GRCm38) |
N765K |
probably damaging |
Het |
Ctnnal1 |
T |
C |
4: 56,847,857 (GRCm38) |
D94G |
probably damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,877,594 (GRCm38) |
N185S |
probably benign |
Het |
Depdc1a |
A |
G |
3: 159,526,706 (GRCm38) |
N698S |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,473,871 (GRCm38) |
I1986N |
probably damaging |
Het |
Dpysl3 |
C |
T |
18: 43,354,802 (GRCm38) |
V159I |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,661,196 (GRCm38) |
Y4047H |
probably damaging |
Het |
E130308A19Rik |
C |
T |
4: 59,691,057 (GRCm38) |
P297L |
probably benign |
Het |
E2f5 |
A |
G |
3: 14,587,319 (GRCm38) |
T72A |
probably benign |
Het |
Ephb6 |
G |
T |
6: 41,616,139 (GRCm38) |
R437L |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,298,314 (GRCm38) |
H615R |
probably damaging |
Het |
Erbin |
T |
C |
13: 103,884,206 (GRCm38) |
T82A |
probably damaging |
Het |
Eri2 |
T |
C |
7: 119,785,680 (GRCm38) |
N533D |
probably benign |
Het |
Fkbp9 |
A |
G |
6: 56,850,716 (GRCm38) |
N174S |
probably damaging |
Het |
Fsbp |
C |
T |
4: 11,583,709 (GRCm38) |
T136I |
possibly damaging |
Het |
Fubp3 |
C |
A |
2: 31,583,211 (GRCm38) |
D47E |
probably damaging |
Het |
Gm21850 |
G |
A |
2: 154,056,499 (GRCm38) |
|
noncoding transcript |
Het |
Gm5141 |
T |
A |
13: 62,774,950 (GRCm38) |
Y135F |
unknown |
Het |
Gm7353 |
T |
A |
7: 3,110,725 (GRCm38) |
|
noncoding transcript |
Het |
Gm8765 |
C |
A |
13: 50,701,080 (GRCm38) |
S251R |
probably damaging |
Het |
Gm9925 |
T |
C |
18: 74,065,273 (GRCm38) |
|
probably benign |
Het |
Greb1l |
T |
C |
18: 10,541,792 (GRCm38) |
S1180P |
probably benign |
Het |
Hist1h2ag |
G |
A |
13: 22,042,909 (GRCm38) |
Q7* |
probably null |
Het |
Kiz |
A |
G |
2: 146,889,246 (GRCm38) |
T192A |
possibly damaging |
Het |
Klhl24 |
T |
A |
16: 20,106,958 (GRCm38) |
C79S |
probably damaging |
Het |
Map3k11 |
A |
G |
19: 5,690,938 (GRCm38) |
H231R |
probably damaging |
Het |
Mbd4 |
C |
A |
6: 115,849,384 (GRCm38) |
R194S |
probably benign |
Het |
Mettl21e |
A |
C |
1: 44,211,143 (GRCm38) |
S34R |
probably benign |
Het |
Mrps5 |
T |
C |
2: 127,598,241 (GRCm38) |
V245A |
probably benign |
Het |
Mtrf1 |
T |
C |
14: 79,401,688 (GRCm38) |
Y87H |
probably benign |
Het |
Myh15 |
T |
C |
16: 49,120,057 (GRCm38) |
I790T |
probably benign |
Het |
Necab1 |
T |
G |
4: 14,989,248 (GRCm38) |
I176L |
probably benign |
Het |
Nfkb2 |
T |
A |
19: 46,309,922 (GRCm38) |
L555Q |
probably damaging |
Het |
Nhlrc3 |
T |
A |
3: 53,458,567 (GRCm38) |
E168D |
probably benign |
Het |
Nlrp5 |
T |
A |
7: 23,435,778 (GRCm38) |
C949S |
probably damaging |
Het |
Nup155 |
C |
A |
15: 8,157,703 (GRCm38) |
A1372E |
probably benign |
Het |
Nynrin |
G |
T |
14: 55,863,263 (GRCm38) |
R170L |
probably damaging |
Het |
Ogfrl1 |
T |
A |
1: 23,370,321 (GRCm38) |
N275Y |
probably damaging |
Het |
Olfr1110 |
C |
T |
2: 87,135,877 (GRCm38) |
S148N |
probably damaging |
Het |
Olfr1302 |
A |
G |
2: 111,780,845 (GRCm38) |
D175G |
probably damaging |
Het |
Olfr1480 |
A |
G |
19: 13,529,955 (GRCm38) |
N138S |
probably benign |
Het |
Olfr912 |
A |
G |
9: 38,581,969 (GRCm38) |
T231A |
possibly damaging |
Het |
Olr1 |
A |
T |
6: 129,488,876 (GRCm38) |
S56T |
probably damaging |
Het |
Ovol2 |
A |
T |
2: 144,331,283 (GRCm38) |
|
probably benign |
Het |
Pcdha6 |
A |
T |
18: 36,969,853 (GRCm38) |
I700F |
probably damaging |
Het |
Prkcz |
C |
T |
4: 155,289,702 (GRCm38) |
V86M |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,586,773 (GRCm38) |
T2124A |
probably benign |
Het |
Ranbp3 |
G |
T |
17: 56,673,346 (GRCm38) |
|
probably benign |
Het |
Rapgef2 |
A |
G |
3: 79,169,769 (GRCm38) |
|
probably benign |
Het |
Rbl1 |
A |
G |
2: 157,174,804 (GRCm38) |
V625A |
probably benign |
Het |
Rbm38 |
G |
T |
2: 173,022,151 (GRCm38) |
G38C |
probably damaging |
Het |
Reg1 |
T |
G |
6: 78,426,350 (GRCm38) |
F7C |
possibly damaging |
Het |
Retnlg |
A |
T |
16: 48,874,334 (GRCm38) |
Q115L |
possibly damaging |
Het |
Rhobtb1 |
G |
A |
10: 69,270,153 (GRCm38) |
V183I |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,291,105 (GRCm38) |
Q1186R |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 29,095,097 (GRCm38) |
F1246L |
possibly damaging |
Het |
Samm50 |
A |
G |
15: 84,210,610 (GRCm38) |
N401S |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,506,193 (GRCm38) |
I690F |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,959,238 (GRCm38) |
D304G |
probably damaging |
Het |
Skint6 |
T |
C |
4: 113,236,397 (GRCm38) |
Y183C |
probably damaging |
Het |
Slamf1 |
A |
T |
1: 171,777,261 (GRCm38) |
T200S |
probably benign |
Het |
Slc34a2 |
C |
T |
5: 53,069,451 (GRCm38) |
R639C |
probably damaging |
Het |
Smap1 |
A |
T |
1: 23,853,436 (GRCm38) |
M149K |
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,143,981 (GRCm38) |
|
probably benign |
Het |
Sp140 |
T |
A |
1: 85,610,828 (GRCm38) |
D95E |
possibly damaging |
Het |
Spata13 |
G |
A |
14: 60,753,907 (GRCm38) |
W366* |
probably null |
Het |
Strip1 |
G |
A |
3: 107,626,998 (GRCm38) |
T136I |
probably benign |
Het |
Tacr1 |
A |
T |
6: 82,557,072 (GRCm38) |
T360S |
probably benign |
Het |
Tbc1d14 |
T |
A |
5: 36,571,256 (GRCm38) |
|
probably benign |
Het |
Tcaf2 |
T |
C |
6: 42,628,062 (GRCm38) |
Y596C |
probably damaging |
Het |
Tspoap1 |
C |
T |
11: 87,778,443 (GRCm38) |
T1454I |
possibly damaging |
Het |
Ttc30a2 |
A |
C |
2: 75,977,576 (GRCm38) |
C197W |
probably benign |
Het |
Ttn |
A |
T |
2: 76,914,583 (GRCm38) |
M5374K |
probably benign |
Het |
Uts2r |
G |
A |
11: 121,160,879 (GRCm38) |
V190I |
possibly damaging |
Het |
Vmn1r181 |
A |
G |
7: 23,984,583 (GRCm38) |
T158A |
possibly damaging |
Het |
Wdr35 |
A |
T |
12: 9,018,150 (GRCm38) |
T778S |
probably benign |
Het |
Xrn1 |
A |
T |
9: 95,974,744 (GRCm38) |
|
probably benign |
Het |
Zfp35 |
A |
T |
18: 24,003,269 (GRCm38) |
K223N |
probably damaging |
Het |
Zfp764 |
T |
C |
7: 127,404,771 (GRCm38) |
Q396R |
probably benign |
Het |
Zfyve1 |
T |
C |
12: 83,558,647 (GRCm38) |
Y11C |
probably damaging |
Het |
|
Other mutations in Dnah7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Dnah7b
|
APN |
1 |
46,142,149 (GRCm38) |
missense |
probably benign |
0.04 |
IGL00796:Dnah7b
|
APN |
1 |
46,211,337 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL00825:Dnah7b
|
APN |
1 |
46,224,651 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00910:Dnah7b
|
APN |
1 |
46,066,729 (GRCm38) |
unclassified |
probably benign |
|
IGL00950:Dnah7b
|
APN |
1 |
46,214,322 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01142:Dnah7b
|
APN |
1 |
46,195,378 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01350:Dnah7b
|
APN |
1 |
46,081,432 (GRCm38) |
splice site |
probably benign |
|
IGL01392:Dnah7b
|
APN |
1 |
46,126,788 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01403:Dnah7b
|
APN |
1 |
46,116,300 (GRCm38) |
splice site |
probably benign |
|
IGL01460:Dnah7b
|
APN |
1 |
46,139,704 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL01576:Dnah7b
|
APN |
1 |
46,268,653 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01693:Dnah7b
|
APN |
1 |
46,358,147 (GRCm38) |
missense |
probably benign |
0.29 |
IGL01838:Dnah7b
|
APN |
1 |
46,358,137 (GRCm38) |
nonsense |
probably null |
|
IGL01906:Dnah7b
|
APN |
1 |
46,175,453 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01960:Dnah7b
|
APN |
1 |
46,124,337 (GRCm38) |
splice site |
probably benign |
|
IGL01989:Dnah7b
|
APN |
1 |
46,289,534 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02127:Dnah7b
|
APN |
1 |
46,139,875 (GRCm38) |
missense |
probably benign |
|
IGL02213:Dnah7b
|
APN |
1 |
46,233,592 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02267:Dnah7b
|
APN |
1 |
46,226,930 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02349:Dnah7b
|
APN |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
IGL02381:Dnah7b
|
APN |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02473:Dnah7b
|
APN |
1 |
46,234,193 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02484:Dnah7b
|
APN |
1 |
46,195,318 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02590:Dnah7b
|
APN |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02655:Dnah7b
|
APN |
1 |
46,116,301 (GRCm38) |
splice site |
probably benign |
|
IGL02704:Dnah7b
|
APN |
1 |
46,142,133 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02719:Dnah7b
|
APN |
1 |
46,099,608 (GRCm38) |
splice site |
probably benign |
|
IGL02745:Dnah7b
|
APN |
1 |
46,195,029 (GRCm38) |
splice site |
probably benign |
|
IGL02818:Dnah7b
|
APN |
1 |
46,290,808 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02892:Dnah7b
|
APN |
1 |
46,119,298 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL03285:Dnah7b
|
APN |
1 |
46,182,375 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03354:Dnah7b
|
APN |
1 |
46,085,689 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03355:Dnah7b
|
APN |
1 |
46,119,304 (GRCm38) |
missense |
probably benign |
0.18 |
BB001:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
BB011:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
PIT4305001:Dnah7b
|
UTSW |
1 |
46,373,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0116:Dnah7b
|
UTSW |
1 |
46,213,360 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0145:Dnah7b
|
UTSW |
1 |
46,223,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R0230:Dnah7b
|
UTSW |
1 |
46,219,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0302:Dnah7b
|
UTSW |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.26 |
R0313:Dnah7b
|
UTSW |
1 |
46,207,643 (GRCm38) |
missense |
probably damaging |
1.00 |
R0317:Dnah7b
|
UTSW |
1 |
46,134,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R0347:Dnah7b
|
UTSW |
1 |
46,240,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R0352:Dnah7b
|
UTSW |
1 |
46,277,126 (GRCm38) |
missense |
probably damaging |
0.98 |
R0363:Dnah7b
|
UTSW |
1 |
46,236,788 (GRCm38) |
missense |
probably damaging |
0.99 |
R0379:Dnah7b
|
UTSW |
1 |
46,140,176 (GRCm38) |
missense |
probably benign |
0.00 |
R0502:Dnah7b
|
UTSW |
1 |
46,219,544 (GRCm38) |
missense |
probably damaging |
0.96 |
R0602:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0631:Dnah7b
|
UTSW |
1 |
46,240,992 (GRCm38) |
missense |
probably benign |
0.02 |
R0664:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0882:Dnah7b
|
UTSW |
1 |
46,340,132 (GRCm38) |
missense |
probably benign |
0.00 |
R0931:Dnah7b
|
UTSW |
1 |
46,099,612 (GRCm38) |
splice site |
probably benign |
|
R1035:Dnah7b
|
UTSW |
1 |
46,124,448 (GRCm38) |
missense |
probably benign |
|
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1166:Dnah7b
|
UTSW |
1 |
46,325,810 (GRCm38) |
missense |
probably damaging |
1.00 |
R1219:Dnah7b
|
UTSW |
1 |
46,340,120 (GRCm38) |
missense |
probably benign |
0.00 |
R1318:Dnah7b
|
UTSW |
1 |
46,099,509 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1334:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1429:Dnah7b
|
UTSW |
1 |
46,289,656 (GRCm38) |
missense |
possibly damaging |
0.84 |
R1440:Dnah7b
|
UTSW |
1 |
46,078,593 (GRCm38) |
splice site |
probably benign |
|
R1484:Dnah7b
|
UTSW |
1 |
46,137,543 (GRCm38) |
missense |
probably benign |
0.00 |
R1529:Dnah7b
|
UTSW |
1 |
46,177,281 (GRCm38) |
missense |
probably damaging |
1.00 |
R1544:Dnah7b
|
UTSW |
1 |
46,066,797 (GRCm38) |
missense |
unknown |
|
R1607:Dnah7b
|
UTSW |
1 |
46,290,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R1609:Dnah7b
|
UTSW |
1 |
46,352,966 (GRCm38) |
missense |
probably damaging |
1.00 |
R1652:Dnah7b
|
UTSW |
1 |
46,175,390 (GRCm38) |
nonsense |
probably null |
|
R1681:Dnah7b
|
UTSW |
1 |
46,324,712 (GRCm38) |
nonsense |
probably null |
|
R1716:Dnah7b
|
UTSW |
1 |
46,191,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R1753:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1834:Dnah7b
|
UTSW |
1 |
46,233,759 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1838:Dnah7b
|
UTSW |
1 |
46,277,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R1838:Dnah7b
|
UTSW |
1 |
46,116,177 (GRCm38) |
missense |
probably benign |
0.04 |
R1898:Dnah7b
|
UTSW |
1 |
46,236,714 (GRCm38) |
missense |
probably benign |
0.02 |
R1962:Dnah7b
|
UTSW |
1 |
46,242,103 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2001:Dnah7b
|
UTSW |
1 |
46,142,087 (GRCm38) |
missense |
possibly damaging |
0.69 |
R2049:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2076:Dnah7b
|
UTSW |
1 |
46,242,321 (GRCm38) |
nonsense |
probably null |
|
R2083:Dnah7b
|
UTSW |
1 |
46,241,067 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2140:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2141:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2142:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2165:Dnah7b
|
UTSW |
1 |
46,097,992 (GRCm38) |
splice site |
probably benign |
|
R2172:Dnah7b
|
UTSW |
1 |
46,124,512 (GRCm38) |
missense |
probably benign |
0.12 |
R2239:Dnah7b
|
UTSW |
1 |
46,201,184 (GRCm38) |
splice site |
probably benign |
|
R2247:Dnah7b
|
UTSW |
1 |
46,277,063 (GRCm38) |
missense |
probably damaging |
1.00 |
R2267:Dnah7b
|
UTSW |
1 |
46,233,915 (GRCm38) |
missense |
probably damaging |
1.00 |
R2405:Dnah7b
|
UTSW |
1 |
46,362,954 (GRCm38) |
missense |
probably benign |
0.31 |
R2509:Dnah7b
|
UTSW |
1 |
46,195,287 (GRCm38) |
missense |
probably damaging |
0.96 |
R2895:Dnah7b
|
UTSW |
1 |
46,139,741 (GRCm38) |
missense |
probably damaging |
1.00 |
R2965:Dnah7b
|
UTSW |
1 |
46,207,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R3013:Dnah7b
|
UTSW |
1 |
46,188,687 (GRCm38) |
critical splice donor site |
probably null |
|
R3022:Dnah7b
|
UTSW |
1 |
46,182,423 (GRCm38) |
missense |
probably damaging |
0.99 |
R3056:Dnah7b
|
UTSW |
1 |
46,268,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R3107:Dnah7b
|
UTSW |
1 |
46,352,873 (GRCm38) |
missense |
probably benign |
0.00 |
R3735:Dnah7b
|
UTSW |
1 |
46,299,875 (GRCm38) |
missense |
probably benign |
0.05 |
R3898:Dnah7b
|
UTSW |
1 |
46,243,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R3944:Dnah7b
|
UTSW |
1 |
46,137,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R3983:Dnah7b
|
UTSW |
1 |
46,233,711 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4041:Dnah7b
|
UTSW |
1 |
46,081,495 (GRCm38) |
missense |
probably benign |
|
R4172:Dnah7b
|
UTSW |
1 |
46,226,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R4210:Dnah7b
|
UTSW |
1 |
46,137,418 (GRCm38) |
missense |
possibly damaging |
0.63 |
R4306:Dnah7b
|
UTSW |
1 |
46,221,772 (GRCm38) |
missense |
probably damaging |
0.99 |
R4391:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
R4414:Dnah7b
|
UTSW |
1 |
46,126,680 (GRCm38) |
missense |
probably benign |
0.00 |
R4495:Dnah7b
|
UTSW |
1 |
46,085,632 (GRCm38) |
missense |
probably benign |
0.00 |
R4660:Dnah7b
|
UTSW |
1 |
46,289,536 (GRCm38) |
missense |
probably damaging |
1.00 |
R4670:Dnah7b
|
UTSW |
1 |
46,078,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R4675:Dnah7b
|
UTSW |
1 |
46,217,157 (GRCm38) |
missense |
possibly damaging |
0.89 |
R4685:Dnah7b
|
UTSW |
1 |
46,211,328 (GRCm38) |
missense |
probably damaging |
1.00 |
R4727:Dnah7b
|
UTSW |
1 |
46,207,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R4735:Dnah7b
|
UTSW |
1 |
46,066,955 (GRCm38) |
missense |
unknown |
|
R4828:Dnah7b
|
UTSW |
1 |
46,128,112 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4859:Dnah7b
|
UTSW |
1 |
46,356,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R4865:Dnah7b
|
UTSW |
1 |
46,195,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R4871:Dnah7b
|
UTSW |
1 |
46,081,444 (GRCm38) |
missense |
probably benign |
0.21 |
R4881:Dnah7b
|
UTSW |
1 |
46,201,318 (GRCm38) |
missense |
probably damaging |
1.00 |
R4902:Dnah7b
|
UTSW |
1 |
46,290,775 (GRCm38) |
missense |
probably benign |
0.04 |
R4960:Dnah7b
|
UTSW |
1 |
46,233,726 (GRCm38) |
missense |
probably benign |
|
R5000:Dnah7b
|
UTSW |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
R5005:Dnah7b
|
UTSW |
1 |
46,242,028 (GRCm38) |
missense |
probably damaging |
0.99 |
R5026:Dnah7b
|
UTSW |
1 |
46,187,363 (GRCm38) |
missense |
probably damaging |
0.99 |
R5080:Dnah7b
|
UTSW |
1 |
46,182,380 (GRCm38) |
nonsense |
probably null |
|
R5174:Dnah7b
|
UTSW |
1 |
46,243,349 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5178:Dnah7b
|
UTSW |
1 |
46,358,216 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5244:Dnah7b
|
UTSW |
1 |
46,233,858 (GRCm38) |
missense |
probably damaging |
1.00 |
R5250:Dnah7b
|
UTSW |
1 |
46,373,354 (GRCm38) |
missense |
probably damaging |
1.00 |
R5350:Dnah7b
|
UTSW |
1 |
46,233,689 (GRCm38) |
missense |
probably benign |
0.16 |
R5380:Dnah7b
|
UTSW |
1 |
46,217,191 (GRCm38) |
missense |
probably benign |
0.18 |
R5387:Dnah7b
|
UTSW |
1 |
46,188,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R5423:Dnah7b
|
UTSW |
1 |
46,358,271 (GRCm38) |
missense |
probably benign |
0.01 |
R5426:Dnah7b
|
UTSW |
1 |
46,242,206 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5451:Dnah7b
|
UTSW |
1 |
46,242,019 (GRCm38) |
missense |
possibly damaging |
0.73 |
R5459:Dnah7b
|
UTSW |
1 |
46,109,312 (GRCm38) |
missense |
probably null |
|
R5479:Dnah7b
|
UTSW |
1 |
46,223,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R5583:Dnah7b
|
UTSW |
1 |
46,242,199 (GRCm38) |
missense |
probably benign |
0.06 |
R5637:Dnah7b
|
UTSW |
1 |
46,356,514 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5641:Dnah7b
|
UTSW |
1 |
46,268,764 (GRCm38) |
splice site |
probably null |
|
R5659:Dnah7b
|
UTSW |
1 |
46,352,849 (GRCm38) |
missense |
probably damaging |
1.00 |
R5739:Dnah7b
|
UTSW |
1 |
46,233,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R5759:Dnah7b
|
UTSW |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R5821:Dnah7b
|
UTSW |
1 |
46,142,132 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5874:Dnah7b
|
UTSW |
1 |
46,191,725 (GRCm38) |
missense |
probably damaging |
1.00 |
R5892:Dnah7b
|
UTSW |
1 |
46,337,593 (GRCm38) |
critical splice donor site |
probably null |
|
R5918:Dnah7b
|
UTSW |
1 |
46,221,643 (GRCm38) |
missense |
probably benign |
|
R5941:Dnah7b
|
UTSW |
1 |
46,187,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R5965:Dnah7b
|
UTSW |
1 |
46,362,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R5987:Dnah7b
|
UTSW |
1 |
46,119,398 (GRCm38) |
splice site |
probably null |
|
R6041:Dnah7b
|
UTSW |
1 |
46,289,645 (GRCm38) |
missense |
probably benign |
0.04 |
R6043:Dnah7b
|
UTSW |
1 |
46,139,789 (GRCm38) |
missense |
probably benign |
|
R6049:Dnah7b
|
UTSW |
1 |
46,085,602 (GRCm38) |
missense |
probably benign |
|
R6131:Dnah7b
|
UTSW |
1 |
46,253,466 (GRCm38) |
missense |
probably damaging |
1.00 |
R6168:Dnah7b
|
UTSW |
1 |
46,290,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R6195:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6219:Dnah7b
|
UTSW |
1 |
46,233,585 (GRCm38) |
missense |
probably benign |
0.03 |
R6226:Dnah7b
|
UTSW |
1 |
46,126,668 (GRCm38) |
missense |
probably benign |
0.01 |
R6233:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6247:Dnah7b
|
UTSW |
1 |
46,225,888 (GRCm38) |
missense |
probably benign |
|
R6273:Dnah7b
|
UTSW |
1 |
46,242,316 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6279:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6300:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6330:Dnah7b
|
UTSW |
1 |
46,340,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R6476:Dnah7b
|
UTSW |
1 |
46,242,204 (GRCm38) |
nonsense |
probably null |
|
R6494:Dnah7b
|
UTSW |
1 |
46,099,431 (GRCm38) |
missense |
probably damaging |
1.00 |
R6762:Dnah7b
|
UTSW |
1 |
46,224,742 (GRCm38) |
missense |
probably benign |
0.12 |
R6800:Dnah7b
|
UTSW |
1 |
46,340,217 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6838:Dnah7b
|
UTSW |
1 |
46,191,788 (GRCm38) |
missense |
probably damaging |
1.00 |
R6937:Dnah7b
|
UTSW |
1 |
46,195,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R6940:Dnah7b
|
UTSW |
1 |
46,119,268 (GRCm38) |
missense |
probably benign |
0.12 |
R6969:Dnah7b
|
UTSW |
1 |
46,358,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R6993:Dnah7b
|
UTSW |
1 |
46,195,139 (GRCm38) |
critical splice donor site |
probably null |
|
R7040:Dnah7b
|
UTSW |
1 |
46,236,809 (GRCm38) |
missense |
probably benign |
0.01 |
R7117:Dnah7b
|
UTSW |
1 |
46,352,813 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7135:Dnah7b
|
UTSW |
1 |
46,139,710 (GRCm38) |
missense |
probably damaging |
0.99 |
R7153:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.05 |
R7189:Dnah7b
|
UTSW |
1 |
46,242,142 (GRCm38) |
missense |
probably damaging |
1.00 |
R7237:Dnah7b
|
UTSW |
1 |
46,139,966 (GRCm38) |
missense |
probably damaging |
0.98 |
R7243:Dnah7b
|
UTSW |
1 |
46,083,754 (GRCm38) |
missense |
probably benign |
|
R7244:Dnah7b
|
UTSW |
1 |
46,277,143 (GRCm38) |
missense |
probably damaging |
0.99 |
R7248:Dnah7b
|
UTSW |
1 |
46,142,085 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7318:Dnah7b
|
UTSW |
1 |
46,195,372 (GRCm38) |
missense |
probably damaging |
1.00 |
R7375:Dnah7b
|
UTSW |
1 |
46,303,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7483:Dnah7b
|
UTSW |
1 |
46,175,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R7486:Dnah7b
|
UTSW |
1 |
46,290,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R7498:Dnah7b
|
UTSW |
1 |
46,325,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R7501:Dnah7b
|
UTSW |
1 |
46,356,554 (GRCm38) |
missense |
probably damaging |
1.00 |
R7513:Dnah7b
|
UTSW |
1 |
46,124,346 (GRCm38) |
missense |
probably benign |
0.06 |
R7547:Dnah7b
|
UTSW |
1 |
46,214,413 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7620:Dnah7b
|
UTSW |
1 |
46,268,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7670:Dnah7b
|
UTSW |
1 |
46,109,302 (GRCm38) |
missense |
probably benign |
|
R7676:Dnah7b
|
UTSW |
1 |
46,234,164 (GRCm38) |
nonsense |
probably null |
|
R7731:Dnah7b
|
UTSW |
1 |
46,139,745 (GRCm38) |
missense |
probably benign |
0.00 |
R7760:Dnah7b
|
UTSW |
1 |
46,201,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R7768:Dnah7b
|
UTSW |
1 |
46,137,474 (GRCm38) |
missense |
probably benign |
|
R7807:Dnah7b
|
UTSW |
1 |
46,214,367 (GRCm38) |
missense |
probably benign |
|
R7895:Dnah7b
|
UTSW |
1 |
46,249,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R7911:Dnah7b
|
UTSW |
1 |
46,139,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R7924:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
R7944:Dnah7b
|
UTSW |
1 |
46,227,003 (GRCm38) |
missense |
probably benign |
|
R7946:Dnah7b
|
UTSW |
1 |
46,233,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R7983:Dnah7b
|
UTSW |
1 |
46,243,424 (GRCm38) |
missense |
probably damaging |
1.00 |
R8012:Dnah7b
|
UTSW |
1 |
46,243,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R8069:Dnah7b
|
UTSW |
1 |
46,224,706 (GRCm38) |
nonsense |
probably null |
|
R8094:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.01 |
R8137:Dnah7b
|
UTSW |
1 |
46,233,753 (GRCm38) |
missense |
probably damaging |
1.00 |
R8167:Dnah7b
|
UTSW |
1 |
46,253,511 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8268:Dnah7b
|
UTSW |
1 |
46,356,576 (GRCm38) |
missense |
probably benign |
0.43 |
R8309:Dnah7b
|
UTSW |
1 |
46,139,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R8313:Dnah7b
|
UTSW |
1 |
46,175,296 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8410:Dnah7b
|
UTSW |
1 |
46,356,659 (GRCm38) |
critical splice donor site |
probably null |
|
R8438:Dnah7b
|
UTSW |
1 |
46,188,679 (GRCm38) |
missense |
probably damaging |
1.00 |
R8446:Dnah7b
|
UTSW |
1 |
46,290,715 (GRCm38) |
missense |
probably damaging |
1.00 |
R8471:Dnah7b
|
UTSW |
1 |
46,099,490 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8551:Dnah7b
|
UTSW |
1 |
46,116,200 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8711:Dnah7b
|
UTSW |
1 |
46,175,438 (GRCm38) |
missense |
probably damaging |
1.00 |
R8745:Dnah7b
|
UTSW |
1 |
46,182,464 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8765:Dnah7b
|
UTSW |
1 |
46,352,999 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8797:Dnah7b
|
UTSW |
1 |
46,123,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R8805:Dnah7b
|
UTSW |
1 |
46,234,145 (GRCm38) |
missense |
possibly damaging |
0.90 |
R8830:Dnah7b
|
UTSW |
1 |
46,191,793 (GRCm38) |
missense |
probably damaging |
1.00 |
R8861:Dnah7b
|
UTSW |
1 |
46,241,076 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8905:Dnah7b
|
UTSW |
1 |
46,253,374 (GRCm38) |
missense |
probably damaging |
0.99 |
R9009:Dnah7b
|
UTSW |
1 |
46,223,072 (GRCm38) |
missense |
probably benign |
0.00 |
R9058:Dnah7b
|
UTSW |
1 |
46,243,415 (GRCm38) |
missense |
probably damaging |
1.00 |
R9130:Dnah7b
|
UTSW |
1 |
46,134,514 (GRCm38) |
missense |
probably benign |
0.01 |
R9131:Dnah7b
|
UTSW |
1 |
46,227,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R9181:Dnah7b
|
UTSW |
1 |
46,142,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R9182:Dnah7b
|
UTSW |
1 |
46,290,878 (GRCm38) |
missense |
probably benign |
0.06 |
R9223:Dnah7b
|
UTSW |
1 |
46,322,260 (GRCm38) |
missense |
probably benign |
0.12 |
R9391:Dnah7b
|
UTSW |
1 |
46,233,754 (GRCm38) |
nonsense |
probably null |
|
R9392:Dnah7b
|
UTSW |
1 |
46,123,738 (GRCm38) |
nonsense |
probably null |
|
R9456:Dnah7b
|
UTSW |
1 |
46,126,793 (GRCm38) |
missense |
possibly damaging |
0.82 |
R9498:Dnah7b
|
UTSW |
1 |
46,214,404 (GRCm38) |
missense |
probably benign |
0.27 |
R9553:Dnah7b
|
UTSW |
1 |
46,225,796 (GRCm38) |
missense |
probably damaging |
0.99 |
R9598:Dnah7b
|
UTSW |
1 |
46,253,461 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9653:Dnah7b
|
UTSW |
1 |
46,213,384 (GRCm38) |
missense |
possibly damaging |
0.55 |
R9781:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
RF020:Dnah7b
|
UTSW |
1 |
46,373,261 (GRCm38) |
missense |
possibly damaging |
0.84 |
V8831:Dnah7b
|
UTSW |
1 |
46,373,298 (GRCm38) |
nonsense |
probably null |
|
X0023:Dnah7b
|
UTSW |
1 |
46,303,577 (GRCm38) |
missense |
probably benign |
0.04 |
|