Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610042L04Rik |
T |
C |
14: 4,348,902 (GRCm38) |
I21T |
probably damaging |
Het |
Adgrf1 |
A |
C |
17: 43,611,693 (GRCm39) |
E186D |
probably damaging |
Het |
Adgrf4 |
C |
T |
17: 42,977,789 (GRCm39) |
R518Q |
possibly damaging |
Het |
Afdn |
A |
G |
17: 14,030,695 (GRCm39) |
E202G |
probably damaging |
Het |
Agfg2 |
T |
A |
5: 137,665,378 (GRCm39) |
R126W |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,263,777 (GRCm39) |
V77I |
probably benign |
Het |
Alppl2 |
A |
G |
1: 87,015,419 (GRCm39) |
S381P |
probably benign |
Het |
Aqp2 |
A |
G |
15: 99,477,247 (GRCm39) |
T72A |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,779,302 (GRCm39) |
C1123R |
probably damaging |
Het |
AU016765 |
T |
A |
17: 64,826,995 (GRCm39) |
|
noncoding transcript |
Het |
Bscl2 |
T |
C |
19: 8,822,684 (GRCm39) |
|
probably null |
Het |
Ccdc80 |
A |
T |
16: 44,947,809 (GRCm39) |
Y929F |
probably damaging |
Het |
Cenpj |
T |
C |
14: 56,764,389 (GRCm39) |
D1341G |
probably damaging |
Het |
Cfap300 |
T |
C |
9: 8,022,478 (GRCm39) |
D248G |
probably damaging |
Het |
Cir1 |
A |
T |
2: 73,142,781 (GRCm39) |
S18T |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
Het |
Crb1 |
T |
C |
1: 139,164,750 (GRCm39) |
I1125V |
probably benign |
Het |
Cyp3a13 |
A |
T |
5: 137,919,716 (GRCm39) |
V20D |
possibly damaging |
Het |
Dars1 |
T |
A |
1: 128,299,899 (GRCm39) |
M362L |
probably benign |
Het |
Dck |
T |
C |
5: 88,920,582 (GRCm39) |
C101R |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 117,972,545 (GRCm39) |
T2880A |
probably benign |
Het |
Eef1a2 |
C |
T |
2: 180,790,535 (GRCm39) |
E374K |
probably benign |
Het |
Eif3a |
A |
T |
19: 60,763,832 (GRCm39) |
|
probably benign |
Het |
Esco1 |
A |
G |
18: 10,574,873 (GRCm39) |
|
probably null |
Het |
Exoc8 |
C |
T |
8: 125,624,154 (GRCm39) |
R71Q |
possibly damaging |
Het |
Far1 |
G |
A |
7: 113,165,667 (GRCm39) |
V445M |
possibly damaging |
Het |
Fbn1 |
C |
A |
2: 125,185,730 (GRCm39) |
C1648F |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,425,393 (GRCm39) |
K1189R |
probably benign |
Het |
Foxl2 |
C |
A |
9: 98,838,540 (GRCm39) |
P276H |
unknown |
Het |
Fpr3 |
T |
A |
17: 18,190,879 (GRCm39) |
V50E |
probably damaging |
Het |
Garem1 |
T |
A |
18: 21,262,431 (GRCm39) |
R794S |
probably damaging |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Glyatl3 |
T |
C |
17: 41,221,975 (GRCm39) |
D93G |
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,425,336 (GRCm39) |
I274T |
probably benign |
Het |
Gucy1a1 |
C |
T |
3: 82,026,193 (GRCm39) |
|
probably null |
Het |
Hook1 |
GATGAATGA |
GATGA |
4: 95,901,549 (GRCm39) |
503 |
probably null |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Ints13 |
A |
G |
6: 146,477,929 (GRCm39) |
S7P |
probably damaging |
Het |
Kat5 |
T |
A |
19: 5,655,713 (GRCm39) |
|
probably null |
Het |
Kcnma1 |
A |
C |
14: 23,364,288 (GRCm39) |
L988R |
probably damaging |
Het |
Kcnq3 |
C |
A |
15: 65,877,827 (GRCm39) |
|
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,392,231 (GRCm39) |
E273G |
possibly damaging |
Het |
Krt82 |
T |
A |
15: 101,453,591 (GRCm39) |
Q265L |
probably damaging |
Het |
Lama2 |
A |
T |
10: 26,930,690 (GRCm39) |
|
probably null |
Het |
Laptm4b |
G |
T |
15: 34,238,478 (GRCm39) |
M3I |
probably benign |
Het |
Lmtk2 |
A |
G |
5: 144,084,433 (GRCm39) |
Y156C |
probably damaging |
Het |
Lrrc58 |
G |
A |
16: 37,701,771 (GRCm39) |
E350K |
probably damaging |
Het |
Lrrk1 |
A |
T |
7: 65,980,498 (GRCm39) |
D227E |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,248,895 (GRCm39) |
C7210Y |
probably damaging |
Het |
Madd |
A |
G |
2: 90,982,854 (GRCm39) |
I1363T |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,883,334 (GRCm39) |
V295A |
probably benign |
Het |
Mki67 |
A |
G |
7: 135,297,321 (GRCm39) |
I2571T |
possibly damaging |
Het |
Mtrr |
C |
T |
13: 68,717,059 (GRCm39) |
A385T |
possibly damaging |
Het |
Myh7b |
A |
G |
2: 155,462,043 (GRCm39) |
Y313C |
probably damaging |
Het |
Myot |
A |
T |
18: 44,487,192 (GRCm39) |
H343L |
possibly damaging |
Het |
Myt1 |
C |
A |
2: 181,467,772 (GRCm39) |
Q1069K |
probably damaging |
Het |
Nid1 |
T |
A |
13: 13,674,253 (GRCm39) |
D877E |
probably damaging |
Het |
Nle1 |
A |
G |
11: 82,796,394 (GRCm39) |
V159A |
probably damaging |
Het |
Nmbr |
C |
A |
10: 14,646,186 (GRCm39) |
Y353* |
probably null |
Het |
Nos1ap |
T |
A |
1: 170,156,735 (GRCm39) |
D241V |
probably damaging |
Het |
Nostrin |
A |
C |
2: 68,996,347 (GRCm39) |
Y209S |
probably damaging |
Het |
Or14j4 |
T |
G |
17: 37,921,362 (GRCm39) |
E93D |
probably benign |
Het |
Or1e19 |
A |
T |
11: 73,316,707 (GRCm39) |
M34K |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5d40 |
A |
T |
2: 88,015,439 (GRCm39) |
S73C |
probably benign |
Het |
Or8h9 |
A |
T |
2: 86,789,625 (GRCm39) |
M59K |
probably damaging |
Het |
Or8s2 |
G |
A |
15: 98,276,277 (GRCm39) |
T238I |
possibly damaging |
Het |
Pcdh7 |
T |
A |
5: 58,286,338 (GRCm39) |
V1138E |
probably damaging |
Het |
Pglyrp3 |
T |
G |
3: 91,933,874 (GRCm39) |
V173G |
probably benign |
Het |
Plec |
T |
C |
15: 76,067,374 (GRCm39) |
T1331A |
probably benign |
Het |
Plxnb2 |
T |
C |
15: 89,040,765 (GRCm39) |
D1787G |
probably benign |
Het |
Pms1 |
T |
A |
1: 53,321,147 (GRCm39) |
I29F |
probably damaging |
Het |
Ptprt |
G |
A |
2: 161,653,908 (GRCm39) |
T574I |
probably damaging |
Het |
R3hdm1 |
A |
G |
1: 128,118,430 (GRCm39) |
Y561C |
probably damaging |
Het |
Rab17 |
A |
G |
1: 90,887,800 (GRCm39) |
F120S |
probably benign |
Het |
Rab7b |
T |
A |
1: 131,626,157 (GRCm39) |
W62R |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,575,493 (GRCm39) |
G4835E |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,705,493 (GRCm39) |
V807A |
probably benign |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Slc23a1 |
C |
T |
18: 35,759,487 (GRCm39) |
R26Q |
unknown |
Het |
Slc7a4 |
C |
A |
16: 17,392,408 (GRCm39) |
R342L |
possibly damaging |
Het |
Slfn9 |
C |
T |
11: 82,875,481 (GRCm39) |
C367Y |
possibly damaging |
Het |
Slitrk6 |
T |
G |
14: 110,988,226 (GRCm39) |
T494P |
probably benign |
Het |
Tasor |
C |
T |
14: 27,201,992 (GRCm39) |
T1462I |
probably damaging |
Het |
Tiam1 |
A |
G |
16: 89,646,533 (GRCm39) |
|
probably benign |
Het |
Tiparp |
C |
A |
3: 65,436,673 (GRCm39) |
|
probably benign |
Het |
Tmem39b |
T |
C |
4: 129,572,481 (GRCm39) |
T374A |
probably benign |
Het |
Trim5 |
G |
A |
7: 103,925,998 (GRCm39) |
R188* |
probably null |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Vmn2r26 |
A |
T |
6: 124,038,196 (GRCm39) |
E590D |
probably benign |
Het |
Wwc1 |
A |
G |
11: 35,761,355 (GRCm39) |
F650S |
probably benign |
Het |
Xrcc6 |
T |
A |
15: 81,907,178 (GRCm39) |
F167I |
probably damaging |
Het |
Zfp1005 |
A |
T |
2: 150,111,281 (GRCm39) |
H657L |
probably benign |
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 |
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 |
|