Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700022I11Rik |
A |
T |
4: 42,974,171 (GRCm38) |
D1168V |
probably benign |
Het |
4930430A15Rik |
T |
C |
2: 111,200,418 (GRCm38) |
E382G |
probably damaging |
Het |
9130011E15Rik |
A |
T |
19: 45,965,381 (GRCm38) |
I188K |
probably damaging |
Het |
Ace |
C |
T |
11: 105,976,623 (GRCm38) |
Q484* |
probably null |
Het |
Ackr3 |
T |
C |
1: 90,213,981 (GRCm38) |
I54T |
probably damaging |
Het |
Aco1 |
G |
A |
4: 40,183,605 (GRCm38) |
G508S |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,332,483 (GRCm38) |
R511H |
probably damaging |
Het |
Ankef1 |
T |
C |
2: 136,545,738 (GRCm38) |
S192P |
possibly damaging |
Het |
Ankrd16 |
T |
G |
2: 11,789,748 (GRCm38) |
C315G |
possibly damaging |
Het |
Ankzf1 |
T |
C |
1: 75,196,243 (GRCm38) |
S328P |
probably damaging |
Het |
Aqp2 |
A |
G |
15: 99,583,100 (GRCm38) |
I176V |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 80,027,180 (GRCm38) |
Y730C |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,493,779 (GRCm38) |
E316G |
probably damaging |
Het |
Btbd17 |
A |
T |
11: 114,791,952 (GRCm38) |
|
probably null |
Het |
Calu |
A |
G |
6: 29,372,615 (GRCm38) |
Y263C |
probably damaging |
Het |
Ccdc122 |
T |
C |
14: 77,068,951 (GRCm38) |
|
probably null |
Het |
Cenpf |
T |
C |
1: 189,656,901 (GRCm38) |
K1578R |
probably damaging |
Het |
Cep120 |
A |
G |
18: 53,719,312 (GRCm38) |
V498A |
possibly damaging |
Het |
Ces1a |
T |
A |
8: 93,048,075 (GRCm38) |
N12Y |
probably benign |
Het |
Chmp1a |
A |
T |
8: 123,208,022 (GRCm38) |
M65K |
probably damaging |
Het |
Cnot1 |
G |
T |
8: 95,739,833 (GRCm38) |
T1592K |
possibly damaging |
Het |
Cps1 |
T |
A |
1: 67,204,638 (GRCm38) |
I1091N |
probably benign |
Het |
Dhx32 |
T |
C |
7: 133,721,292 (GRCm38) |
N731S |
probably benign |
Het |
Dhx33 |
G |
A |
11: 70,999,843 (GRCm38) |
R177W |
probably damaging |
Het |
Dmd |
G |
C |
X: 84,312,483 (GRCm38) |
A2257P |
probably benign |
Het |
Dnah10 |
T |
C |
5: 124,814,674 (GRCm38) |
S3259P |
probably damaging |
Het |
Dock3 |
A |
G |
9: 106,993,463 (GRCm38) |
F584S |
possibly damaging |
Het |
Dtnb |
A |
G |
12: 3,781,273 (GRCm38) |
T658A |
probably benign |
Het |
Duox2 |
T |
A |
2: 122,295,158 (GRCm38) |
S323C |
probably damaging |
Het |
Elovl3 |
A |
T |
19: 46,132,167 (GRCm38) |
E33V |
probably damaging |
Het |
Enpp5 |
T |
C |
17: 44,085,373 (GRCm38) |
F392S |
probably benign |
Het |
Eogt |
T |
C |
6: 97,131,376 (GRCm38) |
T235A |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,536,219 (GRCm38) |
V370A |
probably benign |
Het |
Ewsr1 |
C |
T |
11: 5,071,555 (GRCm38) |
R466H |
unknown |
Het |
Fam208a |
T |
A |
14: 27,461,213 (GRCm38) |
I543K |
probably benign |
Het |
Fcgbp |
G |
A |
7: 28,120,389 (GRCm38) |
G2514S |
probably damaging |
Het |
Flt1 |
A |
T |
5: 147,599,606 (GRCm38) |
D808E |
possibly damaging |
Het |
Glg1 |
C |
T |
8: 111,168,671 (GRCm38) |
G836E |
probably damaging |
Het |
Gm17334 |
A |
G |
11: 53,772,828 (GRCm38) |
|
probably benign |
Het |
Gpbp1 |
A |
T |
13: 111,453,407 (GRCm38) |
D51E |
probably benign |
Het |
Il12rb2 |
C |
G |
6: 67,360,552 (GRCm38) |
C115S |
probably damaging |
Het |
Il1rl1 |
T |
C |
1: 40,462,044 (GRCm38) |
S527P |
probably damaging |
Het |
Ireb2 |
A |
G |
9: 54,881,449 (GRCm38) |
D69G |
probably benign |
Het |
Kif5a |
T |
C |
10: 127,245,369 (GRCm38) |
D232G |
probably damaging |
Het |
M1ap |
A |
G |
6: 82,981,882 (GRCm38) |
I165V |
probably benign |
Het |
Mff |
T |
A |
1: 82,751,700 (GRCm38) |
L287H |
probably damaging |
Het |
Mmp27 |
A |
G |
9: 7,577,739 (GRCm38) |
M311V |
possibly damaging |
Het |
Mpped2 |
T |
A |
2: 106,744,802 (GRCm38) |
Y77* |
probably null |
Het |
Mybbp1a |
G |
A |
11: 72,441,445 (GRCm38) |
S21N |
probably benign |
Het |
Obscn |
T |
C |
11: 59,132,652 (GRCm38) |
D633G |
probably damaging |
Het |
Obscn |
G |
C |
11: 59,069,281 (GRCm38) |
I3253M |
probably damaging |
Het |
Olfr1247 |
A |
G |
2: 89,609,478 (GRCm38) |
V208A |
probably benign |
Het |
Olfr1404 |
A |
T |
1: 173,215,810 (GRCm38) |
D53V |
probably damaging |
Het |
Olr1 |
C |
T |
6: 129,502,094 (GRCm38) |
V54I |
probably benign |
Het |
Phlpp2 |
T |
C |
8: 109,928,492 (GRCm38) |
S605P |
possibly damaging |
Het |
Plekhg4 |
TAGTCGATGCCCGAGTC |
TAGTC |
8: 105,376,452 (GRCm38) |
|
probably benign |
Het |
Prss8 |
C |
A |
7: 127,927,094 (GRCm38) |
R148L |
possibly damaging |
Het |
Psg27 |
T |
C |
7: 18,560,417 (GRCm38) |
D355G |
probably damaging |
Het |
Rabgef1 |
C |
A |
5: 130,187,561 (GRCm38) |
Q52K |
probably benign |
Het |
Rnf6 |
C |
T |
5: 146,210,906 (GRCm38) |
R434H |
probably damaging |
Het |
Rpl26 |
A |
G |
11: 68,903,273 (GRCm38) |
E88G |
probably benign |
Het |
Rpn1 |
T |
A |
6: 88,100,962 (GRCm38) |
L460Q |
probably damaging |
Het |
Sap130 |
T |
A |
18: 31,648,279 (GRCm38) |
I165N |
probably damaging |
Het |
Sash1 |
A |
G |
10: 8,756,697 (GRCm38) |
V258A |
probably damaging |
Het |
Scarb1 |
G |
T |
5: 125,294,143 (GRCm38) |
N288K |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,440,239 (GRCm38) |
I588T |
probably damaging |
Het |
Shank2 |
C |
A |
7: 144,409,540 (GRCm38) |
S295Y |
probably damaging |
Het |
Slc15a3 |
T |
C |
19: 10,857,299 (GRCm38) |
S515P |
probably damaging |
Het |
Slc25a13 |
A |
T |
6: 6,114,017 (GRCm38) |
M285K |
probably benign |
Het |
Slc39a11 |
A |
G |
11: 113,463,974 (GRCm38) |
I143T |
probably null |
Het |
Smarcd2 |
A |
T |
11: 106,265,307 (GRCm38) |
L42* |
probably null |
Het |
Smc3 |
A |
G |
19: 53,631,533 (GRCm38) |
D620G |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,790,776 (GRCm38) |
D456N |
probably damaging |
Het |
Taar4 |
A |
C |
10: 23,961,173 (GRCm38) |
Q227P |
probably benign |
Het |
Tecta |
G |
T |
9: 42,337,279 (GRCm38) |
Y1937* |
probably null |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm38) |
R637Q |
probably benign |
Het |
Tmem130 |
T |
A |
5: 144,755,274 (GRCm38) |
T107S |
possibly damaging |
Het |
Tmem132d |
T |
C |
5: 128,269,131 (GRCm38) |
D109G |
probably damaging |
Het |
Tmem81 |
A |
G |
1: 132,507,906 (GRCm38) |
Y150C |
probably damaging |
Het |
Tnrc18 |
C |
T |
5: 142,759,706 (GRCm38) |
|
probably null |
Het |
Trim43a |
A |
G |
9: 88,586,094 (GRCm38) |
K256R |
possibly damaging |
Het |
Trpm6 |
A |
G |
19: 18,877,739 (GRCm38) |
T1921A |
probably damaging |
Het |
Tubb3 |
C |
T |
8: 123,421,270 (GRCm38) |
A314V |
probably damaging |
Het |
Ube3b |
A |
C |
5: 114,415,255 (GRCm38) |
N896T |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,679,744 (GRCm38) |
|
probably null |
Het |
Upb1 |
A |
G |
10: 75,424,513 (GRCm38) |
T134A |
probably damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,286,753 (GRCm38) |
M695K |
possibly damaging |
Het |
Wwc1 |
G |
T |
11: 35,889,353 (GRCm38) |
D258E |
possibly damaging |
Het |
Zfp619 |
T |
A |
7: 39,534,761 (GRCm38) |
Y72N |
probably benign |
Het |
Zfp672 |
G |
T |
11: 58,316,636 (GRCm38) |
H286Q |
possibly damaging |
Het |
|
Other mutations in Dnah7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Dnah7a
|
APN |
1 |
53,419,684 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00510:Dnah7a
|
APN |
1 |
53,501,542 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00545:Dnah7a
|
APN |
1 |
53,457,746 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL01320:Dnah7a
|
APN |
1 |
53,434,046 (GRCm38) |
missense |
probably benign |
0.32 |
IGL01322:Dnah7a
|
APN |
1 |
53,434,046 (GRCm38) |
missense |
probably benign |
0.32 |
IGL01357:Dnah7a
|
APN |
1 |
53,662,381 (GRCm38) |
missense |
probably benign |
|
IGL01417:Dnah7a
|
APN |
1 |
53,584,600 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01508:Dnah7a
|
APN |
1 |
53,627,072 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01511:Dnah7a
|
APN |
1 |
53,419,595 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01545:Dnah7a
|
APN |
1 |
53,518,782 (GRCm38) |
missense |
probably benign |
|
IGL01575:Dnah7a
|
APN |
1 |
53,427,820 (GRCm38) |
splice site |
probably benign |
|
IGL01667:Dnah7a
|
APN |
1 |
53,547,292 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01712:Dnah7a
|
APN |
1 |
53,423,270 (GRCm38) |
missense |
probably benign |
0.23 |
IGL01824:Dnah7a
|
APN |
1 |
53,504,270 (GRCm38) |
missense |
probably benign |
|
IGL01829:Dnah7a
|
APN |
1 |
53,618,068 (GRCm38) |
missense |
possibly damaging |
0.64 |
IGL01861:Dnah7a
|
APN |
1 |
53,584,449 (GRCm38) |
splice site |
probably benign |
|
IGL01861:Dnah7a
|
APN |
1 |
53,640,349 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01984:Dnah7a
|
APN |
1 |
53,702,015 (GRCm38) |
splice site |
probably null |
|
IGL02056:Dnah7a
|
APN |
1 |
53,504,342 (GRCm38) |
missense |
probably benign |
0.17 |
IGL02069:Dnah7a
|
APN |
1 |
53,561,894 (GRCm38) |
splice site |
probably benign |
|
IGL02072:Dnah7a
|
APN |
1 |
53,605,827 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02110:Dnah7a
|
APN |
1 |
53,411,580 (GRCm38) |
missense |
possibly damaging |
0.52 |
IGL02120:Dnah7a
|
APN |
1 |
53,495,717 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02128:Dnah7a
|
APN |
1 |
53,437,513 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02135:Dnah7a
|
APN |
1 |
53,623,473 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02151:Dnah7a
|
APN |
1 |
53,472,864 (GRCm38) |
missense |
probably benign |
0.08 |
IGL02156:Dnah7a
|
APN |
1 |
53,419,723 (GRCm38) |
missense |
probably benign |
0.27 |
IGL02270:Dnah7a
|
APN |
1 |
53,472,893 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02282:Dnah7a
|
APN |
1 |
53,643,510 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02328:Dnah7a
|
APN |
1 |
53,524,937 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02370:Dnah7a
|
APN |
1 |
53,635,397 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02420:Dnah7a
|
APN |
1 |
53,686,543 (GRCm38) |
missense |
probably benign |
|
IGL02458:Dnah7a
|
APN |
1 |
53,618,328 (GRCm38) |
nonsense |
probably null |
|
IGL02489:Dnah7a
|
APN |
1 |
53,647,322 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL02554:Dnah7a
|
APN |
1 |
53,618,046 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02578:Dnah7a
|
APN |
1 |
53,432,915 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02646:Dnah7a
|
APN |
1 |
53,525,035 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02675:Dnah7a
|
APN |
1 |
53,504,024 (GRCm38) |
missense |
possibly damaging |
0.96 |
IGL02688:Dnah7a
|
APN |
1 |
53,444,472 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02858:Dnah7a
|
APN |
1 |
53,472,959 (GRCm38) |
splice site |
probably benign |
|
IGL02874:Dnah7a
|
APN |
1 |
53,605,814 (GRCm38) |
missense |
possibly damaging |
0.70 |
IGL02887:Dnah7a
|
APN |
1 |
53,522,360 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02894:Dnah7a
|
APN |
1 |
53,577,328 (GRCm38) |
missense |
probably benign |
0.27 |
IGL02926:Dnah7a
|
APN |
1 |
53,495,950 (GRCm38) |
missense |
possibly damaging |
0.64 |
IGL03113:Dnah7a
|
APN |
1 |
53,433,004 (GRCm38) |
missense |
possibly damaging |
0.64 |
IGL03156:Dnah7a
|
APN |
1 |
53,605,824 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL03195:Dnah7a
|
APN |
1 |
53,419,607 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03209:Dnah7a
|
APN |
1 |
53,686,614 (GRCm38) |
splice site |
probably benign |
|
IGL03214:Dnah7a
|
APN |
1 |
53,522,209 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03242:Dnah7a
|
APN |
1 |
53,620,723 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03251:Dnah7a
|
APN |
1 |
53,647,274 (GRCm38) |
missense |
probably benign |
|
IGL03265:Dnah7a
|
APN |
1 |
53,528,848 (GRCm38) |
missense |
probably benign |
|
IGL03277:Dnah7a
|
APN |
1 |
53,630,322 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03278:Dnah7a
|
APN |
1 |
53,496,965 (GRCm38) |
missense |
probably benign |
0.07 |
IGL03356:Dnah7a
|
APN |
1 |
53,503,934 (GRCm38) |
missense |
probably benign |
0.01 |
PIT4378001:Dnah7a
|
UTSW |
1 |
53,531,203 (GRCm38) |
missense |
probably damaging |
0.99 |
R0046:Dnah7a
|
UTSW |
1 |
53,456,874 (GRCm38) |
splice site |
probably null |
|
R0051:Dnah7a
|
UTSW |
1 |
53,521,086 (GRCm38) |
splice site |
probably benign |
|
R0082:Dnah7a
|
UTSW |
1 |
53,518,708 (GRCm38) |
missense |
probably damaging |
1.00 |
R0111:Dnah7a
|
UTSW |
1 |
53,468,684 (GRCm38) |
missense |
probably benign |
0.03 |
R0122:Dnah7a
|
UTSW |
1 |
53,397,142 (GRCm38) |
missense |
probably damaging |
1.00 |
R0245:Dnah7a
|
UTSW |
1 |
53,501,526 (GRCm38) |
missense |
probably damaging |
1.00 |
R0278:Dnah7a
|
UTSW |
1 |
53,504,146 (GRCm38) |
missense |
probably benign |
0.00 |
R0309:Dnah7a
|
UTSW |
1 |
53,405,690 (GRCm38) |
missense |
probably damaging |
0.97 |
R0334:Dnah7a
|
UTSW |
1 |
53,433,054 (GRCm38) |
missense |
possibly damaging |
0.61 |
R0392:Dnah7a
|
UTSW |
1 |
53,504,198 (GRCm38) |
missense |
probably damaging |
0.97 |
R0452:Dnah7a
|
UTSW |
1 |
53,605,819 (GRCm38) |
missense |
probably benign |
0.00 |
R0511:Dnah7a
|
UTSW |
1 |
53,497,126 (GRCm38) |
missense |
probably benign |
|
R0576:Dnah7a
|
UTSW |
1 |
53,636,087 (GRCm38) |
missense |
probably benign |
0.12 |
R0592:Dnah7a
|
UTSW |
1 |
53,456,612 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0628:Dnah7a
|
UTSW |
1 |
53,497,105 (GRCm38) |
missense |
probably benign |
0.18 |
R0689:Dnah7a
|
UTSW |
1 |
53,620,681 (GRCm38) |
nonsense |
probably null |
|
R0735:Dnah7a
|
UTSW |
1 |
53,544,511 (GRCm38) |
missense |
possibly damaging |
0.70 |
R0800:Dnah7a
|
UTSW |
1 |
53,565,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R0829:Dnah7a
|
UTSW |
1 |
53,504,079 (GRCm38) |
missense |
probably benign |
0.07 |
R0842:Dnah7a
|
UTSW |
1 |
53,501,674 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0879:Dnah7a
|
UTSW |
1 |
53,427,860 (GRCm38) |
missense |
possibly damaging |
0.85 |
R1331:Dnah7a
|
UTSW |
1 |
53,468,669 (GRCm38) |
missense |
probably damaging |
0.99 |
R1418:Dnah7a
|
UTSW |
1 |
53,647,236 (GRCm38) |
splice site |
probably benign |
|
R1421:Dnah7a
|
UTSW |
1 |
53,540,873 (GRCm38) |
splice site |
probably benign |
|
R1445:Dnah7a
|
UTSW |
1 |
53,528,797 (GRCm38) |
missense |
probably benign |
0.02 |
R1473:Dnah7a
|
UTSW |
1 |
53,496,014 (GRCm38) |
missense |
probably benign |
0.00 |
R1538:Dnah7a
|
UTSW |
1 |
53,495,989 (GRCm38) |
missense |
possibly damaging |
0.71 |
R1742:Dnah7a
|
UTSW |
1 |
53,456,684 (GRCm38) |
missense |
probably benign |
0.39 |
R1754:Dnah7a
|
UTSW |
1 |
53,561,900 (GRCm38) |
critical splice donor site |
probably null |
|
R1754:Dnah7a
|
UTSW |
1 |
53,504,185 (GRCm38) |
missense |
probably benign |
0.18 |
R1773:Dnah7a
|
UTSW |
1 |
53,432,887 (GRCm38) |
splice site |
probably null |
|
R1779:Dnah7a
|
UTSW |
1 |
53,577,223 (GRCm38) |
missense |
probably benign |
|
R1816:Dnah7a
|
UTSW |
1 |
53,631,742 (GRCm38) |
splice site |
probably benign |
|
R1817:Dnah7a
|
UTSW |
1 |
53,559,148 (GRCm38) |
missense |
probably benign |
|
R1818:Dnah7a
|
UTSW |
1 |
53,559,148 (GRCm38) |
missense |
probably benign |
|
R1819:Dnah7a
|
UTSW |
1 |
53,559,148 (GRCm38) |
missense |
probably benign |
|
R1873:Dnah7a
|
UTSW |
1 |
53,456,532 (GRCm38) |
splice site |
probably benign |
|
R1875:Dnah7a
|
UTSW |
1 |
53,456,532 (GRCm38) |
splice site |
probably benign |
|
R1884:Dnah7a
|
UTSW |
1 |
53,541,000 (GRCm38) |
missense |
probably damaging |
0.99 |
R1902:Dnah7a
|
UTSW |
1 |
53,535,478 (GRCm38) |
missense |
probably damaging |
1.00 |
R1903:Dnah7a
|
UTSW |
1 |
53,535,478 (GRCm38) |
missense |
probably damaging |
1.00 |
R1908:Dnah7a
|
UTSW |
1 |
53,631,562 (GRCm38) |
missense |
probably benign |
|
R1959:Dnah7a
|
UTSW |
1 |
53,684,983 (GRCm38) |
missense |
probably benign |
0.00 |
R1960:Dnah7a
|
UTSW |
1 |
53,684,983 (GRCm38) |
missense |
probably benign |
0.00 |
R1985:Dnah7a
|
UTSW |
1 |
53,503,934 (GRCm38) |
missense |
probably benign |
0.01 |
R1992:Dnah7a
|
UTSW |
1 |
53,582,676 (GRCm38) |
missense |
possibly damaging |
0.91 |
R2037:Dnah7a
|
UTSW |
1 |
53,582,582 (GRCm38) |
missense |
probably benign |
0.00 |
R2076:Dnah7a
|
UTSW |
1 |
53,503,809 (GRCm38) |
missense |
probably benign |
0.01 |
R2124:Dnah7a
|
UTSW |
1 |
53,496,942 (GRCm38) |
missense |
possibly damaging |
0.58 |
R2191:Dnah7a
|
UTSW |
1 |
53,605,875 (GRCm38) |
missense |
possibly damaging |
0.54 |
R2211:Dnah7a
|
UTSW |
1 |
53,479,773 (GRCm38) |
missense |
probably benign |
0.21 |
R2220:Dnah7a
|
UTSW |
1 |
53,521,174 (GRCm38) |
missense |
probably benign |
|
R2355:Dnah7a
|
UTSW |
1 |
53,582,502 (GRCm38) |
missense |
probably benign |
0.00 |
R2495:Dnah7a
|
UTSW |
1 |
53,605,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R2901:Dnah7a
|
UTSW |
1 |
53,427,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R2911:Dnah7a
|
UTSW |
1 |
53,427,824 (GRCm38) |
critical splice donor site |
probably null |
|
R2993:Dnah7a
|
UTSW |
1 |
53,503,554 (GRCm38) |
missense |
probably damaging |
1.00 |
R3522:Dnah7a
|
UTSW |
1 |
53,618,116 (GRCm38) |
missense |
probably damaging |
1.00 |
R3683:Dnah7a
|
UTSW |
1 |
53,444,516 (GRCm38) |
missense |
probably benign |
|
R3723:Dnah7a
|
UTSW |
1 |
53,447,346 (GRCm38) |
missense |
probably benign |
0.04 |
R3847:Dnah7a
|
UTSW |
1 |
53,501,656 (GRCm38) |
missense |
probably benign |
0.01 |
R4002:Dnah7a
|
UTSW |
1 |
53,631,681 (GRCm38) |
missense |
probably benign |
|
R4009:Dnah7a
|
UTSW |
1 |
53,525,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R4063:Dnah7a
|
UTSW |
1 |
53,425,217 (GRCm38) |
missense |
probably benign |
|
R4193:Dnah7a
|
UTSW |
1 |
53,447,334 (GRCm38) |
missense |
probably benign |
0.00 |
R4236:Dnah7a
|
UTSW |
1 |
53,447,365 (GRCm38) |
missense |
probably benign |
0.00 |
R4399:Dnah7a
|
UTSW |
1 |
53,518,727 (GRCm38) |
missense |
probably damaging |
1.00 |
R4469:Dnah7a
|
UTSW |
1 |
53,444,526 (GRCm38) |
missense |
probably benign |
0.01 |
R4494:Dnah7a
|
UTSW |
1 |
53,449,038 (GRCm38) |
missense |
probably benign |
0.01 |
R4569:Dnah7a
|
UTSW |
1 |
53,411,659 (GRCm38) |
missense |
probably benign |
0.01 |
R4609:Dnah7a
|
UTSW |
1 |
53,456,657 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4632:Dnah7a
|
UTSW |
1 |
53,427,951 (GRCm38) |
missense |
probably damaging |
0.97 |
R4703:Dnah7a
|
UTSW |
1 |
53,447,317 (GRCm38) |
critical splice donor site |
probably null |
|
R4781:Dnah7a
|
UTSW |
1 |
53,425,208 (GRCm38) |
missense |
probably benign |
0.28 |
R4854:Dnah7a
|
UTSW |
1 |
53,706,729 (GRCm38) |
utr 5 prime |
probably benign |
|
R4932:Dnah7a
|
UTSW |
1 |
53,503,578 (GRCm38) |
missense |
possibly damaging |
0.90 |
R4976:Dnah7a
|
UTSW |
1 |
53,698,692 (GRCm38) |
missense |
probably benign |
|
R5000:Dnah7a
|
UTSW |
1 |
53,567,042 (GRCm38) |
missense |
probably damaging |
1.00 |
R5023:Dnah7a
|
UTSW |
1 |
53,647,248 (GRCm38) |
nonsense |
probably null |
|
R5026:Dnah7a
|
UTSW |
1 |
53,662,498 (GRCm38) |
missense |
probably damaging |
0.99 |
R5050:Dnah7a
|
UTSW |
1 |
53,497,096 (GRCm38) |
missense |
probably benign |
0.01 |
R5119:Dnah7a
|
UTSW |
1 |
53,698,692 (GRCm38) |
missense |
probably benign |
|
R5151:Dnah7a
|
UTSW |
1 |
53,620,770 (GRCm38) |
missense |
probably benign |
0.00 |
R5155:Dnah7a
|
UTSW |
1 |
53,643,495 (GRCm38) |
missense |
probably benign |
0.01 |
R5180:Dnah7a
|
UTSW |
1 |
53,423,287 (GRCm38) |
missense |
probably damaging |
0.97 |
R5228:Dnah7a
|
UTSW |
1 |
53,437,609 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5237:Dnah7a
|
UTSW |
1 |
53,447,531 (GRCm38) |
splice site |
probably null |
|
R5267:Dnah7a
|
UTSW |
1 |
53,479,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R5334:Dnah7a
|
UTSW |
1 |
53,503,646 (GRCm38) |
missense |
probably benign |
0.00 |
R5358:Dnah7a
|
UTSW |
1 |
53,547,172 (GRCm38) |
missense |
probably damaging |
1.00 |
R5401:Dnah7a
|
UTSW |
1 |
53,631,653 (GRCm38) |
missense |
probably benign |
0.01 |
R5412:Dnah7a
|
UTSW |
1 |
53,635,344 (GRCm38) |
missense |
probably benign |
|
R5496:Dnah7a
|
UTSW |
1 |
53,457,768 (GRCm38) |
missense |
probably benign |
|
R5531:Dnah7a
|
UTSW |
1 |
53,419,748 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5536:Dnah7a
|
UTSW |
1 |
53,425,253 (GRCm38) |
missense |
probably benign |
|
R5543:Dnah7a
|
UTSW |
1 |
53,504,069 (GRCm38) |
missense |
probably damaging |
1.00 |
R5597:Dnah7a
|
UTSW |
1 |
53,534,452 (GRCm38) |
missense |
probably benign |
0.00 |
R5609:Dnah7a
|
UTSW |
1 |
53,582,594 (GRCm38) |
missense |
probably benign |
0.03 |
R5643:Dnah7a
|
UTSW |
1 |
53,405,707 (GRCm38) |
missense |
probably benign |
|
R5644:Dnah7a
|
UTSW |
1 |
53,540,979 (GRCm38) |
missense |
probably benign |
0.33 |
R5689:Dnah7a
|
UTSW |
1 |
53,405,698 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5715:Dnah7a
|
UTSW |
1 |
53,413,778 (GRCm38) |
missense |
probably damaging |
1.00 |
R5780:Dnah7a
|
UTSW |
1 |
53,483,319 (GRCm38) |
missense |
probably benign |
0.03 |
R5893:Dnah7a
|
UTSW |
1 |
53,457,785 (GRCm38) |
missense |
possibly damaging |
0.66 |
R5946:Dnah7a
|
UTSW |
1 |
53,559,308 (GRCm38) |
missense |
probably damaging |
1.00 |
R5995:Dnah7a
|
UTSW |
1 |
53,620,670 (GRCm38) |
missense |
probably benign |
0.00 |
R6102:Dnah7a
|
UTSW |
1 |
53,559,140 (GRCm38) |
missense |
probably benign |
0.00 |
R6108:Dnah7a
|
UTSW |
1 |
53,456,845 (GRCm38) |
missense |
probably damaging |
1.00 |
R6133:Dnah7a
|
UTSW |
1 |
53,419,655 (GRCm38) |
missense |
probably benign |
0.05 |
R6168:Dnah7a
|
UTSW |
1 |
53,411,568 (GRCm38) |
missense |
probably damaging |
1.00 |
R6175:Dnah7a
|
UTSW |
1 |
53,433,022 (GRCm38) |
missense |
probably damaging |
1.00 |
R6211:Dnah7a
|
UTSW |
1 |
53,419,636 (GRCm38) |
missense |
probably damaging |
0.99 |
R6282:Dnah7a
|
UTSW |
1 |
53,503,601 (GRCm38) |
missense |
probably damaging |
1.00 |
R6329:Dnah7a
|
UTSW |
1 |
53,541,114 (GRCm38) |
missense |
probably damaging |
1.00 |
R6344:Dnah7a
|
UTSW |
1 |
53,397,190 (GRCm38) |
missense |
probably benign |
0.02 |
R6530:Dnah7a
|
UTSW |
1 |
53,503,697 (GRCm38) |
missense |
probably benign |
0.04 |
R6574:Dnah7a
|
UTSW |
1 |
53,456,534 (GRCm38) |
critical splice donor site |
probably null |
|
R6608:Dnah7a
|
UTSW |
1 |
53,525,118 (GRCm38) |
missense |
probably benign |
|
R6625:Dnah7a
|
UTSW |
1 |
53,565,757 (GRCm38) |
missense |
probably benign |
0.05 |
R6661:Dnah7a
|
UTSW |
1 |
53,623,450 (GRCm38) |
missense |
probably benign |
0.00 |
R6681:Dnah7a
|
UTSW |
1 |
53,521,226 (GRCm38) |
critical splice acceptor site |
probably null |
|
R6747:Dnah7a
|
UTSW |
1 |
53,636,062 (GRCm38) |
missense |
probably benign |
0.01 |
R6774:Dnah7a
|
UTSW |
1 |
53,698,651 (GRCm38) |
missense |
probably benign |
|
R6823:Dnah7a
|
UTSW |
1 |
53,456,704 (GRCm38) |
missense |
probably benign |
|
R6900:Dnah7a
|
UTSW |
1 |
53,662,351 (GRCm38) |
missense |
probably damaging |
0.97 |
R6940:Dnah7a
|
UTSW |
1 |
53,631,677 (GRCm38) |
missense |
probably benign |
0.09 |
R6956:Dnah7a
|
UTSW |
1 |
53,577,287 (GRCm38) |
missense |
probably benign |
0.02 |
R6978:Dnah7a
|
UTSW |
1 |
53,662,367 (GRCm38) |
missense |
probably null |
|
R6988:Dnah7a
|
UTSW |
1 |
53,582,625 (GRCm38) |
missense |
possibly damaging |
0.62 |
R7026:Dnah7a
|
UTSW |
1 |
53,504,289 (GRCm38) |
missense |
probably benign |
|
R7027:Dnah7a
|
UTSW |
1 |
53,631,506 (GRCm38) |
missense |
probably benign |
0.01 |
R7033:Dnah7a
|
UTSW |
1 |
53,479,661 (GRCm38) |
missense |
probably damaging |
1.00 |
R7072:Dnah7a
|
UTSW |
1 |
53,419,753 (GRCm38) |
missense |
probably benign |
0.00 |
R7096:Dnah7a
|
UTSW |
1 |
53,483,440 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7142:Dnah7a
|
UTSW |
1 |
53,413,768 (GRCm38) |
nonsense |
probably null |
|
R7144:Dnah7a
|
UTSW |
1 |
53,698,708 (GRCm38) |
splice site |
probably null |
|
R7167:Dnah7a
|
UTSW |
1 |
53,503,776 (GRCm38) |
missense |
probably benign |
0.00 |
R7182:Dnah7a
|
UTSW |
1 |
53,620,461 (GRCm38) |
splice site |
probably null |
|
R7196:Dnah7a
|
UTSW |
1 |
53,684,841 (GRCm38) |
missense |
probably benign |
0.00 |
R7206:Dnah7a
|
UTSW |
1 |
53,698,633 (GRCm38) |
nonsense |
probably null |
|
R7215:Dnah7a
|
UTSW |
1 |
53,618,350 (GRCm38) |
missense |
probably damaging |
0.99 |
R7224:Dnah7a
|
UTSW |
1 |
53,397,261 (GRCm38) |
missense |
probably benign |
0.00 |
R7264:Dnah7a
|
UTSW |
1 |
53,518,814 (GRCm38) |
missense |
probably benign |
|
R7282:Dnah7a
|
UTSW |
1 |
53,684,900 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7365:Dnah7a
|
UTSW |
1 |
53,497,138 (GRCm38) |
missense |
probably benign |
|
R7392:Dnah7a
|
UTSW |
1 |
53,501,661 (GRCm38) |
missense |
probably benign |
0.00 |
R7454:Dnah7a
|
UTSW |
1 |
53,518,764 (GRCm38) |
missense |
probably benign |
|
R7471:Dnah7a
|
UTSW |
1 |
53,419,699 (GRCm38) |
missense |
probably damaging |
1.00 |
R7547:Dnah7a
|
UTSW |
1 |
53,663,837 (GRCm38) |
missense |
probably benign |
0.00 |
R7554:Dnah7a
|
UTSW |
1 |
53,528,698 (GRCm38) |
missense |
possibly damaging |
0.87 |
R7655:Dnah7a
|
UTSW |
1 |
53,496,005 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7656:Dnah7a
|
UTSW |
1 |
53,496,005 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7666:Dnah7a
|
UTSW |
1 |
53,547,297 (GRCm38) |
missense |
probably benign |
0.00 |
R7721:Dnah7a
|
UTSW |
1 |
53,631,683 (GRCm38) |
missense |
probably benign |
|
R7813:Dnah7a
|
UTSW |
1 |
53,618,086 (GRCm38) |
missense |
probably benign |
|
R7839:Dnah7a
|
UTSW |
1 |
53,567,175 (GRCm38) |
missense |
probably benign |
0.08 |
R7959:Dnah7a
|
UTSW |
1 |
53,643,462 (GRCm38) |
missense |
probably benign |
0.00 |
R7984:Dnah7a
|
UTSW |
1 |
53,504,218 (GRCm38) |
missense |
probably benign |
0.01 |
R7985:Dnah7a
|
UTSW |
1 |
53,518,727 (GRCm38) |
missense |
probably damaging |
1.00 |
R8116:Dnah7a
|
UTSW |
1 |
53,503,890 (GRCm38) |
missense |
probably benign |
|
R8140:Dnah7a
|
UTSW |
1 |
53,501,589 (GRCm38) |
missense |
probably benign |
0.02 |
R8184:Dnah7a
|
UTSW |
1 |
53,627,035 (GRCm38) |
missense |
probably benign |
0.03 |
R8339:Dnah7a
|
UTSW |
1 |
53,685,019 (GRCm38) |
missense |
probably benign |
|
R8352:Dnah7a
|
UTSW |
1 |
53,427,827 (GRCm38) |
missense |
probably null |
0.01 |
R8423:Dnah7a
|
UTSW |
1 |
53,472,904 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8428:Dnah7a
|
UTSW |
1 |
53,472,953 (GRCm38) |
missense |
probably damaging |
0.98 |
R8432:Dnah7a
|
UTSW |
1 |
53,618,036 (GRCm38) |
missense |
possibly damaging |
0.46 |
R8452:Dnah7a
|
UTSW |
1 |
53,427,827 (GRCm38) |
missense |
probably null |
0.01 |
R8458:Dnah7a
|
UTSW |
1 |
53,617,983 (GRCm38) |
missense |
probably benign |
0.01 |
R8493:Dnah7a
|
UTSW |
1 |
53,472,908 (GRCm38) |
missense |
probably damaging |
1.00 |
R8498:Dnah7a
|
UTSW |
1 |
53,617,980 (GRCm38) |
missense |
probably benign |
0.01 |
R8502:Dnah7a
|
UTSW |
1 |
53,640,361 (GRCm38) |
missense |
probably benign |
0.39 |
R8692:Dnah7a
|
UTSW |
1 |
53,433,016 (GRCm38) |
missense |
probably benign |
0.00 |
R8700:Dnah7a
|
UTSW |
1 |
53,495,929 (GRCm38) |
missense |
possibly damaging |
0.62 |
R8709:Dnah7a
|
UTSW |
1 |
53,635,317 (GRCm38) |
missense |
probably benign |
|
R8856:Dnah7a
|
UTSW |
1 |
53,423,263 (GRCm38) |
missense |
probably damaging |
1.00 |
R8875:Dnah7a
|
UTSW |
1 |
53,643,523 (GRCm38) |
missense |
probably benign |
0.10 |
R8967:Dnah7a
|
UTSW |
1 |
53,643,435 (GRCm38) |
splice site |
probably benign |
|
R8982:Dnah7a
|
UTSW |
1 |
53,531,142 (GRCm38) |
missense |
probably benign |
|
R8984:Dnah7a
|
UTSW |
1 |
53,635,277 (GRCm38) |
nonsense |
probably null |
|
R8993:Dnah7a
|
UTSW |
1 |
53,504,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R9008:Dnah7a
|
UTSW |
1 |
53,662,342 (GRCm38) |
missense |
possibly damaging |
0.81 |
R9022:Dnah7a
|
UTSW |
1 |
53,472,957 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9028:Dnah7a
|
UTSW |
1 |
53,521,138 (GRCm38) |
missense |
probably benign |
0.00 |
R9077:Dnah7a
|
UTSW |
1 |
53,702,059 (GRCm38) |
missense |
unknown |
|
R9167:Dnah7a
|
UTSW |
1 |
53,618,211 (GRCm38) |
missense |
probably benign |
0.00 |
R9206:Dnah7a
|
UTSW |
1 |
53,501,598 (GRCm38) |
missense |
probably benign |
0.11 |
R9226:Dnah7a
|
UTSW |
1 |
53,521,167 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9251:Dnah7a
|
UTSW |
1 |
53,582,512 (GRCm38) |
missense |
probably damaging |
1.00 |
R9265:Dnah7a
|
UTSW |
1 |
53,635,346 (GRCm38) |
missense |
probably benign |
|
R9350:Dnah7a
|
UTSW |
1 |
53,397,148 (GRCm38) |
missense |
probably benign |
0.19 |
R9369:Dnah7a
|
UTSW |
1 |
53,525,063 (GRCm38) |
missense |
possibly damaging |
0.72 |
R9369:Dnah7a
|
UTSW |
1 |
53,504,262 (GRCm38) |
missense |
probably benign |
|
R9372:Dnah7a
|
UTSW |
1 |
53,504,315 (GRCm38) |
missense |
probably benign |
|
R9376:Dnah7a
|
UTSW |
1 |
53,528,899 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9378:Dnah7a
|
UTSW |
1 |
53,582,617 (GRCm38) |
missense |
probably benign |
0.32 |
R9401:Dnah7a
|
UTSW |
1 |
53,528,867 (GRCm38) |
missense |
probably benign |
0.01 |
R9431:Dnah7a
|
UTSW |
1 |
53,411,653 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9529:Dnah7a
|
UTSW |
1 |
53,522,336 (GRCm38) |
missense |
probably damaging |
1.00 |
R9701:Dnah7a
|
UTSW |
1 |
53,522,229 (GRCm38) |
missense |
probably benign |
0.03 |
R9712:Dnah7a
|
UTSW |
1 |
53,559,140 (GRCm38) |
missense |
probably benign |
0.00 |
R9799:Dnah7a
|
UTSW |
1 |
53,518,809 (GRCm38) |
missense |
probably benign |
0.00 |
R9802:Dnah7a
|
UTSW |
1 |
53,522,229 (GRCm38) |
missense |
probably benign |
0.03 |
X0027:Dnah7a
|
UTSW |
1 |
53,472,930 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Dnah7a
|
UTSW |
1 |
53,468,643 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,483,463 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,419,699 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Dnah7a
|
UTSW |
1 |
53,559,102 (GRCm38) |
missense |
probably benign |
0.21 |
Z1177:Dnah7a
|
UTSW |
1 |
53,411,656 (GRCm38) |
missense |
probably benign |
0.08 |
Z1177:Dnah7a
|
UTSW |
1 |
53,643,457 (GRCm38) |
missense |
possibly damaging |
0.92 |
|