Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
G |
3: 124,200,163 (GRCm39) |
L476F |
probably damaging |
Het |
4930432E11Rik |
A |
T |
7: 29,278,591 (GRCm39) |
|
noncoding transcript |
Het |
A930011G23Rik |
A |
T |
5: 99,370,897 (GRCm39) |
|
probably benign |
Het |
Abcd3 |
A |
G |
3: 121,575,612 (GRCm39) |
Y217H |
probably damaging |
Het |
Abraxas1 |
A |
T |
5: 100,965,822 (GRCm39) |
|
probably benign |
Het |
Acsbg1 |
T |
C |
9: 54,523,346 (GRCm39) |
Y427C |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adam10 |
T |
A |
9: 70,683,651 (GRCm39) |
|
probably benign |
Het |
Adam24 |
G |
A |
8: 41,134,004 (GRCm39) |
V491I |
possibly damaging |
Het |
Adamts2 |
T |
G |
11: 50,647,524 (GRCm39) |
V299G |
probably damaging |
Het |
Adh7 |
A |
G |
3: 137,929,752 (GRCm39) |
T143A |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,581,419 (GRCm39) |
S81P |
probably benign |
Het |
Arhgap20 |
C |
A |
9: 51,761,215 (GRCm39) |
T986K |
probably benign |
Het |
Atp13a5 |
A |
T |
16: 29,133,478 (GRCm39) |
I391N |
possibly damaging |
Het |
Atp6v0a1 |
C |
A |
11: 100,917,511 (GRCm39) |
A143E |
probably benign |
Het |
Calcrl |
A |
G |
2: 84,181,629 (GRCm39) |
I173T |
probably damaging |
Het |
Casz1 |
A |
G |
4: 149,017,394 (GRCm39) |
T228A |
probably benign |
Het |
Cckar |
A |
G |
5: 53,857,321 (GRCm39) |
I292T |
probably damaging |
Het |
Ccn5 |
G |
A |
2: 163,670,906 (GRCm39) |
V138M |
probably damaging |
Het |
Cfhr2 |
T |
A |
1: 139,786,383 (GRCm39) |
|
probably null |
Het |
Chkb |
T |
C |
15: 89,313,260 (GRCm39) |
I109V |
possibly damaging |
Het |
Clec2i |
T |
C |
6: 128,865,069 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
A |
6: 123,000,934 (GRCm39) |
W216R |
probably damaging |
Het |
Cntnap1 |
A |
C |
11: 101,077,337 (GRCm39) |
I1000L |
probably damaging |
Het |
Cp |
C |
A |
3: 20,011,549 (GRCm39) |
D34E |
possibly damaging |
Het |
Cse1l |
T |
C |
2: 166,782,044 (GRCm39) |
|
probably null |
Het |
Dennd3 |
T |
C |
15: 73,394,357 (GRCm39) |
|
probably null |
Het |
Eaf2 |
A |
G |
16: 36,630,832 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
A |
11: 104,611,765 (GRCm39) |
S536T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,421,136 (GRCm39) |
T405A |
possibly damaging |
Het |
Fam117a |
G |
A |
11: 95,269,779 (GRCm39) |
V348M |
probably damaging |
Het |
Fh1 |
T |
C |
1: 175,428,990 (GRCm39) |
*167W |
probably null |
Het |
Fmo9 |
T |
A |
1: 166,490,868 (GRCm39) |
I486F |
probably benign |
Het |
Gabbr1 |
T |
A |
17: 37,365,771 (GRCm39) |
I150N |
probably damaging |
Het |
Gfpt1 |
T |
C |
6: 87,054,179 (GRCm39) |
V478A |
possibly damaging |
Het |
Gm2663 |
A |
T |
6: 40,974,894 (GRCm39) |
V59E |
probably damaging |
Het |
Gm4868 |
T |
A |
5: 125,925,176 (GRCm39) |
|
noncoding transcript |
Het |
Heatr4 |
T |
A |
12: 84,026,934 (GRCm39) |
T108S |
probably benign |
Het |
Hells |
G |
T |
19: 38,935,286 (GRCm39) |
A319S |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,876,780 (GRCm39) |
V1238A |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,880,252 (GRCm39) |
Q488L |
possibly damaging |
Het |
Hkdc1 |
A |
G |
10: 62,227,162 (GRCm39) |
F765S |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,245,820 (GRCm39) |
W938R |
probably damaging |
Het |
Itpr2 |
G |
A |
6: 146,060,399 (GRCm39) |
R2473* |
probably null |
Het |
Kctd1 |
C |
T |
18: 15,194,839 (GRCm39) |
V595I |
probably benign |
Het |
Krt7 |
A |
G |
15: 101,321,290 (GRCm39) |
Y369C |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,689,364 (GRCm39) |
T323A |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,801,122 (GRCm39) |
L58P |
unknown |
Het |
Liph |
C |
A |
16: 21,786,800 (GRCm39) |
R272L |
probably benign |
Het |
Lrrc9 |
A |
T |
12: 72,502,772 (GRCm39) |
K248* |
probably null |
Het |
Mei4 |
T |
A |
9: 81,809,195 (GRCm39) |
S93T |
probably damaging |
Het |
Mgll |
T |
A |
6: 88,790,930 (GRCm39) |
Y183* |
probably null |
Het |
Myo5b |
A |
G |
18: 74,875,218 (GRCm39) |
M1541V |
probably benign |
Het |
Napg |
A |
G |
18: 63,115,762 (GRCm39) |
E66G |
probably benign |
Het |
Npr3 |
T |
C |
15: 11,851,572 (GRCm39) |
D406G |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,136,224 (GRCm39) |
T355A |
possibly damaging |
Het |
Or13j1 |
G |
A |
4: 43,706,041 (GRCm39) |
H176Y |
probably damaging |
Het |
Or4a71 |
A |
T |
2: 89,357,989 (GRCm39) |
I255K |
probably benign |
Het |
Or51m1 |
G |
T |
7: 103,578,668 (GRCm39) |
V213L |
probably benign |
Het |
Or51v8 |
A |
G |
7: 103,319,845 (GRCm39) |
I131T |
probably benign |
Het |
Or52z13 |
A |
T |
7: 103,247,107 (GRCm39) |
I195F |
probably damaging |
Het |
Or5b107 |
T |
C |
19: 13,142,404 (GRCm39) |
Y9H |
probably benign |
Het |
Or8d1 |
A |
G |
9: 38,766,846 (GRCm39) |
M163V |
possibly damaging |
Het |
Orai2 |
T |
C |
5: 136,179,793 (GRCm39) |
E80G |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,582,535 (GRCm39) |
V547E |
probably damaging |
Het |
Pcdhb15 |
T |
C |
18: 37,609,084 (GRCm39) |
I772T |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,244,630 (GRCm39) |
Q1150R |
probably damaging |
Het |
Pdcd6 |
A |
G |
13: 74,453,700 (GRCm39) |
I146T |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,621,988 (GRCm39) |
D664V |
probably damaging |
Het |
Pik3ap1 |
A |
T |
19: 41,320,673 (GRCm39) |
V182E |
probably damaging |
Het |
Pip4k2a |
A |
G |
2: 18,852,433 (GRCm39) |
V283A |
probably benign |
Het |
Pkdrej |
A |
G |
15: 85,705,372 (GRCm39) |
V188A |
possibly damaging |
Het |
Pnpla6 |
T |
C |
8: 3,591,404 (GRCm39) |
W1151R |
probably damaging |
Het |
Ppp1r14c |
A |
G |
10: 3,316,890 (GRCm39) |
Y75C |
probably damaging |
Het |
Prl2b1 |
C |
T |
13: 27,567,452 (GRCm39) |
D224N |
probably benign |
Het |
Ptgis |
A |
G |
2: 167,056,778 (GRCm39) |
S270P |
probably benign |
Het |
Rgs11 |
C |
A |
17: 26,429,640 (GRCm39) |
A446D |
probably damaging |
Het |
Rims2 |
A |
G |
15: 39,545,098 (GRCm39) |
T1531A |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,526,580 (GRCm39) |
|
probably benign |
Het |
Scarb2 |
C |
G |
5: 92,596,416 (GRCm39) |
M409I |
probably benign |
Het |
Scube3 |
C |
T |
17: 28,387,353 (GRCm39) |
|
probably benign |
Het |
Slc44a4 |
T |
C |
17: 35,140,901 (GRCm39) |
I180T |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,781,803 (GRCm39) |
M344T |
probably damaging |
Het |
Smc3 |
A |
T |
19: 53,627,800 (GRCm39) |
T860S |
probably benign |
Het |
Snrpa |
A |
G |
7: 26,891,174 (GRCm39) |
I99T |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,163,481 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,902,778 (GRCm39) |
|
probably null |
Het |
Suds3 |
T |
C |
5: 117,243,309 (GRCm39) |
K143R |
probably benign |
Het |
Supt20 |
A |
T |
3: 54,622,164 (GRCm39) |
M424L |
probably benign |
Het |
Tgtp2 |
T |
C |
11: 48,949,751 (GRCm39) |
M274V |
probably benign |
Het |
Tmem158 |
T |
A |
9: 123,088,974 (GRCm39) |
M213L |
probably benign |
Het |
Tnks |
C |
A |
8: 35,324,672 (GRCm39) |
R639L |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt10c |
A |
C |
16: 55,854,938 (GRCm39) |
N232K |
possibly damaging |
Het |
Trpm6 |
C |
T |
19: 18,833,581 (GRCm39) |
R1587W |
probably damaging |
Het |
Trrap |
G |
A |
5: 144,765,400 (GRCm39) |
V2539I |
probably benign |
Het |
Tsg101 |
A |
G |
7: 46,556,835 (GRCm39) |
S115P |
probably benign |
Het |
Ttll13 |
G |
T |
7: 79,910,256 (GRCm39) |
V800L |
probably benign |
Het |
Vmn1r57 |
A |
G |
7: 5,223,576 (GRCm39) |
T34A |
possibly damaging |
Het |
Vmn2r118 |
T |
A |
17: 55,918,530 (GRCm39) |
T121S |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,035,772 (GRCm39) |
I238M |
possibly damaging |
Het |
Zfp81 |
T |
A |
17: 33,554,080 (GRCm39) |
T245S |
probably benign |
Het |
Zfyve26 |
G |
T |
12: 79,325,237 (GRCm39) |
P824Q |
probably damaging |
Het |
|
Other mutations in Dnah7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Dnah7a
|
APN |
1 |
53,458,843 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00510:Dnah7a
|
APN |
1 |
53,540,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00545:Dnah7a
|
APN |
1 |
53,496,905 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01320:Dnah7a
|
APN |
1 |
53,473,205 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01322:Dnah7a
|
APN |
1 |
53,473,205 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01357:Dnah7a
|
APN |
1 |
53,701,540 (GRCm39) |
missense |
probably benign |
|
IGL01417:Dnah7a
|
APN |
1 |
53,623,759 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01508:Dnah7a
|
APN |
1 |
53,666,231 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01511:Dnah7a
|
APN |
1 |
53,458,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01545:Dnah7a
|
APN |
1 |
53,557,941 (GRCm39) |
missense |
probably benign |
|
IGL01575:Dnah7a
|
APN |
1 |
53,466,979 (GRCm39) |
splice site |
probably benign |
|
IGL01667:Dnah7a
|
APN |
1 |
53,586,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01712:Dnah7a
|
APN |
1 |
53,462,429 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01824:Dnah7a
|
APN |
1 |
53,543,429 (GRCm39) |
missense |
probably benign |
|
IGL01829:Dnah7a
|
APN |
1 |
53,657,227 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01861:Dnah7a
|
APN |
1 |
53,623,608 (GRCm39) |
splice site |
probably benign |
|
IGL01861:Dnah7a
|
APN |
1 |
53,679,508 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01984:Dnah7a
|
APN |
1 |
53,741,174 (GRCm39) |
splice site |
probably null |
|
IGL02056:Dnah7a
|
APN |
1 |
53,543,501 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02069:Dnah7a
|
APN |
1 |
53,601,053 (GRCm39) |
splice site |
probably benign |
|
IGL02072:Dnah7a
|
APN |
1 |
53,644,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Dnah7a
|
APN |
1 |
53,450,739 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02120:Dnah7a
|
APN |
1 |
53,534,876 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02128:Dnah7a
|
APN |
1 |
53,476,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Dnah7a
|
APN |
1 |
53,662,632 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02151:Dnah7a
|
APN |
1 |
53,512,023 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02156:Dnah7a
|
APN |
1 |
53,458,882 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02270:Dnah7a
|
APN |
1 |
53,512,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02282:Dnah7a
|
APN |
1 |
53,682,669 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02328:Dnah7a
|
APN |
1 |
53,564,096 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02370:Dnah7a
|
APN |
1 |
53,674,556 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02420:Dnah7a
|
APN |
1 |
53,725,702 (GRCm39) |
missense |
probably benign |
|
IGL02458:Dnah7a
|
APN |
1 |
53,657,487 (GRCm39) |
nonsense |
probably null |
|
IGL02489:Dnah7a
|
APN |
1 |
53,686,481 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02554:Dnah7a
|
APN |
1 |
53,657,205 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02578:Dnah7a
|
APN |
1 |
53,472,074 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02646:Dnah7a
|
APN |
1 |
53,564,194 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02675:Dnah7a
|
APN |
1 |
53,543,183 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02688:Dnah7a
|
APN |
1 |
53,483,631 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02858:Dnah7a
|
APN |
1 |
53,512,118 (GRCm39) |
splice site |
probably benign |
|
IGL02874:Dnah7a
|
APN |
1 |
53,644,973 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02887:Dnah7a
|
APN |
1 |
53,561,519 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02894:Dnah7a
|
APN |
1 |
53,616,487 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02926:Dnah7a
|
APN |
1 |
53,535,109 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03113:Dnah7a
|
APN |
1 |
53,472,163 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03156:Dnah7a
|
APN |
1 |
53,644,983 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03195:Dnah7a
|
APN |
1 |
53,458,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Dnah7a
|
APN |
1 |
53,725,773 (GRCm39) |
splice site |
probably benign |
|
IGL03214:Dnah7a
|
APN |
1 |
53,561,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03242:Dnah7a
|
APN |
1 |
53,659,882 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03251:Dnah7a
|
APN |
1 |
53,686,433 (GRCm39) |
missense |
probably benign |
|
IGL03265:Dnah7a
|
APN |
1 |
53,568,007 (GRCm39) |
missense |
probably benign |
|
IGL03277:Dnah7a
|
APN |
1 |
53,669,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03278:Dnah7a
|
APN |
1 |
53,536,124 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03356:Dnah7a
|
APN |
1 |
53,543,093 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4378001:Dnah7a
|
UTSW |
1 |
53,570,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Dnah7a
|
UTSW |
1 |
53,496,033 (GRCm39) |
splice site |
probably null |
|
R0051:Dnah7a
|
UTSW |
1 |
53,560,245 (GRCm39) |
splice site |
probably benign |
|
R0082:Dnah7a
|
UTSW |
1 |
53,557,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Dnah7a
|
UTSW |
1 |
53,507,843 (GRCm39) |
missense |
probably benign |
0.03 |
R0122:Dnah7a
|
UTSW |
1 |
53,436,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Dnah7a
|
UTSW |
1 |
53,540,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0278:Dnah7a
|
UTSW |
1 |
53,543,305 (GRCm39) |
missense |
probably benign |
0.00 |
R0309:Dnah7a
|
UTSW |
1 |
53,444,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R0334:Dnah7a
|
UTSW |
1 |
53,472,213 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0392:Dnah7a
|
UTSW |
1 |
53,543,357 (GRCm39) |
missense |
probably damaging |
0.97 |
R0452:Dnah7a
|
UTSW |
1 |
53,644,978 (GRCm39) |
missense |
probably benign |
0.00 |
R0511:Dnah7a
|
UTSW |
1 |
53,536,285 (GRCm39) |
missense |
probably benign |
|
R0576:Dnah7a
|
UTSW |
1 |
53,675,246 (GRCm39) |
missense |
probably benign |
0.12 |
R0592:Dnah7a
|
UTSW |
1 |
53,495,771 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0628:Dnah7a
|
UTSW |
1 |
53,536,264 (GRCm39) |
missense |
probably benign |
0.18 |
R0689:Dnah7a
|
UTSW |
1 |
53,659,840 (GRCm39) |
nonsense |
probably null |
|
R0735:Dnah7a
|
UTSW |
1 |
53,583,670 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0800:Dnah7a
|
UTSW |
1 |
53,604,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Dnah7a
|
UTSW |
1 |
53,543,238 (GRCm39) |
missense |
probably benign |
0.07 |
R0842:Dnah7a
|
UTSW |
1 |
53,540,833 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0879:Dnah7a
|
UTSW |
1 |
53,467,019 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1331:Dnah7a
|
UTSW |
1 |
53,507,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R1418:Dnah7a
|
UTSW |
1 |
53,686,395 (GRCm39) |
splice site |
probably benign |
|
R1421:Dnah7a
|
UTSW |
1 |
53,580,032 (GRCm39) |
splice site |
probably benign |
|
R1445:Dnah7a
|
UTSW |
1 |
53,567,956 (GRCm39) |
missense |
probably benign |
0.02 |
R1473:Dnah7a
|
UTSW |
1 |
53,535,173 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Dnah7a
|
UTSW |
1 |
53,535,148 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1742:Dnah7a
|
UTSW |
1 |
53,495,843 (GRCm39) |
missense |
probably benign |
0.39 |
R1754:Dnah7a
|
UTSW |
1 |
53,601,059 (GRCm39) |
critical splice donor site |
probably null |
|
R1754:Dnah7a
|
UTSW |
1 |
53,543,344 (GRCm39) |
missense |
probably benign |
0.18 |
R1773:Dnah7a
|
UTSW |
1 |
53,472,046 (GRCm39) |
splice site |
probably null |
|
R1816:Dnah7a
|
UTSW |
1 |
53,670,901 (GRCm39) |
splice site |
probably benign |
|
R1817:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1818:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1819:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1873:Dnah7a
|
UTSW |
1 |
53,495,691 (GRCm39) |
splice site |
probably benign |
|
R1875:Dnah7a
|
UTSW |
1 |
53,495,691 (GRCm39) |
splice site |
probably benign |
|
R1884:Dnah7a
|
UTSW |
1 |
53,580,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R1902:Dnah7a
|
UTSW |
1 |
53,574,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Dnah7a
|
UTSW |
1 |
53,574,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Dnah7a
|
UTSW |
1 |
53,670,721 (GRCm39) |
missense |
probably benign |
|
R1959:Dnah7a
|
UTSW |
1 |
53,724,142 (GRCm39) |
missense |
probably benign |
0.00 |
R1960:Dnah7a
|
UTSW |
1 |
53,724,142 (GRCm39) |
missense |
probably benign |
0.00 |
R1985:Dnah7a
|
UTSW |
1 |
53,543,093 (GRCm39) |
missense |
probably benign |
0.01 |
R1992:Dnah7a
|
UTSW |
1 |
53,621,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2037:Dnah7a
|
UTSW |
1 |
53,621,741 (GRCm39) |
missense |
probably benign |
0.00 |
R2074:Dnah7a
|
UTSW |
1 |
53,496,855 (GRCm39) |
missense |
probably benign |
0.45 |
R2076:Dnah7a
|
UTSW |
1 |
53,542,968 (GRCm39) |
missense |
probably benign |
0.01 |
R2124:Dnah7a
|
UTSW |
1 |
53,536,101 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2191:Dnah7a
|
UTSW |
1 |
53,645,034 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2211:Dnah7a
|
UTSW |
1 |
53,518,932 (GRCm39) |
missense |
probably benign |
0.21 |
R2220:Dnah7a
|
UTSW |
1 |
53,560,333 (GRCm39) |
missense |
probably benign |
|
R2355:Dnah7a
|
UTSW |
1 |
53,621,661 (GRCm39) |
missense |
probably benign |
0.00 |
R2495:Dnah7a
|
UTSW |
1 |
53,645,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R2901:Dnah7a
|
UTSW |
1 |
53,467,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R2911:Dnah7a
|
UTSW |
1 |
53,466,983 (GRCm39) |
critical splice donor site |
probably null |
|
R2993:Dnah7a
|
UTSW |
1 |
53,542,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Dnah7a
|
UTSW |
1 |
53,657,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Dnah7a
|
UTSW |
1 |
53,483,675 (GRCm39) |
missense |
probably benign |
|
R3723:Dnah7a
|
UTSW |
1 |
53,486,505 (GRCm39) |
missense |
probably benign |
0.04 |
R3847:Dnah7a
|
UTSW |
1 |
53,540,815 (GRCm39) |
missense |
probably benign |
0.01 |
R4002:Dnah7a
|
UTSW |
1 |
53,670,840 (GRCm39) |
missense |
probably benign |
|
R4009:Dnah7a
|
UTSW |
1 |
53,564,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Dnah7a
|
UTSW |
1 |
53,464,376 (GRCm39) |
missense |
probably benign |
|
R4193:Dnah7a
|
UTSW |
1 |
53,486,493 (GRCm39) |
missense |
probably benign |
0.00 |
R4236:Dnah7a
|
UTSW |
1 |
53,486,524 (GRCm39) |
missense |
probably benign |
0.00 |
R4399:Dnah7a
|
UTSW |
1 |
53,557,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Dnah7a
|
UTSW |
1 |
53,483,685 (GRCm39) |
missense |
probably benign |
0.01 |
R4494:Dnah7a
|
UTSW |
1 |
53,488,197 (GRCm39) |
missense |
probably benign |
0.01 |
R4569:Dnah7a
|
UTSW |
1 |
53,450,818 (GRCm39) |
missense |
probably benign |
0.01 |
R4609:Dnah7a
|
UTSW |
1 |
53,495,816 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4632:Dnah7a
|
UTSW |
1 |
53,467,110 (GRCm39) |
missense |
probably damaging |
0.97 |
R4703:Dnah7a
|
UTSW |
1 |
53,486,476 (GRCm39) |
critical splice donor site |
probably null |
|
R4781:Dnah7a
|
UTSW |
1 |
53,464,367 (GRCm39) |
missense |
probably benign |
0.28 |
R4854:Dnah7a
|
UTSW |
1 |
53,745,888 (GRCm39) |
utr 5 prime |
probably benign |
|
R4932:Dnah7a
|
UTSW |
1 |
53,542,737 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4976:Dnah7a
|
UTSW |
1 |
53,737,851 (GRCm39) |
missense |
probably benign |
|
R5000:Dnah7a
|
UTSW |
1 |
53,606,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Dnah7a
|
UTSW |
1 |
53,686,407 (GRCm39) |
nonsense |
probably null |
|
R5026:Dnah7a
|
UTSW |
1 |
53,701,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R5050:Dnah7a
|
UTSW |
1 |
53,536,255 (GRCm39) |
missense |
probably benign |
0.01 |
R5119:Dnah7a
|
UTSW |
1 |
53,737,851 (GRCm39) |
missense |
probably benign |
|
R5151:Dnah7a
|
UTSW |
1 |
53,659,929 (GRCm39) |
missense |
probably benign |
0.00 |
R5155:Dnah7a
|
UTSW |
1 |
53,682,654 (GRCm39) |
missense |
probably benign |
0.01 |
R5180:Dnah7a
|
UTSW |
1 |
53,462,446 (GRCm39) |
missense |
probably damaging |
0.97 |
R5228:Dnah7a
|
UTSW |
1 |
53,476,768 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5237:Dnah7a
|
UTSW |
1 |
53,486,690 (GRCm39) |
splice site |
probably null |
|
R5267:Dnah7a
|
UTSW |
1 |
53,518,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Dnah7a
|
UTSW |
1 |
53,542,805 (GRCm39) |
missense |
probably benign |
0.00 |
R5358:Dnah7a
|
UTSW |
1 |
53,586,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Dnah7a
|
UTSW |
1 |
53,670,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5412:Dnah7a
|
UTSW |
1 |
53,674,503 (GRCm39) |
missense |
probably benign |
|
R5496:Dnah7a
|
UTSW |
1 |
53,496,927 (GRCm39) |
missense |
probably benign |
|
R5531:Dnah7a
|
UTSW |
1 |
53,458,907 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5536:Dnah7a
|
UTSW |
1 |
53,464,412 (GRCm39) |
missense |
probably benign |
|
R5543:Dnah7a
|
UTSW |
1 |
53,543,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R5597:Dnah7a
|
UTSW |
1 |
53,573,611 (GRCm39) |
missense |
probably benign |
0.00 |
R5609:Dnah7a
|
UTSW |
1 |
53,621,753 (GRCm39) |
missense |
probably benign |
0.03 |
R5643:Dnah7a
|
UTSW |
1 |
53,444,866 (GRCm39) |
missense |
probably benign |
|
R5644:Dnah7a
|
UTSW |
1 |
53,580,138 (GRCm39) |
missense |
probably benign |
0.33 |
R5689:Dnah7a
|
UTSW |
1 |
53,444,857 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5715:Dnah7a
|
UTSW |
1 |
53,452,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Dnah7a
|
UTSW |
1 |
53,522,478 (GRCm39) |
missense |
probably benign |
0.03 |
R5893:Dnah7a
|
UTSW |
1 |
53,496,944 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5946:Dnah7a
|
UTSW |
1 |
53,598,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Dnah7a
|
UTSW |
1 |
53,659,829 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Dnah7a
|
UTSW |
1 |
53,598,299 (GRCm39) |
missense |
probably benign |
0.00 |
R6108:Dnah7a
|
UTSW |
1 |
53,496,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Dnah7a
|
UTSW |
1 |
53,458,814 (GRCm39) |
missense |
probably benign |
0.05 |
R6168:Dnah7a
|
UTSW |
1 |
53,450,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Dnah7a
|
UTSW |
1 |
53,472,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Dnah7a
|
UTSW |
1 |
53,458,795 (GRCm39) |
missense |
probably damaging |
0.99 |
R6282:Dnah7a
|
UTSW |
1 |
53,542,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Dnah7a
|
UTSW |
1 |
53,580,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6344:Dnah7a
|
UTSW |
1 |
53,436,349 (GRCm39) |
missense |
probably benign |
0.02 |
R6530:Dnah7a
|
UTSW |
1 |
53,542,856 (GRCm39) |
missense |
probably benign |
0.04 |
R6574:Dnah7a
|
UTSW |
1 |
53,495,693 (GRCm39) |
critical splice donor site |
probably null |
|
R6608:Dnah7a
|
UTSW |
1 |
53,564,277 (GRCm39) |
missense |
probably benign |
|
R6625:Dnah7a
|
UTSW |
1 |
53,604,916 (GRCm39) |
missense |
probably benign |
0.05 |
R6661:Dnah7a
|
UTSW |
1 |
53,662,609 (GRCm39) |
missense |
probably benign |
0.00 |
R6681:Dnah7a
|
UTSW |
1 |
53,560,385 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6747:Dnah7a
|
UTSW |
1 |
53,675,221 (GRCm39) |
missense |
probably benign |
0.01 |
R6774:Dnah7a
|
UTSW |
1 |
53,737,810 (GRCm39) |
missense |
probably benign |
|
R6823:Dnah7a
|
UTSW |
1 |
53,495,863 (GRCm39) |
missense |
probably benign |
|
R6900:Dnah7a
|
UTSW |
1 |
53,701,510 (GRCm39) |
missense |
probably damaging |
0.97 |
R6940:Dnah7a
|
UTSW |
1 |
53,670,836 (GRCm39) |
missense |
probably benign |
0.09 |
R6956:Dnah7a
|
UTSW |
1 |
53,616,446 (GRCm39) |
missense |
probably benign |
0.02 |
R6978:Dnah7a
|
UTSW |
1 |
53,701,526 (GRCm39) |
missense |
probably null |
|
R6988:Dnah7a
|
UTSW |
1 |
53,621,784 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7026:Dnah7a
|
UTSW |
1 |
53,543,448 (GRCm39) |
missense |
probably benign |
|
R7027:Dnah7a
|
UTSW |
1 |
53,670,665 (GRCm39) |
missense |
probably benign |
0.01 |
R7033:Dnah7a
|
UTSW |
1 |
53,518,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Dnah7a
|
UTSW |
1 |
53,458,912 (GRCm39) |
missense |
probably benign |
0.00 |
R7096:Dnah7a
|
UTSW |
1 |
53,522,599 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7142:Dnah7a
|
UTSW |
1 |
53,452,927 (GRCm39) |
nonsense |
probably null |
|
R7144:Dnah7a
|
UTSW |
1 |
53,737,867 (GRCm39) |
splice site |
probably null |
|
R7167:Dnah7a
|
UTSW |
1 |
53,542,935 (GRCm39) |
missense |
probably benign |
0.00 |
R7182:Dnah7a
|
UTSW |
1 |
53,659,620 (GRCm39) |
splice site |
probably null |
|
R7196:Dnah7a
|
UTSW |
1 |
53,724,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7206:Dnah7a
|
UTSW |
1 |
53,737,792 (GRCm39) |
nonsense |
probably null |
|
R7215:Dnah7a
|
UTSW |
1 |
53,657,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R7224:Dnah7a
|
UTSW |
1 |
53,436,420 (GRCm39) |
missense |
probably benign |
0.00 |
R7264:Dnah7a
|
UTSW |
1 |
53,557,973 (GRCm39) |
missense |
probably benign |
|
R7282:Dnah7a
|
UTSW |
1 |
53,724,059 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7365:Dnah7a
|
UTSW |
1 |
53,536,297 (GRCm39) |
missense |
probably benign |
|
R7392:Dnah7a
|
UTSW |
1 |
53,540,820 (GRCm39) |
missense |
probably benign |
0.00 |
R7454:Dnah7a
|
UTSW |
1 |
53,557,923 (GRCm39) |
missense |
probably benign |
|
R7471:Dnah7a
|
UTSW |
1 |
53,458,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7547:Dnah7a
|
UTSW |
1 |
53,702,996 (GRCm39) |
missense |
probably benign |
0.00 |
R7554:Dnah7a
|
UTSW |
1 |
53,567,857 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7655:Dnah7a
|
UTSW |
1 |
53,535,164 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7656:Dnah7a
|
UTSW |
1 |
53,535,164 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7666:Dnah7a
|
UTSW |
1 |
53,586,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7721:Dnah7a
|
UTSW |
1 |
53,670,842 (GRCm39) |
missense |
probably benign |
|
R7813:Dnah7a
|
UTSW |
1 |
53,657,245 (GRCm39) |
missense |
probably benign |
|
R7839:Dnah7a
|
UTSW |
1 |
53,606,334 (GRCm39) |
missense |
probably benign |
0.08 |
R7959:Dnah7a
|
UTSW |
1 |
53,682,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Dnah7a
|
UTSW |
1 |
53,543,377 (GRCm39) |
missense |
probably benign |
0.01 |
R7985:Dnah7a
|
UTSW |
1 |
53,557,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Dnah7a
|
UTSW |
1 |
53,543,049 (GRCm39) |
missense |
probably benign |
|
R8140:Dnah7a
|
UTSW |
1 |
53,540,748 (GRCm39) |
missense |
probably benign |
0.02 |
R8184:Dnah7a
|
UTSW |
1 |
53,666,194 (GRCm39) |
missense |
probably benign |
0.03 |
R8339:Dnah7a
|
UTSW |
1 |
53,724,178 (GRCm39) |
missense |
probably benign |
|
R8352:Dnah7a
|
UTSW |
1 |
53,466,986 (GRCm39) |
missense |
probably null |
0.01 |
R8423:Dnah7a
|
UTSW |
1 |
53,512,063 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8428:Dnah7a
|
UTSW |
1 |
53,512,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R8432:Dnah7a
|
UTSW |
1 |
53,657,195 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8452:Dnah7a
|
UTSW |
1 |
53,466,986 (GRCm39) |
missense |
probably null |
0.01 |
R8458:Dnah7a
|
UTSW |
1 |
53,657,142 (GRCm39) |
missense |
probably benign |
0.01 |
R8493:Dnah7a
|
UTSW |
1 |
53,512,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8498:Dnah7a
|
UTSW |
1 |
53,657,139 (GRCm39) |
missense |
probably benign |
0.01 |
R8502:Dnah7a
|
UTSW |
1 |
53,679,520 (GRCm39) |
missense |
probably benign |
0.39 |
R8692:Dnah7a
|
UTSW |
1 |
53,472,175 (GRCm39) |
missense |
probably benign |
0.00 |
R8700:Dnah7a
|
UTSW |
1 |
53,535,088 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8709:Dnah7a
|
UTSW |
1 |
53,674,476 (GRCm39) |
missense |
probably benign |
|
R8856:Dnah7a
|
UTSW |
1 |
53,462,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Dnah7a
|
UTSW |
1 |
53,682,682 (GRCm39) |
missense |
probably benign |
0.10 |
R8967:Dnah7a
|
UTSW |
1 |
53,682,594 (GRCm39) |
splice site |
probably benign |
|
R8982:Dnah7a
|
UTSW |
1 |
53,570,301 (GRCm39) |
missense |
probably benign |
|
R8984:Dnah7a
|
UTSW |
1 |
53,674,436 (GRCm39) |
nonsense |
probably null |
|
R8993:Dnah7a
|
UTSW |
1 |
53,543,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Dnah7a
|
UTSW |
1 |
53,701,501 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9022:Dnah7a
|
UTSW |
1 |
53,512,116 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9028:Dnah7a
|
UTSW |
1 |
53,560,297 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Dnah7a
|
UTSW |
1 |
53,741,218 (GRCm39) |
missense |
unknown |
|
R9167:Dnah7a
|
UTSW |
1 |
53,657,370 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Dnah7a
|
UTSW |
1 |
53,540,757 (GRCm39) |
missense |
probably benign |
0.11 |
R9226:Dnah7a
|
UTSW |
1 |
53,560,326 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9251:Dnah7a
|
UTSW |
1 |
53,621,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R9265:Dnah7a
|
UTSW |
1 |
53,674,505 (GRCm39) |
missense |
probably benign |
|
R9350:Dnah7a
|
UTSW |
1 |
53,436,307 (GRCm39) |
missense |
probably benign |
0.19 |
R9369:Dnah7a
|
UTSW |
1 |
53,564,222 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9369:Dnah7a
|
UTSW |
1 |
53,543,421 (GRCm39) |
missense |
probably benign |
|
R9372:Dnah7a
|
UTSW |
1 |
53,543,474 (GRCm39) |
missense |
probably benign |
|
R9376:Dnah7a
|
UTSW |
1 |
53,568,058 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9378:Dnah7a
|
UTSW |
1 |
53,621,776 (GRCm39) |
missense |
probably benign |
0.32 |
R9401:Dnah7a
|
UTSW |
1 |
53,568,026 (GRCm39) |
missense |
probably benign |
0.01 |
R9431:Dnah7a
|
UTSW |
1 |
53,450,812 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9529:Dnah7a
|
UTSW |
1 |
53,561,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Dnah7a
|
UTSW |
1 |
53,561,388 (GRCm39) |
missense |
probably benign |
0.03 |
R9712:Dnah7a
|
UTSW |
1 |
53,598,299 (GRCm39) |
missense |
probably benign |
0.00 |
R9799:Dnah7a
|
UTSW |
1 |
53,557,968 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Dnah7a
|
UTSW |
1 |
53,561,388 (GRCm39) |
missense |
probably benign |
0.03 |
X0027:Dnah7a
|
UTSW |
1 |
53,512,089 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dnah7a
|
UTSW |
1 |
53,507,802 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,522,622 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,458,858 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah7a
|
UTSW |
1 |
53,598,261 (GRCm39) |
missense |
probably benign |
0.21 |
Z1177:Dnah7a
|
UTSW |
1 |
53,450,815 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Dnah7a
|
UTSW |
1 |
53,682,616 (GRCm39) |
missense |
possibly damaging |
0.92 |
|