Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 9,010,657 (GRCm38) |
K3102E |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,702,154 (GRCm38) |
|
probably null |
Het |
Akp3 |
A |
T |
1: 87,127,763 (GRCm38) |
T511S |
unknown |
Het |
Alkal2 |
T |
A |
12: 30,884,890 (GRCm38) |
L36Q |
probably damaging |
Het |
Arhgef17 |
A |
T |
7: 100,880,011 (GRCm38) |
V523E |
probably damaging |
Het |
Asah1 |
G |
T |
8: 41,360,295 (GRCm38) |
T27K |
possibly damaging |
Het |
Bag2 |
A |
G |
1: 33,746,953 (GRCm38) |
V96A |
probably damaging |
Het |
Bicd1 |
C |
T |
6: 149,520,403 (GRCm38) |
A874V |
probably damaging |
Het |
C4b |
T |
C |
17: 34,742,417 (GRCm38) |
I189M |
probably benign |
Het |
Calcr |
A |
G |
6: 3,708,538 (GRCm38) |
I216T |
probably damaging |
Het |
Cdk5rap2 |
T |
A |
4: 70,266,733 (GRCm38) |
D1160V |
probably damaging |
Het |
Cep128 |
A |
T |
12: 91,348,851 (GRCm38) |
I87K |
probably damaging |
Het |
Cep170b |
C |
G |
12: 112,740,841 (GRCm38) |
H1256Q |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,484,484 (GRCm38) |
V705E |
probably damaging |
Het |
Clec12b |
T |
A |
6: 129,379,960 (GRCm38) |
I172L |
probably benign |
Het |
Cobl |
A |
T |
11: 12,306,948 (GRCm38) |
|
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,390,042 (GRCm38) |
D972V |
probably damaging |
Het |
Csrp1 |
A |
T |
1: 135,751,059 (GRCm38) |
N174I |
probably damaging |
Het |
Dnajc21 |
A |
T |
15: 10,461,915 (GRCm38) |
D133E |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,526,276 (GRCm38) |
I353N |
probably damaging |
Het |
Elavl3 |
A |
T |
9: 22,018,733 (GRCm38) |
S292T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,771,612 (GRCm38) |
N52S |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,280,535 (GRCm38) |
M671K |
possibly damaging |
Het |
Gabrg3 |
T |
C |
7: 56,773,284 (GRCm38) |
D222G |
possibly damaging |
Het |
Gk5 |
C |
T |
9: 96,140,656 (GRCm38) |
Q182* |
probably null |
Het |
Gm14403 |
A |
T |
2: 177,507,261 (GRCm38) |
H50L |
possibly damaging |
Het |
Gzma |
T |
C |
13: 113,098,260 (GRCm38) |
T66A |
probably damaging |
Het |
Hint2 |
T |
C |
4: 43,656,445 (GRCm38) |
|
probably benign |
Het |
Hnmt |
A |
T |
2: 24,014,239 (GRCm38) |
W137R |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,059,963 (GRCm38) |
V90A |
probably benign |
Het |
Idua |
A |
T |
5: 108,680,224 (GRCm38) |
|
probably benign |
Het |
Kif1a |
A |
C |
1: 93,055,767 (GRCm38) |
S669R |
probably damaging |
Het |
Klhdc7b |
A |
T |
15: 89,387,659 (GRCm38) |
M915L |
possibly damaging |
Het |
Klhl41 |
A |
G |
2: 69,670,471 (GRCm38) |
Y92C |
probably damaging |
Het |
Klrc2 |
A |
T |
6: 129,656,457 (GRCm38) |
C186S |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 101,929,336 (GRCm38) |
|
probably benign |
Het |
Lrriq1 |
T |
C |
10: 103,215,440 (GRCm38) |
M484V |
probably benign |
Het |
Lzts1 |
A |
G |
8: 69,139,077 (GRCm38) |
S140P |
possibly damaging |
Het |
Mgat5b |
T |
A |
11: 116,973,400 (GRCm38) |
V464E |
probably damaging |
Het |
Mms19 |
A |
T |
19: 41,955,866 (GRCm38) |
D298E |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,793,715 (GRCm38) |
|
probably null |
Het |
Mycbp2 |
T |
A |
14: 103,287,334 (GRCm38) |
K597I |
probably damaging |
Het |
Myo18a |
C |
A |
11: 77,854,687 (GRCm38) |
D1619E |
probably benign |
Het |
Nfx1 |
T |
C |
4: 40,984,973 (GRCm38) |
W366R |
probably null |
Het |
Nipbl |
C |
T |
15: 8,358,907 (GRCm38) |
V410I |
probably benign |
Het |
Olfr1037 |
T |
C |
2: 86,085,159 (GRCm38) |
N206S |
probably damaging |
Het |
Olfr116 |
T |
A |
17: 37,624,432 (GRCm38) |
I68F |
probably benign |
Het |
Olfr1188 |
T |
A |
2: 88,559,505 (GRCm38) |
M1K |
probably null |
Het |
Olfr1313 |
A |
T |
2: 112,071,668 (GRCm38) |
M305K |
probably benign |
Het |
Olfr1443 |
A |
T |
19: 12,680,972 (GRCm38) |
Y288F |
probably damaging |
Het |
Olfr648 |
T |
C |
7: 104,179,884 (GRCm38) |
I175V |
probably benign |
Het |
Olfr850 |
A |
T |
9: 19,477,557 (GRCm38) |
M231K |
probably benign |
Het |
Otog |
A |
T |
7: 46,287,447 (GRCm38) |
T1527S |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,218,095 (GRCm38) |
M53K |
possibly damaging |
Het |
Pask |
A |
G |
1: 93,337,343 (GRCm38) |
|
probably null |
Het |
Pcca |
G |
A |
14: 122,887,069 (GRCm38) |
C684Y |
probably damaging |
Het |
Pcdhb10 |
A |
G |
18: 37,413,166 (GRCm38) |
T432A |
possibly damaging |
Het |
Peak1 |
T |
C |
9: 56,258,755 (GRCm38) |
N630D |
probably damaging |
Het |
Plbd2 |
A |
T |
5: 120,493,166 (GRCm38) |
|
probably null |
Het |
Plekhg5 |
T |
C |
4: 152,104,340 (GRCm38) |
V200A |
probably benign |
Het |
Pola2 |
A |
G |
19: 5,961,170 (GRCm38) |
V42A |
probably benign |
Het |
Ppfibp2 |
T |
A |
7: 107,737,890 (GRCm38) |
W572R |
probably damaging |
Het |
Ppp6r1 |
C |
T |
7: 4,633,772 (GRCm38) |
E679K |
probably benign |
Het |
Pramef6 |
A |
T |
4: 143,895,767 (GRCm38) |
H339Q |
probably damaging |
Het |
Prdx3 |
G |
A |
19: 60,871,525 (GRCm38) |
A70V |
probably damaging |
Het |
Prkd2 |
T |
C |
7: 16,843,792 (GRCm38) |
F57L |
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,506,746 (GRCm38) |
T324A |
possibly damaging |
Het |
Ptdss1 |
T |
C |
13: 66,972,540 (GRCm38) |
F267L |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,593,051 (GRCm38) |
H169L |
probably benign |
Het |
Rere |
A |
G |
4: 150,617,243 (GRCm38) |
H1360R |
probably damaging |
Het |
Rfc3 |
C |
T |
5: 151,649,979 (GRCm38) |
V40I |
probably benign |
Het |
Rims1 |
T |
A |
1: 22,538,509 (GRCm38) |
T219S |
probably damaging |
Het |
Rnf169 |
T |
C |
7: 99,927,131 (GRCm38) |
R289G |
possibly damaging |
Het |
Senp7 |
T |
C |
16: 56,184,149 (GRCm38) |
|
silent |
Het |
Sfmbt2 |
A |
T |
2: 10,568,373 (GRCm38) |
I571F |
probably damaging |
Het |
Slc11a2 |
C |
A |
15: 100,403,187 (GRCm38) |
K328N |
probably benign |
Het |
Slc25a10 |
A |
G |
11: 120,496,376 (GRCm38) |
|
probably benign |
Het |
Slc38a8 |
T |
C |
8: 119,480,749 (GRCm38) |
*433W |
probably null |
Het |
Slco1a5 |
A |
C |
6: 142,237,594 (GRCm38) |
|
probably null |
Het |
Smc6 |
T |
A |
12: 11,289,994 (GRCm38) |
N434K |
probably benign |
Het |
Syndig1 |
A |
T |
2: 149,899,508 (GRCm38) |
I5F |
possibly damaging |
Het |
Syt5 |
T |
C |
7: 4,543,019 (GRCm38) |
Q124R |
probably benign |
Het |
Taok3 |
A |
C |
5: 117,206,720 (GRCm38) |
M171L |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,649,413 (GRCm38) |
D389G |
probably benign |
Het |
Tcaf2 |
G |
A |
6: 42,642,773 (GRCm38) |
R107C |
possibly damaging |
Het |
Tex14 |
C |
A |
11: 87,535,626 (GRCm38) |
H1159Q |
probably damaging |
Het |
Tmprss11d |
T |
A |
5: 86,326,529 (GRCm38) |
M190L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,938,523 (GRCm38) |
T2856S |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,444,687 (GRCm38) |
M2997K |
probably damaging |
Het |
Unc5c |
C |
T |
3: 141,678,125 (GRCm38) |
A88V |
probably damaging |
Het |
Use1 |
T |
C |
8: 71,367,754 (GRCm38) |
|
probably benign |
Het |
Vmn1r43 |
T |
C |
6: 89,870,372 (GRCm38) |
N44S |
probably damaging |
Het |
Vmn1r89 |
T |
A |
7: 13,220,219 (GRCm38) |
V294D |
possibly damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,047,003 (GRCm38) |
V819E |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,524,977 (GRCm38) |
M271L |
probably benign |
Het |
Vmn2r52 |
T |
C |
7: 10,171,132 (GRCm38) |
Y260C |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 85,149,943 (GRCm38) |
R519* |
probably null |
Het |
Vmn2r69 |
T |
A |
7: 85,407,196 (GRCm38) |
D578V |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,426,474 (GRCm38) |
Y132C |
probably damaging |
Het |
Wdr74 |
T |
A |
19: 8,737,876 (GRCm38) |
V133E |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,409,244 (GRCm38) |
|
probably benign |
Het |
Zfp810 |
A |
T |
9: 22,283,171 (GRCm38) |
S74T |
probably benign |
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 |
R2074:Dnah7a
|
UTSW |
1 |
53,457,696 (GRCm38) |
missense |
probably benign |
0.45 |
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 |
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 |
|