Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,988,021 (GRCm39) |
K3102E |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,351,902 (GRCm39) |
|
probably null |
Het |
Akp3 |
A |
T |
1: 87,055,485 (GRCm39) |
T511S |
unknown |
Het |
Alkal2 |
T |
A |
12: 30,934,889 (GRCm39) |
L36Q |
probably damaging |
Het |
Arhgef17 |
A |
T |
7: 100,529,218 (GRCm39) |
V523E |
probably damaging |
Het |
Asah1 |
G |
T |
8: 41,813,332 (GRCm39) |
T27K |
possibly damaging |
Het |
Bag2 |
A |
G |
1: 33,786,034 (GRCm39) |
V96A |
probably damaging |
Het |
Bicd1 |
C |
T |
6: 149,421,901 (GRCm39) |
A874V |
probably damaging |
Het |
C4b |
T |
C |
17: 34,961,391 (GRCm39) |
I189M |
probably benign |
Het |
Calcr |
A |
G |
6: 3,708,538 (GRCm39) |
I216T |
probably damaging |
Het |
Cdk5rap2 |
T |
A |
4: 70,184,970 (GRCm39) |
D1160V |
probably damaging |
Het |
Cep128 |
A |
T |
12: 91,315,625 (GRCm39) |
I87K |
probably damaging |
Het |
Cep170b |
C |
G |
12: 112,707,275 (GRCm39) |
H1256Q |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,134,232 (GRCm39) |
V705E |
probably damaging |
Het |
Clec12b |
T |
A |
6: 129,356,923 (GRCm39) |
I172L |
probably benign |
Het |
Cobl |
A |
T |
11: 12,256,948 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,429,202 (GRCm39) |
D972V |
probably damaging |
Het |
Csrp1 |
A |
T |
1: 135,678,797 (GRCm39) |
N174I |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,444,866 (GRCm39) |
H3946L |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,462,001 (GRCm39) |
D133E |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,345,026 (GRCm39) |
I353N |
probably damaging |
Het |
Elavl3 |
A |
T |
9: 21,930,029 (GRCm39) |
S292T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,498,923 (GRCm39) |
N52S |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,171,361 (GRCm39) |
M671K |
possibly damaging |
Het |
Gabrg3 |
T |
C |
7: 56,423,032 (GRCm39) |
D222G |
possibly damaging |
Het |
Gk5 |
C |
T |
9: 96,022,709 (GRCm39) |
Q182* |
probably null |
Het |
Gm14403 |
A |
T |
2: 177,199,054 (GRCm39) |
H50L |
possibly damaging |
Het |
Gzma |
T |
C |
13: 113,234,794 (GRCm39) |
T66A |
probably damaging |
Het |
Hint2 |
T |
C |
4: 43,656,445 (GRCm39) |
|
probably benign |
Het |
Hnmt |
A |
T |
2: 23,904,251 (GRCm39) |
W137R |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,048,402 (GRCm39) |
V90A |
probably benign |
Het |
Idua |
A |
T |
5: 108,828,090 (GRCm39) |
|
probably benign |
Het |
Kif1a |
A |
C |
1: 92,983,489 (GRCm39) |
S669R |
probably damaging |
Het |
Klhdc7b |
A |
T |
15: 89,271,862 (GRCm39) |
M915L |
possibly damaging |
Het |
Klhl41 |
A |
G |
2: 69,500,815 (GRCm39) |
Y92C |
probably damaging |
Het |
Klrc2 |
A |
T |
6: 129,633,420 (GRCm39) |
C186S |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 102,166,772 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
C |
10: 103,051,301 (GRCm39) |
M484V |
probably benign |
Het |
Lzts1 |
A |
G |
8: 69,591,729 (GRCm39) |
S140P |
possibly damaging |
Het |
Mgat5b |
T |
A |
11: 116,864,226 (GRCm39) |
V464E |
probably damaging |
Het |
Mms19 |
A |
T |
19: 41,944,305 (GRCm39) |
D298E |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,347,452 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
T |
A |
14: 103,524,770 (GRCm39) |
K597I |
probably damaging |
Het |
Myo18a |
C |
A |
11: 77,745,513 (GRCm39) |
D1619E |
probably benign |
Het |
Nfx1 |
T |
C |
4: 40,984,973 (GRCm39) |
W366R |
probably null |
Het |
Nipbl |
C |
T |
15: 8,388,391 (GRCm39) |
V410I |
probably benign |
Het |
Or14j10 |
T |
A |
17: 37,935,323 (GRCm39) |
I68F |
probably benign |
Het |
Or4c101 |
T |
A |
2: 88,389,849 (GRCm39) |
M1K |
probably null |
Het |
Or4f60 |
A |
T |
2: 111,902,013 (GRCm39) |
M305K |
probably benign |
Het |
Or52h1 |
T |
C |
7: 103,829,091 (GRCm39) |
I175V |
probably benign |
Het |
Or5b95 |
A |
T |
19: 12,658,336 (GRCm39) |
Y288F |
probably damaging |
Het |
Or7g32 |
A |
T |
9: 19,388,853 (GRCm39) |
M231K |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,503 (GRCm39) |
N206S |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,125,516 (GRCm39) |
M53K |
possibly damaging |
Het |
Pask |
A |
G |
1: 93,265,065 (GRCm39) |
|
probably null |
Het |
Pcca |
G |
A |
14: 123,124,481 (GRCm39) |
C684Y |
probably damaging |
Het |
Pcdhb10 |
A |
G |
18: 37,546,219 (GRCm39) |
T432A |
possibly damaging |
Het |
Peak1 |
T |
C |
9: 56,166,039 (GRCm39) |
N630D |
probably damaging |
Het |
Plbd2 |
A |
T |
5: 120,631,231 (GRCm39) |
|
probably null |
Het |
Plekhg5 |
T |
C |
4: 152,188,797 (GRCm39) |
V200A |
probably benign |
Het |
Pola2 |
A |
G |
19: 6,011,198 (GRCm39) |
V42A |
probably benign |
Het |
Ppfibp2 |
T |
A |
7: 107,337,097 (GRCm39) |
W572R |
probably damaging |
Het |
Ppp6r1 |
C |
T |
7: 4,636,771 (GRCm39) |
E679K |
probably benign |
Het |
Pramel11 |
A |
T |
4: 143,622,337 (GRCm39) |
H339Q |
probably damaging |
Het |
Prdx3 |
G |
A |
19: 60,859,963 (GRCm39) |
A70V |
probably damaging |
Het |
Prkd2 |
T |
C |
7: 16,577,717 (GRCm39) |
F57L |
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,206,171 (GRCm39) |
T324A |
possibly damaging |
Het |
Ptdss1 |
T |
C |
13: 67,120,604 (GRCm39) |
F267L |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,593,137 (GRCm39) |
H169L |
probably benign |
Het |
Rere |
A |
G |
4: 150,701,700 (GRCm39) |
H1360R |
probably damaging |
Het |
Rfc3 |
C |
T |
5: 151,573,444 (GRCm39) |
V40I |
probably benign |
Het |
Rims1 |
T |
A |
1: 22,577,590 (GRCm39) |
T219S |
probably damaging |
Het |
Rnf169 |
T |
C |
7: 99,576,338 (GRCm39) |
R289G |
possibly damaging |
Het |
Senp7 |
T |
C |
16: 56,004,512 (GRCm39) |
|
silent |
Het |
Sfmbt2 |
A |
T |
2: 10,573,184 (GRCm39) |
I571F |
probably damaging |
Het |
Slc11a2 |
C |
A |
15: 100,301,068 (GRCm39) |
K328N |
probably benign |
Het |
Slc25a10 |
A |
G |
11: 120,387,202 (GRCm39) |
|
probably benign |
Het |
Slc38a8 |
T |
C |
8: 120,207,488 (GRCm39) |
*433W |
probably null |
Het |
Slco1a5 |
A |
C |
6: 142,183,320 (GRCm39) |
|
probably null |
Het |
Smc6 |
T |
A |
12: 11,339,995 (GRCm39) |
N434K |
probably benign |
Het |
Syndig1 |
A |
T |
2: 149,741,428 (GRCm39) |
I5F |
possibly damaging |
Het |
Syt5 |
T |
C |
7: 4,546,018 (GRCm39) |
Q124R |
probably benign |
Het |
Taok3 |
A |
C |
5: 117,344,785 (GRCm39) |
M171L |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,560,709 (GRCm39) |
D389G |
probably benign |
Het |
Tcaf2 |
G |
A |
6: 42,619,707 (GRCm39) |
R107C |
possibly damaging |
Het |
Tex14 |
C |
A |
11: 87,426,452 (GRCm39) |
H1159Q |
probably damaging |
Het |
Tmprss11d |
T |
A |
5: 86,474,388 (GRCm39) |
M190L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,768,867 (GRCm39) |
T2856S |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,171,998 (GRCm39) |
M2997K |
probably damaging |
Het |
Unc5c |
C |
T |
3: 141,383,886 (GRCm39) |
A88V |
probably damaging |
Het |
Use1 |
T |
C |
8: 71,820,398 (GRCm39) |
|
probably benign |
Het |
Vmn1r43 |
T |
C |
6: 89,847,354 (GRCm39) |
N44S |
probably damaging |
Het |
Vmn1r89 |
T |
A |
7: 12,954,146 (GRCm39) |
V294D |
possibly damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,194,869 (GRCm39) |
V819E |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,977 (GRCm39) |
M271L |
probably benign |
Het |
Vmn2r52 |
T |
C |
7: 9,905,059 (GRCm39) |
Y260C |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 84,799,151 (GRCm39) |
R519* |
probably null |
Het |
Vmn2r69 |
T |
A |
7: 85,056,404 (GRCm39) |
D578V |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,262,343 (GRCm39) |
Y132C |
probably damaging |
Het |
Wdr74 |
T |
A |
19: 8,715,240 (GRCm39) |
V133E |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,720,170 (GRCm39) |
|
probably benign |
Het |
Zfp810 |
A |
T |
9: 22,194,467 (GRCm39) |
S74T |
probably benign |
Het |
|
Other mutations in Otog |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Otog
|
APN |
7 |
45,900,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00725:Otog
|
APN |
7 |
45,923,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00757:Otog
|
APN |
7 |
45,939,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00822:Otog
|
APN |
7 |
45,945,304 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01354:Otog
|
APN |
7 |
45,939,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01567:Otog
|
APN |
7 |
45,926,039 (GRCm39) |
splice site |
probably benign |
|
IGL02034:Otog
|
APN |
7 |
45,945,417 (GRCm39) |
nonsense |
probably null |
|
IGL02090:Otog
|
APN |
7 |
45,949,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02132:Otog
|
APN |
7 |
45,954,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02148:Otog
|
APN |
7 |
45,950,011 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02173:Otog
|
APN |
7 |
45,926,165 (GRCm39) |
splice site |
probably benign |
|
IGL02199:Otog
|
APN |
7 |
45,926,775 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02216:Otog
|
APN |
7 |
45,950,892 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02322:Otog
|
APN |
7 |
45,950,881 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02330:Otog
|
APN |
7 |
45,937,493 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02529:Otog
|
APN |
7 |
45,909,381 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02898:Otog
|
APN |
7 |
45,959,562 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02970:Otog
|
APN |
7 |
45,945,291 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03085:Otog
|
APN |
7 |
45,955,346 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03108:Otog
|
APN |
7 |
45,900,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03275:Otog
|
APN |
7 |
45,955,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282_Otog_616
|
UTSW |
7 |
45,926,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0636_otog_678
|
UTSW |
7 |
45,913,652 (GRCm39) |
critical splice donor site |
probably null |
|
R1029_otog_141
|
UTSW |
7 |
45,924,019 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Otog
|
UTSW |
7 |
45,959,571 (GRCm39) |
missense |
probably damaging |
1.00 |
BB020:Otog
|
UTSW |
7 |
45,959,571 (GRCm39) |
missense |
probably damaging |
1.00 |
I1329:Otog
|
UTSW |
7 |
45,895,927 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02984:Otog
|
UTSW |
7 |
45,954,932 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4472001:Otog
|
UTSW |
7 |
45,945,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0032:Otog
|
UTSW |
7 |
45,937,637 (GRCm39) |
nonsense |
probably null |
|
R0105:Otog
|
UTSW |
7 |
45,937,790 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0164:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0164:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0165:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0166:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0167:Otog
|
UTSW |
7 |
45,953,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R0240:Otog
|
UTSW |
7 |
45,913,456 (GRCm39) |
splice site |
probably null |
|
R0240:Otog
|
UTSW |
7 |
45,913,456 (GRCm39) |
splice site |
probably null |
|
R0242:Otog
|
UTSW |
7 |
45,916,805 (GRCm39) |
missense |
probably damaging |
0.98 |
R0242:Otog
|
UTSW |
7 |
45,916,805 (GRCm39) |
missense |
probably damaging |
0.98 |
R0282:Otog
|
UTSW |
7 |
45,926,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0392:Otog
|
UTSW |
7 |
45,899,499 (GRCm39) |
missense |
probably benign |
0.00 |
R0436:Otog
|
UTSW |
7 |
45,915,360 (GRCm39) |
splice site |
probably benign |
|
R0441:Otog
|
UTSW |
7 |
45,955,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Otog
|
UTSW |
7 |
45,923,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Otog
|
UTSW |
7 |
45,947,668 (GRCm39) |
missense |
probably damaging |
0.98 |
R0541:Otog
|
UTSW |
7 |
45,918,673 (GRCm39) |
splice site |
probably benign |
|
R0600:Otog
|
UTSW |
7 |
45,900,819 (GRCm39) |
splice site |
probably benign |
|
R0626:Otog
|
UTSW |
7 |
45,920,797 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0636:Otog
|
UTSW |
7 |
45,913,652 (GRCm39) |
critical splice donor site |
probably null |
|
R0764:Otog
|
UTSW |
7 |
45,949,918 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Otog
|
UTSW |
7 |
45,918,786 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0836:Otog
|
UTSW |
7 |
45,918,786 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0844:Otog
|
UTSW |
7 |
45,937,252 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1029:Otog
|
UTSW |
7 |
45,924,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Otog
|
UTSW |
7 |
45,950,025 (GRCm39) |
splice site |
probably benign |
|
R1134:Otog
|
UTSW |
7 |
45,947,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Otog
|
UTSW |
7 |
45,939,179 (GRCm39) |
missense |
probably benign |
0.41 |
R1204:Otog
|
UTSW |
7 |
45,909,335 (GRCm39) |
missense |
probably benign |
0.16 |
R1301:Otog
|
UTSW |
7 |
45,939,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R1344:Otog
|
UTSW |
7 |
45,924,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Otog
|
UTSW |
7 |
45,923,119 (GRCm39) |
splice site |
probably benign |
|
R1418:Otog
|
UTSW |
7 |
45,924,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Otog
|
UTSW |
7 |
45,950,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1479:Otog
|
UTSW |
7 |
45,945,402 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1521:Otog
|
UTSW |
7 |
45,908,688 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1589:Otog
|
UTSW |
7 |
45,933,332 (GRCm39) |
missense |
probably benign |
0.18 |
R1671:Otog
|
UTSW |
7 |
45,911,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Otog
|
UTSW |
7 |
45,937,583 (GRCm39) |
missense |
probably benign |
0.28 |
R1806:Otog
|
UTSW |
7 |
45,940,361 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1843:Otog
|
UTSW |
7 |
45,895,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R1873:Otog
|
UTSW |
7 |
45,918,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R1923:Otog
|
UTSW |
7 |
45,895,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Otog
|
UTSW |
7 |
45,895,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R2008:Otog
|
UTSW |
7 |
45,913,498 (GRCm39) |
missense |
probably benign |
0.43 |
R2048:Otog
|
UTSW |
7 |
45,937,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Otog
|
UTSW |
7 |
45,899,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Otog
|
UTSW |
7 |
45,952,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Otog
|
UTSW |
7 |
45,890,453 (GRCm39) |
start codon destroyed |
probably null |
|
R2278:Otog
|
UTSW |
7 |
45,949,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Otog
|
UTSW |
7 |
45,890,964 (GRCm39) |
missense |
probably benign |
0.10 |
R2424:Otog
|
UTSW |
7 |
45,947,593 (GRCm39) |
nonsense |
probably null |
|
R2513:Otog
|
UTSW |
7 |
45,955,014 (GRCm39) |
critical splice donor site |
probably null |
|
R2863:Otog
|
UTSW |
7 |
45,918,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R3148:Otog
|
UTSW |
7 |
45,939,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Otog
|
UTSW |
7 |
45,937,792 (GRCm39) |
missense |
probably benign |
0.03 |
R3732:Otog
|
UTSW |
7 |
45,937,792 (GRCm39) |
missense |
probably benign |
0.03 |
R3733:Otog
|
UTSW |
7 |
45,937,792 (GRCm39) |
missense |
probably benign |
0.03 |
R3734:Otog
|
UTSW |
7 |
45,937,792 (GRCm39) |
missense |
probably benign |
0.03 |
R3855:Otog
|
UTSW |
7 |
45,923,184 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3880:Otog
|
UTSW |
7 |
45,937,445 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4081:Otog
|
UTSW |
7 |
45,937,723 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4349:Otog
|
UTSW |
7 |
45,923,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R4382:Otog
|
UTSW |
7 |
45,939,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Otog
|
UTSW |
7 |
45,934,548 (GRCm39) |
missense |
probably damaging |
0.98 |
R4520:Otog
|
UTSW |
7 |
45,890,477 (GRCm39) |
unclassified |
probably benign |
|
R4569:Otog
|
UTSW |
7 |
45,959,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Otog
|
UTSW |
7 |
45,937,225 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4672:Otog
|
UTSW |
7 |
45,939,210 (GRCm39) |
missense |
probably damaging |
0.98 |
R4764:Otog
|
UTSW |
7 |
45,937,943 (GRCm39) |
missense |
probably benign |
0.29 |
R4910:Otog
|
UTSW |
7 |
45,947,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Otog
|
UTSW |
7 |
45,913,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4913:Otog
|
UTSW |
7 |
45,913,526 (GRCm39) |
missense |
probably benign |
0.31 |
R4975:Otog
|
UTSW |
7 |
45,937,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4996:Otog
|
UTSW |
7 |
45,954,934 (GRCm39) |
nonsense |
probably null |
|
R4996:Otog
|
UTSW |
7 |
45,948,030 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5116:Otog
|
UTSW |
7 |
45,923,191 (GRCm39) |
missense |
probably benign |
0.34 |
R5138:Otog
|
UTSW |
7 |
45,899,430 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5169:Otog
|
UTSW |
7 |
45,947,572 (GRCm39) |
missense |
probably benign |
0.06 |
R5239:Otog
|
UTSW |
7 |
45,936,859 (GRCm39) |
missense |
probably benign |
0.15 |
R5277:Otog
|
UTSW |
7 |
45,896,045 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5287:Otog
|
UTSW |
7 |
45,918,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R5299:Otog
|
UTSW |
7 |
45,938,275 (GRCm39) |
missense |
probably benign |
0.16 |
R5378:Otog
|
UTSW |
7 |
45,904,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Otog
|
UTSW |
7 |
45,898,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5487:Otog
|
UTSW |
7 |
45,938,192 (GRCm39) |
missense |
probably benign |
0.27 |
R5507:Otog
|
UTSW |
7 |
45,911,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Otog
|
UTSW |
7 |
45,923,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5757:Otog
|
UTSW |
7 |
45,890,545 (GRCm39) |
critical splice donor site |
probably null |
|
R5910:Otog
|
UTSW |
7 |
45,948,022 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6019:Otog
|
UTSW |
7 |
45,938,374 (GRCm39) |
missense |
probably benign |
0.00 |
R6150:Otog
|
UTSW |
7 |
45,913,483 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6225:Otog
|
UTSW |
7 |
45,898,458 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6271:Otog
|
UTSW |
7 |
45,901,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Otog
|
UTSW |
7 |
45,950,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Otog
|
UTSW |
7 |
45,955,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R6640:Otog
|
UTSW |
7 |
45,911,167 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6753:Otog
|
UTSW |
7 |
45,898,495 (GRCm39) |
missense |
probably benign |
0.06 |
R6788:Otog
|
UTSW |
7 |
45,947,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Otog
|
UTSW |
7 |
45,923,205 (GRCm39) |
missense |
probably damaging |
0.96 |
R7033:Otog
|
UTSW |
7 |
45,916,822 (GRCm39) |
critical splice donor site |
probably null |
|
R7071:Otog
|
UTSW |
7 |
45,916,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7084:Otog
|
UTSW |
7 |
45,947,990 (GRCm39) |
nonsense |
probably null |
|
R7116:Otog
|
UTSW |
7 |
45,947,689 (GRCm39) |
missense |
probably damaging |
0.99 |
R7202:Otog
|
UTSW |
7 |
45,937,474 (GRCm39) |
missense |
probably damaging |
0.97 |
R7365:Otog
|
UTSW |
7 |
45,947,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7468:Otog
|
UTSW |
7 |
45,913,543 (GRCm39) |
missense |
probably benign |
|
R7475:Otog
|
UTSW |
7 |
45,916,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R7502:Otog
|
UTSW |
7 |
45,948,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Otog
|
UTSW |
7 |
45,952,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R7577:Otog
|
UTSW |
7 |
45,937,279 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7651:Otog
|
UTSW |
7 |
45,891,185 (GRCm39) |
missense |
probably benign |
0.00 |
R7689:Otog
|
UTSW |
7 |
45,901,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R7806:Otog
|
UTSW |
7 |
45,935,200 (GRCm39) |
missense |
probably benign |
|
R7933:Otog
|
UTSW |
7 |
45,959,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R8021:Otog
|
UTSW |
7 |
45,916,766 (GRCm39) |
missense |
probably damaging |
0.98 |
R8082:Otog
|
UTSW |
7 |
45,939,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Otog
|
UTSW |
7 |
45,901,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R8772:Otog
|
UTSW |
7 |
45,934,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Otog
|
UTSW |
7 |
45,950,905 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8842:Otog
|
UTSW |
7 |
45,895,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Otog
|
UTSW |
7 |
45,936,878 (GRCm39) |
missense |
probably benign |
0.43 |
R8988:Otog
|
UTSW |
7 |
45,959,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9010:Otog
|
UTSW |
7 |
45,949,894 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Otog
|
UTSW |
7 |
45,937,520 (GRCm39) |
missense |
probably benign |
0.13 |
R9131:Otog
|
UTSW |
7 |
45,952,597 (GRCm39) |
nonsense |
probably null |
|
R9179:Otog
|
UTSW |
7 |
45,937,885 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9334:Otog
|
UTSW |
7 |
45,909,353 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9365:Otog
|
UTSW |
7 |
45,920,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Otog
|
UTSW |
7 |
45,916,721 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9418:Otog
|
UTSW |
7 |
45,938,024 (GRCm39) |
missense |
probably benign |
0.41 |
R9465:Otog
|
UTSW |
7 |
45,955,299 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9496:Otog
|
UTSW |
7 |
45,890,505 (GRCm39) |
missense |
unknown |
|
R9632:Otog
|
UTSW |
7 |
45,915,143 (GRCm39) |
missense |
probably benign |
0.27 |
R9656:Otog
|
UTSW |
7 |
45,959,567 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Otog
|
UTSW |
7 |
45,937,093 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Otog
|
UTSW |
7 |
45,909,345 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Otog
|
UTSW |
7 |
45,939,164 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Otog
|
UTSW |
7 |
45,923,962 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Otog
|
UTSW |
7 |
45,912,276 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:Otog
|
UTSW |
7 |
45,959,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|