Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
C |
A |
9: 46,218,119 (GRCm39) |
|
probably null |
Het |
Actr10 |
G |
A |
12: 71,008,653 (GRCm39) |
G362E |
probably damaging |
Het |
Aldh1a3 |
T |
C |
7: 66,057,600 (GRCm39) |
T278A |
probably damaging |
Het |
Arpp21 |
T |
A |
9: 112,008,152 (GRCm39) |
K116M |
probably damaging |
Het |
Arrdc3 |
T |
C |
13: 81,039,184 (GRCm39) |
Y72H |
probably damaging |
Het |
Atr |
T |
C |
9: 95,819,649 (GRCm39) |
V2212A |
probably benign |
Het |
Bcdin3d |
A |
G |
15: 99,368,932 (GRCm39) |
F89S |
possibly damaging |
Het |
Cacna1d |
C |
A |
14: 30,212,929 (GRCm39) |
A44S |
probably benign |
Het |
Cbx3 |
A |
G |
6: 51,452,269 (GRCm39) |
E28G |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,148,061 (GRCm39) |
F2722L |
probably damaging |
Het |
Clec11a |
A |
G |
7: 43,954,062 (GRCm39) |
V297A |
probably benign |
Het |
Clk2 |
C |
A |
3: 89,082,806 (GRCm39) |
|
probably benign |
Het |
Clybl |
T |
A |
14: 122,608,716 (GRCm39) |
C103S |
possibly damaging |
Het |
Col12a1 |
T |
A |
9: 79,551,248 (GRCm39) |
N2123Y |
probably damaging |
Het |
Corin |
G |
A |
5: 72,496,402 (GRCm39) |
P517L |
probably damaging |
Het |
Ddhd2 |
A |
T |
8: 26,217,726 (GRCm39) |
I717N |
probably damaging |
Het |
Derl2 |
C |
A |
11: 70,905,390 (GRCm39) |
G31* |
probably null |
Het |
Dgcr8 |
A |
G |
16: 18,095,941 (GRCm39) |
V523A |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,984,571 (GRCm39) |
S3090P |
probably damaging |
Het |
Dsp |
C |
A |
13: 38,367,274 (GRCm39) |
H641N |
probably benign |
Het |
Dsp |
A |
T |
13: 38,379,821 (GRCm39) |
T1590S |
possibly damaging |
Het |
Duox2 |
A |
T |
2: 122,128,012 (GRCm39) |
L57Q |
probably damaging |
Het |
Etfdh |
A |
T |
3: 79,530,880 (GRCm39) |
V47D |
probably benign |
Het |
Exoc1 |
T |
C |
5: 76,715,922 (GRCm39) |
Y823H |
probably damaging |
Het |
Fam81a |
C |
T |
9: 70,006,457 (GRCm39) |
R185K |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,811,768 (GRCm39) |
I2696V |
probably benign |
Het |
Glis1 |
GCACACA |
GCACA |
4: 107,480,302 (GRCm39) |
|
probably null |
Het |
Gtf3c1 |
A |
T |
7: 125,246,664 (GRCm39) |
N1548K |
probably benign |
Het |
H3c2 |
G |
A |
13: 23,936,613 (GRCm39) |
R84H |
probably damaging |
Het |
Hkdc1 |
A |
T |
10: 62,234,470 (GRCm39) |
I575N |
probably damaging |
Het |
Ifi208 |
A |
G |
1: 173,518,239 (GRCm39) |
I449V |
probably null |
Het |
Ino80 |
T |
C |
2: 119,213,902 (GRCm39) |
T1223A |
probably damaging |
Het |
Kctd9 |
T |
C |
14: 67,966,197 (GRCm39) |
|
probably null |
Het |
Khdrbs1 |
A |
G |
4: 129,635,647 (GRCm39) |
Y103H |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,707,693 (GRCm39) |
H1752R |
probably damaging |
Het |
Lrp5 |
T |
A |
19: 3,678,319 (GRCm39) |
Q512L |
probably benign |
Het |
Map2k5 |
T |
C |
9: 63,170,440 (GRCm39) |
T293A |
probably damaging |
Het |
Myo7a |
C |
A |
7: 97,732,806 (GRCm39) |
R657L |
probably damaging |
Het |
Myrfl |
A |
G |
10: 116,631,963 (GRCm39) |
|
probably null |
Het |
Nfatc2 |
G |
A |
2: 168,378,229 (GRCm39) |
H258Y |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,202,801 (GRCm39) |
L1336Q |
probably damaging |
Het |
Or10z1 |
A |
G |
1: 174,078,395 (GRCm39) |
S33P |
probably damaging |
Het |
Or4c113 |
T |
C |
2: 88,885,291 (GRCm39) |
I160V |
probably benign |
Het |
Or5an10 |
T |
C |
19: 12,276,140 (GRCm39) |
M119V |
possibly damaging |
Het |
Pcdh17 |
T |
G |
14: 84,684,649 (GRCm39) |
I372S |
probably damaging |
Het |
Pira13 |
A |
T |
7: 3,827,556 (GRCm39) |
Y200* |
probably null |
Het |
Plagl1 |
A |
G |
10: 13,003,919 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
C |
2: 24,931,115 (GRCm39) |
F910S |
possibly damaging |
Het |
Prdm13 |
G |
A |
4: 21,679,507 (GRCm39) |
P328S |
unknown |
Het |
Prdm5 |
C |
T |
6: 65,833,086 (GRCm39) |
Q152* |
probably null |
Het |
Psat1 |
A |
G |
19: 15,892,312 (GRCm39) |
F216S |
possibly damaging |
Het |
Psg21 |
A |
T |
7: 18,390,453 (GRCm39) |
M1K |
probably null |
Het |
Rab11fip3 |
A |
T |
17: 26,210,000 (GRCm39) |
S994T |
probably benign |
Het |
Rax |
A |
G |
18: 66,071,389 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
A |
T |
15: 36,099,934 (GRCm39) |
S260R |
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,675,175 (GRCm39) |
H3317Q |
probably damaging |
Het |
Sc5d |
A |
G |
9: 42,166,811 (GRCm39) |
Y243H |
probably damaging |
Het |
Serpinf1 |
T |
C |
11: 75,305,854 (GRCm39) |
E178G |
probably damaging |
Het |
Slc15a3 |
A |
T |
19: 10,833,369 (GRCm39) |
Y462F |
probably damaging |
Het |
Slc9b1 |
G |
A |
3: 135,063,534 (GRCm39) |
|
probably benign |
Het |
Slit2 |
C |
T |
5: 48,439,309 (GRCm39) |
P1111S |
probably damaging |
Het |
Slit3 |
T |
C |
11: 35,479,812 (GRCm39) |
Y330H |
probably damaging |
Het |
Snw1 |
T |
C |
12: 87,507,205 (GRCm39) |
K204E |
probably benign |
Het |
Steap1 |
A |
G |
5: 5,786,486 (GRCm39) |
I317T |
probably damaging |
Het |
Sval2 |
A |
G |
6: 41,838,879 (GRCm39) |
N20S |
probably damaging |
Het |
Tfrc |
C |
A |
16: 32,434,027 (GRCm39) |
Y85* |
probably null |
Het |
Tmem87a |
T |
C |
2: 120,202,026 (GRCm39) |
T412A |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,583,239 (GRCm39) |
K2705E |
probably damaging |
Het |
Vmn1r230 |
A |
T |
17: 21,067,230 (GRCm39) |
K140* |
probably null |
Het |
Vmn2r62 |
A |
T |
7: 42,414,240 (GRCm39) |
H734Q |
possibly damaging |
Het |
Zbtb8os |
T |
A |
4: 129,240,719 (GRCm39) |
|
probably benign |
Het |
Zfp608 |
A |
T |
18: 55,024,871 (GRCm39) |
H1466Q |
probably damaging |
Het |
Zfp957 |
C |
T |
14: 79,450,362 (GRCm39) |
C479Y |
probably damaging |
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 |
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 |
R5643:Otog
|
UTSW |
7 |
45,936,871 (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 |
|