Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
A |
3: 59,776,435 (GRCm39) |
|
probably null |
Het |
Adam3 |
T |
A |
8: 25,184,321 (GRCm39) |
I560L |
probably benign |
Het |
Agxt |
T |
C |
1: 93,063,436 (GRCm39) |
F113L |
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,688,568 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
A |
18: 65,399,357 (GRCm39) |
K2074* |
probably null |
Het |
Apob |
A |
G |
12: 8,057,848 (GRCm39) |
Y2077C |
probably damaging |
Het |
Arhgap17 |
A |
T |
7: 122,907,600 (GRCm39) |
L254Q |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Arid1b |
T |
A |
17: 5,392,478 (GRCm39) |
S2003T |
probably damaging |
Het |
Armc5 |
T |
G |
7: 127,839,900 (GRCm39) |
L406R |
possibly damaging |
Het |
Arsb |
T |
C |
13: 93,908,485 (GRCm39) |
V67A |
probably benign |
Het |
Aspm |
A |
G |
1: 139,419,281 (GRCm39) |
Y2982C |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,052,348 (GRCm39) |
T3016K |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,774,307 (GRCm39) |
L487P |
probably damaging |
Het |
Card11 |
C |
G |
5: 140,860,169 (GRCm39) |
D1063H |
probably damaging |
Het |
Ccdc186 |
G |
A |
19: 56,787,123 (GRCm39) |
T615M |
probably damaging |
Het |
Cd101 |
T |
A |
3: 100,901,205 (GRCm39) |
T960S |
probably benign |
Het |
Cdca7l |
C |
A |
12: 117,837,520 (GRCm39) |
S191* |
probably null |
Het |
Cemip |
A |
T |
7: 83,646,619 (GRCm39) |
I143N |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,609,829 (GRCm39) |
E161K |
possibly damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chrm2 |
A |
T |
6: 36,501,168 (GRCm39) |
T342S |
probably benign |
Het |
Cib2 |
A |
G |
9: 54,457,163 (GRCm39) |
F34L |
probably benign |
Het |
Cnot1 |
A |
T |
8: 96,459,859 (GRCm39) |
I1836N |
probably benign |
Het |
Col4a3 |
C |
A |
1: 82,650,400 (GRCm39) |
P552Q |
unknown |
Het |
Cp |
T |
A |
3: 20,043,388 (GRCm39) |
|
probably benign |
Het |
Cul3 |
C |
T |
1: 80,267,806 (GRCm39) |
V112I |
probably benign |
Het |
Dcdc5 |
A |
G |
2: 106,195,895 (GRCm39) |
|
noncoding transcript |
Het |
Disp1 |
A |
T |
1: 182,917,027 (GRCm39) |
V133E |
probably damaging |
Het |
Dlg4 |
A |
G |
11: 69,921,751 (GRCm39) |
D30G |
probably damaging |
Het |
Dop1a |
C |
T |
9: 86,374,114 (GRCm39) |
T191I |
probably damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Fbxw8 |
G |
T |
5: 118,263,092 (GRCm39) |
|
probably null |
Het |
Filip1 |
A |
G |
9: 79,725,214 (GRCm39) |
V1135A |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,657,814 (GRCm39) |
K472E |
probably benign |
Het |
Gm10568 |
T |
G |
1: 3,751,164 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gm6871 |
T |
A |
7: 41,223,016 (GRCm39) |
H24L |
probably benign |
Het |
Gpr155 |
G |
A |
2: 73,197,882 (GRCm39) |
Q413* |
probably null |
Het |
Grhl2 |
A |
G |
15: 37,291,920 (GRCm39) |
|
probably null |
Het |
Ighv1-31 |
G |
C |
12: 114,793,128 (GRCm39) |
S36* |
probably null |
Het |
Ighv8-5 |
A |
G |
12: 115,031,462 (GRCm39) |
S26P |
probably damaging |
Het |
Igkv17-134 |
A |
C |
6: 67,697,910 (GRCm39) |
|
probably benign |
Het |
Igkv5-48 |
A |
C |
6: 69,703,833 (GRCm39) |
L24R |
probably damaging |
Het |
Isg20l2 |
T |
A |
3: 87,846,570 (GRCm39) |
V340E |
probably damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,884 (GRCm39) |
Y447C |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,634,287 (GRCm39) |
S855P |
probably damaging |
Het |
Mgat4e |
A |
T |
1: 134,469,602 (GRCm39) |
N147K |
probably damaging |
Het |
Mlc1 |
A |
G |
15: 88,842,415 (GRCm39) |
L315P |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,076,292 (GRCm39) |
V322A |
probably benign |
Het |
Mroh7 |
T |
C |
4: 106,567,152 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
A |
10: 88,391,586 (GRCm39) |
K304* |
probably null |
Het |
Nlrp14 |
A |
C |
7: 106,785,790 (GRCm39) |
D622A |
possibly damaging |
Het |
Nlrp1b |
T |
A |
11: 71,108,103 (GRCm39) |
H466L |
probably benign |
Het |
Nlrp4d |
T |
A |
7: 10,112,336 (GRCm39) |
|
noncoding transcript |
Het |
Nrxn3 |
A |
G |
12: 89,227,130 (GRCm39) |
E628G |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,845,007 (GRCm39) |
S21P |
unknown |
Het |
Or2h2b-ps1 |
T |
C |
17: 37,480,934 (GRCm39) |
I202V |
probably benign |
Het |
Or2l13b |
T |
C |
16: 19,348,768 (GRCm39) |
T301A |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,423 (GRCm39) |
I126K |
possibly damaging |
Het |
Or52e8 |
G |
A |
7: 104,624,686 (GRCm39) |
P169S |
possibly damaging |
Het |
Or5k1 |
T |
A |
16: 58,617,805 (GRCm39) |
T135S |
probably benign |
Het |
Or6c66 |
T |
C |
10: 129,461,676 (GRCm39) |
T85A |
probably damaging |
Het |
Or8c11 |
T |
A |
9: 38,290,038 (GRCm39) |
V287E |
probably null |
Het |
Otogl |
T |
C |
10: 107,715,378 (GRCm39) |
S433G |
probably benign |
Het |
Pcdhb17 |
A |
T |
18: 37,618,212 (GRCm39) |
M1L |
possibly damaging |
Het |
Pde7b |
T |
A |
10: 20,600,480 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
T |
C |
4: 99,820,724 (GRCm39) |
V207A |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,791,661 (GRCm39) |
V1116E |
probably damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,879,360 (GRCm39) |
Y497F |
possibly damaging |
Het |
Pomgnt2 |
T |
C |
9: 121,812,013 (GRCm39) |
N256S |
probably benign |
Het |
Pot1a |
A |
T |
6: 25,746,020 (GRCm39) |
|
probably benign |
Het |
Prdm9 |
T |
C |
17: 15,764,585 (GRCm39) |
T732A |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
C |
6: 137,345,336 (GRCm39) |
V114A |
probably damaging |
Het |
Pyurf |
A |
G |
6: 57,668,933 (GRCm39) |
S20P |
unknown |
Het |
Rasgrf1 |
A |
G |
9: 89,858,805 (GRCm39) |
T488A |
probably benign |
Het |
Rassf8 |
A |
T |
6: 145,761,006 (GRCm39) |
K111* |
probably null |
Het |
Reps1 |
A |
T |
10: 17,983,436 (GRCm39) |
E426D |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,730,666 (GRCm39) |
K982R |
probably damaging |
Het |
Rps23 |
T |
C |
13: 91,071,871 (GRCm39) |
|
probably null |
Het |
Scamp4 |
T |
A |
10: 80,445,505 (GRCm39) |
V56E |
probably damaging |
Het |
Serpina1c |
C |
T |
12: 103,861,291 (GRCm39) |
V408I |
probably benign |
Het |
Sigirr |
A |
G |
7: 140,673,701 (GRCm39) |
W49R |
probably damaging |
Het |
Slc17a6 |
A |
T |
7: 51,308,489 (GRCm39) |
H271L |
possibly damaging |
Het |
Slc7a5 |
G |
T |
8: 122,611,861 (GRCm39) |
T389K |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,191,999 (GRCm39) |
H945L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,523,549 (GRCm39) |
S662P |
probably damaging |
Het |
Snta1 |
C |
A |
2: 154,218,938 (GRCm39) |
E466* |
probably null |
Het |
Sowaha |
A |
G |
11: 53,369,272 (GRCm39) |
L488P |
probably damaging |
Het |
Spata17 |
C |
A |
1: 186,926,208 (GRCm39) |
V41F |
probably damaging |
Het |
Spta1 |
T |
A |
1: 174,045,429 (GRCm39) |
|
probably null |
Het |
Srrm2 |
T |
A |
17: 24,034,362 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,985,992 (GRCm39) |
N388S |
probably benign |
Het |
Stmn3 |
T |
C |
2: 180,950,630 (GRCm39) |
K59E |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,096,276 (GRCm39) |
H1448R |
possibly damaging |
Het |
Sycp2 |
A |
T |
2: 178,000,017 (GRCm39) |
D986E |
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tbkbp1 |
G |
A |
11: 97,029,956 (GRCm39) |
S400L |
probably benign |
Het |
Tesc |
G |
T |
5: 118,194,531 (GRCm39) |
|
probably benign |
Het |
Tjp1 |
C |
T |
7: 64,993,475 (GRCm39) |
G33R |
probably damaging |
Het |
Tlr11 |
C |
A |
14: 50,600,346 (GRCm39) |
F777L |
probably benign |
Het |
Tmem156 |
A |
G |
5: 65,248,805 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
G |
11: 60,643,204 (GRCm39) |
|
probably benign |
Het |
Tpcn1 |
A |
G |
5: 120,694,584 (GRCm39) |
W162R |
probably damaging |
Het |
Tpd52l2 |
A |
T |
2: 181,157,005 (GRCm39) |
|
probably benign |
Het |
Trim80 |
G |
A |
11: 115,337,281 (GRCm39) |
G381D |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Vmn2r117 |
TC |
T |
17: 23,698,487 (GRCm39) |
|
probably null |
Het |
Vmn2r56 |
T |
A |
7: 12,449,462 (GRCm39) |
I259F |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,693,077 (GRCm39) |
T508A |
probably benign |
Het |
Wdr73 |
A |
G |
7: 80,541,456 (GRCm39) |
V362A |
probably damaging |
Het |
Zdhhc21 |
G |
T |
4: 82,738,568 (GRCm39) |
T207K |
possibly damaging |
Het |
Zfp120 |
T |
A |
2: 149,959,872 (GRCm39) |
Q150L |
probably damaging |
Het |
Zfp212 |
C |
A |
6: 47,908,433 (GRCm39) |
Q471K |
possibly damaging |
Het |
Zfp804b |
C |
T |
5: 6,820,540 (GRCm39) |
G841D |
possibly damaging |
Het |
Znfx1 |
A |
T |
2: 166,878,724 (GRCm39) |
M1884K |
probably damaging |
Het |
Znfx1 |
G |
T |
2: 166,879,402 (GRCm39) |
A1658D |
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 |
45,913,486 (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 |
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 |
|