Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,553,223 (GRCm39) |
N178I |
probably damaging |
Het |
Acvr2b |
A |
G |
9: 119,261,874 (GRCm39) |
R437G |
probably damaging |
Het |
Adamtsl3 |
C |
A |
7: 82,227,802 (GRCm39) |
A1329E |
probably damaging |
Het |
Adgrl2 |
T |
C |
3: 148,596,124 (GRCm39) |
I71V |
probably damaging |
Het |
Adra1a |
A |
T |
14: 66,964,981 (GRCm39) |
I324F |
possibly damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Ampd1 |
G |
T |
3: 103,002,194 (GRCm39) |
|
probably null |
Het |
Ankrd16 |
T |
A |
2: 11,788,506 (GRCm39) |
D211E |
probably damaging |
Het |
Aopep |
T |
A |
13: 63,357,963 (GRCm39) |
C656S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Apc |
C |
A |
18: 34,445,098 (GRCm39) |
Q665K |
possibly damaging |
Het |
Arap2 |
T |
C |
5: 62,835,301 (GRCm39) |
N747S |
probably damaging |
Het |
Arsk |
A |
T |
13: 76,239,931 (GRCm39) |
C47* |
probably null |
Het |
Atp8b5 |
T |
A |
4: 43,370,726 (GRCm39) |
F1001I |
probably benign |
Het |
Bap1 |
T |
A |
14: 30,980,288 (GRCm39) |
Y645* |
probably null |
Het |
Brca2 |
A |
G |
5: 150,480,594 (GRCm39) |
Y2760C |
probably damaging |
Het |
Cad |
T |
A |
5: 31,215,416 (GRCm39) |
F76I |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccdc27 |
TTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTC |
4: 154,120,763 (GRCm39) |
|
probably benign |
Het |
Cdkn2c |
A |
C |
4: 109,522,260 (GRCm39) |
N28K |
probably null |
Het |
Celsr1 |
T |
A |
15: 85,847,424 (GRCm39) |
I1438F |
probably benign |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Cldn1 |
G |
C |
16: 26,190,300 (GRCm39) |
A26G |
probably damaging |
Het |
Col20a1 |
T |
A |
2: 180,634,366 (GRCm39) |
F110L |
probably damaging |
Het |
Creg2 |
T |
C |
1: 39,664,146 (GRCm39) |
N204S |
probably benign |
Het |
Cx3cl1 |
C |
A |
8: 95,506,201 (GRCm39) |
Q69K |
probably benign |
Het |
Cyfip2 |
T |
C |
11: 46,176,958 (GRCm39) |
E74G |
possibly damaging |
Het |
Cyp2g1 |
A |
T |
7: 26,520,135 (GRCm39) |
I456F |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,877,345 (GRCm39) |
E528G |
possibly damaging |
Het |
Dapk1 |
T |
A |
13: 60,909,481 (GRCm39) |
W1365R |
possibly damaging |
Het |
Dbt |
T |
A |
3: 116,332,773 (GRCm39) |
D16E |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,148,125 (GRCm39) |
L1469* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,566,982 (GRCm39) |
T2415S |
possibly damaging |
Het |
Dnmbp |
A |
G |
19: 43,842,750 (GRCm39) |
L1210S |
probably damaging |
Het |
Dpyd |
T |
C |
3: 118,468,217 (GRCm39) |
V77A |
probably benign |
Het |
Eps15l1 |
A |
T |
8: 73,140,712 (GRCm39) |
V260D |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,241,198 (GRCm39) |
V573A |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,710,202 (GRCm39) |
S625T |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,831,557 (GRCm39) |
|
probably benign |
Het |
Gabra4 |
G |
T |
5: 71,798,567 (GRCm39) |
D137E |
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gm43302 |
T |
C |
5: 105,422,610 (GRCm39) |
D474G |
probably damaging |
Het |
Golim4 |
A |
T |
3: 75,815,456 (GRCm39) |
V116D |
probably damaging |
Het |
Gpr19 |
T |
C |
6: 134,847,405 (GRCm39) |
M1V |
probably null |
Het |
Hnf4a |
T |
A |
2: 163,389,338 (GRCm39) |
N29K |
probably benign |
Het |
Htt |
A |
G |
5: 35,034,453 (GRCm39) |
R1975G |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Il4i1 |
G |
A |
7: 44,489,494 (GRCm39) |
V420M |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,717,879 (GRCm39) |
|
probably null |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Jmjd4 |
A |
T |
11: 59,345,781 (GRCm39) |
H287L |
probably damaging |
Het |
Kcnj13 |
A |
G |
1: 87,314,256 (GRCm39) |
V322A |
probably benign |
Het |
Kdm5d |
T |
C |
Y: 941,483 (GRCm39) |
L1228P |
probably benign |
Het |
Klra3 |
A |
G |
6: 130,312,738 (GRCm39) |
S9P |
probably benign |
Het |
Ldhd |
C |
T |
8: 112,355,169 (GRCm39) |
|
probably null |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lmo7 |
A |
T |
14: 102,137,674 (GRCm39) |
D670V |
probably damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Lrp5 |
T |
C |
19: 3,672,708 (GRCm39) |
T534A |
possibly damaging |
Het |
Lrrc24 |
A |
T |
15: 76,599,781 (GRCm39) |
F453I |
possibly damaging |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Mcpt8 |
T |
C |
14: 56,319,740 (GRCm39) |
I237V |
probably damaging |
Het |
Med4 |
A |
G |
14: 73,755,436 (GRCm39) |
N248S |
possibly damaging |
Het |
Mest |
C |
T |
6: 30,745,884 (GRCm39) |
L269F |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,739,695 (GRCm39) |
|
probably null |
Het |
Mki67 |
T |
A |
7: 135,305,970 (GRCm39) |
|
probably null |
Het |
Mnx1 |
T |
A |
5: 29,679,187 (GRCm39) |
S299C |
unknown |
Het |
Nbr1 |
T |
A |
11: 101,457,017 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
T |
G |
9: 26,994,642 (GRCm39) |
V1174G |
probably damaging |
Het |
Nyap1 |
A |
C |
5: 137,731,943 (GRCm39) |
|
probably null |
Het |
Olfml3 |
T |
A |
3: 103,643,185 (GRCm39) |
M399L |
probably benign |
Het |
Oosp1 |
T |
C |
19: 11,668,314 (GRCm39) |
D23G |
probably damaging |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or6c205 |
T |
C |
10: 129,086,943 (GRCm39) |
F180S |
probably benign |
Het |
Osbpl6 |
T |
A |
2: 76,416,558 (GRCm39) |
I546K |
probably damaging |
Het |
Pcdhb14 |
C |
A |
18: 37,580,923 (GRCm39) |
Q10K |
probably benign |
Het |
Pcx |
T |
C |
19: 4,652,579 (GRCm39) |
F189L |
probably benign |
Het |
Pde6b |
A |
G |
5: 108,576,069 (GRCm39) |
D718G |
probably damaging |
Het |
Pklr |
C |
A |
3: 89,049,967 (GRCm39) |
P314Q |
probably damaging |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Plekha6 |
C |
A |
1: 133,207,103 (GRCm39) |
|
probably null |
Het |
Plekho1 |
A |
G |
3: 95,896,429 (GRCm39) |
S347P |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,327,058 (GRCm39) |
D331N |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prkra |
A |
T |
2: 76,477,480 (GRCm39) |
I75K |
probably damaging |
Het |
Ptpn11 |
G |
A |
5: 121,310,089 (GRCm39) |
A31V |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,468,124 (GRCm39) |
|
probably null |
Het |
Rbm12 |
A |
T |
2: 155,937,430 (GRCm39) |
C947* |
probably null |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Sarm1 |
A |
T |
11: 78,366,133 (GRCm39) |
C649S |
probably benign |
Het |
Septin12 |
T |
A |
16: 4,809,643 (GRCm39) |
Q223L |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Slc22a21 |
A |
T |
11: 53,870,559 (GRCm39) |
L42Q |
probably damaging |
Het |
Slc44a1 |
GCCC |
GCCCCCCC |
4: 53,563,246 (GRCm39) |
|
probably null |
Het |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Sort1 |
T |
A |
3: 108,259,002 (GRCm39) |
F678Y |
probably benign |
Het |
Spag6 |
T |
A |
2: 18,737,908 (GRCm39) |
C259* |
probably null |
Het |
Spata31e2 |
T |
C |
1: 26,724,935 (GRCm39) |
R82G |
probably benign |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Stk24 |
A |
T |
14: 121,539,623 (GRCm39) |
I191N |
probably damaging |
Het |
Tacc1 |
A |
T |
8: 25,654,509 (GRCm39) |
N271K |
probably damaging |
Het |
Tacc2 |
T |
A |
7: 130,223,587 (GRCm39) |
S91T |
possibly damaging |
Het |
Tacr3 |
T |
C |
3: 134,637,941 (GRCm39) |
V366A |
probably benign |
Het |
Tasor |
A |
G |
14: 27,198,571 (GRCm39) |
N1301S |
possibly damaging |
Het |
Tbccd1 |
A |
G |
16: 22,660,739 (GRCm39) |
S26P |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tor1aip2 |
A |
G |
1: 155,941,095 (GRCm39) |
Y467C |
probably damaging |
Het |
Ttc9b |
T |
A |
7: 27,353,774 (GRCm39) |
|
probably null |
Het |
Tti1 |
T |
C |
2: 157,842,663 (GRCm39) |
R789G |
probably benign |
Het |
Ttn |
A |
T |
2: 76,662,561 (GRCm39) |
|
probably null |
Het |
Txk |
T |
A |
5: 72,853,922 (GRCm39) |
T472S |
probably damaging |
Het |
Ube3d |
A |
T |
9: 86,254,540 (GRCm39) |
|
probably null |
Het |
Vav2 |
C |
A |
2: 27,189,408 (GRCm39) |
R176L |
possibly damaging |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Wdr27 |
T |
A |
17: 15,148,594 (GRCm39) |
D133V |
probably damaging |
Het |
Zc3h7a |
A |
T |
16: 10,968,469 (GRCm39) |
Y503* |
probably null |
Het |
Zdhhc13 |
T |
A |
7: 48,474,392 (GRCm39) |
L548Q |
possibly damaging |
Het |
Zfp467 |
A |
C |
6: 48,419,595 (GRCm39) |
S38A |
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 |
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 |
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 |
|