Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
C |
3: 59,840,161 (GRCm39) |
T78P |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,800,291 (GRCm39) |
K497R |
probably damaging |
Het |
Aldh1a3 |
C |
T |
7: 66,068,927 (GRCm39) |
R19Q |
possibly damaging |
Het |
Bmp2k |
A |
G |
5: 97,234,944 (GRCm39) |
|
probably benign |
Het |
Ccni |
A |
T |
5: 93,335,553 (GRCm39) |
L195Q |
possibly damaging |
Het |
Cdkl4 |
C |
A |
17: 80,832,764 (GRCm39) |
G327* |
probably null |
Het |
Cdsn |
T |
C |
17: 35,866,326 (GRCm39) |
V285A |
possibly damaging |
Het |
Cfap20dc |
A |
G |
14: 8,518,736 (GRCm38) |
V240A |
probably benign |
Het |
Chtf18 |
T |
C |
17: 25,943,540 (GRCm39) |
E352G |
possibly damaging |
Het |
Clasp2 |
T |
A |
9: 113,732,984 (GRCm39) |
I961N |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,949,752 (GRCm39) |
Q128R |
probably damaging |
Het |
Cttnbp2 |
C |
A |
6: 18,406,525 (GRCm39) |
Q1055H |
possibly damaging |
Het |
Cyld |
T |
G |
8: 89,433,860 (GRCm39) |
F216L |
probably benign |
Het |
Cyp3a41a |
A |
G |
5: 145,656,858 (GRCm39) |
M1T |
probably null |
Het |
Disp3 |
C |
T |
4: 148,328,673 (GRCm39) |
R1097H |
possibly damaging |
Het |
Dmap1 |
T |
C |
4: 117,538,233 (GRCm39) |
D67G |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,875,959 (GRCm39) |
F529L |
probably benign |
Het |
Ergic3 |
T |
C |
2: 155,859,638 (GRCm39) |
|
probably null |
Het |
Fkbp14 |
A |
G |
6: 54,569,943 (GRCm39) |
I29T |
probably benign |
Het |
Gm4845 |
T |
A |
1: 141,184,623 (GRCm39) |
|
noncoding transcript |
Het |
Gm7135 |
A |
T |
1: 97,281,801 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,481 (GRCm39) |
I57F |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,809,280 (GRCm39) |
V1722A |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,283,037 (GRCm39) |
D1971G |
possibly damaging |
Het |
Il21 |
C |
A |
3: 37,286,653 (GRCm39) |
S21I |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,614,244 (GRCm39) |
I398N |
probably damaging |
Het |
Kansl1 |
A |
T |
11: 104,226,390 (GRCm39) |
S922R |
probably damaging |
Het |
Krt27 |
G |
A |
11: 99,237,722 (GRCm39) |
Q339* |
probably null |
Het |
Lama1 |
C |
A |
17: 68,045,829 (GRCm39) |
L245I |
possibly damaging |
Het |
Lmo2 |
T |
A |
2: 103,806,488 (GRCm39) |
C60* |
probably null |
Het |
Med16 |
A |
G |
10: 79,738,839 (GRCm39) |
S316P |
possibly damaging |
Het |
Mia3 |
T |
C |
1: 183,111,970 (GRCm39) |
N529S |
probably benign |
Het |
Msi2 |
T |
C |
11: 88,285,481 (GRCm39) |
K188E |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,209,128 (GRCm39) |
K1870R |
probably damaging |
Het |
Nhlrc1 |
A |
G |
13: 47,167,216 (GRCm39) |
V347A |
probably benign |
Het |
Nol6 |
C |
T |
4: 41,120,167 (GRCm39) |
R487H |
probably benign |
Het |
Or4c117 |
T |
C |
2: 88,955,682 (GRCm39) |
Y131C |
probably damaging |
Het |
Or4k41 |
T |
C |
2: 111,280,028 (GRCm39) |
I181T |
probably benign |
Het |
Or52h1 |
A |
T |
7: 103,828,736 (GRCm39) |
V293D |
probably damaging |
Het |
Or5d18 |
T |
C |
2: 87,865,005 (GRCm39) |
I159M |
probably benign |
Het |
Or6c205 |
T |
C |
10: 129,087,141 (GRCm39) |
I246T |
probably damaging |
Het |
Ptprv |
A |
G |
1: 135,046,586 (GRCm39) |
|
noncoding transcript |
Het |
Pus7l |
A |
G |
15: 94,427,369 (GRCm39) |
V471A |
possibly damaging |
Het |
Rab11fip4 |
A |
G |
11: 79,510,497 (GRCm39) |
R68G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,277,428 (GRCm39) |
D264G |
possibly damaging |
Het |
Reln |
A |
G |
5: 22,165,424 (GRCm39) |
S2045P |
probably damaging |
Het |
Rgs22 |
A |
C |
15: 36,055,022 (GRCm39) |
Y593* |
probably null |
Het |
Ror2 |
C |
T |
13: 53,285,954 (GRCm39) |
D87N |
probably damaging |
Het |
Rps6ka4 |
A |
T |
19: 6,817,678 (GRCm39) |
|
probably null |
Het |
Rttn |
T |
A |
18: 89,082,209 (GRCm39) |
|
probably null |
Het |
Runx3 |
A |
G |
4: 134,898,446 (GRCm39) |
T206A |
probably benign |
Het |
Setx |
A |
G |
2: 29,054,562 (GRCm39) |
E2158G |
probably damaging |
Het |
Siglece |
C |
T |
7: 43,308,396 (GRCm39) |
|
probably null |
Het |
Slco1a8 |
T |
C |
6: 141,926,599 (GRCm39) |
S576G |
probably benign |
Het |
Snx1 |
A |
T |
9: 66,012,187 (GRCm39) |
L96* |
probably null |
Het |
Srrm1 |
A |
G |
4: 135,074,031 (GRCm39) |
|
probably benign |
Het |
Stk39 |
A |
T |
2: 68,051,336 (GRCm39) |
|
probably benign |
Het |
Sun3 |
G |
A |
11: 8,988,311 (GRCm39) |
R4* |
probably null |
Het |
Svil |
A |
G |
18: 5,054,025 (GRCm39) |
K347E |
possibly damaging |
Het |
Sybu |
T |
A |
15: 44,541,063 (GRCm39) |
E333V |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,192,520 (GRCm39) |
|
probably benign |
Het |
Tfip11 |
G |
T |
5: 112,483,613 (GRCm39) |
|
probably benign |
Het |
Tmc1 |
A |
C |
19: 20,884,319 (GRCm39) |
D40E |
probably damaging |
Het |
Twf2 |
G |
T |
9: 106,089,539 (GRCm39) |
G121W |
probably damaging |
Het |
Vpreb3 |
A |
G |
10: 75,775,636 (GRCm39) |
V50A |
probably damaging |
Het |
Vps8 |
T |
A |
16: 21,285,219 (GRCm39) |
L400Q |
probably damaging |
Het |
Xylt1 |
A |
T |
7: 117,266,565 (GRCm39) |
Y861F |
probably damaging |
Het |
Zfp608 |
T |
G |
18: 55,022,962 (GRCm39) |
T1485P |
probably damaging |
Het |
Zfp619 |
T |
G |
7: 39,186,504 (GRCm39) |
S845A |
possibly damaging |
Het |
Zscan4d |
A |
T |
7: 10,899,274 (GRCm39) |
M1K |
probably null |
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 |
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 |
|