Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acads |
A |
T |
5: 115,250,845 (GRCm39) |
C151S |
probably damaging |
Het |
Actr8 |
T |
C |
14: 29,708,301 (GRCm39) |
I193T |
probably benign |
Het |
Btbd2 |
T |
C |
10: 80,480,103 (GRCm39) |
N419S |
probably benign |
Het |
Cacna2d1 |
T |
A |
5: 16,561,831 (GRCm39) |
W821R |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,626,646 (GRCm39) |
Y214C |
probably benign |
Het |
Calu |
T |
A |
6: 29,366,162 (GRCm39) |
L180Q |
probably damaging |
Het |
Corin |
C |
T |
5: 72,497,280 (GRCm39) |
V615I |
probably damaging |
Het |
Cyp8b1 |
A |
T |
9: 121,744,983 (GRCm39) |
D116E |
probably benign |
Het |
D630036H23Rik |
C |
A |
12: 36,431,711 (GRCm39) |
A96S |
unknown |
Het |
Ddx24 |
A |
T |
12: 103,377,555 (GRCm39) |
Y717N |
probably damaging |
Het |
Dmap1 |
G |
T |
4: 117,533,308 (GRCm39) |
Q249K |
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,900,508 (GRCm39) |
W3922R |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,517,773 (GRCm39) |
F2036L |
probably benign |
Het |
Dnah14 |
T |
C |
1: 181,625,311 (GRCm39) |
I4064T |
probably benign |
Het |
Dock9 |
A |
C |
14: 121,818,844 (GRCm39) |
V1546G |
probably damaging |
Het |
Eif1ad4 |
A |
T |
12: 87,862,249 (GRCm39) |
Q37L |
possibly damaging |
Het |
Eif3a |
A |
T |
19: 60,755,006 (GRCm39) |
S1059T |
unknown |
Het |
Ep300 |
A |
G |
15: 81,521,026 (GRCm39) |
E1262G |
unknown |
Het |
Evl |
T |
A |
12: 108,652,716 (GRCm39) |
I387N |
probably damaging |
Het |
Fat2 |
A |
C |
11: 55,200,752 (GRCm39) |
V774G |
probably damaging |
Het |
Fez1 |
T |
A |
9: 36,755,093 (GRCm39) |
Y31N |
probably benign |
Het |
Fkbp10 |
A |
G |
11: 100,313,960 (GRCm39) |
I435V |
probably damaging |
Het |
Flnb |
A |
G |
14: 7,929,004 (GRCm38) |
D1911G |
probably benign |
Het |
Fnbp1 |
T |
C |
2: 30,973,038 (GRCm39) |
Y154C |
probably benign |
Het |
Fndc10 |
T |
C |
4: 155,779,496 (GRCm39) |
I180T |
possibly damaging |
Het |
Frmd4a |
G |
A |
2: 4,609,026 (GRCm39) |
V965I |
possibly damaging |
Het |
Gabrr2 |
A |
G |
4: 33,071,352 (GRCm39) |
H64R |
possibly damaging |
Het |
Glis3 |
T |
C |
19: 28,508,403 (GRCm39) |
D527G |
probably damaging |
Het |
H2-Ob |
T |
A |
17: 34,459,989 (GRCm39) |
F33L |
probably damaging |
Het |
Hbb-bh1 |
C |
T |
7: 103,492,239 (GRCm39) |
E27K |
probably benign |
Het |
Ifnb1 |
T |
A |
4: 88,440,915 (GRCm39) |
T33S |
probably benign |
Het |
Igkv4-80 |
T |
A |
6: 68,993,766 (GRCm39) |
T42S |
probably damaging |
Het |
Irs2 |
C |
T |
8: 11,057,334 (GRCm39) |
G366D |
probably damaging |
Het |
Kcnk2 |
CAAA |
CAA |
1: 188,988,891 (GRCm39) |
|
probably null |
Het |
Krtap5-3 |
T |
A |
7: 141,756,068 (GRCm39) |
C302S |
unknown |
Het |
Lgi1 |
A |
G |
19: 38,294,757 (GRCm39) |
K510E |
probably benign |
Het |
Lgi2 |
T |
A |
5: 52,695,936 (GRCm39) |
D341V |
probably benign |
Het |
Lin7c |
T |
C |
2: 109,724,813 (GRCm39) |
I14T |
probably benign |
Het |
Lrrc19 |
A |
T |
4: 94,531,573 (GRCm39) |
M13K |
probably benign |
Het |
Lrrc69 |
T |
C |
4: 14,666,012 (GRCm39) |
I315M |
probably benign |
Het |
Mtcl3 |
G |
A |
10: 29,072,969 (GRCm39) |
D754N |
probably damaging |
Het |
Myo5c |
A |
T |
9: 75,204,770 (GRCm39) |
D1541V |
probably damaging |
Het |
Mypn |
T |
G |
10: 63,003,019 (GRCm39) |
M373L |
probably benign |
Het |
Nckipsd |
C |
A |
9: 108,689,837 (GRCm39) |
H333N |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,157,401 (GRCm39) |
L428Q |
probably null |
Het |
Or13a20 |
T |
C |
7: 140,231,904 (GRCm39) |
L4S |
probably benign |
Het |
Or2b28 |
C |
A |
13: 21,531,587 (GRCm39) |
T163K |
probably damaging |
Het |
Or5an11 |
T |
C |
19: 12,245,735 (GRCm39) |
I47T |
possibly damaging |
Het |
Papln |
A |
T |
12: 83,838,618 (GRCm39) |
Q1249L |
probably benign |
Het |
Plxna2 |
G |
T |
1: 194,327,202 (GRCm39) |
G379C |
probably damaging |
Het |
Pofut2 |
T |
C |
10: 77,095,260 (GRCm39) |
I35T |
probably benign |
Het |
Pros1 |
A |
G |
16: 62,744,887 (GRCm39) |
T501A |
possibly damaging |
Het |
Rapgef1 |
T |
C |
2: 29,625,821 (GRCm39) |
S1042P |
possibly damaging |
Het |
Rps6kb1 |
C |
T |
11: 86,408,443 (GRCm39) |
E185K |
probably damaging |
Het |
Slc13a2 |
A |
T |
11: 78,294,233 (GRCm39) |
L216Q |
probably damaging |
Het |
Slc22a14 |
T |
C |
9: 119,009,615 (GRCm39) |
Y160C |
probably damaging |
Het |
Slc22a4 |
T |
A |
11: 53,879,773 (GRCm39) |
I429F |
possibly damaging |
Het |
Slc26a3 |
A |
G |
12: 31,511,785 (GRCm39) |
K457E |
probably damaging |
Het |
Slc47a2 |
T |
C |
11: 61,227,060 (GRCm39) |
I169M |
possibly damaging |
Het |
Slco1a1 |
C |
T |
6: 141,854,672 (GRCm39) |
V660I |
probably benign |
Het |
Smyd1 |
A |
G |
6: 71,202,450 (GRCm39) |
Y252H |
probably damaging |
Het |
Spp2 |
A |
T |
1: 88,334,695 (GRCm39) |
|
probably benign |
Het |
Stra8 |
T |
A |
6: 34,911,121 (GRCm39) |
W250R |
probably damaging |
Het |
Syne1 |
A |
C |
10: 5,170,359 (GRCm39) |
L5183R |
probably damaging |
Het |
Tdrd9 |
T |
C |
12: 112,012,684 (GRCm39) |
S1203P |
probably damaging |
Het |
Th |
C |
A |
7: 142,453,620 (GRCm39) |
E27* |
probably null |
Het |
Thada |
C |
A |
17: 84,736,619 (GRCm39) |
L887F |
probably damaging |
Het |
Timm23 |
T |
C |
14: 31,902,586 (GRCm39) |
T186A |
probably benign |
Het |
Tmem132b |
A |
T |
5: 125,860,420 (GRCm39) |
E555V |
probably damaging |
Het |
Tnik |
A |
T |
3: 28,649,093 (GRCm39) |
Q457L |
unknown |
Het |
Uba7 |
C |
A |
9: 107,861,037 (GRCm39) |
H942Q |
probably benign |
Het |
Upf2 |
T |
C |
2: 5,966,078 (GRCm39) |
S233P |
unknown |
Het |
Urm1 |
T |
A |
2: 29,732,760 (GRCm39) |
N72K |
probably damaging |
Het |
Usp10 |
T |
C |
8: 120,675,504 (GRCm39) |
S508P |
possibly damaging |
Het |
Usp37 |
G |
A |
1: 74,499,081 (GRCm39) |
P632S |
probably damaging |
Het |
Wdr77 |
T |
A |
3: 105,872,404 (GRCm39) |
N209K |
probably benign |
Het |
Zbtb24 |
C |
T |
10: 41,327,429 (GRCm39) |
T105M |
probably benign |
Het |
Zfp341 |
T |
A |
2: 154,485,763 (GRCm39) |
I671N |
probably damaging |
Het |
Zfp414 |
A |
G |
17: 33,848,984 (GRCm39) |
T73A |
probably benign |
Het |
Zfp574 |
A |
T |
7: 24,781,404 (GRCm39) |
I809F |
possibly damaging |
Het |
Zfp62 |
T |
C |
11: 49,108,108 (GRCm39) |
I733T |
probably damaging |
Het |
Zfp719 |
A |
G |
7: 43,239,581 (GRCm39) |
I390V |
possibly damaging |
Het |
|
Other mutations in Otogl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
H8562:Otogl
|
UTSW |
10 |
107,746,817 (GRCm39) |
missense |
probably benign |
0.00 |
R0084:Otogl
|
UTSW |
10 |
107,737,202 (GRCm39) |
missense |
probably damaging |
0.96 |
R0164:Otogl
|
UTSW |
10 |
107,710,391 (GRCm39) |
missense |
probably damaging |
0.97 |
R0164:Otogl
|
UTSW |
10 |
107,710,391 (GRCm39) |
missense |
probably damaging |
0.97 |
R0238:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0238:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0294:Otogl
|
UTSW |
10 |
107,613,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Otogl
|
UTSW |
10 |
107,606,511 (GRCm39) |
splice site |
probably benign |
|
R0442:Otogl
|
UTSW |
10 |
107,712,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Otogl
|
UTSW |
10 |
107,639,466 (GRCm39) |
missense |
probably benign |
0.02 |
R0507:Otogl
|
UTSW |
10 |
107,702,601 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0573:Otogl
|
UTSW |
10 |
107,616,849 (GRCm39) |
missense |
probably benign |
0.00 |
R0581:Otogl
|
UTSW |
10 |
107,624,901 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0613:Otogl
|
UTSW |
10 |
107,652,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R0614:Otogl
|
UTSW |
10 |
107,634,216 (GRCm39) |
missense |
probably benign |
0.14 |
R0742:Otogl
|
UTSW |
10 |
107,702,601 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0846:Otogl
|
UTSW |
10 |
107,608,157 (GRCm39) |
missense |
probably benign |
0.40 |
R1146:Otogl
|
UTSW |
10 |
107,722,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Otogl
|
UTSW |
10 |
107,722,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Otogl
|
UTSW |
10 |
107,615,113 (GRCm39) |
missense |
probably benign |
0.02 |
R1457:Otogl
|
UTSW |
10 |
107,714,013 (GRCm39) |
splice site |
probably null |
|
R1526:Otogl
|
UTSW |
10 |
107,705,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Otogl
|
UTSW |
10 |
107,634,218 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1664:Otogl
|
UTSW |
10 |
107,642,437 (GRCm39) |
missense |
probably benign |
0.00 |
R1667:Otogl
|
UTSW |
10 |
107,649,826 (GRCm39) |
nonsense |
probably null |
|
R1695:Otogl
|
UTSW |
10 |
107,649,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R1731:Otogl
|
UTSW |
10 |
107,652,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1733:Otogl
|
UTSW |
10 |
107,619,573 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1764:Otogl
|
UTSW |
10 |
107,735,322 (GRCm39) |
nonsense |
probably null |
|
R1824:Otogl
|
UTSW |
10 |
107,615,692 (GRCm39) |
missense |
probably benign |
|
R1850:Otogl
|
UTSW |
10 |
107,713,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Otogl
|
UTSW |
10 |
107,690,125 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1875:Otogl
|
UTSW |
10 |
107,735,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Otogl
|
UTSW |
10 |
107,613,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R1986:Otogl
|
UTSW |
10 |
107,630,051 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2072:Otogl
|
UTSW |
10 |
107,616,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Otogl
|
UTSW |
10 |
107,694,779 (GRCm39) |
missense |
probably benign |
0.06 |
R2219:Otogl
|
UTSW |
10 |
107,692,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Otogl
|
UTSW |
10 |
107,710,361 (GRCm39) |
missense |
probably damaging |
0.99 |
R2883:Otogl
|
UTSW |
10 |
107,604,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Otogl
|
UTSW |
10 |
107,655,865 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3620:Otogl
|
UTSW |
10 |
107,710,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R3621:Otogl
|
UTSW |
10 |
107,710,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R3735:Otogl
|
UTSW |
10 |
107,735,390 (GRCm39) |
nonsense |
probably null |
|
R3812:Otogl
|
UTSW |
10 |
107,735,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R3880:Otogl
|
UTSW |
10 |
107,663,565 (GRCm39) |
missense |
probably damaging |
0.96 |
R3958:Otogl
|
UTSW |
10 |
107,657,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Otogl
|
UTSW |
10 |
107,626,510 (GRCm39) |
missense |
probably benign |
0.02 |
R4064:Otogl
|
UTSW |
10 |
107,626,510 (GRCm39) |
missense |
probably benign |
0.02 |
R4108:Otogl
|
UTSW |
10 |
107,607,105 (GRCm39) |
missense |
probably benign |
0.01 |
R4352:Otogl
|
UTSW |
10 |
107,705,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4526:Otogl
|
UTSW |
10 |
107,722,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Otogl
|
UTSW |
10 |
107,727,985 (GRCm39) |
nonsense |
probably null |
|
R4703:Otogl
|
UTSW |
10 |
107,657,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4741:Otogl
|
UTSW |
10 |
107,615,121 (GRCm39) |
missense |
probably benign |
0.00 |
R4790:Otogl
|
UTSW |
10 |
107,657,894 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4801:Otogl
|
UTSW |
10 |
107,737,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Otogl
|
UTSW |
10 |
107,737,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Otogl
|
UTSW |
10 |
107,715,378 (GRCm39) |
missense |
probably benign |
0.05 |
R4913:Otogl
|
UTSW |
10 |
107,712,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R5238:Otogl
|
UTSW |
10 |
107,604,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R5261:Otogl
|
UTSW |
10 |
107,613,453 (GRCm39) |
missense |
probably benign |
0.16 |
R5387:Otogl
|
UTSW |
10 |
107,616,794 (GRCm39) |
missense |
probably benign |
0.03 |
R5395:Otogl
|
UTSW |
10 |
107,652,999 (GRCm39) |
missense |
probably benign |
0.39 |
R5403:Otogl
|
UTSW |
10 |
107,644,617 (GRCm39) |
missense |
probably benign |
0.08 |
R5482:Otogl
|
UTSW |
10 |
107,657,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R5547:Otogl
|
UTSW |
10 |
107,617,909 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5611:Otogl
|
UTSW |
10 |
107,622,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Otogl
|
UTSW |
10 |
107,722,413 (GRCm39) |
missense |
probably benign |
0.44 |
R5690:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5711:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5731:Otogl
|
UTSW |
10 |
107,717,325 (GRCm39) |
missense |
probably damaging |
0.98 |
R5743:Otogl
|
UTSW |
10 |
107,692,862 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5782:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5820:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5897:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6004:Otogl
|
UTSW |
10 |
107,715,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6146:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6147:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6149:Otogl
|
UTSW |
10 |
107,717,314 (GRCm39) |
missense |
probably benign |
0.36 |
R6226:Otogl
|
UTSW |
10 |
107,607,067 (GRCm39) |
nonsense |
probably null |
|
R6283:Otogl
|
UTSW |
10 |
107,626,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R6414:Otogl
|
UTSW |
10 |
107,617,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Otogl
|
UTSW |
10 |
107,657,895 (GRCm39) |
splice site |
probably null |
|
R6634:Otogl
|
UTSW |
10 |
107,698,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R6727:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6755:Otogl
|
UTSW |
10 |
107,689,164 (GRCm39) |
nonsense |
probably null |
|
R6795:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6797:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6864:Otogl
|
UTSW |
10 |
107,663,667 (GRCm39) |
missense |
probably damaging |
0.96 |
R6924:Otogl
|
UTSW |
10 |
107,644,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Otogl
|
UTSW |
10 |
107,649,911 (GRCm39) |
missense |
probably benign |
0.01 |
R7000:Otogl
|
UTSW |
10 |
107,615,692 (GRCm39) |
missense |
probably benign |
|
R7075:Otogl
|
UTSW |
10 |
107,614,790 (GRCm39) |
missense |
probably benign |
0.16 |
R7122:Otogl
|
UTSW |
10 |
107,702,515 (GRCm39) |
missense |
probably benign |
0.08 |
R7176:Otogl
|
UTSW |
10 |
107,614,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Otogl
|
UTSW |
10 |
107,599,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Otogl
|
UTSW |
10 |
107,710,394 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7252:Otogl
|
UTSW |
10 |
107,657,804 (GRCm39) |
missense |
probably benign |
0.06 |
R7286:Otogl
|
UTSW |
10 |
107,606,471 (GRCm39) |
missense |
probably benign |
0.00 |
R7373:Otogl
|
UTSW |
10 |
107,737,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Otogl
|
UTSW |
10 |
107,639,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Otogl
|
UTSW |
10 |
107,657,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Otogl
|
UTSW |
10 |
107,722,843 (GRCm39) |
missense |
probably benign |
0.06 |
R7659:Otogl
|
UTSW |
10 |
107,612,981 (GRCm39) |
missense |
probably benign |
0.19 |
R7732:Otogl
|
UTSW |
10 |
107,642,525 (GRCm39) |
missense |
probably benign |
0.01 |
R7754:Otogl
|
UTSW |
10 |
107,705,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Otogl
|
UTSW |
10 |
107,712,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Otogl
|
UTSW |
10 |
107,722,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R7864:Otogl
|
UTSW |
10 |
107,705,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Otogl
|
UTSW |
10 |
107,612,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7941:Otogl
|
UTSW |
10 |
107,642,663 (GRCm39) |
splice site |
probably null |
|
R7956:Otogl
|
UTSW |
10 |
107,713,887 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7988:Otogl
|
UTSW |
10 |
107,731,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Otogl
|
UTSW |
10 |
107,644,476 (GRCm39) |
missense |
probably benign |
0.00 |
R8058:Otogl
|
UTSW |
10 |
107,598,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R8127:Otogl
|
UTSW |
10 |
107,731,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Otogl
|
UTSW |
10 |
107,642,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Otogl
|
UTSW |
10 |
107,613,461 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8319:Otogl
|
UTSW |
10 |
107,689,127 (GRCm39) |
critical splice donor site |
probably null |
|
R8339:Otogl
|
UTSW |
10 |
107,625,397 (GRCm39) |
missense |
probably benign |
0.34 |
R8339:Otogl
|
UTSW |
10 |
107,625,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R8394:Otogl
|
UTSW |
10 |
107,722,326 (GRCm39) |
critical splice donor site |
probably null |
|
R8428:Otogl
|
UTSW |
10 |
107,634,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Otogl
|
UTSW |
10 |
107,692,975 (GRCm39) |
missense |
probably benign |
0.01 |
R8501:Otogl
|
UTSW |
10 |
107,626,421 (GRCm39) |
missense |
probably benign |
|
R8503:Otogl
|
UTSW |
10 |
107,727,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Otogl
|
UTSW |
10 |
107,747,936 (GRCm39) |
critical splice donor site |
probably null |
|
R9025:Otogl
|
UTSW |
10 |
107,613,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R9090:Otogl
|
UTSW |
10 |
107,652,974 (GRCm39) |
missense |
probably null |
0.99 |
R9223:Otogl
|
UTSW |
10 |
107,690,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R9268:Otogl
|
UTSW |
10 |
107,616,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Otogl
|
UTSW |
10 |
107,652,974 (GRCm39) |
missense |
probably null |
0.99 |
R9356:Otogl
|
UTSW |
10 |
107,617,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Otogl
|
UTSW |
10 |
107,737,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Otogl
|
UTSW |
10 |
107,598,364 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9731:Otogl
|
UTSW |
10 |
107,735,328 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Otogl
|
UTSW |
10 |
107,731,643 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Otogl
|
UTSW |
10 |
107,702,538 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Otogl
|
UTSW |
10 |
107,614,734 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Otogl
|
UTSW |
10 |
107,613,074 (GRCm39) |
missense |
probably benign |
|
Z1176:Otogl
|
UTSW |
10 |
107,624,893 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Otogl
|
UTSW |
10 |
107,689,258 (GRCm39) |
missense |
possibly damaging |
0.78 |
Z1177:Otogl
|
UTSW |
10 |
107,599,119 (GRCm39) |
nonsense |
probably null |
|
Z1177:Otogl
|
UTSW |
10 |
107,712,764 (GRCm39) |
missense |
probably benign |
0.14 |
|