Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,242,134 (GRCm39) |
E1332D |
probably benign |
Het |
Abca5 |
C |
A |
11: 110,220,043 (GRCm39) |
V8L |
probably benign |
Het |
Abcc8 |
C |
T |
7: 45,773,339 (GRCm39) |
E797K |
probably benign |
Het |
Acd |
C |
A |
8: 106,425,039 (GRCm39) |
|
probably null |
Het |
Adam34l |
A |
T |
8: 44,078,132 (GRCm39) |
Y697* |
probably null |
Het |
Adamts12 |
T |
C |
15: 11,311,240 (GRCm39) |
S1166P |
probably benign |
Het |
Alox12b |
T |
C |
11: 69,049,199 (GRCm39) |
Y83H |
possibly damaging |
Het |
Antxr2 |
A |
T |
5: 98,178,297 (GRCm39) |
S38T |
probably damaging |
Het |
Arpc1a |
T |
A |
5: 145,043,901 (GRCm39) |
C344S |
possibly damaging |
Het |
Bcan |
T |
C |
3: 87,902,908 (GRCm39) |
Y290C |
probably damaging |
Het |
Bod1l |
G |
A |
5: 41,991,018 (GRCm39) |
S179F |
possibly damaging |
Het |
Catsper3 |
A |
C |
13: 55,953,561 (GRCm39) |
D224A |
probably damaging |
Het |
Ccar2 |
A |
G |
14: 70,377,946 (GRCm39) |
S680P |
probably damaging |
Het |
Ccdc18 |
A |
G |
5: 108,368,703 (GRCm39) |
H1275R |
possibly damaging |
Het |
Ccdc40 |
T |
C |
11: 119,150,730 (GRCm39) |
M1011T |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,263,386 (GRCm39) |
D17V |
probably damaging |
Het |
Csn1s2a |
T |
C |
5: 87,926,058 (GRCm39) |
F45L |
probably benign |
Het |
Cwf19l2 |
T |
G |
9: 3,458,802 (GRCm39) |
N750K |
possibly damaging |
Het |
Cyb5r4 |
A |
G |
9: 86,922,462 (GRCm39) |
D157G |
probably benign |
Het |
D130040H23Rik |
T |
A |
8: 69,755,354 (GRCm39) |
I253N |
probably benign |
Het |
Dennd4a |
C |
T |
9: 64,804,516 (GRCm39) |
A1285V |
probably benign |
Het |
Dlat |
A |
G |
9: 50,548,874 (GRCm39) |
S561P |
probably damaging |
Het |
Dlgap2 |
T |
A |
8: 14,823,347 (GRCm39) |
V522E |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,331,859 (GRCm39) |
Y2148* |
probably null |
Het |
Dnase2a |
T |
C |
8: 85,635,392 (GRCm39) |
|
probably benign |
Het |
Elapor2 |
A |
G |
5: 9,468,007 (GRCm39) |
E225G |
probably damaging |
Het |
Fam83f |
T |
C |
15: 80,574,113 (GRCm39) |
|
probably benign |
Het |
Firrm |
G |
A |
1: 163,792,363 (GRCm39) |
L545F |
probably damaging |
Het |
Foxi1 |
A |
T |
11: 34,157,937 (GRCm39) |
N29K |
possibly damaging |
Het |
Galk2 |
T |
C |
2: 125,817,183 (GRCm39) |
L324P |
probably benign |
Het |
Gdpd4 |
G |
A |
7: 97,622,162 (GRCm39) |
V214I |
probably benign |
Het |
Gfra3 |
C |
T |
18: 34,844,373 (GRCm39) |
A56T |
probably damaging |
Het |
Glyctk |
A |
G |
9: 106,032,547 (GRCm39) |
S489P |
probably damaging |
Het |
Izumo4 |
A |
T |
10: 80,539,569 (GRCm39) |
I135F |
probably damaging |
Het |
Krt87 |
T |
A |
15: 101,385,071 (GRCm39) |
T342S |
probably benign |
Het |
L1td1 |
T |
A |
4: 98,625,714 (GRCm39) |
D636E |
possibly damaging |
Het |
Letm2 |
A |
G |
8: 26,086,460 (GRCm39) |
|
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,591,744 (GRCm39) |
F828L |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,511,431 (GRCm39) |
D179G |
unknown |
Het |
Mdn1 |
T |
A |
4: 32,763,339 (GRCm39) |
D5146E |
probably damaging |
Het |
Megf10 |
T |
A |
18: 57,324,257 (GRCm39) |
Y99* |
probably null |
Het |
Men1 |
A |
G |
19: 6,387,660 (GRCm39) |
D285G |
probably damaging |
Het |
Mertk |
T |
G |
2: 128,643,116 (GRCm39) |
D838E |
probably benign |
Het |
Mta1 |
T |
C |
12: 113,091,694 (GRCm39) |
S266P |
possibly damaging |
Het |
Mta3 |
G |
A |
17: 84,089,397 (GRCm39) |
V320M |
probably damaging |
Het |
Nlrp9c |
G |
A |
7: 26,084,245 (GRCm39) |
Q445* |
probably null |
Het |
Or2m12 |
A |
T |
16: 19,105,357 (GRCm39) |
N45K |
probably damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,961 (GRCm39) |
I165T |
possibly damaging |
Het |
Or8b38 |
A |
T |
9: 37,972,646 (GRCm39) |
K10I |
probably benign |
Het |
Or8d6 |
T |
G |
9: 39,854,117 (GRCm39) |
I187R |
probably damaging |
Het |
Pbrm1 |
T |
A |
14: 30,828,132 (GRCm39) |
L1320I |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,457,972 (GRCm39) |
T297K |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,882,795 (GRCm39) |
D782G |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,426,185 (GRCm39) |
|
probably null |
Het |
Pira2 |
T |
C |
7: 3,847,452 (GRCm39) |
N79S |
probably damaging |
Het |
Pkdrej |
G |
T |
15: 85,700,632 (GRCm39) |
T1768K |
probably damaging |
Het |
Plcb3 |
T |
C |
19: 6,940,353 (GRCm39) |
I439V |
probably benign |
Het |
Pold4 |
T |
A |
19: 4,282,593 (GRCm39) |
Y58* |
probably null |
Het |
Ppef2 |
T |
G |
5: 92,398,371 (GRCm39) |
Q49P |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,723,817 (GRCm39) |
I2026F |
possibly damaging |
Het |
Rest |
T |
A |
5: 77,416,209 (GRCm39) |
V141E |
possibly damaging |
Het |
Rnf139 |
T |
C |
15: 58,771,202 (GRCm39) |
V409A |
probably benign |
Het |
Rnpc3 |
T |
C |
3: 113,404,704 (GRCm39) |
|
probably benign |
Het |
S100a10 |
A |
T |
3: 93,468,377 (GRCm39) |
E36V |
probably benign |
Het |
S1pr3 |
A |
C |
13: 51,573,952 (GRCm39) |
K378Q |
probably benign |
Het |
Scaper |
T |
A |
9: 55,593,222 (GRCm39) |
I472F |
probably damaging |
Het |
Sgcg |
G |
A |
14: 61,477,896 (GRCm39) |
|
probably benign |
Het |
Shank1 |
A |
T |
7: 43,991,539 (GRCm39) |
R69* |
probably null |
Het |
Shoc1 |
G |
A |
4: 59,054,142 (GRCm39) |
|
probably benign |
Het |
Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
Slc25a54 |
T |
A |
3: 108,987,932 (GRCm39) |
Y24* |
probably null |
Het |
Slc29a4 |
T |
C |
5: 142,707,243 (GRCm39) |
*529R |
probably null |
Het |
Slc41a2 |
G |
A |
10: 83,137,029 (GRCm39) |
Q293* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,737,509 (GRCm38) |
|
probably null |
Het |
Slfn9 |
G |
T |
11: 82,872,402 (GRCm39) |
T778N |
probably benign |
Het |
Ssr2 |
T |
C |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Tecrl |
T |
A |
5: 83,502,706 (GRCm39) |
T33S |
probably benign |
Het |
Tnfrsf9 |
T |
A |
4: 151,018,804 (GRCm39) |
C158* |
probably null |
Het |
Tradd |
T |
C |
8: 105,985,792 (GRCm39) |
E253G |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,314,479 (GRCm39) |
H807R |
probably benign |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r27 |
T |
C |
6: 124,201,170 (GRCm39) |
I262M |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,737,316 (GRCm39) |
V91A |
probably damaging |
Het |
Vwf |
C |
T |
6: 125,619,902 (GRCm39) |
R1527C |
probably damaging |
Het |
Wwc1 |
C |
T |
11: 35,752,772 (GRCm39) |
G763D |
probably damaging |
Het |
Zfp526 |
T |
G |
7: 24,924,594 (GRCm39) |
D284E |
possibly damaging |
Het |
Zfp646 |
T |
C |
7: 127,483,021 (GRCm39) |
F1733L |
possibly damaging |
Het |
Zfp90 |
A |
G |
8: 107,145,755 (GRCm39) |
H29R |
probably benign |
Het |
Zkscan4 |
A |
G |
13: 21,668,104 (GRCm39) |
E185G |
probably benign |
Het |
|
Other mutations in Aox1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Aox1
|
APN |
1 |
58,098,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01014:Aox1
|
APN |
1 |
58,361,960 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01077:Aox1
|
APN |
1 |
58,096,569 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Aox1
|
APN |
1 |
58,333,566 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01335:Aox1
|
APN |
1 |
58,121,312 (GRCm39) |
nonsense |
probably null |
|
IGL01383:Aox1
|
APN |
1 |
58,333,464 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01410:Aox1
|
APN |
1 |
58,145,184 (GRCm39) |
splice site |
probably null |
|
IGL01684:Aox1
|
APN |
1 |
58,116,740 (GRCm39) |
splice site |
probably null |
|
IGL01727:Aox1
|
APN |
1 |
58,112,387 (GRCm39) |
nonsense |
probably null |
|
IGL01734:Aox1
|
APN |
1 |
58,393,469 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01793:Aox1
|
APN |
1 |
58,375,783 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01805:Aox1
|
APN |
1 |
58,120,672 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01834:Aox1
|
APN |
1 |
58,348,183 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01924:Aox1
|
APN |
1 |
58,326,902 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01996:Aox1
|
APN |
1 |
58,121,225 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02060:Aox1
|
APN |
1 |
58,137,114 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02206:Aox1
|
APN |
1 |
58,104,499 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02591:Aox1
|
APN |
1 |
58,398,158 (GRCm39) |
nonsense |
probably null |
|
IGL02645:Aox1
|
APN |
1 |
58,373,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Aox1
|
APN |
1 |
58,373,928 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02801:Aox1
|
APN |
1 |
58,393,336 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02839:Aox1
|
APN |
1 |
58,107,943 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02975:Aox1
|
APN |
1 |
58,107,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Aox1
|
APN |
1 |
58,376,509 (GRCm39) |
missense |
probably benign |
|
IGL03062:Aox1
|
APN |
1 |
58,117,624 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03104:Aox1
|
APN |
1 |
58,321,918 (GRCm39) |
missense |
probably benign |
|
IGL03121:Aox1
|
APN |
1 |
58,398,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03191:Aox1
|
APN |
1 |
58,398,228 (GRCm39) |
missense |
probably null |
0.98 |
IGL03236:Aox1
|
APN |
1 |
58,349,156 (GRCm39) |
nonsense |
probably null |
|
IGL03286:Aox1
|
APN |
1 |
58,088,543 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03335:Aox1
|
APN |
1 |
58,115,319 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03395:Aox1
|
APN |
1 |
58,107,884 (GRCm39) |
splice site |
probably benign |
|
IGL03409:Aox1
|
APN |
1 |
58,393,588 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4362001:Aox1
|
UTSW |
1 |
58,321,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Aox1
|
UTSW |
1 |
58,393,581 (GRCm39) |
missense |
probably benign |
0.00 |
R0035:Aox1
|
UTSW |
1 |
58,393,581 (GRCm39) |
missense |
probably benign |
0.00 |
R0048:Aox1
|
UTSW |
1 |
58,112,371 (GRCm39) |
missense |
probably damaging |
0.98 |
R0144:Aox1
|
UTSW |
1 |
58,109,233 (GRCm39) |
missense |
probably benign |
0.00 |
R0207:Aox1
|
UTSW |
1 |
58,144,173 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0267:Aox1
|
UTSW |
1 |
58,378,605 (GRCm39) |
splice site |
probably benign |
|
R0357:Aox1
|
UTSW |
1 |
58,131,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Aox1
|
UTSW |
1 |
58,100,400 (GRCm39) |
missense |
probably benign |
0.00 |
R0388:Aox1
|
UTSW |
1 |
58,393,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Aox1
|
UTSW |
1 |
58,108,008 (GRCm39) |
splice site |
probably null |
|
R0409:Aox1
|
UTSW |
1 |
58,375,783 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0465:Aox1
|
UTSW |
1 |
58,101,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Aox1
|
UTSW |
1 |
58,082,810 (GRCm39) |
splice site |
probably benign |
|
R0547:Aox1
|
UTSW |
1 |
58,349,201 (GRCm39) |
missense |
probably damaging |
0.96 |
R0630:Aox1
|
UTSW |
1 |
58,376,480 (GRCm39) |
splice site |
probably benign |
|
R0726:Aox1
|
UTSW |
1 |
58,373,941 (GRCm39) |
splice site |
probably benign |
|
R0734:Aox1
|
UTSW |
1 |
58,344,500 (GRCm39) |
missense |
probably benign |
0.22 |
R0831:Aox1
|
UTSW |
1 |
58,378,842 (GRCm39) |
missense |
probably benign |
0.28 |
R0961:Aox1
|
UTSW |
1 |
58,349,230 (GRCm39) |
missense |
probably benign |
0.00 |
R1005:Aox1
|
UTSW |
1 |
58,104,511 (GRCm39) |
missense |
probably benign |
0.00 |
R1404:Aox1
|
UTSW |
1 |
58,385,371 (GRCm39) |
splice site |
probably benign |
|
R1507:Aox1
|
UTSW |
1 |
58,143,610 (GRCm39) |
missense |
probably benign |
0.01 |
R1512:Aox1
|
UTSW |
1 |
58,346,510 (GRCm39) |
missense |
probably benign |
0.00 |
R1573:Aox1
|
UTSW |
1 |
58,348,186 (GRCm39) |
missense |
probably benign |
0.00 |
R1592:Aox1
|
UTSW |
1 |
58,339,853 (GRCm39) |
missense |
probably benign |
0.00 |
R1597:Aox1
|
UTSW |
1 |
58,086,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R1693:Aox1
|
UTSW |
1 |
58,124,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Aox1
|
UTSW |
1 |
58,116,633 (GRCm39) |
missense |
probably benign |
|
R1747:Aox1
|
UTSW |
1 |
58,378,751 (GRCm39) |
missense |
probably benign |
0.01 |
R1768:Aox1
|
UTSW |
1 |
58,393,354 (GRCm39) |
missense |
probably benign |
0.00 |
R1809:Aox1
|
UTSW |
1 |
58,333,484 (GRCm39) |
missense |
probably benign |
|
R1823:Aox1
|
UTSW |
1 |
58,351,518 (GRCm39) |
missense |
probably benign |
0.02 |
R1834:Aox1
|
UTSW |
1 |
58,348,150 (GRCm39) |
missense |
probably benign |
0.08 |
R1835:Aox1
|
UTSW |
1 |
58,348,150 (GRCm39) |
missense |
probably benign |
0.08 |
R1836:Aox1
|
UTSW |
1 |
58,348,150 (GRCm39) |
missense |
probably benign |
0.08 |
R1869:Aox1
|
UTSW |
1 |
58,115,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Aox1
|
UTSW |
1 |
58,117,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Aox1
|
UTSW |
1 |
58,141,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Aox1
|
UTSW |
1 |
58,086,300 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2062:Aox1
|
UTSW |
1 |
58,098,351 (GRCm39) |
splice site |
probably null |
|
R2065:Aox1
|
UTSW |
1 |
58,098,351 (GRCm39) |
splice site |
probably null |
|
R2219:Aox1
|
UTSW |
1 |
58,388,289 (GRCm39) |
splice site |
probably null |
|
R2220:Aox1
|
UTSW |
1 |
58,388,289 (GRCm39) |
splice site |
probably null |
|
R2265:Aox1
|
UTSW |
1 |
58,120,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Aox1
|
UTSW |
1 |
58,382,832 (GRCm39) |
missense |
probably benign |
0.38 |
R2942:Aox1
|
UTSW |
1 |
58,376,540 (GRCm39) |
missense |
probably benign |
0.03 |
R2967:Aox1
|
UTSW |
1 |
58,361,993 (GRCm39) |
missense |
probably damaging |
0.96 |
R3082:Aox1
|
UTSW |
1 |
58,322,759 (GRCm39) |
splice site |
probably benign |
|
R3161:Aox1
|
UTSW |
1 |
58,343,597 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3408:Aox1
|
UTSW |
1 |
58,382,827 (GRCm39) |
missense |
probably benign |
0.32 |
R3713:Aox1
|
UTSW |
1 |
58,095,374 (GRCm39) |
missense |
probably benign |
0.01 |
R3778:Aox1
|
UTSW |
1 |
58,092,862 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3803:Aox1
|
UTSW |
1 |
58,329,058 (GRCm39) |
splice site |
probably null |
|
R3894:Aox1
|
UTSW |
1 |
58,373,837 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4198:Aox1
|
UTSW |
1 |
58,124,766 (GRCm39) |
missense |
probably benign |
|
R4214:Aox1
|
UTSW |
1 |
58,346,603 (GRCm39) |
critical splice donor site |
probably null |
|
R4249:Aox1
|
UTSW |
1 |
58,338,978 (GRCm39) |
missense |
probably benign |
0.01 |
R4296:Aox1
|
UTSW |
1 |
58,096,559 (GRCm39) |
splice site |
probably null |
|
R4562:Aox1
|
UTSW |
1 |
58,098,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R4666:Aox1
|
UTSW |
1 |
58,343,756 (GRCm39) |
nonsense |
probably null |
|
R4668:Aox1
|
UTSW |
1 |
58,373,853 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4703:Aox1
|
UTSW |
1 |
58,398,116 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4758:Aox1
|
UTSW |
1 |
58,371,741 (GRCm39) |
missense |
probably benign |
0.00 |
R4858:Aox1
|
UTSW |
1 |
58,143,640 (GRCm39) |
missense |
probably benign |
|
R4862:Aox1
|
UTSW |
1 |
58,134,316 (GRCm39) |
missense |
probably damaging |
0.98 |
R4890:Aox1
|
UTSW |
1 |
58,373,862 (GRCm39) |
missense |
probably benign |
0.11 |
R4900:Aox1
|
UTSW |
1 |
58,344,544 (GRCm39) |
missense |
probably benign |
|
R4924:Aox1
|
UTSW |
1 |
58,344,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Aox1
|
UTSW |
1 |
58,349,254 (GRCm39) |
splice site |
probably null |
|
R5048:Aox1
|
UTSW |
1 |
58,098,641 (GRCm39) |
splice site |
probably benign |
|
R5112:Aox1
|
UTSW |
1 |
58,349,254 (GRCm39) |
splice site |
probably null |
|
R5127:Aox1
|
UTSW |
1 |
58,069,185 (GRCm39) |
missense |
probably benign |
0.00 |
R5139:Aox1
|
UTSW |
1 |
58,100,456 (GRCm39) |
missense |
probably benign |
0.03 |
R5157:Aox1
|
UTSW |
1 |
58,109,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Aox1
|
UTSW |
1 |
58,088,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Aox1
|
UTSW |
1 |
58,107,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5235:Aox1
|
UTSW |
1 |
58,096,714 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5289:Aox1
|
UTSW |
1 |
58,131,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R5466:Aox1
|
UTSW |
1 |
58,080,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Aox1
|
UTSW |
1 |
58,143,569 (GRCm39) |
missense |
probably benign |
0.03 |
R5615:Aox1
|
UTSW |
1 |
58,136,125 (GRCm39) |
missense |
probably benign |
|
R5652:Aox1
|
UTSW |
1 |
58,134,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Aox1
|
UTSW |
1 |
58,088,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R5987:Aox1
|
UTSW |
1 |
58,346,518 (GRCm39) |
missense |
probably benign |
0.00 |
R6008:Aox1
|
UTSW |
1 |
58,116,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Aox1
|
UTSW |
1 |
58,143,668 (GRCm39) |
critical splice donor site |
probably null |
|
R6215:Aox1
|
UTSW |
1 |
58,124,620 (GRCm39) |
missense |
probably benign |
|
R6239:Aox1
|
UTSW |
1 |
58,344,550 (GRCm39) |
critical splice donor site |
probably null |
|
R6273:Aox1
|
UTSW |
1 |
58,378,831 (GRCm39) |
missense |
probably benign |
0.00 |
R6291:Aox1
|
UTSW |
1 |
58,369,965 (GRCm39) |
missense |
probably damaging |
0.98 |
R6334:Aox1
|
UTSW |
1 |
58,346,566 (GRCm39) |
nonsense |
probably null |
|
R6403:Aox1
|
UTSW |
1 |
58,107,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6440:Aox1
|
UTSW |
1 |
58,133,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Aox1
|
UTSW |
1 |
58,102,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Aox1
|
UTSW |
1 |
58,096,705 (GRCm39) |
missense |
probably benign |
0.40 |
R6752:Aox1
|
UTSW |
1 |
58,086,398 (GRCm39) |
missense |
probably benign |
0.00 |
R6764:Aox1
|
UTSW |
1 |
58,389,441 (GRCm39) |
missense |
probably damaging |
0.97 |
R6766:Aox1
|
UTSW |
1 |
58,388,227 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6789:Aox1
|
UTSW |
1 |
58,343,644 (GRCm39) |
missense |
probably benign |
0.01 |
R6804:Aox1
|
UTSW |
1 |
58,343,757 (GRCm39) |
missense |
probably benign |
0.04 |
R6989:Aox1
|
UTSW |
1 |
58,124,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Aox1
|
UTSW |
1 |
58,370,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7015:Aox1
|
UTSW |
1 |
58,321,917 (GRCm39) |
missense |
probably benign |
0.00 |
R7042:Aox1
|
UTSW |
1 |
58,141,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R7055:Aox1
|
UTSW |
1 |
58,338,927 (GRCm39) |
missense |
probably benign |
0.08 |
R7089:Aox1
|
UTSW |
1 |
58,375,808 (GRCm39) |
missense |
probably benign |
0.01 |
R7157:Aox1
|
UTSW |
1 |
58,322,651 (GRCm39) |
missense |
probably benign |
0.00 |
R7303:Aox1
|
UTSW |
1 |
58,373,924 (GRCm39) |
nonsense |
probably null |
|
R7426:Aox1
|
UTSW |
1 |
58,329,142 (GRCm39) |
nonsense |
probably null |
|
R7442:Aox1
|
UTSW |
1 |
58,121,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7506:Aox1
|
UTSW |
1 |
58,088,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7563:Aox1
|
UTSW |
1 |
58,086,304 (GRCm39) |
missense |
probably benign |
0.32 |
R7589:Aox1
|
UTSW |
1 |
58,080,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Aox1
|
UTSW |
1 |
58,107,451 (GRCm39) |
missense |
probably benign |
0.01 |
R7762:Aox1
|
UTSW |
1 |
58,388,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Aox1
|
UTSW |
1 |
58,124,626 (GRCm39) |
missense |
probably benign |
|
R7876:Aox1
|
UTSW |
1 |
58,101,330 (GRCm39) |
nonsense |
probably null |
|
R7899:Aox1
|
UTSW |
1 |
58,320,396 (GRCm39) |
splice site |
probably null |
|
R7905:Aox1
|
UTSW |
1 |
58,143,557 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7908:Aox1
|
UTSW |
1 |
58,145,227 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7942:Aox1
|
UTSW |
1 |
58,376,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R7975:Aox1
|
UTSW |
1 |
58,348,187 (GRCm39) |
missense |
probably benign |
0.02 |
R8029:Aox1
|
UTSW |
1 |
58,382,827 (GRCm39) |
missense |
probably benign |
0.32 |
R8032:Aox1
|
UTSW |
1 |
58,389,442 (GRCm39) |
missense |
probably benign |
0.01 |
R8116:Aox1
|
UTSW |
1 |
58,115,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8147:Aox1
|
UTSW |
1 |
58,339,821 (GRCm39) |
missense |
probably benign |
0.02 |
R8165:Aox1
|
UTSW |
1 |
58,348,088 (GRCm39) |
missense |
probably benign |
0.08 |
R8179:Aox1
|
UTSW |
1 |
58,137,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Aox1
|
UTSW |
1 |
58,092,873 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8284:Aox1
|
UTSW |
1 |
58,115,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Aox1
|
UTSW |
1 |
58,335,046 (GRCm39) |
missense |
probably benign |
|
R8415:Aox1
|
UTSW |
1 |
58,080,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Aox1
|
UTSW |
1 |
58,378,763 (GRCm39) |
missense |
probably benign |
0.10 |
R8946:Aox1
|
UTSW |
1 |
58,145,227 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8973:Aox1
|
UTSW |
1 |
58,329,113 (GRCm39) |
missense |
probably benign |
0.34 |
R8988:Aox1
|
UTSW |
1 |
58,088,625 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9015:Aox1
|
UTSW |
1 |
58,382,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R9097:Aox1
|
UTSW |
1 |
58,326,887 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9101:Aox1
|
UTSW |
1 |
58,371,796 (GRCm39) |
missense |
probably benign |
0.03 |
R9108:Aox1
|
UTSW |
1 |
58,321,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R9180:Aox1
|
UTSW |
1 |
58,378,777 (GRCm39) |
nonsense |
probably null |
|
R9258:Aox1
|
UTSW |
1 |
58,351,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Aox1
|
UTSW |
1 |
58,361,953 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9296:Aox1
|
UTSW |
1 |
58,124,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Aox1
|
UTSW |
1 |
58,104,501 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9461:Aox1
|
UTSW |
1 |
58,116,736 (GRCm39) |
critical splice donor site |
probably null |
|
R9519:Aox1
|
UTSW |
1 |
58,373,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R9581:Aox1
|
UTSW |
1 |
58,370,055 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Aox1
|
UTSW |
1 |
58,120,701 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Aox1
|
UTSW |
1 |
58,393,556 (GRCm39) |
missense |
possibly damaging |
0.69 |
|