Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,297,257 (GRCm39) |
L2411R |
probably damaging |
Het |
Als2 |
A |
G |
1: 59,245,746 (GRCm39) |
W577R |
probably damaging |
Het |
Areg |
A |
T |
5: 91,294,577 (GRCm39) |
H245L |
possibly damaging |
Het |
Arhgap35 |
T |
C |
7: 16,297,392 (GRCm39) |
T558A |
possibly damaging |
Het |
Arhgef28 |
A |
T |
13: 98,073,368 (GRCm39) |
C1322* |
probably null |
Het |
Arhgef38 |
T |
C |
3: 132,912,719 (GRCm39) |
R107G |
possibly damaging |
Het |
Atf7ip |
T |
A |
6: 136,548,500 (GRCm39) |
F695L |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Bche |
T |
G |
3: 73,556,011 (GRCm39) |
Q549P |
possibly damaging |
Het |
Blnk |
A |
G |
19: 40,917,733 (GRCm39) |
F417L |
possibly damaging |
Het |
Bloc1s1 |
T |
G |
10: 128,759,255 (GRCm39) |
K17T |
probably damaging |
Het |
C330018D20Rik |
G |
T |
18: 57,090,968 (GRCm39) |
T65K |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,096,417 (GRCm39) |
N1560K |
probably benign |
Het |
Cers1 |
T |
A |
8: 70,774,228 (GRCm39) |
S162T |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,686,832 (GRCm39) |
K157E |
probably benign |
Het |
Cldn7 |
G |
A |
11: 69,858,494 (GRCm39) |
R196Q |
probably benign |
Het |
Clrn2 |
C |
A |
5: 45,611,369 (GRCm39) |
Q73K |
probably benign |
Het |
Cmss1 |
A |
G |
16: 57,122,608 (GRCm39) |
V262A |
probably benign |
Het |
Cpb2 |
T |
A |
14: 75,498,128 (GRCm39) |
V97E |
probably damaging |
Het |
Ctnnd2 |
G |
A |
15: 30,683,387 (GRCm39) |
V463I |
probably benign |
Het |
Cyp7a1 |
A |
T |
4: 6,268,476 (GRCm39) |
S416R |
probably benign |
Het |
Dip2b |
C |
T |
15: 100,087,960 (GRCm39) |
R965C |
probably damaging |
Het |
Dkk3 |
T |
C |
7: 111,749,865 (GRCm39) |
T102A |
probably benign |
Het |
Dmap1 |
C |
A |
4: 117,538,039 (GRCm39) |
|
probably null |
Het |
Dnah12 |
C |
A |
14: 26,608,828 (GRCm39) |
D3872E |
possibly damaging |
Het |
Dnah7b |
A |
G |
1: 46,158,558 (GRCm39) |
|
probably null |
Het |
Dnai1 |
C |
T |
4: 41,632,391 (GRCm39) |
T575I |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,464,599 (GRCm39) |
Y365N |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,936,215 (GRCm39) |
K18* |
probably null |
Het |
E2f2 |
A |
T |
4: 135,900,245 (GRCm39) |
T52S |
probably benign |
Het |
Elavl4 |
A |
G |
4: 110,147,841 (GRCm39) |
L13S |
probably benign |
Het |
Epor |
T |
C |
9: 21,873,572 (GRCm39) |
D59G |
possibly damaging |
Het |
Eral1 |
A |
G |
11: 77,971,059 (GRCm39) |
C43R |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,362,697 (GRCm39) |
V228A |
probably benign |
Het |
Gba1 |
T |
C |
3: 89,113,129 (GRCm39) |
S187P |
probably damaging |
Het |
Gcc2 |
G |
T |
10: 58,091,669 (GRCm39) |
|
probably benign |
Het |
Gdap2 |
C |
A |
3: 100,109,572 (GRCm39) |
|
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Gpr160 |
T |
C |
3: 30,950,612 (GRCm39) |
L228P |
probably benign |
Het |
Gsdmc2 |
A |
C |
15: 63,702,715 (GRCm39) |
V184G |
probably benign |
Het |
Gtf2e2 |
A |
T |
8: 34,266,080 (GRCm39) |
K252M |
probably damaging |
Het |
Gtf2e2 |
G |
T |
8: 34,266,081 (GRCm39) |
K252N |
probably benign |
Het |
Gys1 |
T |
C |
7: 45,087,529 (GRCm39) |
Y102H |
probably benign |
Het |
H4c2 |
A |
G |
13: 23,941,209 (GRCm39) |
D69G |
probably damaging |
Het |
Ifit3b |
A |
C |
19: 34,589,598 (GRCm39) |
D258A |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,323,575 (GRCm39) |
M1200K |
probably damaging |
Het |
Kcng4 |
A |
T |
8: 120,353,098 (GRCm39) |
F271I |
probably damaging |
Het |
Klhdc2 |
C |
T |
12: 69,350,387 (GRCm39) |
S144L |
possibly damaging |
Het |
Lhcgr |
A |
G |
17: 89,063,006 (GRCm39) |
F222S |
probably damaging |
Het |
Lrp5 |
C |
G |
19: 3,678,299 (GRCm39) |
G519R |
probably damaging |
Het |
Magel2 |
T |
C |
7: 62,028,515 (GRCm39) |
V473A |
probably benign |
Het |
Map1a |
T |
C |
2: 121,134,776 (GRCm39) |
V1864A |
possibly damaging |
Het |
Mast4 |
T |
A |
13: 102,895,242 (GRCm39) |
Q760H |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,613,294 (GRCm39) |
N437D |
probably benign |
Het |
Mettl18 |
G |
A |
1: 163,824,344 (GRCm39) |
V222I |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,934,155 (GRCm39) |
T782M |
probably benign |
Het |
Mocos |
T |
A |
18: 24,819,750 (GRCm39) |
V664E |
probably damaging |
Het |
Neb |
G |
T |
2: 52,185,306 (GRCm39) |
N975K |
probably benign |
Het |
Nectin3 |
A |
T |
16: 46,284,508 (GRCm39) |
S59T |
probably benign |
Het |
Nelfb |
A |
T |
2: 25,093,900 (GRCm39) |
M11K |
probably damaging |
Het |
Nrp1 |
A |
G |
8: 129,202,650 (GRCm39) |
N545S |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,687,478 (GRCm39) |
D53G |
probably damaging |
Het |
Or2g1 |
T |
A |
17: 38,107,248 (GRCm39) |
N304K |
probably benign |
Het |
Or51b4 |
T |
A |
7: 103,530,907 (GRCm39) |
D181V |
probably damaging |
Het |
Or5b117 |
A |
T |
19: 13,431,324 (GRCm39) |
S186T |
possibly damaging |
Het |
Or5p67 |
T |
A |
7: 107,922,254 (GRCm39) |
T210S |
probably benign |
Het |
Or6c70 |
A |
T |
10: 129,710,390 (GRCm39) |
F79I |
probably damaging |
Het |
Or8g53 |
T |
C |
9: 39,683,836 (GRCm39) |
T87A |
probably benign |
Het |
P3h1 |
A |
G |
4: 119,103,862 (GRCm39) |
H587R |
probably damaging |
Het |
Paqr4 |
A |
G |
17: 23,958,832 (GRCm39) |
|
probably null |
Het |
Pde12 |
A |
G |
14: 26,390,253 (GRCm39) |
V152A |
probably benign |
Het |
Ppip5k1 |
C |
A |
2: 121,180,972 (GRCm39) |
E45* |
probably null |
Het |
Ptch2 |
C |
T |
4: 116,967,254 (GRCm39) |
A677V |
probably benign |
Het |
Rgs12 |
A |
G |
5: 35,177,689 (GRCm39) |
N93S |
probably damaging |
Het |
Rif1 |
C |
G |
2: 51,985,856 (GRCm39) |
L614V |
probably damaging |
Het |
Rnf32 |
T |
C |
5: 29,408,145 (GRCm39) |
S125P |
probably damaging |
Het |
Robo4 |
A |
G |
9: 37,322,696 (GRCm39) |
I850V |
probably damaging |
Het |
Scap |
T |
A |
9: 110,210,219 (GRCm39) |
I876N |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,034,484 (GRCm39) |
D1219G |
possibly damaging |
Het |
Skint5 |
T |
C |
4: 113,743,005 (GRCm39) |
E354G |
unknown |
Het |
Spart |
A |
G |
3: 55,033,962 (GRCm39) |
D396G |
probably benign |
Het |
Spindoc |
G |
A |
19: 7,351,024 (GRCm39) |
S311L |
probably benign |
Het |
Spta1 |
G |
T |
1: 174,050,894 (GRCm39) |
R1791L |
probably damaging |
Het |
Tbck |
T |
C |
3: 132,507,278 (GRCm39) |
I750T |
possibly damaging |
Het |
Tmem191 |
T |
C |
16: 17,094,334 (GRCm39) |
|
probably null |
Het |
Trgv1 |
A |
T |
13: 19,524,474 (GRCm39) |
Y66F |
probably benign |
Het |
Vmn2r125 |
A |
G |
4: 156,702,292 (GRCm39) |
Y26C |
probably damaging |
Het |
Zbtb17 |
T |
C |
4: 141,192,128 (GRCm39) |
C358R |
possibly damaging |
Het |
Zfp180 |
G |
A |
7: 23,804,859 (GRCm39) |
G426E |
probably damaging |
Het |
Zfp445 |
A |
G |
9: 122,682,951 (GRCm39) |
V330A |
probably benign |
Het |
Zfp595 |
A |
G |
13: 67,465,688 (GRCm39) |
C192R |
probably damaging |
Het |
Zkscan4 |
A |
G |
13: 21,668,623 (GRCm39) |
H387R |
probably damaging |
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 |
R1870: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 |
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 |
|