Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
T |
C |
16: 88,424,081 (GRCm39) |
M137V |
probably benign |
Het |
Aak1 |
T |
A |
6: 86,932,172 (GRCm39) |
I381N |
probably benign |
Het |
Abcd4 |
C |
T |
12: 84,658,533 (GRCm39) |
M223I |
probably benign |
Het |
Adgrf2 |
A |
G |
17: 43,023,979 (GRCm39) |
V164A |
probably damaging |
Het |
Ahdc1 |
G |
A |
4: 132,793,297 (GRCm39) |
A1513T |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,235,929 (GRCm39) |
M168T |
probably damaging |
Het |
Aqr |
A |
G |
2: 113,949,150 (GRCm39) |
|
probably benign |
Het |
Astn1 |
A |
G |
1: 158,495,102 (GRCm39) |
E1042G |
possibly damaging |
Het |
Azi2 |
A |
G |
9: 117,876,508 (GRCm39) |
D8G |
possibly damaging |
Het |
Bcam |
T |
C |
7: 19,498,118 (GRCm39) |
T302A |
probably benign |
Het |
Cct6b |
A |
T |
11: 82,651,183 (GRCm39) |
I110N |
probably damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,493,263 (GRCm39) |
S762N |
possibly damaging |
Het |
Cecr2 |
T |
C |
6: 120,735,221 (GRCm39) |
L819P |
probably damaging |
Het |
Cers3 |
G |
T |
7: 66,435,823 (GRCm39) |
A261S |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,121,538 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
G |
T |
9: 108,793,508 (GRCm39) |
G1357* |
probably null |
Het |
Cux1 |
A |
G |
5: 136,594,397 (GRCm39) |
|
probably benign |
Het |
Cwh43 |
A |
T |
5: 73,595,835 (GRCm39) |
I535F |
probably damaging |
Het |
Dexi |
A |
T |
16: 10,360,553 (GRCm39) |
M1K |
probably null |
Het |
Dnah12 |
T |
C |
14: 26,534,747 (GRCm39) |
V2081A |
probably benign |
Het |
Efcab5 |
A |
T |
11: 77,007,008 (GRCm39) |
L872Q |
probably damaging |
Het |
Enpp7 |
A |
G |
11: 118,881,344 (GRCm39) |
Y163C |
probably damaging |
Het |
Fam221a |
T |
C |
6: 49,349,548 (GRCm39) |
Y38H |
probably damaging |
Het |
Foxred1 |
A |
G |
9: 35,122,186 (GRCm39) |
M1T |
probably null |
Het |
Fscn3 |
C |
T |
6: 28,428,091 (GRCm39) |
T26I |
possibly damaging |
Het |
Galp |
A |
T |
7: 6,216,836 (GRCm39) |
D72V |
probably damaging |
Het |
Gm9843 |
A |
G |
16: 76,200,419 (GRCm39) |
|
noncoding transcript |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Lmbrd1 |
T |
C |
1: 24,732,076 (GRCm39) |
Y98H |
probably damaging |
Het |
Lrrc63 |
T |
G |
14: 75,344,776 (GRCm39) |
Y437S |
probably benign |
Het |
Macc1 |
A |
G |
12: 119,410,576 (GRCm39) |
E448G |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,504,194 (GRCm39) |
H404R |
probably benign |
Het |
Mink1 |
G |
T |
11: 70,499,776 (GRCm39) |
R773L |
possibly damaging |
Het |
Mroh2b |
A |
G |
15: 4,973,131 (GRCm39) |
I1045V |
probably benign |
Het |
Mroh3 |
T |
C |
1: 136,113,714 (GRCm39) |
T692A |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,370,057 (GRCm39) |
E939V |
possibly damaging |
Het |
Naip2 |
A |
G |
13: 100,298,410 (GRCm39) |
F542S |
probably damaging |
Het |
Napsa |
A |
G |
7: 44,230,852 (GRCm39) |
Y73C |
probably damaging |
Het |
Ndst4 |
A |
T |
3: 125,355,154 (GRCm39) |
H354L |
possibly damaging |
Het |
Neil1 |
A |
T |
9: 57,054,254 (GRCm39) |
V22E |
probably damaging |
Het |
Nol4 |
T |
C |
18: 23,172,994 (GRCm39) |
I36V |
probably damaging |
Het |
Nprl3 |
G |
A |
11: 32,205,464 (GRCm39) |
T111I |
probably damaging |
Het |
Or12k8 |
A |
G |
2: 36,975,517 (GRCm39) |
M81T |
possibly damaging |
Het |
Or1e26 |
A |
T |
11: 73,479,731 (GRCm39) |
Y278N |
probably damaging |
Het |
Or4p22 |
C |
A |
2: 88,317,787 (GRCm39) |
T237N |
probably damaging |
Het |
Pald1 |
G |
A |
10: 61,178,144 (GRCm39) |
T624I |
possibly damaging |
Het |
Pcdhb13 |
C |
T |
18: 37,576,786 (GRCm39) |
P388L |
probably damaging |
Het |
Pcdhga6 |
T |
C |
18: 37,840,976 (GRCm39) |
V232A |
probably damaging |
Het |
Pde6b |
A |
G |
5: 108,570,928 (GRCm39) |
I388V |
probably damaging |
Het |
Phactr2 |
C |
A |
10: 13,264,476 (GRCm39) |
|
probably benign |
Het |
Prdx5 |
T |
C |
19: 6,885,477 (GRCm39) |
D56G |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,574,969 (GRCm39) |
I350N |
probably damaging |
Het |
Rangap1 |
C |
A |
15: 81,594,661 (GRCm39) |
E389D |
probably benign |
Het |
Reln |
A |
G |
5: 22,109,732 (GRCm39) |
V3126A |
probably damaging |
Het |
Rpl21 |
G |
A |
5: 146,771,847 (GRCm39) |
G59S |
possibly damaging |
Het |
Rsph6a |
G |
A |
7: 18,791,475 (GRCm39) |
V215M |
probably damaging |
Het |
Smcp |
T |
C |
3: 92,491,431 (GRCm39) |
K139E |
unknown |
Het |
Stag1 |
A |
G |
9: 100,771,671 (GRCm39) |
T699A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,338,700 (GRCm39) |
|
probably null |
Het |
Tle1 |
G |
T |
4: 72,044,659 (GRCm39) |
H459Q |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,561,363 (GRCm39) |
P27302S |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,571,610 (GRCm39) |
V26428I |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,742,968 (GRCm39) |
E656G |
probably benign |
Het |
Vmn1r218 |
A |
T |
13: 23,321,081 (GRCm39) |
N63Y |
probably damaging |
Het |
Vmn1r79 |
A |
G |
7: 11,910,139 (GRCm39) |
N40S |
possibly damaging |
Het |
Wdr35 |
A |
G |
12: 9,077,648 (GRCm39) |
D1107G |
possibly damaging |
Het |
Zfp101 |
A |
G |
17: 33,600,880 (GRCm39) |
M292T |
probably benign |
Het |
Zfp108 |
T |
A |
7: 23,961,270 (GRCm39) |
C620* |
probably null |
Het |
Zscan4b |
T |
C |
7: 10,635,818 (GRCm39) |
T170A |
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 |
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 |
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 |
|