Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,000,614 (GRCm39) |
|
probably benign |
Het |
Adamts20 |
C |
T |
15: 94,238,968 (GRCm39) |
S750N |
probably damaging |
Het |
Adh6a |
G |
A |
3: 138,036,722 (GRCm39) |
R370H |
possibly damaging |
Het |
Akr1b7 |
A |
G |
6: 34,396,046 (GRCm39) |
N183D |
probably damaging |
Het |
Aktip |
A |
T |
8: 91,856,348 (GRCm39) |
I43N |
probably damaging |
Het |
Ankrd26 |
A |
T |
6: 118,502,883 (GRCm39) |
|
probably benign |
Het |
Ano9 |
G |
A |
7: 140,688,717 (GRCm39) |
T144I |
possibly damaging |
Het |
Anpep |
G |
T |
7: 79,491,571 (GRCm39) |
D143E |
probably benign |
Het |
Ap1g1 |
C |
G |
8: 110,559,814 (GRCm39) |
|
probably benign |
Het |
Arhgef4 |
G |
A |
1: 34,849,636 (GRCm39) |
|
probably null |
Het |
Arsj |
A |
G |
3: 126,231,944 (GRCm39) |
Y230C |
possibly damaging |
Het |
Asmt |
C |
T |
X: 169,109,480 (GRCm39) |
|
probably benign |
Het |
Astl |
A |
T |
2: 127,187,405 (GRCm39) |
K72N |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,780,704 (GRCm39) |
|
probably benign |
Het |
Baiap2l1 |
A |
C |
5: 144,261,365 (GRCm39) |
|
probably null |
Het |
C7 |
A |
T |
15: 5,063,821 (GRCm39) |
N193K |
probably damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,247,785 (GRCm39) |
R362L |
probably damaging |
Het |
Cct4 |
T |
A |
11: 22,947,615 (GRCm39) |
D189E |
probably benign |
Het |
Cd300lg |
G |
A |
11: 101,933,938 (GRCm39) |
G62S |
probably benign |
Het |
Cdk14 |
T |
A |
5: 5,060,901 (GRCm39) |
M307L |
probably damaging |
Het |
Cfi |
G |
A |
3: 129,666,768 (GRCm39) |
|
probably null |
Het |
Clec2g |
G |
T |
6: 128,957,273 (GRCm39) |
|
probably null |
Het |
Cntnap2 |
T |
C |
6: 46,965,609 (GRCm39) |
S807P |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,755,671 (GRCm39) |
H206L |
probably damaging |
Het |
Ct55 |
A |
G |
X: 52,735,716 (GRCm39) |
E99G |
probably benign |
Het |
Cyp2c23 |
A |
T |
19: 44,009,997 (GRCm39) |
|
probably benign |
Het |
Degs1l |
T |
C |
1: 180,887,252 (GRCm39) |
I279T |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,965,767 (GRCm39) |
V1058A |
probably benign |
Het |
Dpp9 |
A |
G |
17: 56,506,038 (GRCm39) |
Y454H |
probably damaging |
Het |
Drosha |
G |
A |
15: 12,890,198 (GRCm39) |
G920R |
probably null |
Het |
Duox2 |
A |
G |
2: 122,114,378 (GRCm39) |
S1142P |
possibly damaging |
Het |
Fam13a |
C |
T |
6: 58,942,045 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
G |
16: 57,327,023 (GRCm39) |
R18G |
probably benign |
Het |
Foxa1 |
A |
G |
12: 57,589,527 (GRCm39) |
V231A |
probably damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,303 (GRCm39) |
M285K |
possibly damaging |
Het |
Gm5084 |
T |
A |
13: 60,360,320 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
G |
A |
19: 28,740,586 (GRCm39) |
|
noncoding transcript |
Het |
Gm9922 |
G |
T |
14: 101,966,841 (GRCm39) |
|
probably benign |
Het |
Gtf3c4 |
A |
T |
2: 28,723,988 (GRCm39) |
Y440* |
probably null |
Het |
Helq |
A |
G |
5: 100,921,820 (GRCm39) |
S795P |
probably damaging |
Het |
Helz |
T |
A |
11: 107,489,997 (GRCm39) |
S151T |
possibly damaging |
Het |
Irgm1 |
T |
C |
11: 48,757,440 (GRCm39) |
T124A |
probably benign |
Het |
Itgam |
C |
T |
7: 127,670,109 (GRCm39) |
P134S |
possibly damaging |
Het |
Kdm6a |
T |
C |
X: 18,102,923 (GRCm39) |
Y217H |
probably benign |
Het |
Kif6 |
T |
C |
17: 50,208,812 (GRCm39) |
L744P |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,489,190 (GRCm39) |
R1203H |
probably damaging |
Het |
Ksr2 |
A |
G |
5: 117,693,535 (GRCm39) |
T328A |
probably damaging |
Het |
Lig1 |
T |
C |
7: 13,034,281 (GRCm39) |
|
probably benign |
Het |
Lpar3 |
G |
A |
3: 145,946,303 (GRCm39) |
|
probably benign |
Het |
Lrrk2 |
T |
C |
15: 91,584,095 (GRCm39) |
F285S |
possibly damaging |
Het |
Marchf7 |
A |
G |
2: 60,062,637 (GRCm39) |
D148G |
probably benign |
Het |
Mcee |
T |
C |
7: 64,050,049 (GRCm39) |
L60S |
probably damaging |
Het |
Mob2 |
A |
G |
7: 141,570,111 (GRCm39) |
I81T |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,909,909 (GRCm39) |
D87E |
probably damaging |
Het |
Msantd5f9 |
A |
G |
4: 73,835,754 (GRCm39) |
F237L |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,462,283 (GRCm39) |
T560A |
probably benign |
Het |
Nagk |
C |
T |
6: 83,774,169 (GRCm39) |
T42I |
probably benign |
Het |
Naip1 |
G |
T |
13: 100,562,747 (GRCm39) |
T806K |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,195,857 (GRCm39) |
|
probably benign |
Het |
Ocln |
G |
T |
13: 100,647,967 (GRCm39) |
Y401* |
probably null |
Het |
Odad2 |
T |
A |
18: 7,211,630 (GRCm39) |
Y748F |
probably benign |
Het |
Oma1 |
T |
A |
4: 103,182,374 (GRCm39) |
N292K |
probably damaging |
Het |
Or8b55 |
G |
A |
9: 38,727,443 (GRCm39) |
V215I |
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,389,412 (GRCm39) |
|
probably null |
Het |
Pcdhb16 |
T |
C |
18: 37,611,441 (GRCm39) |
F134L |
probably damaging |
Het |
Pipox |
A |
T |
11: 77,772,360 (GRCm39) |
Y337N |
probably benign |
Het |
Polr3b |
A |
G |
10: 84,528,865 (GRCm39) |
D763G |
probably damaging |
Het |
Pygo1 |
T |
A |
9: 72,852,078 (GRCm39) |
N88K |
probably damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,862,251 (GRCm39) |
M674T |
probably damaging |
Het |
Rbm25 |
T |
C |
12: 83,719,501 (GRCm39) |
|
probably benign |
Het |
Rbm26 |
C |
T |
14: 105,354,542 (GRCm39) |
|
probably benign |
Het |
Rbms2 |
G |
A |
10: 127,974,055 (GRCm39) |
T187I |
possibly damaging |
Het |
Rnase11 |
T |
A |
14: 51,287,184 (GRCm39) |
R123S |
probably benign |
Het |
Rngtt |
A |
G |
4: 33,443,614 (GRCm39) |
N485D |
probably benign |
Het |
Rp1l1 |
A |
T |
14: 64,265,415 (GRCm39) |
M334L |
probably benign |
Het |
Rps9 |
T |
A |
7: 3,707,726 (GRCm39) |
L56Q |
probably damaging |
Het |
Saysd1 |
C |
A |
14: 20,133,170 (GRCm39) |
|
probably benign |
Het |
Sema4d |
C |
T |
13: 51,867,727 (GRCm39) |
|
probably null |
Het |
Shisa5 |
A |
T |
9: 108,869,998 (GRCm39) |
D34V |
probably damaging |
Het |
Skil |
A |
G |
3: 31,171,655 (GRCm39) |
D547G |
probably damaging |
Het |
Slc2a5 |
T |
A |
4: 150,227,514 (GRCm39) |
F444L |
probably damaging |
Het |
Slc9b2 |
T |
G |
3: 135,022,892 (GRCm39) |
C10G |
possibly damaging |
Het |
Sorcs2 |
G |
T |
5: 36,386,564 (GRCm39) |
|
probably benign |
Het |
Stk17b |
T |
G |
1: 53,805,140 (GRCm39) |
K140N |
possibly damaging |
Het |
Stradb |
T |
A |
1: 59,033,549 (GRCm39) |
L404Q |
possibly damaging |
Het |
Synj2 |
T |
C |
17: 6,076,826 (GRCm39) |
M432T |
possibly damaging |
Het |
Tanc1 |
G |
T |
2: 59,630,441 (GRCm39) |
R800L |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,522,987 (GRCm39) |
M1473V |
probably benign |
Het |
Tesc |
A |
G |
5: 118,199,667 (GRCm39) |
I190V |
probably benign |
Het |
Tex15 |
T |
C |
8: 34,064,262 (GRCm39) |
F1231L |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,332 (GRCm39) |
I127V |
probably benign |
Het |
Tlr6 |
A |
T |
5: 65,111,055 (GRCm39) |
C617* |
probably null |
Het |
Trank1 |
A |
T |
9: 111,221,893 (GRCm39) |
I2877F |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,406,552 (GRCm39) |
H1373Q |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,024,496 (GRCm39) |
S274P |
probably damaging |
Het |
Ucp2 |
T |
A |
7: 100,147,606 (GRCm39) |
V195E |
probably damaging |
Het |
Vars2 |
T |
C |
17: 35,973,108 (GRCm39) |
T394A |
probably damaging |
Het |
Vmn1r1 |
A |
G |
1: 181,985,371 (GRCm39) |
V98A |
possibly damaging |
Het |
Vmn1r225 |
A |
G |
17: 20,722,918 (GRCm39) |
I120V |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,881 (GRCm39) |
M299L |
probably benign |
Het |
Vmn2r25 |
A |
G |
6: 123,802,337 (GRCm39) |
V522A |
probably benign |
Het |
Vmn2r70 |
T |
C |
7: 85,215,130 (GRCm39) |
I135V |
probably benign |
Het |
Vwf |
T |
C |
6: 125,567,138 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
T |
C |
7: 12,713,048 (GRCm39) |
F29L |
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 |
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 |
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 |
|