Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
G |
A |
8: 25,362,646 (GRCm39) |
S17L |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
Ankrd34c |
A |
G |
9: 89,611,381 (GRCm39) |
V320A |
probably benign |
Het |
Arap2 |
A |
C |
5: 62,834,443 (GRCm39) |
|
probably null |
Het |
Atm |
A |
T |
9: 53,401,582 (GRCm39) |
I1429N |
probably damaging |
Het |
Ccdc68 |
A |
G |
18: 70,099,861 (GRCm39) |
N290D |
probably damaging |
Het |
Chst1 |
T |
C |
2: 92,443,542 (GRCm39) |
W5R |
probably damaging |
Het |
Clip1 |
G |
T |
5: 123,752,827 (GRCm39) |
|
probably benign |
Het |
Crebbp |
T |
C |
16: 3,935,364 (GRCm39) |
T842A |
probably damaging |
Het |
Cyp2b13 |
T |
C |
7: 25,781,236 (GRCm39) |
|
probably null |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,358,522 (GRCm39) |
|
probably null |
Het |
Dst |
A |
G |
1: 34,333,564 (GRCm39) |
I4800V |
probably damaging |
Het |
Efcab7 |
CAAGTAAAGTAA |
CAAGTAA |
4: 99,735,161 (GRCm39) |
|
probably null |
Het |
Epb41l2 |
C |
T |
10: 25,348,990 (GRCm39) |
Q382* |
probably null |
Het |
Fam83e |
A |
G |
7: 45,376,070 (GRCm39) |
D261G |
probably damaging |
Het |
Ifnk |
T |
G |
4: 35,152,134 (GRCm39) |
S21A |
possibly damaging |
Het |
Ift122 |
A |
G |
6: 115,903,204 (GRCm39) |
H1157R |
probably benign |
Het |
Ighv1-67 |
T |
C |
12: 115,567,654 (GRCm39) |
K67R |
possibly damaging |
Het |
Inpp4a |
C |
A |
1: 37,411,422 (GRCm39) |
A97D |
probably damaging |
Het |
Insm1 |
T |
A |
2: 146,065,346 (GRCm39) |
Y387* |
probably null |
Het |
Irgm1 |
T |
C |
11: 48,756,928 (GRCm39) |
I294M |
possibly damaging |
Het |
Isoc2b |
C |
T |
7: 4,854,061 (GRCm39) |
V104M |
probably damaging |
Het |
Kif2c |
A |
C |
4: 117,024,280 (GRCm39) |
S311R |
probably benign |
Het |
Morn3 |
G |
A |
5: 123,179,270 (GRCm39) |
A60V |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,274,534 (GRCm39) |
N89D |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,293 (GRCm39) |
N141I |
probably damaging |
Het |
Or4c116 |
G |
T |
2: 88,942,640 (GRCm39) |
T72N |
possibly damaging |
Het |
Or4c127 |
T |
C |
2: 89,832,876 (GRCm39) |
V42A |
probably benign |
Het |
Or5d44 |
T |
A |
2: 88,142,095 (GRCm39) |
Q15L |
noncoding transcript |
Het |
Or8b48 |
A |
C |
9: 38,493,069 (GRCm39) |
R165S |
probably damaging |
Het |
Pan2 |
C |
A |
10: 128,150,381 (GRCm39) |
N708K |
possibly damaging |
Het |
Parp1 |
T |
A |
1: 180,425,927 (GRCm39) |
V886E |
probably damaging |
Het |
Pcdha8 |
C |
A |
18: 37,127,753 (GRCm39) |
A745E |
probably benign |
Het |
Pcyox1 |
C |
T |
6: 86,371,390 (GRCm39) |
|
probably null |
Het |
Prl2c2 |
A |
T |
13: 13,176,713 (GRCm39) |
|
probably null |
Het |
Samd1 |
T |
C |
8: 84,726,361 (GRCm39) |
S473P |
possibly damaging |
Het |
Slc26a1 |
A |
T |
5: 108,819,773 (GRCm39) |
D475E |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,493,535 (GRCm39) |
V239A |
possibly damaging |
Het |
Smo |
T |
A |
6: 29,736,044 (GRCm39) |
L12Q |
unknown |
Homo |
Srpk1 |
C |
T |
17: 28,821,727 (GRCm39) |
R229Q |
possibly damaging |
Het |
Syn2 |
T |
A |
6: 115,216,362 (GRCm39) |
F191L |
probably damaging |
Het |
Syngr2 |
T |
C |
11: 117,704,261 (GRCm39) |
V182A |
probably benign |
Het |
Tarbp1 |
G |
A |
8: 127,174,139 (GRCm39) |
A889V |
probably benign |
Het |
Tbc1d2b |
T |
C |
9: 90,108,262 (GRCm39) |
T430A |
probably benign |
Het |
Tmem217 |
T |
A |
17: 29,745,484 (GRCm39) |
Y82F |
probably damaging |
Het |
Ttll9 |
T |
A |
2: 152,841,220 (GRCm39) |
Y272* |
probably null |
Het |
Uts2r |
A |
G |
11: 121,052,033 (GRCm39) |
Y299C |
probably damaging |
Het |
Vsig8 |
T |
A |
1: 172,388,143 (GRCm39) |
M37K |
probably benign |
Het |
Vwf |
G |
T |
6: 125,616,339 (GRCm39) |
D1218Y |
unknown |
Het |
Wdr11 |
T |
G |
7: 129,226,036 (GRCm39) |
M727R |
probably benign |
Het |
Wwc2 |
A |
G |
8: 48,353,826 (GRCm39) |
Y103H |
possibly damaging |
Het |
Yod1 |
T |
A |
1: 130,647,008 (GRCm39) |
L295* |
probably null |
Het |
Zfp113 |
G |
T |
5: 138,143,608 (GRCm39) |
S214* |
probably null |
Het |
Zfp438 |
T |
A |
18: 5,213,780 (GRCm39) |
M393L |
probably benign |
Het |
Zfp946 |
G |
A |
17: 22,674,752 (GRCm39) |
C502Y |
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 |
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 |
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 |
|