Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
A |
G |
19: 57,068,271 (GRCm39) |
S263P |
possibly damaging |
Het |
Ahnak2 |
T |
C |
12: 112,750,610 (GRCm39) |
E104G |
probably null |
Het |
Apof |
T |
A |
10: 128,105,086 (GRCm39) |
M80K |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,283,285 (GRCm39) |
R208H |
probably damaging |
Het |
Arhgef33 |
A |
G |
17: 80,657,018 (GRCm39) |
|
probably null |
Het |
Atxn2l |
CCAGCAGCAGCAGCAGCAGC |
CCAGCAGCAGCAGCAGC |
7: 126,093,420 (GRCm39) |
|
probably benign |
Het |
Cabcoco1 |
T |
C |
10: 68,352,211 (GRCm39) |
K34E |
probably damaging |
Het |
Col4a4 |
C |
A |
1: 82,444,253 (GRCm39) |
G1338V |
unknown |
Het |
Coq9 |
T |
A |
8: 95,579,814 (GRCm39) |
D256E |
probably damaging |
Het |
Dnajc18 |
A |
T |
18: 35,833,963 (GRCm39) |
C41S |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,472,795 (GRCm39) |
I307M |
probably damaging |
Het |
Emg1 |
A |
G |
6: 124,688,870 (GRCm39) |
V46A |
probably damaging |
Het |
Eya3 |
A |
G |
4: 132,408,174 (GRCm39) |
S157G |
probably damaging |
Het |
Eya4 |
T |
C |
10: 23,027,910 (GRCm39) |
N274S |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,878,296 (GRCm39) |
V3395A |
probably damaging |
Het |
Fchsd1 |
A |
T |
18: 38,092,897 (GRCm39) |
|
probably null |
Het |
Gm4846 |
A |
G |
1: 166,325,082 (GRCm39) |
V3A |
probably benign |
Het |
Hecw2 |
T |
A |
1: 53,907,992 (GRCm39) |
|
probably null |
Het |
Herc3 |
T |
A |
6: 58,867,108 (GRCm39) |
I10N |
probably damaging |
Het |
Hhatl |
C |
T |
9: 121,618,588 (GRCm39) |
R138H |
probably benign |
Het |
Hspa9 |
A |
T |
18: 35,085,765 (GRCm39) |
H35Q |
probably benign |
Het |
Irgq |
T |
A |
7: 24,233,115 (GRCm39) |
S319T |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,277,053 (GRCm39) |
M1337V |
probably benign |
Het |
Ksr2 |
T |
A |
5: 117,894,449 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
C |
10: 103,036,559 (GRCm39) |
I865V |
probably damaging |
Het |
Map2k1 |
A |
G |
9: 64,094,577 (GRCm39) |
L355P |
probably damaging |
Het |
Muc16 |
A |
G |
9: 18,551,812 (GRCm39) |
I4827T |
probably benign |
Het |
Myh1 |
T |
C |
11: 67,112,202 (GRCm39) |
V1752A |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,986,909 (GRCm39) |
V282A |
probably damaging |
Het |
Nrg1 |
T |
A |
8: 32,308,561 (GRCm39) |
E485V |
probably damaging |
Het |
Ofcc1 |
T |
C |
13: 40,441,455 (GRCm39) |
D2G |
probably damaging |
Het |
Or10d3 |
CAGAG |
CAG |
9: 39,462,088 (GRCm39) |
|
probably null |
Het |
Pclo |
T |
C |
5: 14,729,146 (GRCm39) |
|
probably benign |
Het |
Pom121 |
T |
C |
5: 135,420,537 (GRCm39) |
K295E |
unknown |
Het |
Rb1 |
A |
C |
14: 73,515,894 (GRCm39) |
I294R |
probably benign |
Het |
Schip1 |
C |
A |
3: 68,402,227 (GRCm39) |
S101R |
probably benign |
Het |
Sec24c |
T |
A |
14: 20,740,868 (GRCm39) |
Y629N |
probably damaging |
Het |
Shkbp1 |
T |
A |
7: 27,049,963 (GRCm39) |
H305L |
probably benign |
Het |
Spag9 |
T |
C |
11: 93,959,801 (GRCm39) |
I187T |
probably damaging |
Het |
Srp72 |
C |
A |
5: 77,135,838 (GRCm39) |
T256K |
probably damaging |
Het |
Stk32c |
T |
A |
7: 138,685,190 (GRCm39) |
N320I |
probably damaging |
Het |
Stxbp4 |
A |
T |
11: 90,497,811 (GRCm39) |
S163T |
probably benign |
Het |
Sycp1 |
T |
G |
3: 102,832,569 (GRCm39) |
Y199S |
probably damaging |
Het |
Tpk1 |
T |
C |
6: 43,445,961 (GRCm39) |
D159G |
probably benign |
Het |
Trav21-dv12 |
C |
T |
14: 54,114,191 (GRCm39) |
H104Y |
probably benign |
Het |
Trip4 |
A |
T |
9: 65,788,302 (GRCm39) |
Y48N |
probably damaging |
Het |
Trmt10b |
A |
G |
4: 45,314,322 (GRCm39) |
T255A |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,747,232 (GRCm39) |
Q4606* |
probably null |
Het |
Vcan |
T |
A |
13: 89,838,806 (GRCm39) |
K2246M |
possibly damaging |
Het |
Zfp438 |
C |
A |
18: 5,213,603 (GRCm39) |
G452C |
probably damaging |
Het |
Zfp54 |
T |
A |
17: 21,654,004 (GRCm39) |
I166N |
probably benign |
Het |
Zfp735 |
T |
C |
11: 73,602,478 (GRCm39) |
V474A |
probably benign |
Het |
Zfp831 |
G |
T |
2: 174,488,360 (GRCm39) |
G1012W |
possibly damaging |
Het |
|
Other mutations in Abca7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01063:Abca7
|
APN |
10 |
79,847,131 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01074:Abca7
|
APN |
10 |
79,849,726 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01313:Abca7
|
APN |
10 |
79,838,957 (GRCm39) |
splice site |
probably benign |
|
IGL01372:Abca7
|
APN |
10 |
79,842,089 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01387:Abca7
|
APN |
10 |
79,835,596 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01468:Abca7
|
APN |
10 |
79,839,711 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01648:Abca7
|
APN |
10 |
79,846,914 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01796:Abca7
|
APN |
10 |
79,849,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01977:Abca7
|
APN |
10 |
79,841,986 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01982:Abca7
|
APN |
10 |
79,838,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Abca7
|
APN |
10 |
79,833,913 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02437:Abca7
|
APN |
10 |
79,844,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02721:Abca7
|
APN |
10 |
79,849,469 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02812:Abca7
|
APN |
10 |
79,841,881 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02823:Abca7
|
APN |
10 |
79,844,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02827:Abca7
|
APN |
10 |
79,845,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Abca7
|
APN |
10 |
79,837,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02952:Abca7
|
APN |
10 |
79,843,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Abca7
|
UTSW |
10 |
79,838,655 (GRCm39) |
splice site |
probably benign |
|
R0528:Abca7
|
UTSW |
10 |
79,838,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0541:Abca7
|
UTSW |
10 |
79,843,185 (GRCm39) |
missense |
probably benign |
0.01 |
R0584:Abca7
|
UTSW |
10 |
79,847,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Abca7
|
UTSW |
10 |
79,837,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Abca7
|
UTSW |
10 |
79,849,577 (GRCm39) |
nonsense |
probably null |
|
R1520:Abca7
|
UTSW |
10 |
79,844,664 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1536:Abca7
|
UTSW |
10 |
79,850,064 (GRCm39) |
missense |
probably benign |
0.39 |
R1619:Abca7
|
UTSW |
10 |
79,844,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Abca7
|
UTSW |
10 |
79,844,832 (GRCm39) |
missense |
probably benign |
|
R1752:Abca7
|
UTSW |
10 |
79,842,468 (GRCm39) |
missense |
probably benign |
0.17 |
R1762:Abca7
|
UTSW |
10 |
79,835,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Abca7
|
UTSW |
10 |
79,844,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Abca7
|
UTSW |
10 |
79,840,874 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1911:Abca7
|
UTSW |
10 |
79,842,468 (GRCm39) |
missense |
probably benign |
0.17 |
R2032:Abca7
|
UTSW |
10 |
79,844,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2188:Abca7
|
UTSW |
10 |
79,838,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Abca7
|
UTSW |
10 |
79,844,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R2974:Abca7
|
UTSW |
10 |
79,844,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R3055:Abca7
|
UTSW |
10 |
79,835,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4496:Abca7
|
UTSW |
10 |
79,838,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Abca7
|
UTSW |
10 |
79,842,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R4581:Abca7
|
UTSW |
10 |
79,842,402 (GRCm39) |
missense |
probably benign |
0.03 |
R4588:Abca7
|
UTSW |
10 |
79,833,701 (GRCm39) |
splice site |
probably null |
|
R4628:Abca7
|
UTSW |
10 |
79,851,022 (GRCm39) |
critical splice donor site |
probably null |
|
R4641:Abca7
|
UTSW |
10 |
79,841,615 (GRCm39) |
critical splice donor site |
probably null |
|
R4888:Abca7
|
UTSW |
10 |
79,838,562 (GRCm39) |
missense |
probably damaging |
0.97 |
R4911:Abca7
|
UTSW |
10 |
79,848,022 (GRCm39) |
critical splice donor site |
probably null |
|
R4979:Abca7
|
UTSW |
10 |
79,840,617 (GRCm39) |
nonsense |
probably null |
|
R4997:Abca7
|
UTSW |
10 |
79,843,154 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5147:Abca7
|
UTSW |
10 |
79,851,149 (GRCm39) |
missense |
probably benign |
0.02 |
R5176:Abca7
|
UTSW |
10 |
79,834,123 (GRCm39) |
missense |
probably benign |
0.35 |
R5190:Abca7
|
UTSW |
10 |
79,835,427 (GRCm39) |
critical splice donor site |
probably null |
|
R5358:Abca7
|
UTSW |
10 |
79,849,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R5409:Abca7
|
UTSW |
10 |
79,850,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5705:Abca7
|
UTSW |
10 |
79,851,276 (GRCm39) |
missense |
probably benign |
|
R6246:Abca7
|
UTSW |
10 |
79,850,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Abca7
|
UTSW |
10 |
79,838,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Abca7
|
UTSW |
10 |
79,844,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Abca7
|
UTSW |
10 |
79,833,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Abca7
|
UTSW |
10 |
79,841,992 (GRCm39) |
missense |
probably benign |
0.04 |
R6284:Abca7
|
UTSW |
10 |
79,840,244 (GRCm39) |
missense |
probably benign |
|
R6307:Abca7
|
UTSW |
10 |
79,843,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Abca7
|
UTSW |
10 |
79,842,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Abca7
|
UTSW |
10 |
79,850,984 (GRCm39) |
missense |
probably null |
0.69 |
R6560:Abca7
|
UTSW |
10 |
79,843,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R6565:Abca7
|
UTSW |
10 |
79,847,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Abca7
|
UTSW |
10 |
79,844,598 (GRCm39) |
missense |
probably damaging |
0.98 |
R6814:Abca7
|
UTSW |
10 |
79,838,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Abca7
|
UTSW |
10 |
79,845,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Abca7
|
UTSW |
10 |
79,850,822 (GRCm39) |
missense |
probably benign |
0.17 |
R7493:Abca7
|
UTSW |
10 |
79,837,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R7535:Abca7
|
UTSW |
10 |
79,837,463 (GRCm39) |
missense |
probably benign |
0.04 |
R7602:Abca7
|
UTSW |
10 |
79,833,846 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7607:Abca7
|
UTSW |
10 |
79,847,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Abca7
|
UTSW |
10 |
79,836,656 (GRCm39) |
missense |
probably benign |
0.00 |
R7821:Abca7
|
UTSW |
10 |
79,838,424 (GRCm39) |
small deletion |
probably benign |
|
R7863:Abca7
|
UTSW |
10 |
79,844,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Abca7
|
UTSW |
10 |
79,840,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Abca7
|
UTSW |
10 |
79,840,867 (GRCm39) |
missense |
probably benign |
0.00 |
R8114:Abca7
|
UTSW |
10 |
79,844,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Abca7
|
UTSW |
10 |
79,842,360 (GRCm39) |
missense |
probably benign |
0.05 |
R8439:Abca7
|
UTSW |
10 |
79,841,995 (GRCm39) |
missense |
probably benign |
0.03 |
R8456:Abca7
|
UTSW |
10 |
79,842,360 (GRCm39) |
missense |
probably benign |
0.05 |
R8830:Abca7
|
UTSW |
10 |
79,844,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Abca7
|
UTSW |
10 |
79,841,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9066:Abca7
|
UTSW |
10 |
79,849,188 (GRCm39) |
missense |
probably damaging |
0.98 |
R9116:Abca7
|
UTSW |
10 |
79,838,973 (GRCm39) |
missense |
|
|
R9128:Abca7
|
UTSW |
10 |
79,838,352 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9141:Abca7
|
UTSW |
10 |
79,851,264 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9184:Abca7
|
UTSW |
10 |
79,838,690 (GRCm39) |
missense |
probably damaging |
0.97 |
R9246:Abca7
|
UTSW |
10 |
79,838,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9320:Abca7
|
UTSW |
10 |
79,833,471 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9426:Abca7
|
UTSW |
10 |
79,851,264 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9490:Abca7
|
UTSW |
10 |
79,834,601 (GRCm39) |
missense |
probably benign |
|
R9561:Abca7
|
UTSW |
10 |
79,837,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9672:Abca7
|
UTSW |
10 |
79,838,563 (GRCm39) |
missense |
probably null |
1.00 |
Z1176:Abca7
|
UTSW |
10 |
79,842,393 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Abca7
|
UTSW |
10 |
79,835,266 (GRCm39) |
nonsense |
probably null |
|
|