Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
G |
A |
17: 57,750,918 (GRCm39) |
V531I |
probably benign |
Het |
Aldoart2 |
A |
G |
12: 55,612,801 (GRCm39) |
Q242R |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,735,589 (GRCm39) |
|
probably benign |
Het |
Ank3 |
C |
T |
10: 69,733,947 (GRCm39) |
A737V |
probably damaging |
Het |
Ankle2 |
A |
G |
5: 110,401,704 (GRCm39) |
I789V |
probably benign |
Het |
Ankrd13c |
T |
C |
3: 157,711,410 (GRCm39) |
V510A |
probably damaging |
Het |
Arid1b |
T |
A |
17: 5,393,118 (GRCm39) |
M2216K |
probably damaging |
Het |
Arrdc1 |
A |
G |
2: 24,815,860 (GRCm39) |
V380A |
probably benign |
Het |
B3galt1 |
C |
A |
2: 67,948,913 (GRCm39) |
N209K |
possibly damaging |
Het |
Cd300c2 |
A |
T |
11: 114,887,731 (GRCm39) |
C224S |
probably benign |
Het |
Cdk4 |
T |
C |
10: 126,900,759 (GRCm39) |
|
probably null |
Het |
Cdk5rap1 |
T |
C |
2: 154,210,794 (GRCm39) |
T115A |
possibly damaging |
Het |
Clvs1 |
A |
T |
4: 9,281,831 (GRCm39) |
R92* |
probably null |
Het |
Cnga1 |
A |
G |
5: 72,762,107 (GRCm39) |
V469A |
probably damaging |
Het |
Ctns |
A |
G |
11: 73,087,479 (GRCm39) |
F16L |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,204,429 (GRCm39) |
C1299S |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,530,783 (GRCm39) |
Y3690F |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,326,703 (GRCm39) |
M1971V |
probably damaging |
Het |
Dnah5 |
G |
A |
15: 28,388,050 (GRCm39) |
V3170M |
probably damaging |
Het |
Dpp8 |
T |
C |
9: 64,963,200 (GRCm39) |
Y485H |
probably benign |
Het |
Dsc2 |
T |
C |
18: 20,183,214 (GRCm39) |
D68G |
probably damaging |
Het |
Eeig2 |
A |
G |
3: 108,887,544 (GRCm39) |
V240A |
probably benign |
Het |
Elavl1 |
A |
T |
8: 4,351,752 (GRCm39) |
D121E |
probably benign |
Het |
Ermap |
A |
G |
4: 119,040,505 (GRCm39) |
V311A |
probably damaging |
Het |
Fbxw11 |
C |
T |
11: 32,689,226 (GRCm39) |
R437C |
probably damaging |
Het |
Gas2l3 |
T |
C |
10: 89,249,634 (GRCm39) |
M495V |
probably benign |
Het |
Hacd1 |
C |
T |
2: 14,049,948 (GRCm39) |
|
probably null |
Het |
Itgav |
A |
G |
2: 83,619,327 (GRCm39) |
R596G |
probably benign |
Het |
Kars1 |
T |
C |
8: 112,728,352 (GRCm39) |
H215R |
possibly damaging |
Het |
Kif26a |
G |
A |
12: 112,144,228 (GRCm39) |
R1494H |
probably damaging |
Het |
Klf12 |
G |
A |
14: 100,260,393 (GRCm39) |
S112L |
possibly damaging |
Het |
Krt77 |
T |
C |
15: 101,777,998 (GRCm39) |
Y19C |
unknown |
Het |
Lrrc4c |
A |
G |
2: 97,460,834 (GRCm39) |
T487A |
probably benign |
Het |
Lrrn1 |
A |
G |
6: 107,545,851 (GRCm39) |
M550V |
probably benign |
Het |
Lsr |
C |
A |
7: 30,657,634 (GRCm39) |
R442L |
probably benign |
Het |
Lysmd2 |
A |
C |
9: 75,542,728 (GRCm39) |
T112P |
probably damaging |
Het |
Mctp2 |
A |
T |
7: 71,909,017 (GRCm39) |
S99T |
probably benign |
Het |
Mettl4 |
A |
G |
17: 95,047,960 (GRCm39) |
V227A |
probably benign |
Het |
Mill2 |
T |
A |
7: 18,590,608 (GRCm39) |
|
probably null |
Het |
Mpp3 |
T |
C |
11: 101,895,848 (GRCm39) |
N476D |
probably benign |
Het |
Mtmr6 |
C |
T |
14: 60,517,638 (GRCm39) |
P83L |
possibly damaging |
Het |
Myh3 |
T |
C |
11: 66,984,364 (GRCm39) |
I1067T |
probably benign |
Het |
Myh9 |
C |
A |
15: 77,657,540 (GRCm39) |
Q1068H |
probably damaging |
Het |
Narf |
T |
A |
11: 121,141,179 (GRCm39) |
H304Q |
possibly damaging |
Het |
Nfatc2ip |
G |
T |
7: 125,995,784 (GRCm39) |
P35Q |
possibly damaging |
Het |
Npas3 |
C |
A |
12: 54,112,618 (GRCm39) |
P426Q |
probably damaging |
Het |
Or10aa3 |
T |
G |
1: 173,878,400 (GRCm39) |
S154A |
possibly damaging |
Het |
Or4e1 |
G |
A |
14: 52,700,740 (GRCm39) |
T242I |
probably damaging |
Het |
Or4f4b |
T |
C |
2: 111,314,311 (GRCm39) |
Y207H |
possibly damaging |
Het |
Or51i1 |
T |
A |
7: 103,671,219 (GRCm39) |
Q102L |
probably damaging |
Het |
Or5p5 |
A |
G |
7: 107,414,589 (GRCm39) |
H266R |
possibly damaging |
Het |
Pcdh10 |
A |
T |
3: 45,333,917 (GRCm39) |
E77V |
probably damaging |
Het |
Pcnt |
C |
T |
10: 76,192,019 (GRCm39) |
R2764Q |
probably damaging |
Het |
Pgbd5 |
T |
C |
8: 125,097,324 (GRCm39) |
D493G |
possibly damaging |
Het |
Piezo2 |
G |
T |
18: 63,290,333 (GRCm39) |
T142N |
probably benign |
Het |
Plcb1 |
A |
G |
2: 135,187,015 (GRCm39) |
I761V |
probably benign |
Het |
Plekhg4 |
T |
G |
8: 106,108,628 (GRCm39) |
D1196E |
probably null |
Het |
Pparg |
A |
G |
6: 115,427,989 (GRCm39) |
K159E |
probably damaging |
Het |
Psmb1 |
A |
T |
17: 15,718,478 (GRCm39) |
M16K |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,361,595 (GRCm39) |
I2139V |
probably benign |
Het |
Ralgapb |
T |
A |
2: 158,282,887 (GRCm39) |
S239T |
probably damaging |
Het |
Serpina11 |
A |
G |
12: 103,950,923 (GRCm39) |
V266A |
probably damaging |
Het |
Sf3a2 |
C |
G |
10: 80,639,947 (GRCm39) |
|
probably benign |
Het |
Smim18 |
T |
C |
8: 34,232,587 (GRCm39) |
T11A |
possibly damaging |
Het |
Snx6 |
G |
A |
12: 54,817,528 (GRCm39) |
T7I |
probably damaging |
Het |
Srcin1 |
T |
A |
11: 97,442,768 (GRCm39) |
D75V |
probably damaging |
Het |
Srsf12 |
T |
A |
4: 33,231,174 (GRCm39) |
S223T |
probably damaging |
Het |
Taf4b |
G |
T |
18: 14,946,599 (GRCm39) |
C474F |
probably damaging |
Het |
Tango6 |
T |
A |
8: 107,444,722 (GRCm39) |
C542* |
probably null |
Het |
Tbc1d24 |
A |
G |
17: 24,427,510 (GRCm39) |
S151P |
possibly damaging |
Het |
Tssk6 |
T |
C |
8: 70,355,714 (GRCm39) |
S253P |
probably benign |
Het |
Ttc39c |
G |
A |
18: 12,857,999 (GRCm39) |
W300* |
probably null |
Het |
Ttc6 |
T |
A |
12: 57,689,926 (GRCm39) |
W539R |
probably benign |
Het |
Ttn |
T |
C |
2: 76,582,770 (GRCm39) |
T22708A |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,749,053 (GRCm39) |
E3999* |
probably null |
Het |
Vill |
T |
G |
9: 118,897,508 (GRCm39) |
L261R |
probably damaging |
Het |
Vmn1r20 |
T |
C |
6: 57,409,159 (GRCm39) |
S162P |
probably damaging |
Het |
Zfp516 |
T |
C |
18: 82,974,219 (GRCm39) |
I139T |
probably benign |
Het |
|
Other mutations in Abca8a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Abca8a
|
APN |
11 |
109,941,765 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01099:Abca8a
|
APN |
11 |
109,965,031 (GRCm39) |
splice site |
probably benign |
|
IGL01100:Abca8a
|
APN |
11 |
109,949,249 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01310:Abca8a
|
APN |
11 |
109,950,801 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01357:Abca8a
|
APN |
11 |
109,922,398 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01554:Abca8a
|
APN |
11 |
109,932,992 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01937:Abca8a
|
APN |
11 |
109,974,130 (GRCm39) |
splice site |
probably benign |
|
IGL01945:Abca8a
|
APN |
11 |
109,974,130 (GRCm39) |
splice site |
probably benign |
|
IGL01987:Abca8a
|
APN |
11 |
109,964,981 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02023:Abca8a
|
APN |
11 |
109,953,942 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02208:Abca8a
|
APN |
11 |
109,950,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02378:Abca8a
|
APN |
11 |
109,969,641 (GRCm39) |
unclassified |
probably benign |
|
IGL02380:Abca8a
|
APN |
11 |
109,969,641 (GRCm39) |
unclassified |
probably benign |
|
IGL02387:Abca8a
|
APN |
11 |
109,969,641 (GRCm39) |
unclassified |
probably benign |
|
IGL02388:Abca8a
|
APN |
11 |
109,969,641 (GRCm39) |
unclassified |
probably benign |
|
IGL02524:Abca8a
|
APN |
11 |
109,969,641 (GRCm39) |
unclassified |
probably benign |
|
IGL02551:Abca8a
|
APN |
11 |
109,975,068 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02831:Abca8a
|
APN |
11 |
109,943,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Abca8a
|
APN |
11 |
109,961,177 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02934:Abca8a
|
APN |
11 |
109,931,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02946:Abca8a
|
APN |
11 |
109,919,041 (GRCm39) |
splice site |
probably benign |
|
IGL02967:Abca8a
|
APN |
11 |
109,941,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02997:Abca8a
|
APN |
11 |
109,966,359 (GRCm39) |
splice site |
probably benign |
|
IGL03265:Abca8a
|
APN |
11 |
109,943,929 (GRCm39) |
missense |
probably benign |
0.01 |
G5030:Abca8a
|
UTSW |
11 |
109,961,165 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Abca8a
|
UTSW |
11 |
109,933,835 (GRCm39) |
missense |
probably benign |
|
PIT4445001:Abca8a
|
UTSW |
11 |
109,966,377 (GRCm39) |
missense |
probably damaging |
0.99 |
R0060:Abca8a
|
UTSW |
11 |
109,961,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Abca8a
|
UTSW |
11 |
109,961,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R0084:Abca8a
|
UTSW |
11 |
109,927,423 (GRCm39) |
splice site |
probably benign |
|
R0394:Abca8a
|
UTSW |
11 |
109,917,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R0477:Abca8a
|
UTSW |
11 |
109,956,051 (GRCm39) |
missense |
probably benign |
|
R0593:Abca8a
|
UTSW |
11 |
109,958,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Abca8a
|
UTSW |
11 |
109,931,390 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0764:Abca8a
|
UTSW |
11 |
109,950,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Abca8a
|
UTSW |
11 |
109,933,814 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0836:Abca8a
|
UTSW |
11 |
109,931,390 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0848:Abca8a
|
UTSW |
11 |
109,919,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0894:Abca8a
|
UTSW |
11 |
109,941,792 (GRCm39) |
missense |
probably benign |
0.00 |
R1163:Abca8a
|
UTSW |
11 |
109,962,356 (GRCm39) |
missense |
probably benign |
0.01 |
R1224:Abca8a
|
UTSW |
11 |
109,931,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Abca8a
|
UTSW |
11 |
109,960,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1596:Abca8a
|
UTSW |
11 |
109,958,886 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1708:Abca8a
|
UTSW |
11 |
109,943,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R1715:Abca8a
|
UTSW |
11 |
109,982,406 (GRCm39) |
missense |
probably damaging |
0.98 |
R1795:Abca8a
|
UTSW |
11 |
109,941,792 (GRCm39) |
missense |
probably benign |
0.00 |
R1832:Abca8a
|
UTSW |
11 |
109,962,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R1852:Abca8a
|
UTSW |
11 |
109,960,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Abca8a
|
UTSW |
11 |
109,980,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Abca8a
|
UTSW |
11 |
109,982,433 (GRCm39) |
missense |
probably benign |
0.20 |
R1917:Abca8a
|
UTSW |
11 |
109,982,341 (GRCm39) |
splice site |
probably benign |
|
R1943:Abca8a
|
UTSW |
11 |
109,960,689 (GRCm39) |
missense |
probably benign |
0.00 |
R1962:Abca8a
|
UTSW |
11 |
109,917,731 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2016:Abca8a
|
UTSW |
11 |
109,961,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R2037:Abca8a
|
UTSW |
11 |
109,980,810 (GRCm39) |
splice site |
probably null |
|
R2098:Abca8a
|
UTSW |
11 |
109,927,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Abca8a
|
UTSW |
11 |
109,958,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Abca8a
|
UTSW |
11 |
109,921,743 (GRCm39) |
missense |
probably null |
1.00 |
R2220:Abca8a
|
UTSW |
11 |
109,917,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Abca8a
|
UTSW |
11 |
109,917,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2395:Abca8a
|
UTSW |
11 |
109,959,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R2847:Abca8a
|
UTSW |
11 |
109,932,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Abca8a
|
UTSW |
11 |
109,932,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Abca8a
|
UTSW |
11 |
109,953,991 (GRCm39) |
missense |
probably benign |
|
R3974:Abca8a
|
UTSW |
11 |
109,974,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Abca8a
|
UTSW |
11 |
109,980,933 (GRCm39) |
missense |
probably damaging |
0.98 |
R4163:Abca8a
|
UTSW |
11 |
109,941,808 (GRCm39) |
missense |
probably benign |
0.00 |
R4274:Abca8a
|
UTSW |
11 |
109,980,930 (GRCm39) |
missense |
probably damaging |
0.96 |
R4507:Abca8a
|
UTSW |
11 |
109,953,851 (GRCm39) |
missense |
probably benign |
0.19 |
R4571:Abca8a
|
UTSW |
11 |
109,920,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Abca8a
|
UTSW |
11 |
109,962,702 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4700:Abca8a
|
UTSW |
11 |
109,961,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Abca8a
|
UTSW |
11 |
109,962,341 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4955:Abca8a
|
UTSW |
11 |
109,927,338 (GRCm39) |
missense |
probably benign |
0.00 |
R5186:Abca8a
|
UTSW |
11 |
109,982,425 (GRCm39) |
missense |
probably null |
0.31 |
R5190:Abca8a
|
UTSW |
11 |
109,980,735 (GRCm39) |
critical splice donor site |
probably null |
|
R5597:Abca8a
|
UTSW |
11 |
109,927,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Abca8a
|
UTSW |
11 |
109,929,225 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5757:Abca8a
|
UTSW |
11 |
109,933,794 (GRCm39) |
missense |
probably benign |
0.28 |
R5822:Abca8a
|
UTSW |
11 |
109,921,705 (GRCm39) |
missense |
probably damaging |
0.98 |
R5925:Abca8a
|
UTSW |
11 |
109,948,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Abca8a
|
UTSW |
11 |
109,954,048 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6122:Abca8a
|
UTSW |
11 |
109,961,249 (GRCm39) |
missense |
probably benign |
0.40 |
R6189:Abca8a
|
UTSW |
11 |
109,921,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Abca8a
|
UTSW |
11 |
109,980,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R6374:Abca8a
|
UTSW |
11 |
109,974,216 (GRCm39) |
nonsense |
probably null |
|
R7022:Abca8a
|
UTSW |
11 |
109,974,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Abca8a
|
UTSW |
11 |
109,964,968 (GRCm39) |
missense |
probably benign |
0.09 |
R7198:Abca8a
|
UTSW |
11 |
109,969,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7220:Abca8a
|
UTSW |
11 |
109,980,793 (GRCm39) |
missense |
probably benign |
0.00 |
R7290:Abca8a
|
UTSW |
11 |
109,921,714 (GRCm39) |
missense |
probably benign |
0.03 |
R7381:Abca8a
|
UTSW |
11 |
109,920,913 (GRCm39) |
splice site |
probably null |
|
R7437:Abca8a
|
UTSW |
11 |
109,941,790 (GRCm39) |
missense |
probably benign |
|
R7733:Abca8a
|
UTSW |
11 |
109,945,413 (GRCm39) |
missense |
probably benign |
0.02 |
R7785:Abca8a
|
UTSW |
11 |
109,965,032 (GRCm39) |
splice site |
probably null |
|
R7917:Abca8a
|
UTSW |
11 |
109,958,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7948:Abca8a
|
UTSW |
11 |
109,941,805 (GRCm39) |
missense |
probably benign |
|
R7957:Abca8a
|
UTSW |
11 |
109,982,439 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R7958:Abca8a
|
UTSW |
11 |
109,922,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7981:Abca8a
|
UTSW |
11 |
109,980,739 (GRCm39) |
missense |
probably benign |
0.00 |
R8033:Abca8a
|
UTSW |
11 |
109,927,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Abca8a
|
UTSW |
11 |
109,980,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R8116:Abca8a
|
UTSW |
11 |
109,982,420 (GRCm39) |
missense |
probably benign |
0.27 |
R8289:Abca8a
|
UTSW |
11 |
109,927,515 (GRCm39) |
intron |
probably benign |
|
R8334:Abca8a
|
UTSW |
11 |
109,959,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Abca8a
|
UTSW |
11 |
109,945,473 (GRCm39) |
missense |
probably benign |
0.31 |
R8406:Abca8a
|
UTSW |
11 |
109,977,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8438:Abca8a
|
UTSW |
11 |
109,966,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R8670:Abca8a
|
UTSW |
11 |
109,966,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R8807:Abca8a
|
UTSW |
11 |
109,974,252 (GRCm39) |
missense |
probably benign |
0.35 |
R8821:Abca8a
|
UTSW |
11 |
109,949,362 (GRCm39) |
missense |
probably damaging |
0.98 |
R8838:Abca8a
|
UTSW |
11 |
109,920,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Abca8a
|
UTSW |
11 |
109,964,941 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8885:Abca8a
|
UTSW |
11 |
109,960,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Abca8a
|
UTSW |
11 |
109,969,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Abca8a
|
UTSW |
11 |
109,962,245 (GRCm39) |
critical splice donor site |
probably null |
|
R9272:Abca8a
|
UTSW |
11 |
109,953,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R9331:Abca8a
|
UTSW |
11 |
109,917,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Abca8a
|
UTSW |
11 |
109,921,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Abca8a
|
UTSW |
11 |
109,977,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R9529:Abca8a
|
UTSW |
11 |
109,947,167 (GRCm39) |
nonsense |
probably null |
|
R9564:Abca8a
|
UTSW |
11 |
109,965,010 (GRCm39) |
missense |
probably benign |
0.04 |
X0022:Abca8a
|
UTSW |
11 |
109,921,923 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Abca8a
|
UTSW |
11 |
109,974,161 (GRCm39) |
missense |
probably damaging |
1.00 |
X0053:Abca8a
|
UTSW |
11 |
109,974,310 (GRCm39) |
missense |
probably damaging |
0.98 |
|