Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449E01Rik |
T |
C |
14: 105,736,380 (GRCm39) |
|
noncoding transcript |
Het |
Akp3 |
G |
A |
1: 87,055,593 (GRCm39) |
G547R |
unknown |
Het |
Anln |
A |
G |
9: 22,262,214 (GRCm39) |
|
probably null |
Het |
Anpep |
T |
G |
7: 79,485,165 (GRCm39) |
Q607P |
probably benign |
Het |
Arl13b |
A |
C |
16: 62,633,640 (GRCm39) |
|
probably null |
Het |
Asxl3 |
T |
C |
18: 22,650,044 (GRCm39) |
S678P |
probably damaging |
Het |
Atf6b |
C |
T |
17: 34,866,702 (GRCm39) |
Q58* |
probably null |
Het |
Camsap3 |
A |
G |
8: 3,648,740 (GRCm39) |
T20A |
probably benign |
Het |
Cfap46 |
T |
A |
7: 139,232,726 (GRCm39) |
M782L |
probably benign |
Het |
Cngb3 |
T |
C |
4: 19,364,260 (GRCm39) |
S155P |
probably benign |
Het |
Coro1a |
T |
C |
7: 126,300,719 (GRCm39) |
I162V |
probably benign |
Het |
Cry1 |
T |
A |
10: 84,982,318 (GRCm39) |
I343F |
probably damaging |
Het |
Csnk1e |
A |
T |
15: 79,309,050 (GRCm39) |
M292K |
probably benign |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Cul9 |
A |
T |
17: 46,836,818 (GRCm39) |
M1069K |
probably benign |
Het |
Cyp2c67 |
C |
A |
19: 39,631,708 (GRCm39) |
|
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,979,200 (GRCm39) |
I2633V |
probably damaging |
Het |
Eif4g3 |
C |
A |
4: 137,933,369 (GRCm39) |
D1731E |
probably damaging |
Het |
Epb41l4b |
T |
C |
4: 57,032,204 (GRCm39) |
T592A |
probably benign |
Het |
Evi5 |
T |
C |
5: 107,946,984 (GRCm39) |
|
probably benign |
Het |
Exo1 |
T |
A |
1: 175,728,952 (GRCm39) |
M672K |
probably benign |
Het |
Fcho1 |
T |
C |
8: 72,163,047 (GRCm39) |
S661G |
probably damaging |
Het |
Fnip2 |
A |
G |
3: 79,415,475 (GRCm39) |
Y188H |
possibly damaging |
Het |
Foxb1 |
T |
C |
9: 69,667,293 (GRCm39) |
D79G |
probably damaging |
Het |
Fyco1 |
T |
C |
9: 123,658,346 (GRCm39) |
Y610C |
probably damaging |
Het |
Gm3095 |
T |
A |
14: 15,170,441 (GRCm39) |
Y97N |
probably damaging |
Het |
Gm3095 |
C |
A |
14: 15,170,440 (GRCm39) |
N96K |
probably damaging |
Het |
Gmfb |
A |
T |
14: 47,049,237 (GRCm39) |
L128* |
probably null |
Het |
Gprc5c |
T |
A |
11: 114,755,220 (GRCm39) |
V299D |
possibly damaging |
Het |
Hsfy2 |
C |
T |
1: 56,676,388 (GRCm39) |
V50I |
probably benign |
Het |
Hspa12b |
A |
C |
2: 130,982,849 (GRCm39) |
K236Q |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,080,221 (GRCm39) |
Y566C |
probably damaging |
Het |
Itpr3 |
A |
C |
17: 27,335,581 (GRCm39) |
|
probably null |
Het |
Kprp |
G |
A |
3: 92,732,783 (GRCm39) |
T89I |
probably damaging |
Het |
Lcmt2 |
T |
C |
2: 120,969,133 (GRCm39) |
E650G |
probably damaging |
Het |
Lrch1 |
T |
C |
14: 75,051,144 (GRCm39) |
D331G |
probably damaging |
Het |
Mroh9 |
T |
A |
1: 162,852,110 (GRCm39) |
I860F |
probably benign |
Het |
Mylk |
G |
C |
16: 34,699,845 (GRCm39) |
E403Q |
possibly damaging |
Het |
Myt1l |
A |
G |
12: 29,877,396 (GRCm39) |
D349G |
unknown |
Het |
Ndufs2 |
T |
C |
1: 171,073,690 (GRCm39) |
T31A |
probably benign |
Het |
Ndufs3 |
A |
T |
2: 90,729,016 (GRCm39) |
S157T |
probably benign |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Noct |
T |
A |
3: 51,155,251 (GRCm39) |
S6R |
probably damaging |
Het |
Npas2 |
T |
A |
1: 39,339,808 (GRCm39) |
H119Q |
probably damaging |
Het |
Oprl1 |
A |
T |
2: 181,360,646 (GRCm39) |
Y207F |
probably benign |
Het |
Or2n1e |
G |
A |
17: 38,586,557 (GRCm39) |
|
probably null |
Het |
Or4c11 |
A |
G |
2: 88,695,871 (GRCm39) |
|
probably null |
Het |
Or8k30 |
T |
G |
2: 86,339,193 (GRCm39) |
L130R |
probably damaging |
Het |
Palm3 |
G |
T |
8: 84,756,291 (GRCm39) |
S601I |
possibly damaging |
Het |
Plscr1 |
T |
A |
9: 92,148,548 (GRCm39) |
C163S |
probably damaging |
Het |
Ptprk |
A |
T |
10: 28,369,166 (GRCm39) |
M713L |
probably benign |
Het |
Rdm1 |
A |
G |
11: 101,519,217 (GRCm39) |
D72G |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,265,366 (GRCm39) |
D442G |
probably benign |
Het |
Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
Sbno1 |
T |
C |
5: 124,542,279 (GRCm39) |
Y338C |
probably damaging |
Het |
Seh1l |
T |
G |
18: 67,921,806 (GRCm39) |
V222G |
probably damaging |
Het |
Septin12 |
T |
C |
16: 4,814,340 (GRCm39) |
K43R |
probably damaging |
Het |
Slc25a18 |
A |
C |
6: 120,763,303 (GRCm39) |
|
probably benign |
Het |
Slc33a1 |
T |
C |
3: 63,855,650 (GRCm39) |
T332A |
possibly damaging |
Het |
Slc35d3 |
A |
G |
10: 19,724,909 (GRCm39) |
S316P |
probably benign |
Het |
Spmip7 |
A |
G |
11: 11,438,641 (GRCm39) |
|
probably benign |
Het |
Srrm2 |
T |
A |
17: 24,037,906 (GRCm39) |
|
probably benign |
Het |
Srsf12 |
C |
T |
4: 33,230,974 (GRCm39) |
S156L |
probably damaging |
Het |
Syce3 |
A |
G |
15: 89,274,606 (GRCm39) |
M49T |
probably benign |
Het |
Tjp3 |
T |
C |
10: 81,112,094 (GRCm39) |
|
probably benign |
Het |
Tnks |
G |
T |
8: 35,342,430 (GRCm39) |
N373K |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,013,847 (GRCm39) |
N366S |
possibly damaging |
Het |
Trpm1 |
G |
A |
7: 63,890,283 (GRCm39) |
R962H |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,854,995 (GRCm39) |
M1885L |
possibly damaging |
Het |
Tshz3 |
A |
G |
7: 36,471,221 (GRCm39) |
D1070G |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,546,421 (GRCm39) |
M3399T |
probably benign |
Het |
Utp15 |
G |
A |
13: 98,393,695 (GRCm39) |
T196I |
probably benign |
Het |
Vmn1r168 |
T |
C |
7: 23,240,725 (GRCm39) |
I194T |
probably benign |
Het |
Vmn2r73 |
C |
T |
7: 85,525,120 (GRCm39) |
W9* |
probably null |
Het |
Wdr17 |
T |
C |
8: 55,092,930 (GRCm39) |
Y1076C |
probably damaging |
Het |
Zan |
T |
C |
5: 137,382,092 (GRCm39) |
T5152A |
unknown |
Het |
Zbtb46 |
A |
T |
2: 181,066,042 (GRCm39) |
V36E |
possibly damaging |
Het |
Zfp558 |
T |
C |
9: 18,380,579 (GRCm39) |
I9M |
possibly damaging |
Het |
Zscan2 |
T |
A |
7: 80,525,534 (GRCm39) |
Y418* |
probably null |
Het |
|
Other mutations in Abca8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00862:Abca8b
|
APN |
11 |
109,844,374 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00952:Abca8b
|
APN |
11 |
109,859,886 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01141:Abca8b
|
APN |
11 |
109,828,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Abca8b
|
APN |
11 |
109,867,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Abca8b
|
APN |
11 |
109,827,580 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01862:Abca8b
|
APN |
11 |
109,837,997 (GRCm39) |
nonsense |
probably null |
|
IGL01963:Abca8b
|
APN |
11 |
109,862,589 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02169:Abca8b
|
APN |
11 |
109,843,408 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02536:Abca8b
|
APN |
11 |
109,872,574 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02658:Abca8b
|
APN |
11 |
109,843,386 (GRCm39) |
missense |
probably benign |
|
IGL02828:Abca8b
|
APN |
11 |
109,871,720 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03118:Abca8b
|
APN |
11 |
109,838,007 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03302:Abca8b
|
APN |
11 |
109,858,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03325:Abca8b
|
APN |
11 |
109,844,422 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0057:Abca8b
|
UTSW |
11 |
109,832,385 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0131:Abca8b
|
UTSW |
11 |
109,833,115 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0226:Abca8b
|
UTSW |
11 |
109,847,844 (GRCm39) |
splice site |
probably null |
|
R0426:Abca8b
|
UTSW |
11 |
109,845,853 (GRCm39) |
splice site |
probably benign |
|
R0432:Abca8b
|
UTSW |
11 |
109,870,841 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0512:Abca8b
|
UTSW |
11 |
109,841,476 (GRCm39) |
missense |
probably benign |
0.32 |
R0589:Abca8b
|
UTSW |
11 |
109,833,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R0690:Abca8b
|
UTSW |
11 |
109,860,634 (GRCm39) |
splice site |
probably benign |
|
R1263:Abca8b
|
UTSW |
11 |
109,832,433 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1371:Abca8b
|
UTSW |
11 |
109,844,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R1497:Abca8b
|
UTSW |
11 |
109,864,647 (GRCm39) |
splice site |
probably benign |
|
R1502:Abca8b
|
UTSW |
11 |
109,865,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1517:Abca8b
|
UTSW |
11 |
109,862,640 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1543:Abca8b
|
UTSW |
11 |
109,865,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R1625:Abca8b
|
UTSW |
11 |
109,857,947 (GRCm39) |
missense |
probably benign |
0.11 |
R1753:Abca8b
|
UTSW |
11 |
109,864,542 (GRCm39) |
missense |
probably benign |
0.00 |
R1819:Abca8b
|
UTSW |
11 |
109,871,882 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1822:Abca8b
|
UTSW |
11 |
109,847,901 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1829:Abca8b
|
UTSW |
11 |
109,833,167 (GRCm39) |
missense |
probably damaging |
0.97 |
R1873:Abca8b
|
UTSW |
11 |
109,870,781 (GRCm39) |
missense |
probably benign |
0.01 |
R1899:Abca8b
|
UTSW |
11 |
109,828,744 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1908:Abca8b
|
UTSW |
11 |
109,847,924 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1962:Abca8b
|
UTSW |
11 |
109,870,724 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Abca8b
|
UTSW |
11 |
109,868,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Abca8b
|
UTSW |
11 |
109,847,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2092:Abca8b
|
UTSW |
11 |
109,857,534 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2100:Abca8b
|
UTSW |
11 |
109,828,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Abca8b
|
UTSW |
11 |
109,845,974 (GRCm39) |
missense |
probably benign |
0.03 |
R2871:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2871:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2872:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2872:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2873:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3711:Abca8b
|
UTSW |
11 |
109,837,081 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3937:Abca8b
|
UTSW |
11 |
109,865,393 (GRCm39) |
missense |
probably benign |
0.01 |
R4052:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4060:Abca8b
|
UTSW |
11 |
109,848,027 (GRCm39) |
missense |
probably benign |
0.04 |
R4207:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4208:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4354:Abca8b
|
UTSW |
11 |
109,862,518 (GRCm39) |
missense |
probably benign |
0.27 |
R4399:Abca8b
|
UTSW |
11 |
109,827,211 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4456:Abca8b
|
UTSW |
11 |
109,833,071 (GRCm39) |
missense |
probably benign |
0.27 |
R4509:Abca8b
|
UTSW |
11 |
109,857,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Abca8b
|
UTSW |
11 |
109,827,274 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4868:Abca8b
|
UTSW |
11 |
109,865,338 (GRCm39) |
missense |
probably benign |
0.05 |
R5002:Abca8b
|
UTSW |
11 |
109,852,623 (GRCm39) |
missense |
probably damaging |
0.96 |
R5007:Abca8b
|
UTSW |
11 |
109,827,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Abca8b
|
UTSW |
11 |
109,840,957 (GRCm39) |
missense |
probably damaging |
0.98 |
R5023:Abca8b
|
UTSW |
11 |
109,865,814 (GRCm39) |
critical splice donor site |
probably null |
|
R5091:Abca8b
|
UTSW |
11 |
109,827,210 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5098:Abca8b
|
UTSW |
11 |
109,847,944 (GRCm39) |
missense |
probably benign |
0.05 |
R5117:Abca8b
|
UTSW |
11 |
109,857,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Abca8b
|
UTSW |
11 |
109,867,420 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5302:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5487:Abca8b
|
UTSW |
11 |
109,844,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R5512:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5564:Abca8b
|
UTSW |
11 |
109,825,407 (GRCm39) |
missense |
probably benign |
0.08 |
R5610:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Abca8b
|
UTSW |
11 |
109,831,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Abca8b
|
UTSW |
11 |
109,844,445 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5827:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5848:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5854:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Abca8b
|
UTSW |
11 |
109,844,423 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5994:Abca8b
|
UTSW |
11 |
109,840,592 (GRCm39) |
splice site |
probably null |
|
R6035:Abca8b
|
UTSW |
11 |
109,862,686 (GRCm39) |
splice site |
probably null |
|
R6035:Abca8b
|
UTSW |
11 |
109,862,686 (GRCm39) |
splice site |
probably null |
|
R6050:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Abca8b
|
UTSW |
11 |
109,864,634 (GRCm39) |
missense |
probably benign |
0.03 |
R6223:Abca8b
|
UTSW |
11 |
109,868,672 (GRCm39) |
missense |
probably benign |
0.00 |
R6349:Abca8b
|
UTSW |
11 |
109,825,544 (GRCm39) |
splice site |
probably null |
|
R7002:Abca8b
|
UTSW |
11 |
109,832,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Abca8b
|
UTSW |
11 |
109,864,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7107:Abca8b
|
UTSW |
11 |
109,867,299 (GRCm39) |
missense |
probably damaging |
0.98 |
R7158:Abca8b
|
UTSW |
11 |
109,825,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Abca8b
|
UTSW |
11 |
109,836,654 (GRCm39) |
missense |
probably benign |
0.09 |
R7197:Abca8b
|
UTSW |
11 |
109,836,648 (GRCm39) |
nonsense |
probably null |
|
R7220:Abca8b
|
UTSW |
11 |
109,872,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Abca8b
|
UTSW |
11 |
109,829,275 (GRCm39) |
missense |
probably benign |
0.01 |
R7590:Abca8b
|
UTSW |
11 |
109,829,341 (GRCm39) |
missense |
probably damaging |
0.97 |
R7658:Abca8b
|
UTSW |
11 |
109,826,543 (GRCm39) |
missense |
probably benign |
0.00 |
R7739:Abca8b
|
UTSW |
11 |
109,865,417 (GRCm39) |
missense |
probably benign |
0.05 |
R7797:Abca8b
|
UTSW |
11 |
109,862,509 (GRCm39) |
critical splice donor site |
probably null |
|
R7934:Abca8b
|
UTSW |
11 |
109,865,865 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8074:Abca8b
|
UTSW |
11 |
109,829,320 (GRCm39) |
missense |
probably benign |
|
R8302:Abca8b
|
UTSW |
11 |
109,853,406 (GRCm39) |
critical splice donor site |
probably null |
|
R8341:Abca8b
|
UTSW |
11 |
109,845,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8486:Abca8b
|
UTSW |
11 |
109,857,937 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8748:Abca8b
|
UTSW |
11 |
109,836,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Abca8b
|
UTSW |
11 |
109,838,003 (GRCm39) |
missense |
probably benign |
0.00 |
R9002:Abca8b
|
UTSW |
11 |
109,843,456 (GRCm39) |
missense |
probably benign |
0.02 |
R9032:Abca8b
|
UTSW |
11 |
109,848,073 (GRCm39) |
missense |
probably benign |
0.04 |
R9099:Abca8b
|
UTSW |
11 |
109,871,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9124:Abca8b
|
UTSW |
11 |
109,828,593 (GRCm39) |
missense |
probably damaging |
0.97 |
R9178:Abca8b
|
UTSW |
11 |
109,840,937 (GRCm39) |
missense |
probably benign |
0.00 |
R9188:Abca8b
|
UTSW |
11 |
109,872,561 (GRCm39) |
nonsense |
probably null |
|
R9277:Abca8b
|
UTSW |
11 |
109,867,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R9340:Abca8b
|
UTSW |
11 |
109,840,939 (GRCm39) |
missense |
probably benign |
0.43 |
R9371:Abca8b
|
UTSW |
11 |
109,858,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Abca8b
|
UTSW |
11 |
109,870,711 (GRCm39) |
missense |
probably benign |
|
R9450:Abca8b
|
UTSW |
11 |
109,859,930 (GRCm39) |
missense |
probably damaging |
0.98 |
R9462:Abca8b
|
UTSW |
11 |
109,844,433 (GRCm39) |
missense |
|
|
R9712:Abca8b
|
UTSW |
11 |
109,833,163 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Abca8b
|
UTSW |
11 |
109,867,308 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Abca8b
|
UTSW |
11 |
109,865,470 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Abca8b
|
UTSW |
11 |
109,852,734 (GRCm39) |
missense |
possibly damaging |
0.52 |
|