Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,770,934 (GRCm39) |
L41P |
probably damaging |
Het |
Acad8 |
A |
T |
9: 26,896,861 (GRCm39) |
Y199* |
probably null |
Het |
Acot12 |
A |
T |
13: 91,908,096 (GRCm39) |
I93L |
probably benign |
Het |
Acsbg3 |
T |
A |
17: 57,191,949 (GRCm39) |
Y542* |
probably null |
Het |
Actn1 |
C |
A |
12: 80,230,291 (GRCm39) |
R321L |
probably benign |
Het |
Ap3s1 |
A |
G |
18: 46,887,469 (GRCm39) |
E34G |
possibly damaging |
Het |
Armh4 |
A |
G |
14: 50,011,459 (GRCm39) |
Y83H |
probably damaging |
Het |
Atp5f1a |
T |
C |
18: 77,870,017 (GRCm39) |
S533P |
probably damaging |
Het |
Bcorl1 |
T |
C |
X: 47,458,081 (GRCm39) |
V538A |
probably benign |
Het |
Cdhr4 |
A |
G |
9: 107,875,206 (GRCm39) |
T689A |
probably damaging |
Het |
Cdk19 |
A |
T |
10: 40,355,726 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
G |
T |
2: 64,928,554 (GRCm39) |
P923Q |
probably damaging |
Het |
Cpt1a |
T |
C |
19: 3,421,585 (GRCm39) |
S456P |
probably benign |
Het |
Cst11 |
T |
C |
2: 148,613,160 (GRCm39) |
Y55C |
probably damaging |
Het |
Ctif |
T |
G |
18: 75,654,452 (GRCm39) |
D358A |
probably benign |
Het |
Cyp2d34 |
T |
G |
15: 82,500,974 (GRCm39) |
E386A |
probably benign |
Het |
Dcxr |
A |
G |
11: 120,617,133 (GRCm39) |
F104L |
probably benign |
Het |
Dmbt1 |
G |
T |
7: 130,703,762 (GRCm39) |
W1107C |
probably damaging |
Het |
Dsg1a |
A |
T |
18: 20,466,830 (GRCm39) |
I567F |
probably damaging |
Het |
Ednrb |
T |
A |
14: 104,058,350 (GRCm39) |
R318* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,527,377 (GRCm39) |
I36T |
possibly damaging |
Het |
Fam83b |
A |
T |
9: 76,399,987 (GRCm39) |
I372N |
probably damaging |
Het |
Fbh1 |
A |
G |
2: 11,763,100 (GRCm39) |
V518A |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,625,162 (GRCm39) |
E308G |
possibly damaging |
Het |
Foxl2 |
A |
C |
9: 98,838,282 (GRCm39) |
Y190S |
probably damaging |
Het |
Gab3 |
TTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTC |
TTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTC |
X: 74,043,585 (GRCm39) |
|
probably benign |
Het |
Galnt17 |
C |
T |
5: 131,114,831 (GRCm39) |
R223Q |
probably damaging |
Het |
Gm14496 |
G |
A |
2: 181,633,127 (GRCm39) |
D37N |
possibly damaging |
Het |
Gpr82 |
T |
C |
X: 13,532,274 (GRCm39) |
V274A |
probably benign |
Het |
Hsp90aa1 |
T |
C |
12: 110,660,566 (GRCm39) |
N292S |
probably damaging |
Het |
Ints1 |
C |
T |
5: 139,741,754 (GRCm39) |
V1826M |
possibly damaging |
Het |
Itgb4 |
A |
G |
11: 115,896,561 (GRCm39) |
D1440G |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,963,200 (GRCm39) |
D1552G |
probably damaging |
Het |
Kel |
G |
A |
6: 41,663,418 (GRCm39) |
T702I |
possibly damaging |
Het |
Klf3 |
T |
C |
5: 64,979,266 (GRCm39) |
V36A |
probably damaging |
Het |
Klhl23 |
A |
T |
2: 69,659,228 (GRCm39) |
I418F |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,510,674 (GRCm39) |
I1329L |
probably benign |
Het |
Krtap2-4 |
T |
C |
11: 99,505,606 (GRCm39) |
|
probably benign |
Het |
Krtap9-5 |
T |
A |
11: 99,840,270 (GRCm39) |
C324S |
unknown |
Het |
Lepr |
T |
C |
4: 101,630,178 (GRCm39) |
V631A |
possibly damaging |
Het |
Lifr |
T |
C |
15: 7,216,404 (GRCm39) |
I793T |
probably damaging |
Het |
Mcoln1 |
G |
A |
8: 3,561,731 (GRCm39) |
R427H |
probably damaging |
Het |
Mgat5b |
G |
A |
11: 116,810,255 (GRCm39) |
|
probably benign |
Het |
Mmp12 |
G |
A |
9: 7,349,802 (GRCm39) |
V78M |
probably damaging |
Het |
Mrgprb8 |
T |
A |
7: 48,038,634 (GRCm39) |
L102M |
possibly damaging |
Het |
Mybphl |
A |
G |
3: 108,282,949 (GRCm39) |
T246A |
possibly damaging |
Het |
Myo7b |
A |
T |
18: 32,133,031 (GRCm39) |
F439L |
probably damaging |
Het |
Myom1 |
A |
T |
17: 71,408,024 (GRCm39) |
D1088V |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,623,471 (GRCm39) |
F1004S |
probably benign |
Het |
Palld |
A |
T |
8: 61,986,467 (GRCm39) |
M788K |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,234,465 (GRCm39) |
Y1423* |
probably null |
Het |
Pfkm |
A |
G |
15: 98,027,171 (GRCm39) |
K615E |
probably damaging |
Het |
Pkd1l2 |
G |
T |
8: 117,808,208 (GRCm39) |
D105E |
probably damaging |
Het |
Plekha5 |
G |
A |
6: 140,518,603 (GRCm39) |
A297T |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,944,810 (GRCm39) |
M2051K |
probably damaging |
Het |
Ppp6r2 |
A |
G |
15: 89,162,949 (GRCm39) |
T524A |
probably damaging |
Het |
Psg26 |
T |
C |
7: 18,209,067 (GRCm39) |
E447G |
probably damaging |
Het |
Rab3gap2 |
A |
G |
1: 185,014,586 (GRCm39) |
D1225G |
probably benign |
Het |
Rep15 |
A |
G |
6: 146,934,403 (GRCm39) |
|
probably null |
Het |
Rgl2 |
G |
A |
17: 34,152,314 (GRCm39) |
|
probably null |
Het |
Rpl7a |
T |
G |
2: 26,801,473 (GRCm39) |
V55G |
possibly damaging |
Het |
Rtp1 |
A |
T |
16: 23,250,108 (GRCm39) |
I158F |
probably benign |
Het |
Scaper |
A |
T |
9: 55,819,334 (GRCm39) |
V127E |
probably benign |
Het |
Sele |
T |
A |
1: 163,881,395 (GRCm39) |
C501S |
probably damaging |
Het |
Serpina11 |
C |
T |
12: 103,949,104 (GRCm39) |
V358I |
probably benign |
Het |
Slc16a4 |
A |
G |
3: 107,211,819 (GRCm39) |
|
probably null |
Het |
Slco6c1 |
T |
C |
1: 97,055,656 (GRCm39) |
I82V |
probably benign |
Het |
Smarca5 |
T |
C |
8: 81,431,304 (GRCm39) |
E971G |
probably damaging |
Het |
Smr2 |
T |
C |
5: 88,256,595 (GRCm39) |
L91P |
probably damaging |
Het |
Spata31f3 |
T |
A |
4: 42,868,558 (GRCm39) |
H355L |
probably benign |
Het |
Spopfm2 |
A |
T |
3: 94,082,973 (GRCm39) |
C279* |
probably null |
Het |
Srrm2 |
A |
G |
17: 24,036,722 (GRCm39) |
|
probably benign |
Het |
Sting1 |
A |
T |
18: 35,868,290 (GRCm39) |
M270K |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,006,514 (GRCm39) |
W7980R |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,074,853 (GRCm39) |
T4598A |
probably benign |
Het |
Tmem171 |
A |
T |
13: 98,828,851 (GRCm39) |
F100I |
probably damaging |
Het |
Tnfrsf10b |
A |
G |
14: 70,013,546 (GRCm39) |
T159A |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,309,834 (GRCm39) |
|
probably null |
Het |
Trim46 |
A |
T |
3: 89,142,504 (GRCm39) |
I638N |
probably damaging |
Het |
Ubl7 |
G |
A |
9: 57,827,825 (GRCm39) |
D171N |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,608,779 (GRCm39) |
Y1514H |
probably damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,129,334 (GRCm39) |
I742V |
probably damaging |
Het |
Xrcc2 |
A |
T |
5: 25,897,505 (GRCm39) |
V148E |
probably damaging |
Het |
Zbed3 |
A |
G |
13: 95,472,615 (GRCm39) |
D13G |
possibly damaging |
Het |
Zdhhc25 |
T |
A |
15: 88,484,962 (GRCm39) |
L99Q |
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 |
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 |
R4946:Abca8a
|
UTSW |
11 |
109,977,300 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|