Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts4 |
C |
A |
1: 171,086,559 (GRCm39) |
P784T |
probably damaging |
Het |
Adamts6 |
T |
C |
13: 104,630,145 (GRCm39) |
L1096P |
probably damaging |
Het |
Ap1b1 |
A |
G |
11: 4,990,290 (GRCm39) |
S849G |
probably benign |
Het |
Arap2 |
T |
C |
5: 62,761,747 (GRCm39) |
S1660G |
probably benign |
Het |
Atp10b |
A |
C |
11: 43,121,174 (GRCm39) |
T946P |
probably damaging |
Het |
Brpf1 |
A |
G |
6: 113,299,381 (GRCm39) |
D1103G |
probably damaging |
Het |
Bub1 |
A |
G |
2: 127,669,339 (GRCm39) |
Y102H |
probably damaging |
Het |
Ccdc182 |
A |
G |
11: 88,185,193 (GRCm39) |
E91G |
probably benign |
Het |
Cd200r4 |
C |
T |
16: 44,653,803 (GRCm39) |
T154M |
probably damaging |
Het |
Cdh20 |
A |
G |
1: 104,881,755 (GRCm39) |
T407A |
probably benign |
Het |
Col6a2 |
T |
C |
10: 76,450,512 (GRCm39) |
I140V |
probably benign |
Het |
Csn3 |
C |
A |
5: 88,077,983 (GRCm39) |
T163K |
probably damaging |
Het |
Dars2 |
A |
T |
1: 160,874,375 (GRCm39) |
L438* |
probably null |
Het |
Dbr1 |
T |
C |
9: 99,464,440 (GRCm39) |
L289P |
probably damaging |
Het |
Ddx46 |
A |
G |
13: 55,811,122 (GRCm39) |
R573G |
possibly damaging |
Het |
Defb10 |
T |
C |
8: 22,348,972 (GRCm39) |
I10T |
possibly damaging |
Het |
Dis3l |
T |
C |
9: 64,233,069 (GRCm39) |
E136G |
possibly damaging |
Het |
Dnajb13 |
T |
C |
7: 100,156,668 (GRCm39) |
Q136R |
probably benign |
Het |
Dse |
A |
T |
10: 34,029,214 (GRCm39) |
S625R |
probably damaging |
Het |
Dvl3 |
A |
G |
16: 20,342,209 (GRCm39) |
D94G |
probably damaging |
Het |
Dynlt2a2 |
A |
G |
17: 15,187,876 (GRCm39) |
F133L |
probably benign |
Het |
E130311K13Rik |
A |
C |
3: 63,822,968 (GRCm39) |
Y225* |
probably null |
Het |
Etnppl |
A |
G |
3: 130,422,438 (GRCm39) |
I222V |
probably benign |
Het |
Evc2 |
T |
C |
5: 37,550,440 (GRCm39) |
L818P |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,205,626 (GRCm39) |
C1083* |
probably null |
Het |
Flnc |
G |
A |
6: 29,438,693 (GRCm39) |
V196I |
probably benign |
Het |
Fscn3 |
A |
G |
6: 28,435,622 (GRCm39) |
D415G |
probably benign |
Het |
Gm4861 |
A |
C |
3: 137,256,381 (GRCm39) |
V75G |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,155,399 (GRCm39) |
T345S |
probably benign |
Het |
Grik4 |
T |
C |
9: 42,432,169 (GRCm39) |
S943G |
probably damaging |
Het |
Grik4 |
C |
T |
9: 42,502,743 (GRCm39) |
R460Q |
probably benign |
Het |
Ifi207 |
A |
C |
1: 173,556,872 (GRCm39) |
L629R |
possibly damaging |
Het |
Ift52 |
G |
A |
2: 162,871,782 (GRCm39) |
|
probably null |
Het |
Insl3 |
A |
G |
8: 72,142,876 (GRCm39) |
D79G |
probably damaging |
Het |
Kif5a |
A |
T |
10: 127,081,310 (GRCm39) |
I208N |
probably damaging |
Het |
Lag3 |
T |
C |
6: 124,886,206 (GRCm39) |
Y249C |
probably damaging |
Het |
Lipe |
T |
C |
7: 25,097,572 (GRCm39) |
N124D |
possibly damaging |
Het |
Lnpep |
A |
G |
17: 17,791,906 (GRCm39) |
Y412H |
probably damaging |
Het |
Lrtm2 |
A |
G |
6: 119,294,235 (GRCm39) |
Y299H |
probably benign |
Het |
Lypd4 |
T |
C |
7: 24,566,253 (GRCm39) |
T24A |
probably benign |
Het |
Magi1 |
T |
A |
6: 93,671,151 (GRCm39) |
I805F |
probably damaging |
Het |
Mfap3 |
T |
C |
11: 57,418,975 (GRCm39) |
L45P |
probably benign |
Het |
Nbea |
G |
A |
3: 55,912,310 (GRCm39) |
P1159L |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,231,407 (GRCm39) |
|
probably benign |
Het |
Notch1 |
A |
T |
2: 26,374,335 (GRCm39) |
N229K |
possibly damaging |
Het |
Nova1 |
A |
G |
12: 46,767,615 (GRCm39) |
I102T |
unknown |
Het |
Npepps |
T |
C |
11: 97,109,401 (GRCm39) |
E725G |
possibly damaging |
Het |
Or11g27 |
A |
T |
14: 50,771,234 (GRCm39) |
M122L |
possibly damaging |
Het |
Or13a1 |
T |
C |
6: 116,471,242 (GRCm39) |
I224T |
probably damaging |
Het |
Or5l14 |
T |
C |
2: 87,792,379 (GRCm39) |
N286D |
probably damaging |
Het |
Or6c69c |
T |
C |
10: 129,910,741 (GRCm39) |
I154T |
probably damaging |
Het |
Pappa2 |
A |
T |
1: 158,784,858 (GRCm39) |
W51R |
probably damaging |
Het |
Pde8a |
T |
C |
7: 80,942,007 (GRCm39) |
S149P |
probably damaging |
Het |
Pgap6 |
A |
G |
17: 26,339,290 (GRCm39) |
T535A |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,785,968 (GRCm39) |
L1052Q |
possibly damaging |
Het |
Pou5f2 |
T |
A |
13: 78,173,370 (GRCm39) |
L104Q |
probably benign |
Het |
Pramel32 |
T |
A |
4: 88,546,269 (GRCm39) |
I358F |
probably benign |
Het |
Psme2b |
A |
T |
11: 48,836,576 (GRCm39) |
W124R |
probably damaging |
Het |
Ptk2b |
G |
A |
14: 66,400,529 (GRCm39) |
S762L |
possibly damaging |
Het |
Ptprs |
T |
C |
17: 56,744,992 (GRCm39) |
N248S |
probably benign |
Het |
Rgs22 |
G |
A |
15: 36,080,997 (GRCm39) |
T705I |
probably damaging |
Het |
Rnf123 |
T |
C |
9: 107,945,709 (GRCm39) |
|
probably null |
Het |
Sel1l2 |
A |
T |
2: 140,231,515 (GRCm39) |
I13N |
probably damaging |
Het |
Slc39a4 |
T |
C |
15: 76,500,793 (GRCm39) |
T57A |
probably benign |
Het |
Smpdl3a |
T |
G |
10: 57,685,187 (GRCm39) |
V319G |
probably damaging |
Het |
Syt9 |
T |
C |
7: 107,035,694 (GRCm39) |
L237P |
probably damaging |
Het |
Tbc1d16 |
G |
T |
11: 119,044,830 (GRCm39) |
A536E |
probably damaging |
Het |
Tcf20 |
T |
C |
15: 82,739,777 (GRCm39) |
D558G |
probably damaging |
Het |
Tdpoz2 |
A |
T |
3: 93,559,453 (GRCm39) |
M173K |
probably benign |
Het |
Tek |
A |
G |
4: 94,669,339 (GRCm39) |
I113M |
probably damaging |
Het |
Tmem50a |
A |
T |
4: 134,636,980 (GRCm39) |
D50E |
probably benign |
Het |
Trappc11 |
A |
T |
8: 47,983,862 (GRCm39) |
V10E |
possibly damaging |
Het |
Vmn1r172 |
C |
T |
7: 23,359,681 (GRCm39) |
R189* |
probably null |
Het |
Vmn2r63 |
A |
T |
7: 42,578,015 (GRCm39) |
D174E |
possibly damaging |
Het |
Zc3h10 |
A |
T |
10: 128,380,151 (GRCm39) |
M402K |
probably damaging |
Het |
Zfp109 |
T |
C |
7: 23,927,588 (GRCm39) |
H615R |
probably damaging |
Het |
Zfp982 |
A |
C |
4: 147,597,126 (GRCm39) |
H161P |
probably benign |
Het |
Zhx1 |
A |
G |
15: 57,917,992 (GRCm39) |
F85L |
probably damaging |
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 |
|
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 |
R1618:Abca8b
|
UTSW |
11 |
109,840,714 (GRCm39) |
splice site |
probably benign |
|
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 |
|