geneid | 10349 |
---|---|
ensemblid | ENSG00000154263.18 |
hgncid | 30 |
symbol | ABCA10 |
name | ATP binding cassette subfamily A member 10 |
refseq_nuc | NM_001377321.1 |
refseq_prot | NP_001364250.1 |
ensembl_nuc | ENST00000690296.1 |
ensembl_prot | ENSP00000509702.1 |
mane_status | MANE Select |
chr | chr17 |
start | 69148007 |
end | 69228824 |
strand | - |
ver | v1.2 |
region | chr17:69148007-69228824 |
region5000 | chr17:69143007-69233824 |
regionname0 | ABCA10_chr17_69148007_69228824 |
regionname5000 | ABCA10_chr17_69143007_69233824 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1543 | 96 | 17 | 11 | 54 | 3 | 10 | 44 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002 | 0/1 | 1543 | 82 | 2 | 19 | 44 | 3 | 13 | 38 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003 | 0/0 | 1543 | 54 | 12 | 14 | 15 | 7 | 6 | 13 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004 | 0/0 | 459 | 42 | 4 | 15 | 17 | 1 | 5 | 12 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005 | 0/0 | 260 | 18 | 17 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006 | 0/0 | 453 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0007 | 0/0 | 458 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0008 | 0/0 | 1543 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009 | 0/0 | 1543 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0010 | 0/0 | 1543 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0011 | 0/0 | 1543 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0012 | 0/0 | 1543 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0013 | 0/0 | 1543 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0014 | 0/0 | 1543 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0015 | 0/0 | 171 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0016 | 0/0 | 1543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0017 | 0/0 | 1543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0018 | 0/0 | 1543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0019 | 0/0 | 1543 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0020 | 0/0 | 1543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0021 | 0/0 | 1543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0022 | 0/0 | 1543 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0023 | 0/0 | 1543 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0024 | 0/0 | 1543 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0025 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0026 | 0/0 | 1543 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 4632 | 94 | 17 | 11 | 53 | 3 | 9 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0002 | 0/1 | 4632 | 80 | 2 | 17 | 44 | 3 | 13 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0003 | 0/0 | 4632 | 52 | 11 | 13 | 15 | 7 | 6 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0004 | 0/0 | 4626 | 29 | 4 | 13 | 6 | 1 | 5 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0005 | 0/0 | 4638 | 14 | 13 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0006 | 0/0 | 4626 | 13 | 0 | 2 | 11 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0007 | 0/0 | 4638 | 11 | 8 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0008 | 0/0 | 4638 | 9 | 6 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0009 | 0/0 | 4632 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0010 | 0/0 | 4632 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0011 | 0/0 | 4632 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0012 | 0/0 | 4632 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0013 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0014 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0015 | 0/0 | 4632 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0016 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0017 | 0/0 | 4632 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0018 | 0/0 | 4632 | 2 | 1 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0019 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0020 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0021 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0022 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0023 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0024 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0025 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0026 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0027 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0028 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0029 | 0/0 | 4630 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0030 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0031 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0032 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0033 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0034 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0035 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0036 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
c0037 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1377 | 134 | 18 | 27 | 56 | 10 | 22 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0002 | 0/0 | 1377 | 92 | 10 | 11 | 60 | 2 | 9 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0003 | 0/0 | 1377 | 40 | 4 | 14 | 16 | 1 | 5 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0004 | 0/0 | 1377 | 24 | 20 | 4 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0005 | 0/0 | 1377 | 12 | 1 | 6 | 4 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0006 | 0/0 | 1377 | 11 | 11 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0007 | 0/0 | 1377 | 9 | 5 | 4 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0008 | 1/0 | 1377 | 8 | 1 | 0 | 4 | 1 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0009 | 0/0 | 1377 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0010 | 0/0 | 1377 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0011 | 0/0 | 1377 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0012 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0013 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0014 | 0/0 | 1377 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0015 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0016 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0017 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
t0018 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4632 | 94 | 17 | 11 | 53 | 3 | 9 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0034 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0035 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002c0002 | 0/1 | 4632 | 80 | 2 | 17 | 44 | 3 | 13 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002c0015 | 0/0 | 4632 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0003 | 0/0 | 4632 | 52 | 11 | 13 | 15 | 7 | 6 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0025 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0028 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0004 | 0/0 | 4626 | 29 | 4 | 13 | 6 | 1 | 5 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0006 | 0/0 | 4626 | 13 | 0 | 2 | 11 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0005 | 0/0 | 4638 | 14 | 13 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0013 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0014 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006c0007 | 0/0 | 4638 | 11 | 8 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006c0016 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0007c0008 | 0/0 | 4638 | 9 | 6 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0008c0009 | 0/0 | 4632 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009c0018 | 0/0 | 4632 | 2 | 1 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009c0022 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0010c0010 | 0/0 | 4632 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0011c0012 | 0/0 | 4632 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0012c0011 | 0/0 | 4632 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0013c0020 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0013c0021 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0014c0017 | 0/0 | 4632 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0015c0030 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0016c0032 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0017c0033 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0018c0036 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0019c0037 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0020c0031 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0021c0023 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0022c0024 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0023c0026 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0024c0027 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0025c0029 | 0/0 | 4630 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0026c0019 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6008 | 81 | 9 | 11 | 51 | 2 | 8 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0001t0006 | 0/0 | 6008 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0001t0008 | 1/0 | 6008 | 5 | 1 | 0 | 1 | 1 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0001t0013 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0001t0017 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0001t0018 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0034t0002 | 0/0 | 6008 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0001c0035t0002 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002c0002t0001 | 0/1 | 6008 | 76 | 2 | 17 | 40 | 3 | 13 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002c0002t0005 | 0/0 | 6008 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0002c0015t0001 | 0/0 | 6008 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0003t0001 | 0/0 | 6008 | 43 | 9 | 7 | 15 | 7 | 5 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0003t0005 | 0/0 | 6008 | 8 | 1 | 6 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0003t0016 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0025t0001 | 0/0 | 6008 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0003c0028t0006 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0004t0003 | 0/0 | 6002 | 28 | 4 | 12 | 6 | 1 | 5 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0004t0011 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0006t0003 | 0/0 | 6002 | 12 | 0 | 2 | 10 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0004c0006t0011 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0005t0004 | 0/0 | 6014 | 13 | 12 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0005t0015 | 0/0 | 6014 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0013t0001 | 0/0 | 6008 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0005c0014t0001 | 0/0 | 6008 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006c0007t0004 | 0/0 | 6014 | 8 | 5 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006c0007t0010 | 0/0 | 6014 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0006c0016t0004 | 0/0 | 6014 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0007c0008t0004 | 0/0 | 6014 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0007c0008t0007 | 0/0 | 6014 | 8 | 5 | 3 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0008c0009t0009 | 0/0 | 6008 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009c0018t0001 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009c0018t0002 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0009c0022t0012 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0010c0010t0006 | 0/0 | 6008 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0011c0012t0008 | 0/0 | 6008 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0012c0011t0002 | 0/0 | 6008 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0013c0020t0006 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0013c0021t0006 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0014c0017t0002 | 0/0 | 6008 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0015c0030t0001 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0016c0032t0002 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0017c0033t0002 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0018c0036t0002 | 0/0 | 6008 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0019c0037t0007 | 0/0 | 6008 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0020c0031t0001 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0021c0023t0001 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0022c0024t0001 | 0/0 | 6008 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0023c0026t0001 | 0/0 | 6008 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0024c0027t0001 | 0/0 | 6008 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0025c0029t0014 | 0/0 | 6006 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
a0026c0019t0001 | 0/0 | 6008 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | copy fasta | chr17 | 69143007 | 69233824 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0008g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0008g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0008g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0017g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0001t0018g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0034t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0001c0035t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0002c0015t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0005g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0003t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0025t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0003c0028t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0004t0011g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0004c0006t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0005t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0013t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0013t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0014t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0005c0014t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0010g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0007t0010g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0016t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0006c0016t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0007c0008t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0008c0009t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0008c0009t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0008c0009t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0008c0009t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0008c0009t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0009c0018t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0009c0018t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0009c0022t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0010c0010t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0010c0010t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0010c0010t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0011c0012t0008g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0011c0012t0008g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0011c0012t0008g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0012c0011t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0012c0011t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0012c0011t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0013c0020t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0013c0021t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0014c0017t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0014c0017t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0015c0030t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0016c0032t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0017c0033t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0018c0036t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0019c0037t0007g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0020c0031t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0021c0023t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0022c0024t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0023c0026t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0024c0027t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0025c0029t0014g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
a0026c0019t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | GBR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0137 | EUR | GBR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00140 | hp1 | a0001 | c0001 | t0008 | g0317 | EUR | GBR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0056 | EUR | GBR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0201 | EUR | FIN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | FIN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0148 | EUR | FIN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | CHS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | CHS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00609 | hp2 | a0004 | c0004 | t0003 | g0239 | EAS | CHS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00639 | hp1 | a0006 | c0007 | t0004 | g0188 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0206 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00733 | hp2 | a0004 | c0004 | t0003 | g0007 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0089 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0133 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01069 | hp1 | a0007 | c0008 | t0007 | g0006 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01069 | hp2 | a0003 | c0025 | t0001 | g0042 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01070 | hp1 | a0004 | c0004 | t0003 | g0208 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01071 | hp1 | a0007 | c0008 | t0007 | g0006 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01071 | hp2 | a0004 | c0004 | t0003 | g0209 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01074 | hp1 | a0004 | c0004 | t0003 | g0235 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01099 | hp2 | a0005 | c0005 | t0004 | g0214 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01106 | hp2 | a0007 | c0008 | t0007 | g0337 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01109 | hp2 | a0006 | c0007 | t0004 | g0185 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01167 | hp2 | a0004 | c0004 | t0003 | g0237 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01169 | hp2 | a0004 | c0004 | t0003 | g0238 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01192 | hp1 | a0004 | c0004 | t0003 | g0234 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01243 | hp1 | a0025 | c0029 | t0014 | g0197 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01243 | hp2 | a0004 | c0004 | t0003 | g0255 | AMR | PUR | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0094 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01257 | hp1 | a0002 | c0015 | t0001 | g0003 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0113 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01258 | hp2 | a0002 | c0015 | t0001 | g0003 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01261 | hp2 | a0003 | c0003 | t0001 | g0057 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0071 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01346 | hp2 | a0019 | c0037 | t0007 | g0331 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01361 | hp2 | a0006 | c0007 | t0004 | g0190 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01433 | hp2 | a0004 | c0004 | t0003 | g0233 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0112 | EUR | IBS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0253 | EUR | IBS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0088 | EUR | IBS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0205 | EUR | IBS | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01884 | hp1 | a0003 | c0028 | t0006 | g0248 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01891 | hp1 | a0010 | c0010 | t0006 | g0140 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01891 | hp2 | a0009 | c0022 | t0012 | g0136 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01928 | hp1 | a0004 | c0004 | t0003 | g0232 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01934 | hp1 | a0004 | c0004 | t0003 | g0236 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01952 | hp2 | a0003 | c0003 | t0005 | g0322 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01975 | hp1 | a0003 | c0003 | t0005 | g0319 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01975 | hp2 | a0004 | c0006 | t0003 | g0269 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01978 | hp2 | a0004 | c0004 | t0011 | g0316 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02004 | hp1 | a0003 | c0003 | t0005 | g0321 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02004 | hp2 | a0004 | c0006 | t0003 | g0050 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02015 | hp2 | a0004 | c0006 | t0011 | g0330 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02027 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02040 | hp2 | a0004 | c0004 | t0003 | g0243 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02055 | hp1 | a0005 | c0005 | t0004 | g0222 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02071 | hp2 | a0004 | c0004 | t0003 | g0304 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02083 | hp2 | a0014 | c0017 | t0002 | g0288 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02145 | hp1 | a0015 | c0030 | t0001 | g0260 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0134 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02148 | hp2 | a0004 | c0004 | t0003 | g0207 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | CDX | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | CDX | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02273 | hp1 | a0003 | c0003 | t0005 | g0309 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02293 | hp1 | a0003 | c0003 | t0005 | g0323 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02300 | hp2 | a0003 | c0003 | t0005 | g0320 | AMR | PEL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02451 | hp1 | a0013 | c0021 | t0006 | g0305 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02451 | hp2 | a0008 | c0009 | t0009 | g0004 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02572 | hp1 | a0008 | c0009 | t0009 | g0200 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02630 | hp1 | a0005 | c0005 | t0004 | g0221 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02630 | hp2 | a0006 | c0007 | t0004 | g0191 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02647 | hp1 | a0007 | c0008 | t0007 | g0336 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02647 | hp2 | a0005 | c0014 | t0001 | g0139 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0129 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02717 | hp2 | a0007 | c0008 | t0007 | g0338 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0127 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02723 | hp2 | a0006 | c0007 | t0010 | g0340 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0118 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02809 | hp1 | a0005 | c0014 | t0001 | g0223 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02809 | hp2 | a0006 | c0007 | t0004 | g0195 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02818 | hp1 | a0005 | c0005 | t0004 | g0184 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02886 | hp1 | a0004 | c0004 | t0003 | g0242 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02886 | hp2 | a0005 | c0005 | t0004 | g0240 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02895 | hp1 | a0004 | c0004 | t0003 | g0074 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02895 | hp2 | a0005 | c0005 | t0004 | g0216 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02896 | hp1 | a0005 | c0005 | t0004 | g0215 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02896 | hp2 | a0006 | c0007 | t0010 | g0339 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02922 | hp1 | a0007 | c0008 | t0004 | g0196 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02965 | hp1 | a0005 | c0005 | t0004 | g0262 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02965 | hp2 | a0005 | c0013 | t0001 | g0039 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0130 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03017 | hp2 | a0004 | c0004 | t0003 | g0005 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03041 | hp2 | a0006 | c0007 | t0010 | g0341 | AFR | GWD | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03098 | hp1 | a0010 | c0010 | t0006 | g0194 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03098 | hp2 | a0008 | c0009 | t0009 | g0245 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03130 | hp2 | a0005 | c0005 | t0004 | g0199 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03139 | hp1 | a0009 | c0018 | t0002 | g0210 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03139 | hp2 | a0020 | c0031 | t0001 | g0069 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0149 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03195 | hp2 | a0006 | c0007 | t0004 | g0111 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03209 | hp1 | a0001 | c0001 | t0017 | g0332 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03209 | hp2 | a0006 | c0007 | t0004 | g0187 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03225 | hp1 | a0008 | c0009 | t0009 | g0004 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03453 | hp1 | a0001 | c0001 | t0018 | g0342 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03453 | hp2 | a0005 | c0005 | t0004 | g0218 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03486 | hp1 | a0003 | c0003 | t0016 | g0308 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03486 | hp2 | a0006 | c0016 | t0004 | g0189 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03490 | hp2 | a0004 | c0004 | t0003 | g0005 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0052 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03516 | hp1 | a0013 | c0020 | t0006 | g0132 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03516 | hp2 | a0010 | c0010 | t0006 | g0135 | AFR | ESN | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03579 | hp1 | a0008 | c0009 | t0009 | g0244 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03579 | hp2 | a0004 | c0004 | t0003 | g0193 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0326 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0249 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03688 | hp1 | a0023 | c0026 | t0001 | g0070 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03688 | hp2 | a0026 | c0019 | t0001 | g0204 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03704 | hp2 | a0003 | c0003 | t0001 | g0302 | SAS | PJL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03831 | hp1 | a0003 | c0003 | t0005 | g0324 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03834 | hp1 | a0001 | c0034 | t0002 | g0109 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03834 | hp2 | a0004 | c0004 | t0003 | g0105 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03942 | hp2 | a0024 | c0027 | t0001 | g0227 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04115 | hp1 | a0004 | c0004 | t0003 | g0141 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04115 | hp2 | a0022 | c0024 | t0001 | g0303 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | BEB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04199 | hp1 | a0004 | c0004 | t0003 | g0280 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04228 | hp1 | a0003 | c0003 | t0001 | g0110 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | STU | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18522 | hp2 | a0006 | c0016 | t0004 | g0186 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18612 | hp2 | a0004 | c0006 | t0003 | g0152 | EAS | CHB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18906 | hp1 | a0003 | c0003 | t0001 | g0128 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18906 | hp2 | a0005 | c0005 | t0004 | g0219 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18943 | hp2 | a0011 | c0012 | t0008 | g0329 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18945 | hp2 | a0004 | c0006 | t0003 | g0121 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18948 | hp2 | a0012 | c0011 | t0002 | g0078 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18953 | hp2 | a0018 | c0036 | t0002 | g0293 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18960 | hp2 | a0011 | c0012 | t0008 | g0325 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18965 | hp1 | a0004 | c0006 | t0003 | g0104 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18965 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18969 | hp2 | a0017 | c0033 | t0002 | g0160 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18971 | hp2 | a0001 | c0035 | t0002 | g0282 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18973 | hp1 | a0011 | c0012 | t0008 | g0328 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18973 | hp2 | a0002 | c0002 | t0005 | g0312 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18974 | hp2 | a0004 | c0006 | t0003 | g0034 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18981 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18983 | hp2 | a0016 | c0032 | t0002 | g0156 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18985 | hp1 | a0001 | c0001 | t0008 | g0311 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18985 | hp2 | a0004 | c0006 | t0003 | g0044 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18988 | hp2 | a0012 | c0011 | t0002 | g0077 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18989 | hp2 | a0004 | c0004 | t0003 | g0272 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18993 | hp2 | a0004 | c0006 | t0003 | g0045 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19000 | hp2 | a0004 | c0006 | t0003 | g0054 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19002 | hp1 | a0002 | c0002 | t0005 | g0314 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19002 | hp2 | a0004 | c0004 | t0003 | g0271 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19004 | hp1 | a0014 | c0017 | t0002 | g0274 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19004 | hp2 | a0002 | c0002 | t0005 | g0315 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19006 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19006 | hp2 | a0012 | c0011 | t0002 | g0055 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19010 | hp1 | a0001 | c0001 | t0013 | g0158 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0225 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19030 | hp2 | a0004 | c0004 | t0003 | g0241 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19043 | hp1 | a0007 | c0008 | t0007 | g0333 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19056 | hp2 | a0009 | c0018 | t0001 | g0102 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19060 | hp2 | a0004 | c0004 | t0003 | g0247 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19065 | hp2 | a0002 | c0002 | t0005 | g0313 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19068 | hp1 | a0004 | c0006 | t0003 | g0122 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19074 | hp1 | a0004 | c0006 | t0003 | g0053 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19086 | hp2 | a0004 | c0006 | t0003 | g0033 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0131 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19240 | hp1 | a0006 | c0007 | t0004 | g0192 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0261 | AFR | YRI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | ASW | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20129 | hp2 | a0007 | c0008 | t0007 | g0334 | AFR | ASW | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20752 | hp1 | a0004 | c0004 | t0003 | g0256 | EUR | TSI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0060 | EUR | TSI | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | GIH | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | GIH | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02486 | hp2 | a0005 | c0005 | t0015 | g0217 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02559 | hp1 | a0005 | c0005 | t0004 | g0213 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG02559 | hp2 | a0005 | c0013 | t0001 | g0049 | AFR | ACB | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03471 | hp1 | a0007 | c0008 | t0007 | g0335 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG06807 | hp1 | a0008 | c0009 | t0009 | g0226 | AFR | USA | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | USA | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20300 | hp1 | a0003 | c0003 | t0005 | g0318 | AFR | USA | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA20300 | hp2 | a0005 | c0005 | t0004 | g0220 | AFR | USA | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA21309 | hp1 | a0021 | c0023 | t0001 | g0211 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0327 | AFR | LWK | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0254 | REF | REF | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0310 | REF | REF | ABCA10_chr17_69143007_69233824 | ABCA10 | chr17 | 69143007 | 69233824 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:69149049
|
TGA | T | 1 | a0004 | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
frameshift_variant | HIGH | c.4515_4516delTC | p.Gln1506fs | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 38/39 | 5072/6008 | 4515/4632 | 1505/1543 | chr17 | 69149049 | ||
chr17:69150035
|
G | A | 1 | a0025 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.4426C>T | p.Pro1476Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/39 | 4982/6008 | 4426/4632 | 1476/1543 | chr17 | 69150035 | ||
chr17:69153832
|
G | A | 1 | a0004 | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
stop_gained&splice_region_variant | HIGH | c.3964C>T | p.Arg1322* | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4520/6008 | 3964/4632 | 1322/1543 | chr17 | 69153832 | ||
chr17:69153849
|
G | C | 1 | a0018 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.3947C>G | p.Ala1316Gly | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4503/6008 | 3947/4632 | 1316/1543 | chr17 | 69153849 | ||
chr17:69153850
|
C | A | 1 | a0018 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.3946G>T | p.Ala1316Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4502/6008 | 3946/4632 | 1316/1543 | chr17 | 69153850 | ||
chr17:69153982
|
C | T | 1 | a0018 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.3814G>A | p.Val1272Ile | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4370/6008 | 3814/4632 | 1272/1543 | chr17 | 69153982 | ||
chr17:69154324
|
C | CACCTGGA others(1): Show |
3 | a0005a0006a0007 | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
frameshift_variant&splice_region_variant | HIGH | c.3695-6_3696dupTTCC others(4): Show |
p.Glu1233fs | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 31/39 | 4252/6008 | 3696/4632 | 1232/1543 | chr17 | 69154324 | ||
chr17:69155824
|
G | C | 1 | a0007 | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
missense_variant | MODERATE | c.3557C>G | p.Thr1186Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/39 | 4113/6008 | 3557/4632 | 1186/1543 | chr17 | 69155824 | ||
chr17:69156852
|
C | T | 1 | a0024 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.3435G>A | p.Met1145Ile | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/39 | 3991/6008 | 3435/4632 | 1145/1543 | chr17 | 69156852 | ||
chr17:69156910
|
C | T | 1 | a0023 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3377G>A | p.Ser1126Asn | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/39 | 3933/6008 | 3377/4632 | 1126/1543 | chr17 | 69156910 | ||
chr17:69174744
|
G | C | 1 | a0011 | 3 | NA18943.hp2 NA18960.hp2 NA18973.hp1 |
missense_variant | MODERATE | c.2911C>G | p.Leu971Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 24/39 | 3467/6008 | 2911/4632 | 971/1543 | chr17 | 69174744 | ||
chr17:69182175
|
A | G | 18 | a0002a0003a0004others(15): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
missense_variant | MODERATE | c.2747T>C | p.Met916Thr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/39 | 3303/6008 | 2747/4632 | 916/1543 | chr17 | 69182175 | ||
chr17:69182232
|
A | G | 1 | a0022 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2690T>C | p.Met897Thr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/39 | 3246/6008 | 2690/4632 | 897/1543 | chr17 | 69182232 | ||
chr17:69182281
|
A | T | 1 | a0010 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.2641T>A | p.Phe881Ile | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/39 | 3197/6008 | 2641/4632 | 881/1543 | chr17 | 69182281 | ||
chr17:69187705
|
C | T | 1 | a0017 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.2306G>A | p.Arg769His | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/39 | 2862/6008 | 2306/4632 | 769/1543 | chr17 | 69187705 | ||
chr17:69190364
|
C | T | 1 | a0014 | 2 | HG02083.hp2 NA19004.hp1 |
missense_variant | MODERATE | c.2125G>A | p.Glu709Lys | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/39 | 2681/6008 | 2125/4632 | 709/1543 | chr17 | 69190364 | ||
chr17:69191199
|
A | G | 1 | a0011 | 3 | NA18943.hp2 NA18960.hp2 NA18973.hp1 |
missense_variant | MODERATE | c.1988T>C | p.Leu663Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/39 | 2544/6008 | 1988/4632 | 663/1543 | chr17 | 69191199 | ||
chr17:69193161
|
G | A | 1 | a0006 | 2 | HG03486.hp2 NA18522.hp2 |
stop_gained | HIGH | c.1729C>T | p.Arg577* | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 15/39 | 2285/6008 | 1729/4632 | 577/1543 | chr17 | 69193161 | ||
chr17:69193976
|
AAT | A | 4 | a0005a0006a0007others(1): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
frameshift_variant | HIGH | c.1357_1358delAT | p.Ile453fs | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/39 | 1914/6008 | 1357/4632 | 453/1543 | chr17 | 69193976 | ||
chr17:69194395
|
AACAG | A | 1 | a0004 | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
frameshift_variant | HIGH | c.1331_1334delCTGT | p.Ser444fs | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 12/39 | 1890/6008 | 1331/4632 | 444/1543 | chr17 | 69194395 | ||
chr17:69194478
|
A | G | 1 | a0013 | 2 | HG02451.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.1252T>C | p.Tyr418His | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 12/39 | 1808/6008 | 1252/4632 | 418/1543 | chr17 | 69194478 | ||
chr17:69201542
|
A | C | 1 | a0016 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1133T>G | p.Phe378Cys | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/39 | 1689/6008 | 1133/4632 | 378/1543 | chr17 | 69201542 | ||
chr17:69201560
|
T | G | 2 | a0008a0019 | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.1115A>C | p.His372Pro | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/39 | 1671/6008 | 1115/4632 | 372/1543 | chr17 | 69201560 | ||
chr17:69214715
|
C | T | 1 | a0021 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.995G>A | p.Arg332Gln | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/39 | 1551/6008 | 995/4632 | 332/1543 | chr17 | 69214715 | ||
chr17:69214851
|
T | C | 3 | a0002a0023a0024 | 84 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
missense_variant&splice_region_variant | MODERATE | c.859A>G | p.Ile287Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/39 | 1415/6008 | 859/4632 | 287/1543 | chr17 | 69214851 | ||
chr17:69215844
|
G | T | 1 | a0020 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.829C>A | p.Pro277Thr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/39 | 1385/6008 | 829/4632 | 277/1543 | chr17 | 69215844 | ||
chr17:69215890
|
A | T | 1 | a0005 | 18 | HG01099.hp2 HG02055.hp1 HG02486.hp2 others(15): Show |
stop_gained | HIGH | c.783T>A | p.Tyr261* | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/39 | 1339/6008 | 783/4632 | 261/1543 | chr17 | 69215890 | ||
chr17:69215982
|
T | C | 1 | a0025 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.691A>G | p.Met231Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/39 | 1247/6008 | 691/4632 | 231/1543 | chr17 | 69215982 | ||
chr17:69216249
|
A | G | 1 | a0012 | 3 | NA18948.hp2 NA18988.hp2 NA19006.hp2 |
missense_variant | MODERATE | c.640T>C | p.Phe214Leu | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 7/39 | 1196/6008 | 640/4632 | 214/1543 | chr17 | 69216249 | ||
chr17:69216282
|
G | A | 11 | a0002a0003a0005others(8): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
missense_variant | MODERATE | c.607C>T | p.Pro203Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 7/39 | 1163/6008 | 607/4632 | 203/1543 | chr17 | 69216282 | ||
chr17:69219561
|
G | A | 1 | a0015 | 1 | HG02145.hp1 | stop_gained | HIGH | c.514C>T | p.Arg172* | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/39 | 1070/6008 | 514/4632 | 172/1543 | chr17 | 69219561 | ||
chr17:69221842
|
G | C | 1 | a0008 | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.253C>G | p.Leu85Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/39 | 809/6008 | 253/4632 | 85/1543 | chr17 | 69221842 | ||
chr17:69222685
|
A | G | 1 | a0026 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.47T>C | p.Ile16Thr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/39 | 603/6008 | 47/4632 | 16/1543 | chr17 | 69222685 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:69153343
|
C | T | 2 | a0005c0013a0008c0009 | 8 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.4098G>A | p.Pro1366Pro | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/39 | 4654/6008 | 4098/4632 | 1366/1543 | chr17 | 69153343 | ||
chr17:69153525
|
G | A | 1 | a0001c0034 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.3987C>T | p.Leu1329Leu | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 33/39 | 4543/6008 | 3987/4632 | 1329/1543 | chr17 | 69153525 | ||
chr17:69153851
|
A | G | 1 | a0018c0036 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.3945T>C | p.Asp1315Asp | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4501/6008 | 3945/4632 | 1315/1543 | chr17 | 69153851 | ||
chr17:69153878
|
T | A | 1 | a0018c0036 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.3918A>T | p.Ala1306Ala | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4474/6008 | 3918/4632 | 1306/1543 | chr17 | 69153878 | ||
chr17:69153977
|
C | T | 2 | a0004c0004a0004c0006 | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
synonymous_variant | LOW | c.3819G>A | p.Arg1273Arg | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4375/6008 | 3819/4632 | 1273/1543 | chr17 | 69153977 | ||
chr17:69153980
|
T | C | 1 | a0001c0035 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.3816A>G | p.Val1272Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4372/6008 | 3816/4632 | 1272/1543 | chr17 | 69153980 | ||
chr17:69153983
|
T | C | 1 | a0018c0036 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.3813A>G | p.Ser1271Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4369/6008 | 3813/4632 | 1271/1543 | chr17 | 69153983 | ||
chr17:69153995
|
G | C | 1 | a0007c0008 | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
synonymous_variant | LOW | c.3801C>G | p.Gly1267Gly | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/39 | 4357/6008 | 3801/4632 | 1267/1543 | chr17 | 69153995 | ||
chr17:69156840
|
T | C | 1 | a0003c0025 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.3447A>G | p.Pro1149Pro | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/39 | 4003/6008 | 3447/4632 | 1149/1543 | chr17 | 69156840 | ||
chr17:69174338
|
T | G | 1 | a0013c0021 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3105A>C | p.Ser1035Ser | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/39 | 3661/6008 | 3105/4632 | 1035/1543 | chr17 | 69174338 | ||
chr17:69174697
|
T | C | 1 | a0015c0030 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.2958A>G | p.Pro986Pro | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 24/39 | 3514/6008 | 2958/4632 | 986/1543 | chr17 | 69174697 | ||
chr17:69185559
|
C | T | 1 | a0010c0010 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.2415G>A | p.Glu805Glu | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/39 | 2971/6008 | 2415/4632 | 805/1543 | chr17 | 69185559 | ||
chr17:69190437
|
T | G | 1 | a0002c0015 | 2 | HG01257.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.2052A>C | p.Ile684Ile | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/39 | 2608/6008 | 2052/4632 | 684/1543 | chr17 | 69190437 | ||
chr17:69193526
|
T | C | 2 | a0008c0009a0019c0037 | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.1608A>G | p.Leu536Leu | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/39 | 2164/6008 | 1608/4632 | 536/1543 | chr17 | 69193526 | ||
chr17:69193832
|
T | C | 1 | a0004c0006 | 13 | HG01975.hp2 HG02004.hp2 HG02015.hp2 others(10): Show |
synonymous_variant | LOW | c.1503A>G | p.Pro501Pro | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/39 | 2059/6008 | 1503/4632 | 501/1543 | chr17 | 69193832 | ||
chr17:69193973
|
A | G | 1 | a0007c0008 | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
synonymous_variant | LOW | c.1362T>C | p.Tyr454Tyr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/39 | 1918/6008 | 1362/4632 | 454/1543 | chr17 | 69193973 | ||
chr17:69215866
|
T | C | 1 | a0003c0028 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.807A>G | p.Gly269Gly | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/39 | 1363/6008 | 807/4632 | 269/1543 | chr17 | 69215866 | ||
chr17:69215890
|
A | G | 10 | a0002c0002a0002c0015a0003c0003others(7): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
synonymous_variant | LOW | c.783T>C | p.Tyr261Tyr | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/39 | 1339/6008 | 783/4632 | 261/1543 | chr17 | 69215890 | ||
chr17:69219571
|
C | T | 22 | a0002c0002a0002c0015a0003c0003others(19): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
synonymous_variant | LOW | c.504G>A | p.Val168Val | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/39 | 1060/6008 | 504/4632 | 168/1543 | chr17 | 69219571 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:69148056
|
G | A | 38 | a0001c0001t0006a0001c0001t0017a0002c0002t0001others(35): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*771C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 771 | chr17 | 69148056 | |||||
chr17:69148059
|
C | T | 1 | a0005c0005t0015 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 768 | chr17 | 69148059 | |||||
chr17:69148179
|
A | G | 1 | a0001c0001t0013 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 648 | chr17 | 69148179 | |||||
chr17:69148254
|
A | G | 5 | a0004c0004t0003a0004c0004t0011a0004c0006t0003others(2): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*573T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 573 | chr17 | 69148254 | |||||
chr17:69148309
|
A | G | 1 | a0025c0029t0014 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 518 | chr17 | 69148309 | |||||
chr17:69148435
|
C | T | 5 | a0004c0004t0003a0004c0004t0011a0004c0006t0003others(2): Show | 43 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*392G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 392 | chr17 | 69148435 | |||||
chr17:69148487
|
C | A | 31 | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(28): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 340 | chr17 | 69148487 | |||||
chr17:69148541
|
G | A | 9 | a0005c0005t0004a0005c0005t0015a0006c0007t0004others(6): Show | 38 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 286 | chr17 | 69148541 | |||||
chr17:69148543
|
T | A | 31 | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(28): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*284A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 284 | chr17 | 69148543 | |||||
chr17:69148743
|
G | T | 17 | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(14): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*84C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 39/39 | 84 | chr17 | 69148743 | |||||
chr17:69225429
|
C | T | 3 | a0001c0001t0017a0007c0008t0007a0019c0037t0007 | 10 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-71G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/39 | 71 | chr17 | 69225429 | |||||
chr17:69228683
|
G | C | 1 | a0003c0003t0016 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-415C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/39 | 3325 | chr17 | 69228683 | |||||
chr17:69228706
|
G | T | 45 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(42): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
5_prime_UTR_variant | MODIFIER | c.-438C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/39 | 3348 | chr17 | 69228706 | |||||
chr17:69228714
|
T | C | 4 | a0001c0001t0017a0006c0007t0010a0007c0008t0007others(1): Show | 13 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-446A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/39 | 3356 | chr17 | 69228714 | |||||
chr17:69228814
|
T | C | 1 | a0001c0001t0018 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-546A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/39 | 3456 | chr17 | 69228814 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:69149100
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.4478-12C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/38 | chr17 | 69149100 | ||||||
chr17:69149149
|
C | T | 10 | a0003c0003t0001g0056a0003c0003t0001g0071a0003c0003t0001g0118others(7): Show | 10 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.4478-61G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/38 | chr17 | 69149149 | ||||||
chr17:69149390
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4478-302T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/38 | chr17 | 69149390 | ||||||
chr17:69149586
|
T | C | 1 | a0010c0010t0006g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4477+398A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/38 | chr17 | 69149586 | ||||||
chr17:69149805
|
C | A | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4477+179G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 37/38 | chr17 | 69149805 | ||||||
chr17:69150147
|
T | C | 2 | a0003c0003t0001g0133a0003c0003t0001g0134 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4398-84A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150147 | ||||||
chr17:69150219
|
T | TA | 4 | a0008c0009t0009g0004a0008c0009t0009g0226a0008c0009t0009g0244others(1): Show | 5 | HG02451.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4398-157dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150219 | ||||||
chr17:69150398
|
T | A | 1 | a0006c0007t0004g0190 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4398-335A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150398 | ||||||
chr17:69150480
|
A | T | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4398-417T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150480 | ||||||
chr17:69150591
|
C | T | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.4398-528G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150591 | ||||||
chr17:69150876
|
C | T | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4398-813G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150876 | ||||||
chr17:69150896
|
T | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.4398-833A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150896 | ||||||
chr17:69150959
|
G | C | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4398-896C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150959 | ||||||
chr17:69150997
|
G | C | 187 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(184): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.4398-934C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69150997 | ||||||
chr17:69151126
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4397+917G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151126 | ||||||
chr17:69151128
|
T | C | 1 | a0003c0003t0001g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4397+915A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151128 | ||||||
chr17:69151137
|
C | T | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4397+906G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151137 | ||||||
chr17:69151237
|
T | A | 1 | a0001c0001t0002g0299 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4397+806A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151237 | ||||||
chr17:69151250
|
G | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.4397+793C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151250 | ||||||
chr17:69151288
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4397+755G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151288 | ||||||
chr17:69151327
|
T | C | 3 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278 | 3 | NA18964.hp2 NA19056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4397+716A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151327 | ||||||
chr17:69151406
|
C | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4397+637G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151406 | ||||||
chr17:69151439
|
C | T | 222 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.4397+604G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151439 | ||||||
chr17:69151505
|
T | C | 1 | a0003c0003t0001g0133 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4397+538A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151505 | ||||||
chr17:69151809
|
A | G | 83 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(80): Show | 85 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.4397+234T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151809 | ||||||
chr17:69151961
|
C | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4397+82G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | 69151961 | ||||||
chr17:69152307
|
G | C | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4256+55C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 35/38 | chr17 | 69152307 | ||||||
chr17:69152622
|
C | T | 1 | a0004c0004t0003g0239 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4137-141G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152622 | ||||||
chr17:69152623
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4137-142T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152623 | ||||||
chr17:69152667
|
G | A | 1 | a0002c0002t0001g0002 | 2 | NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.4137-186C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152667 | ||||||
chr17:69152778
|
C | T | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4137-297G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152778 | ||||||
chr17:69152802
|
G | GTAAA | 3 | a0001c0001t0002g0177a0003c0028t0006g0248a0006c0007t0010g0341 | 3 | HG01884.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4137-325_4137-322d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152802 | ||||||
chr17:69152802
|
GTAAA | G | 202 | a0001c0001t0002g0012a0001c0001t0002g0159a0001c0001t0002g0179others(199): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.4137-325_4137-322d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152802 | ||||||
chr17:69152806
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4137-325T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152806 | ||||||
chr17:69152872
|
G | A | 227 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.4137-391C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69152872 | ||||||
chr17:69153014
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4136+291A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69153014 | ||||||
chr17:69153121
|
A | G | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4136+184T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69153121 | ||||||
chr17:69153157
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4136+148T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 34/38 | chr17 | 69153157 | ||||||
chr17:69153416
|
A | T | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.4042-17T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 33/38 | chr17 | 69153416 | ||||||
chr17:69153604
|
C | A | 3 | a0002c0002t0001g0229a0002c0002t0001g0230a0002c0002t0001g0231 | 3 | NA18955.hp1 NA18975.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.3966-58G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/38 | chr17 | 69153604 | ||||||
chr17:69153700
|
T | C | 1 | a0018c0036t0002g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3965+131A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/38 | chr17 | 69153700 | ||||||
chr17:69153701
|
C | A | 1 | a0018c0036t0002g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3965+130G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/38 | chr17 | 69153701 | ||||||
chr17:69153725
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3965+106G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 32/38 | chr17 | 69153725 | ||||||
chr17:69154010
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0025a0002c0002t0001g0124 | 3 | NA18963.hp2 NA19001.hp1 NA19078.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.3787-1G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 31/38 | chr17 | 69154010 | ||||||
chr17:69154035
|
T | C | 336 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.3787-26A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 31/38 | chr17 | 69154035 | ||||||
chr17:69154420
|
C | CT | 67 | a0001c0001t0002g0300a0001c0001t0006g0009a0001c0001t0006g0010others(64): Show | 68 | HG00609.hp2 HG00639.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.3695-95dupA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | 69154420 | ||||||
chr17:69154420
|
CT | C | 208 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3695-95delA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | 69154420 | ||||||
chr17:69154483
|
G | A | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3695-157C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | 69154483 | ||||||
chr17:69154801
|
G | C | 1 | a0004c0006t0011g0330 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3694+218C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | 69154801 | ||||||
chr17:69154884
|
T | A | 2 | a0003c0003t0001g0127a0021c0023t0001g0211 | 2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3694+135A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | 69154884 | ||||||
chr17:69155153
|
A | C | 1 | a0002c0002t0001g0123 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3577-17T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155153 | ||||||
chr17:69155153
|
A | G | 4 | a0002c0002t0005g0312a0002c0002t0005g0313a0002c0002t0005g0314others(1): Show | 4 | NA18973.hp2 NA19002.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3577-17T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155153 | ||||||
chr17:69155315
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3577-179T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155315 | ||||||
chr17:69155557
|
C | T | 13 | a0006c0007t0004g0111a0006c0007t0004g0185a0006c0007t0004g0187others(10): Show | 13 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.3576+248G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155557 | ||||||
chr17:69155624
|
G | T | 1 | a0024c0027t0001g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3576+181C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155624 | ||||||
chr17:69155631
|
T | A | 1 | a0010c0010t0006g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3576+174A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155631 | ||||||
chr17:69155742
|
T | C | 1 | a0004c0004t0003g0255 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3576+63A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155742 | ||||||
chr17:69155799
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG02698.hp2 | splice_region_variant&intron_variant | LOW | c.3576+6C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 29/38 | chr17 | 69155799 | ||||||
chr17:69156028
|
T | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3456-103A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156028 | ||||||
chr17:69156042
|
T | C | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3456-117A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156042 | ||||||
chr17:69156049
|
C | A | 1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3456-124G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156049 | ||||||
chr17:69156153
|
C | T | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3456-228G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156153 | ||||||
chr17:69156199
|
C | T | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3456-274G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156199 | ||||||
chr17:69156245
|
T | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3456-320A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156245 | ||||||
chr17:69156276
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3456-351T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156276 | ||||||
chr17:69156343
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3456-418C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156343 | ||||||
chr17:69156473
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3455+359G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156473 | ||||||
chr17:69156574
|
T | C | 8 | a0004c0004t0003g0232a0004c0004t0003g0233a0004c0004t0003g0234others(5): Show | 8 | HG01074.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3455+258A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156574 | ||||||
chr17:69156587
|
G | C | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3455+245C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156587 | ||||||
chr17:69156593
|
G | A | 222 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.3455+239C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156593 | ||||||
chr17:69156622
|
C | T | 2 | a0003c0003t0001g0092a0003c0003t0001g0093 | 2 | HG02027.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.3455+210G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156622 | ||||||
chr17:69156752
|
CAAAT | C | 154 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(151): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.3455+76_3455+79del others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 28/38 | chr17 | 69156752 | ||||||
chr17:69157007
|
AGAAGATT others(13): Show |
A | 1 | a0005c0005t0004g0240 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3364-104_3364-85de others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157007 | ||||||
chr17:69157233
|
G | C | 77 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(74): Show | 79 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.3364-310C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157233 | ||||||
chr17:69157245
|
A | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3364-322T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157245 | ||||||
chr17:69157309
|
T | A | 31 | a0004c0004t0003g0105a0004c0004t0003g0141a0004c0004t0003g0232others(28): Show | 31 | HG00609.hp2 HG01074.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.3364-386A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157309 | ||||||
chr17:69157544
|
T | G | 1 | a0003c0003t0001g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3364-621A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157544 | ||||||
chr17:69157560
|
T | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3364-637A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157560 | ||||||
chr17:69157593
|
A | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3364-670T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157593 | ||||||
chr17:69157960
|
T | A | 1 | a0001c0034t0002g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3364-1037A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157960 | ||||||
chr17:69157988
|
A | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3364-1065T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69157988 | ||||||
chr17:69158009
|
C | G | 1 | a0001c0001t0002g0300 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3364-1086G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158009 | ||||||
chr17:69158053
|
AACAAACA others(4): Show |
A | 1 | a0004c0004t0003g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3364-1141_3364-113 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158053 | ||||||
chr17:69158111
|
A | G | 1 | a0003c0003t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3364-1188T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158111 | ||||||
chr17:69158178
|
C | T | 4 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130others(1): Show | 4 | HG02717.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3364-1255G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158178 | ||||||
chr17:69158188
|
G | A | 1 | a0017c0033t0002g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3364-1265C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158188 | ||||||
chr17:69158195
|
C | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3364-1272G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158195 | ||||||
chr17:69158255
|
T | A | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3364-1332A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158255 | ||||||
chr17:69158423
|
T | G | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3364-1500A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158423 | ||||||
chr17:69158551
|
T | A | 1 | a0002c0002t0001g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3364-1628A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158551 | ||||||
chr17:69158556
|
T | G | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3364-1633A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158556 | ||||||
chr17:69158587
|
C | A | 1 | a0001c0001t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3364-1664G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158587 | ||||||
chr17:69158904
|
A | C | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3364-1981T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158904 | ||||||
chr17:69158970
|
C | A | 1 | a0002c0002t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3364-2047G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69158970 | ||||||
chr17:69159019
|
C | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3364-2096G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159019 | ||||||
chr17:69159095
|
G | A | 1 | a0004c0004t0003g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3364-2172C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159095 | ||||||
chr17:69159157
|
G | A | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3364-2234C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159157 | ||||||
chr17:69159220
|
T | G | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3364-2297A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159220 | ||||||
chr17:69159249
|
T | C | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3364-2326A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159249 | ||||||
chr17:69159307
|
G | A | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3364-2384C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159307 | ||||||
chr17:69159352
|
T | C | 2 | a0007c0008t0007g0006a0007c0008t0007g0337 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3364-2429A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159352 | ||||||
chr17:69159379
|
T | A | 3 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0194 | 3 | HG01891.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3364-2456A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159379 | ||||||
chr17:69159425
|
A | C | 2 | a0007c0008t0007g0006a0007c0008t0007g0337 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3364-2502T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159425 | ||||||
chr17:69159483
|
G | A | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3364-2560C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159483 | ||||||
chr17:69159533
|
G | A | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3364-2610C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159533 | ||||||
chr17:69159581
|
A | G | 2 | a0004c0004t0003g0241a0004c0004t0003g0242 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3364-2658T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159581 | ||||||
chr17:69159623
|
G | A | 8 | a0006c0007t0004g0185a0006c0007t0004g0187a0006c0007t0004g0188others(5): Show | 8 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.3364-2700C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159623 | ||||||
chr17:69159713
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3364-2790C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159713 | ||||||
chr17:69159731
|
A | C | 2 | a0001c0001t0002g0257a0001c0001t0002g0259 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3364-2808T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159731 | ||||||
chr17:69159812
|
T | C | 8 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(5): Show | 9 | HG01346.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3364-2889A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69159812 | ||||||
chr17:69160040
|
T | C | 1 | a0004c0006t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3364-3117A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160040 | ||||||
chr17:69160054
|
A | T | 1 | a0004c0004t0003g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3364-3131T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160054 | ||||||
chr17:69160285
|
A | G | 1 | a0002c0002t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3364-3362T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160285 | ||||||
chr17:69160539
|
G | A | 1 | a0018c0036t0002g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3363+3535C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160539 | ||||||
chr17:69160620
|
C | A | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.3363+3454G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160620 | ||||||
chr17:69160687
|
T | A | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363+3387A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160687 | ||||||
chr17:69160742
|
G | T | 2 | a0010c0010t0006g0135a0010c0010t0006g0194 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3363+3332C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160742 | ||||||
chr17:69160860
|
A | C | 1 | a0004c0004t0003g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3363+3214T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69160860 | ||||||
chr17:69161010
|
T | C | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3363+3064A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161010 | ||||||
chr17:69161011
|
T | C | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3363+3063A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161011 | ||||||
chr17:69161073
|
T | C | 1 | a0004c0006t0003g0053 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3363+3001A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161073 | ||||||
chr17:69161186
|
T | C | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3363+2888A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161186 | ||||||
chr17:69161275
|
T | C | 1 | a0002c0002t0001g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3363+2799A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161275 | ||||||
chr17:69161371
|
A | G | 1 | a0004c0004t0003g0255 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3363+2703T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161371 | ||||||
chr17:69161454
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3363+2620C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161454 | ||||||
chr17:69161474
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3363+2600T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161474 | ||||||
chr17:69161524
|
T | A | 2 | a0003c0003t0001g0090a0003c0003t0001g0091 | 2 | NA18965.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.3363+2550A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161524 | ||||||
chr17:69161655
|
C | T | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363+2419G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161655 | ||||||
chr17:69161706
|
G | GGGTACAT others(13): Show |
4 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130others(1): Show | 4 | HG02717.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363+2348_3363+236 others(24): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161706 | ||||||
chr17:69161989
|
T | A | 11 | a0004c0004t0003g0232a0004c0004t0003g0233a0004c0004t0003g0234others(8): Show | 11 | HG00609.hp2 HG01074.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3363+2085A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69161989 | ||||||
chr17:69162241
|
A | G | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3363+1833T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162241 | ||||||
chr17:69162279
|
A | G | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3363+1795T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162279 | ||||||
chr17:69162311
|
G | A | 1 | a0006c0007t0004g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3363+1763C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162311 | ||||||
chr17:69162413
|
C | T | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3363+1661G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162413 | ||||||
chr17:69162512
|
G | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3363+1562C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162512 | ||||||
chr17:69162577
|
G | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3363+1497C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162577 | ||||||
chr17:69162645
|
T | C | 74 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(71): Show | 76 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.3363+1429A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162645 | ||||||
chr17:69162755
|
G | A | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3363+1319C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162755 | ||||||
chr17:69162805
|
A | G | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3363+1269T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162805 | ||||||
chr17:69162808
|
T | TATATAC | 10 | a0001c0001t0002g0035a0001c0001t0002g0040a0001c0001t0002g0066others(7): Show | 10 | HG02165.hp2 HG02523.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.3363+1260_3363+126 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162808
|
T | TATATACA others(5): Show |
1 | a0001c0001t0002g0286 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3363+1254_3363+126 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162808
|
T | TATATACA others(23): Show |
1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3363+1265_3363+126 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162808
|
T | TATATACA others(35): Show |
1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3363+1265_3363+126 others(46): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162808
|
T | TATATACA others(23): Show |
2 | a0022c0024t0001g0303a0023c0026t0001g0070 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3363+1236_3363+126 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162808
|
TATATACA others(5): Show |
T | 2 | a0001c0001t0002g0165a0001c0001t0018g0342 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3363+1254_3363+126 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162808 | ||||||
chr17:69162828
|
T | C | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3363+1246A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162828 | ||||||
chr17:69162838
|
C | CACATACA others(9): Show |
27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(20): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(3): Show |
25 | a0003c0003t0001g0092a0003c0003t0001g0118a0004c0004t0003g0105others(22): Show | 25 | HG00609.hp2 HG01074.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(7): Show |
4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(18): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(9): Show |
22 | a0002c0002t0001g0051a0003c0003t0001g0112a0003c0003t0001g0113others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(20): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(15): Show |
29 | a0002c0002t0001g0061a0002c0002t0001g0064a0002c0002t0001g0082others(26): Show | 29 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(26): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(21): Show |
23 | a0002c0002t0001g0032a0002c0002t0001g0036a0002c0002t0001g0037others(20): Show | 23 | HG00140.hp2 HG01975.hp1 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(27): Show |
18 | a0002c0002t0001g0065a0002c0002t0001g0276a0002c0002t0001g0277others(15): Show | 18 | HG00323.hp1 HG00438.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(38): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(45): Show |
1 | a0003c0003t0001g0088 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3363+1235_3363+123 others(56): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(35): Show |
1 | a0002c0002t0001g0017 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3363+1235_3363+123 others(46): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(29): Show |
5 | a0002c0002t0001g0016a0002c0002t0001g0018a0002c0002t0001g0025others(2): Show | 5 | NA18962.hp2 NA18963.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(40): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(23): Show |
12 | a0002c0002t0001g0014a0002c0002t0001g0019a0002c0002t0001g0022others(9): Show | 13 | HG00438.hp2 HG02129.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(17): Show |
8 | a0002c0002t0001g0002a0002c0002t0001g0062a0002c0002t0001g0095others(5): Show | 9 | HG02083.hp1 HG04184.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(28): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(21): Show |
1 | a0002c0002t0001g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3363+1235_3363+123 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(23): Show |
1 | a0002c0002t0001g0015 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3363+1235_3363+123 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(11): Show |
4 | a0002c0002t0001g0098a0002c0002t0001g0125a0002c0002t0001g0126others(1): Show | 4 | HG02027.hp2 NA18942.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(13): Show |
1 | a0003c0003t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3363+1235_3363+123 others(24): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
C | CATATACA others(5): Show |
2 | a0003c0003t0001g0212a0004c0004t0003g0141 | 2 | HG02976.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3363+1235_3363+123 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162838
|
CAT | C | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0009c0022t0012g0136 | 3 | HG01361.hp1 HG01433.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.3363+1234_3363+123 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162838 | ||||||
chr17:69162840
|
T | C | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3363+1234A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(3): Show |
2 | a0010c0010t0006g0140a0010c0010t0006g0194 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(9): Show |
7 | a0002c0002t0001g0058a0002c0002t0001g0060a0002c0002t0001g0115others(4): Show | 7 | HG01123.hp1 HG01952.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(20): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(15): Show |
14 | a0002c0002t0001g0008a0002c0002t0001g0046a0002c0002t0001g0075others(11): Show | 14 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(26): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(21): Show |
11 | a0002c0002t0001g0024a0002c0002t0001g0038a0002c0002t0001g0076others(8): Show | 11 | HG00609.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(27): Show |
4 | a0002c0002t0001g0116a0002c0002t0001g0138a0002c0002t0001g0183others(1): Show | 5 | HG01257.hp1 HG01258.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(38): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(33): Show |
3 | a0007c0008t0004g0196a0007c0008t0007g0334a0007c0008t0007g0336 | 3 | HG02647.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(44): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162840
|
T | TATACATA others(39): Show |
5 | a0007c0008t0007g0006a0007c0008t0007g0333a0007c0008t0007g0335others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.3363+1233_3363+123 others(50): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162840 | ||||||
chr17:69162852
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3363+1222A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162852 | ||||||
chr17:69162853
|
A | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3363+1221T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162853 | ||||||
chr17:69162861
|
C | T | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3363+1213G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162861 | ||||||
chr17:69162862
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3363+1212C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162862 | ||||||
chr17:69162887
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3363+1187C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162887 | ||||||
chr17:69162902
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3363+1172T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162902 | ||||||
chr17:69162923
|
C | T | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3363+1151G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162923 | ||||||
chr17:69162927
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3363+1147G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162927 | ||||||
chr17:69162941
|
G | A | 225 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(222): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.3363+1133C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162941 | ||||||
chr17:69162976
|
T | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3363+1098A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162976 | ||||||
chr17:69162994
|
C | T | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3363+1080G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162994 | ||||||
chr17:69162995
|
G | T | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3363+1079C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69162995 | ||||||
chr17:69163037
|
A | G | 3 | a0001c0001t0002g0001a0001c0001t0002g0072a0001c0001t0002g0073 | 4 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363+1037T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163037 | ||||||
chr17:69163088
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3363+986G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163088 | ||||||
chr17:69163182
|
T | C | 1 | a0003c0003t0001g0205 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3363+892A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163182 | ||||||
chr17:69163200
|
A | G | 1 | a0004c0004t0003g0236 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3363+874T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163200 | ||||||
chr17:69163220
|
C | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3363+854G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163220 | ||||||
chr17:69163291
|
C | G | 235 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(232): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.3363+783G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163291 | ||||||
chr17:69163349
|
G | T | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3363+725C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163349 | ||||||
chr17:69163412
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3363+662A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163412 | ||||||
chr17:69163420
|
T | C | 4 | a0003c0003t0001g0071a0003c0003t0001g0118a0003c0003t0001g0137others(1): Show | 4 | HG00099.hp2 HG01346.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.3363+654A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163420 | ||||||
chr17:69163551
|
A | C | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3363+523T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163551 | ||||||
chr17:69163592
|
A | G | 2 | a0004c0004t0003g0243a0004c0004t0003g0247 | 2 | HG02040.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3363+482T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163592 | ||||||
chr17:69163697
|
C | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3363+377G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163697 | ||||||
chr17:69163871
|
AC | A | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3363+202delG | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163871 | ||||||
chr17:69163917
|
T | C | 1 | a0004c0004t0003g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3363+157A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69163917 | ||||||
chr17:69164007
|
T | C | 2 | a0002c0002t0001g0116a0002c0015t0001g0003 | 3 | HG01257.hp1 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3363+67A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69164007 | ||||||
chr17:69164045
|
T | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3363+29A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 27/38 | chr17 | 69164045 | ||||||
chr17:69164548
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0068 | 2 | HG02129.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.3283-394A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 26/38 | chr17 | 69164548 | ||||||
chr17:69164552
|
T | C | 1 | a0005c0005t0004g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3283-398A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 26/38 | chr17 | 69164552 | ||||||
chr17:69164566
|
T | A | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3282+398A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 26/38 | chr17 | 69164566 | ||||||
chr17:69165223
|
C | A | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3163-140G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165223 | ||||||
chr17:69165253
|
A | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-170T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165253 | ||||||
chr17:69165286
|
T | C | 1 | a0003c0003t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3163-203A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165286 | ||||||
chr17:69165332
|
C | CA | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-250dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165332 | ||||||
chr17:69165369
|
T | C | 146 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.3163-286A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165369 | ||||||
chr17:69165587
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3163-504G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165587 | ||||||
chr17:69165897
|
C | T | 1 | a0003c0003t0001g0205 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3163-814G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165897 | ||||||
chr17:69165924
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3163-841A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69165924 | ||||||
chr17:69166165
|
C | G | 1 | a0010c0010t0006g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3163-1082G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166165 | ||||||
chr17:69166220
|
C | A | 1 | a0003c0003t0001g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3163-1137G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166220 | ||||||
chr17:69166339
|
C | CA | 147 | a0001c0001t0002g0028a0001c0001t0002g0030a0002c0002t0001g0002others(144): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.3163-1257dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166339 | ||||||
chr17:69166371
|
T | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3163-1288A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166371 | ||||||
chr17:69166438
|
C | T | 10 | a0003c0003t0001g0056a0003c0003t0001g0071a0003c0003t0001g0118others(7): Show | 10 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3163-1355G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166438 | ||||||
chr17:69166534
|
C | T | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3163-1451G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166534 | ||||||
chr17:69166574
|
T | C | 1 | a0003c0003t0001g0205 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3163-1491A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166574 | ||||||
chr17:69166819
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3163-1736C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166819 | ||||||
chr17:69166862
|
G | C | 1 | a0002c0002t0001g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3163-1779C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69166862 | ||||||
chr17:69167071
|
C | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3163-1988G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167071 | ||||||
chr17:69167098
|
C | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-2015G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167098 | ||||||
chr17:69167177
|
C | G | 1 | a0001c0001t0002g0252 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3163-2094G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167177 | ||||||
chr17:69167218
|
T | C | 1 | a0002c0002t0001g0119 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3163-2135A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167218 | ||||||
chr17:69167265
|
A | C | 1 | a0001c0001t0002g0281 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3163-2182T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167265 | ||||||
chr17:69167526
|
C | T | 228 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3163-2443G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167526 | ||||||
chr17:69167778
|
T | C | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-2695A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167778 | ||||||
chr17:69167884
|
T | G | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3163-2801A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167884 | ||||||
chr17:69167890
|
TGTAAA | T | 8 | a0006c0007t0004g0185a0006c0007t0004g0187a0006c0007t0004g0188others(5): Show | 8 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.3163-2812_3163-280 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167890 | ||||||
chr17:69167905
|
T | A | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3163-2822A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69167905 | ||||||
chr17:69168245
|
A | G | 1 | a0005c0005t0004g0240 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3163-3162T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168245 | ||||||
chr17:69168271
|
A | G | 1 | a0001c0001t0006g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3163-3188T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168271 | ||||||
chr17:69168279
|
A | G | 235 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(232): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.3163-3196T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168279 | ||||||
chr17:69168310
|
G | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-3227C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168310 | ||||||
chr17:69168493
|
C | G | 336 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.3163-3410G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168493 | ||||||
chr17:69168578
|
C | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3163-3495G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168578 | ||||||
chr17:69168603
|
C | T | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3163-3520G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168603 | ||||||
chr17:69168694
|
G | C | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3163-3611C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168694 | ||||||
chr17:69168800
|
A | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3163-3717T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69168800 | ||||||
chr17:69169019
|
T | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3163-3936A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169019 | ||||||
chr17:69169043
|
G | A | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3163-3960C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169043 | ||||||
chr17:69169243
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3163-4160T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169243 | ||||||
chr17:69169370
|
T | C | 2 | a0004c0004t0003g0255a0004c0004t0003g0256 | 2 | HG01243.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3163-4287A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169370 | ||||||
chr17:69169549
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3163-4466T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169549 | ||||||
chr17:69169581
|
G | A | 1 | a0007c0008t0004g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3163-4498C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169581 | ||||||
chr17:69169703
|
G | T | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3162+4578C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169703 | ||||||
chr17:69169765
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0072a0001c0001t0002g0073 | 4 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+4516A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169765 | ||||||
chr17:69169867
|
T | C | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3162+4414A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169867 | ||||||
chr17:69169969
|
A | G | 1 | a0005c0005t0004g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3162+4312T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69169969 | ||||||
chr17:69170010
|
G | A | 146 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.3162+4271C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170010 | ||||||
chr17:69170013
|
C | T | 1 | a0005c0005t0004g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3162+4268G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170013 | ||||||
chr17:69170058
|
T | G | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3162+4223A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170058 | ||||||
chr17:69170254
|
C | T | 4 | a0002c0002t0005g0312a0002c0002t0005g0313a0002c0002t0005g0314others(1): Show | 4 | NA18973.hp2 NA19002.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3162+4027G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170254 | ||||||
chr17:69170283
|
G | A | 33 | a0002c0002t0001g0008a0002c0002t0001g0038a0002c0002t0001g0046others(30): Show | 34 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.3162+3998C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170283 | ||||||
chr17:69170287
|
CA | C | 125 | a0001c0001t0002g0147a0001c0001t0002g0295a0002c0002t0001g0002others(122): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.3162+3993delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170287 | ||||||
chr17:69170287
|
CAA | C | 106 | a0003c0003t0001g0056a0003c0003t0001g0071a0003c0003t0001g0088others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3162+3992_3162+399 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170287 | ||||||
chr17:69170307
|
C | T | 1 | a0005c0013t0001g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3162+3974G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170307 | ||||||
chr17:69170437
|
CA | C | 179 | a0001c0001t0017g0332a0002c0002t0001g0002a0002c0002t0001g0008others(176): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.3162+3843delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170437 | ||||||
chr17:69170437
|
CAA | C | 49 | a0003c0028t0006g0248a0004c0004t0003g0005a0004c0004t0003g0007others(46): Show | 51 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.3162+3842_3162+384 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170437 | ||||||
chr17:69170485
|
G | C | 1 | a0003c0003t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3162+3796C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170485 | ||||||
chr17:69170539
|
T | C | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+3742A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170539 | ||||||
chr17:69170753
|
GA | G | 93 | a0003c0003t0001g0056a0003c0003t0001g0071a0003c0003t0001g0118others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.3162+3527delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170753 | ||||||
chr17:69170807
|
C | A | 235 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(232): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.3162+3474G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170807 | ||||||
chr17:69170852
|
A | T | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3162+3429T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69170852 | ||||||
chr17:69171138
|
C | T | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3162+3143G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171138 | ||||||
chr17:69171281
|
A | G | 2 | a0005c0005t0004g0215a0005c0005t0004g0216 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3162+3000T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171281 | ||||||
chr17:69171305
|
A | G | 1 | a0002c0002t0001g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3162+2976T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171305 | ||||||
chr17:69171387
|
A | G | 9 | a0002c0002t0001g0058a0002c0002t0001g0060a0002c0002t0001g0142others(6): Show | 9 | HG01123.hp1 HG01952.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.3162+2894T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171387 | ||||||
chr17:69171534
|
G | A | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3162+2747C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171534 | ||||||
chr17:69171658
|
T | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3162+2623A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171658 | ||||||
chr17:69171736
|
C | T | 13 | a0006c0007t0004g0111a0006c0007t0004g0185a0006c0007t0004g0187others(10): Show | 13 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.3162+2545G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171736 | ||||||
chr17:69171816
|
C | T | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3162+2465G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171816 | ||||||
chr17:69171833
|
T | A | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3162+2448A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171833 | ||||||
chr17:69171917
|
G | T | 1 | a0002c0002t0001g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3162+2364C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171917 | ||||||
chr17:69171934
|
C | CA | 147 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(144): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.3162+2346dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171934 | ||||||
chr17:69171934
|
CA | C | 10 | a0002c0002t0001g0114a0002c0002t0001g0145a0002c0002t0001g0150others(7): Show | 11 | HG01070.hp2 HG01167.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.3162+2346delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69171934 | ||||||
chr17:69172076
|
T | C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3162+2205A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172076 | ||||||
chr17:69172305
|
C | T | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3162+1976G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172305 | ||||||
chr17:69172380
|
A | T | 1 | a0007c0008t0007g0334 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3162+1901T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172380 | ||||||
chr17:69172463
|
T | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3162+1818A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172463 | ||||||
chr17:69172515
|
T | G | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3162+1766A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172515 | ||||||
chr17:69172802
|
G | GGTT | 228 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3162+1476_3162+147 others(7): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172802 | ||||||
chr17:69172903
|
G | A | 6 | a0005c0005t0004g0213a0005c0005t0004g0214a0005c0005t0004g0215others(3): Show | 6 | HG01099.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3162+1378C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69172903 | ||||||
chr17:69173165
|
G | A | 2 | a0003c0003t0001g0020a0004c0004t0011g0316 | 2 | HG01978.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.3162+1116C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173165 | ||||||
chr17:69173269
|
C | T | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3162+1012G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173269 | ||||||
chr17:69173289
|
A | C | 1 | a0003c0003t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3162+992T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173289 | ||||||
chr17:69173359
|
C | T | 235 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(232): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.3162+922G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173359 | ||||||
chr17:69173451
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3162+830G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173451 | ||||||
chr17:69173510
|
A | G | 1 | a0003c0003t0001g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3162+771T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173510 | ||||||
chr17:69173651
|
T | A | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3162+630A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69173651 | ||||||
chr17:69174092
|
A | C | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3162+189T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | 69174092 | ||||||
chr17:69174467
|
A | C | 1 | a0002c0002t0001g0036 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3049-73T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 24/38 | chr17 | 69174467 | ||||||
chr17:69174595
|
A | G | 228 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3048+12T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 24/38 | chr17 | 69174595 | ||||||
chr17:69174778
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01884.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2878-1G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69174778 | ||||||
chr17:69174830
|
G | C | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2878-53C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69174830 | ||||||
chr17:69175312
|
A | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2877+94T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69175312 | ||||||
chr17:69175327
|
G | A | 1 | a0002c0002t0001g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2877+79C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69175327 | ||||||
chr17:69175342
|
A | C | 1 | a0001c0001t0002g0144 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2877+64T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69175342 | ||||||
chr17:69175396
|
T | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2877+10A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 23/38 | chr17 | 69175396 | ||||||
chr17:69175607
|
A | G | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2770-94T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69175607 | ||||||
chr17:69175700
|
A | G | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770-187T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69175700 | ||||||
chr17:69176011
|
G | A | 1 | a0020c0031t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2770-498C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176011 | ||||||
chr17:69176157
|
A | T | 1 | a0003c0003t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2770-644T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176157 | ||||||
chr17:69176334
|
T | C | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2770-821A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176334 | ||||||
chr17:69176480
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2770-967C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176480 | ||||||
chr17:69176527
|
G | C | 1 | a0003c0003t0001g0091 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2770-1014C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176527 | ||||||
chr17:69176789
|
T | G | 1 | a0002c0002t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2770-1276A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176789 | ||||||
chr17:69176847
|
G | A | 9 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(6): Show | 10 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2770-1334C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176847 | ||||||
chr17:69176890
|
A | G | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2770-1377T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176890 | ||||||
chr17:69176914
|
C | T | 2 | a0004c0004t0003g0243a0004c0004t0003g0247 | 2 | HG02040.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2770-1401G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176914 | ||||||
chr17:69176932
|
T | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(338): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.2770-1419A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176932 | ||||||
chr17:69176985
|
C | T | 1 | a0004c0004t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2770-1472G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69176985 | ||||||
chr17:69177433
|
T | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2770-1920A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177433 | ||||||
chr17:69177670
|
G | A | 1 | a0004c0006t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2770-2157C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177670 | ||||||
chr17:69177917
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2770-2404G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177917 | ||||||
chr17:69177928
|
C | A | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2770-2415G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177928 | ||||||
chr17:69177955
|
CA | C | 43 | a0001c0001t0002g0066a0001c0001t0002g0166a0001c0001t0002g0177others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.2770-2443delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177955 | ||||||
chr17:69177955
|
CAA | C | 37 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(34): Show | 38 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2770-2444_2770-244 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177955 | ||||||
chr17:69177955
|
CAAA | C | 8 | a0004c0004t0003g0271a0004c0006t0003g0269a0005c0005t0004g0184others(5): Show | 8 | HG01975.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2770-2445_2770-244 others(7): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177955 | ||||||
chr17:69177955
|
CAAAAAA | C | 7 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.2770-2448_2770-244 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177955 | ||||||
chr17:69177965
|
A | T | 3 | a0008c0009t0009g0004a0008c0009t0009g0226a0008c0009t0009g0244 | 4 | HG02451.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-2452T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177965 | ||||||
chr17:69177967
|
A | T | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2770-2454T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177967 | ||||||
chr17:69177968
|
A | ATTTTTAT others(41): Show |
1 | a0002c0002t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2770-2456_2770-245 others(52): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177968 | ||||||
chr17:69177969
|
A | AATATATA others(41): Show |
3 | a0002c0002t0001g0058a0002c0002t0001g0060a0002c0002t0001g0254 | 3 | HG01123.hp1 NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2770-2457_2770-245 others(52): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177969 | ||||||
chr17:69177969
|
A | AATATATA others(39): Show |
1 | a0002c0002t0001g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2770-2457_2770-245 others(50): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177969 | ||||||
chr17:69177969
|
A | ATATATAT others(40): Show |
3 | a0002c0002t0001g0022a0002c0002t0001g0025a0002c0002t0001g0124 | 3 | NA18963.hp2 NA19001.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2770-2457_2770-245 others(51): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177969 | ||||||
chr17:69177969
|
A | T | 25 | a0002c0002t0001g0145a0002c0002t0001g0183a0003c0003t0001g0056others(22): Show | 26 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.2770-2456T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177969 | ||||||
chr17:69177970
|
A | ATATATAT others(41): Show |
2 | a0002c0002t0001g0143a0005c0014t0001g0223 | 2 | HG02293.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2770-2458_2770-245 others(52): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177970
|
A | ATATATAT others(39): Show |
5 | a0002c0002t0001g0142a0002c0002t0001g0265a0002c0002t0001g0266others(2): Show | 5 | HG01952.hp1 HG01978.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.2770-2458_2770-245 others(50): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177970
|
A | ATATATAT others(37): Show |
1 | a0002c0002t0001g0145 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2770-2458_2770-245 others(48): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177970
|
A | ATATATAT others(60): Show |
1 | a0002c0002t0001g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2770-2458_2770-245 others(71): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177970
|
A | ATATATAT others(83): Show |
1 | a0002c0002t0001g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2770-2458_2770-245 others(94): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177970
|
A | T | 5 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130others(2): Show | 5 | HG02717.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2770-2457T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177970 | ||||||
chr17:69177971
|
A | AATATATA others(43): Show |
1 | a0002c0002t0001g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(54): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | AATATATA others(41): Show |
1 | a0002c0002t0001g0276 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(52): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | AATATATA others(39): Show |
1 | a0002c0002t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(50): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(71): Show |
1 | a0002c0002t0001g0038 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(82): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(69): Show |
1 | a0002c0002t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(80): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(40): Show |
1 | a0024c0027t0001g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(51): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(42): Show |
1 | a0002c0002t0001g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(53): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(44): Show |
2 | a0002c0002t0001g0015a0002c0002t0001g0062 | 2 | NA18951.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(55): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(67): Show |
1 | a0002c0002t0001g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(78): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(63): Show |
1 | a0003c0003t0001g0021 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(74): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(109): Show |
1 | a0003c0003t0005g0322 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(120): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(61): Show |
1 | a0003c0003t0001g0103 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(72): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(105): Show |
1 | a0003c0003t0001g0020 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(116): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(38): Show |
6 | a0002c0002t0001g0017a0002c0002t0001g0024a0002c0002t0001g0228others(3): Show | 6 | HG00609.hp1 HG02717.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(49): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(40): Show |
25 | a0002c0002t0001g0014a0002c0002t0001g0019a0002c0002t0001g0023others(22): Show | 26 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(51): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(42): Show |
8 | a0002c0002t0001g0032a0002c0002t0001g0063a0002c0002t0001g0101others(5): Show | 8 | HG01261.hp1 HG02074.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(53): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(44): Show |
3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0076 | 3 | HG01361.hp1 HG01433.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(55): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(109): Show |
1 | a0003c0003t0005g0318 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(120): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(107): Show |
1 | a0003c0003t0005g0320 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(118): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(61): Show |
3 | a0002c0002t0001g0002a0002c0002t0001g0036a0003c0003t0001g0052 | 4 | HG03492.hp1 NA18969.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(72): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(63): Show |
2 | a0002c0002t0001g0031a0002c0002t0001g0043 | 2 | NA18960.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(74): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(130): Show |
1 | a0003c0003t0005g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(141): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(105): Show |
2 | a0003c0003t0005g0309a0003c0003t0005g0321 | 2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(116): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(103): Show |
1 | a0003c0003t0005g0323 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(114): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(59): Show |
1 | a0002c0002t0001g0123 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(70): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(105): Show |
1 | a0003c0003t0005g0319 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(116): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(36): Show |
1 | a0002c0002t0001g0037 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(47): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(38): Show |
2 | a0002c0002t0001g0018a0002c0002t0001g0279 | 2 | NA19063.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2770-2459_2770-245 others(49): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | ATATATAT others(36): Show |
1 | a0003c0003t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2770-2459_2770-245 others(47): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177971
|
A | T | 57 | a0002c0002t0001g0016a0002c0002t0001g0022a0002c0002t0001g0025others(54): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2770-2458T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177971 | ||||||
chr17:69177972
|
A | ATATATAT others(39): Show |
3 | a0005c0013t0001g0039a0005c0013t0001g0049a0005c0014t0001g0139 | 3 | HG02559.hp2 HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2770-2460_2770-245 others(50): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177972 | ||||||
chr17:69177972
|
A | T | 19 | a0002c0002t0001g0064a0002c0002t0001g0100a0003c0003t0001g0013others(16): Show | 19 | HG00642.hp2 HG00738.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2770-2459T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177972 | ||||||
chr17:69177973
|
A | AAATATAT others(36): Show |
1 | a0003c0003t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(47): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | AAATATAT others(38): Show |
1 | a0003c0003t0001g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(49): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | AAATATAT others(40): Show |
2 | a0002c0002t0001g0075a0002c0002t0001g0097 | 2 | HG01106.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(51): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | AT | 8 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0107others(5): Show | 8 | HG02735.hp2 NA18612.hp1 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(5): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(48): Show |
1 | a0002c0002t0001g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(59): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(63): Show |
1 | a0003c0003t0001g0083 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(74): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(67): Show |
1 | a0003c0003t0001g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(78): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(63): Show |
3 | a0003c0003t0001g0090a0003c0003t0001g0091a0003c0003t0001g0131 | 3 | NA18965.hp2 NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(74): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(61): Show |
2 | a0003c0003t0001g0041a0003c0003t0001g0084 | 2 | NA18948.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(72): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(57): Show |
1 | a0003c0003t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(68): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(59): Show |
1 | a0003c0003t0001g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(70): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(34): Show |
2 | a0003c0003t0001g0133a0003c0003t0001g0134 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(45): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(36): Show |
9 | a0002c0002t0001g0064a0003c0003t0001g0057a0003c0003t0001g0112others(6): Show | 9 | HG00642.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(47): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(38): Show |
4 | a0003c0003t0001g0088a0003c0003t0001g0094a0003c0003t0001g0110others(1): Show | 4 | HG01256.hp1 HG01516.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(49): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(40): Show |
2 | a0002c0002t0001g0099a0002c0002t0001g0278 | 2 | HG03704.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(51): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(59): Show |
3 | a0002c0002t0001g0100a0003c0003t0001g0013a0003c0003t0001g0182 | 3 | NA19060.hp1 NA19082.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2770-2461_2770-246 others(70): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(78): Show |
1 | a0003c0003t0001g0306 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(89): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(93): Show |
1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(104): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(78): Show |
1 | a0021c0023t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(89): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(36): Show |
1 | a0022c0024t0001g0303 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(47): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | ATATATAT others(55): Show |
1 | a0003c0003t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2770-2461_2770-246 others(66): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177973
|
A | T | 194 | a0001c0001t0002g0066a0001c0001t0002g0147a0001c0001t0002g0154others(191): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.2770-2460T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177973 | ||||||
chr17:69177974
|
A | T | 4 | a0003c0003t0001g0092a0003c0003t0001g0133a0003c0003t0001g0134others(1): Show | 4 | HG00738.hp2 HG02145.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-2461T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177974 | ||||||
chr17:69177974
|
AT | A | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2770-2462delA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177974 | ||||||
chr17:69177975
|
T | A | 9 | a0001c0001t0002g0028a0001c0001t0002g0068a0001c0001t0002g0283others(6): Show | 9 | HG03453.hp1 HG03654.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2770-2462A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177975 | ||||||
chr17:69177976
|
A | ATATATAT others(31): Show |
1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2770-2464_2770-246 others(42): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177976 | ||||||
chr17:69177988
|
A | C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2770-2475T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177988 | ||||||
chr17:69177995
|
A | ATATATAT others(58): Show |
1 | a0003c0003t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2770-2483_2770-248 others(69): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(56): Show |
4 | a0003c0003t0001g0071a0003c0003t0001g0137a0003c0003t0001g0205others(1): Show | 4 | HG00099.hp2 HG01346.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770-2483_2770-248 others(67): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(140): Show |
1 | a0003c0003t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2770-2483_2770-248 others(151): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(54): Show |
2 | a0003c0003t0001g0302a0003c0025t0001g0042 | 2 | HG01069.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2770-2483_2770-248 others(65): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(58): Show |
1 | a0003c0003t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2770-2483_2770-248 others(69): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(37): Show |
1 | a0003c0003t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2770-2483_2770-248 others(48): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69177995
|
A | ATATATAT others(52): Show |
1 | a0003c0003t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2770-2483_2770-248 others(63): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69177995 | ||||||
chr17:69178166
|
A | G | 83 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(80): Show | 85 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.2770-2653T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178166 | ||||||
chr17:69178305
|
G | A | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2770-2792C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178305 | ||||||
chr17:69178328
|
C | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2770-2815G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178328 | ||||||
chr17:69178467
|
C | T | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-2954G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178467 | ||||||
chr17:69178568
|
T | G | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-3055A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178568 | ||||||
chr17:69178864
|
C | A | 1 | a0004c0004t0003g0280 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2769+3289G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178864 | ||||||
chr17:69178881
|
T | C | 4 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130others(1): Show | 4 | HG02717.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769+3272A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69178881 | ||||||
chr17:69179009
|
T | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2769+3144A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179009 | ||||||
chr17:69179084
|
A | G | 1 | a0006c0016t0004g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2769+3069T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179084 | ||||||
chr17:69179200
|
C | A | 1 | a0003c0003t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2769+2953G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179200 | ||||||
chr17:69179204
|
A | C | 1 | a0003c0003t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2769+2949T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179204 | ||||||
chr17:69179205
|
C | A | 1 | a0003c0003t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2769+2948G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179205 | ||||||
chr17:69179205
|
C | CA | 148 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(145): Show | 151 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2769+2947dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179205 | ||||||
chr17:69179208
|
A | AAC | 39 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(36): Show | 40 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2769+2944_2769+294 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179208 | ||||||
chr17:69179209
|
C | A | 82 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(79): Show | 85 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.2769+2944G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179209 | ||||||
chr17:69179210
|
A | C | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2769+2943T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179210 | ||||||
chr17:69179213
|
A | C | 1 | a0012c0011t0002g0078 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2769+2940T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179213 | ||||||
chr17:69179214
|
A | C | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2769+2939T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179214 | ||||||
chr17:69179218
|
A | C | 4 | a0002c0002t0001g0046a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG00733.hp1 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2769+2935T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179218 | ||||||
chr17:69179241
|
A | G | 1 | a0001c0001t0018g0342 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2769+2912T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179241 | ||||||
chr17:69179406
|
G | A | 1 | a0001c0034t0002g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2769+2747C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179406 | ||||||
chr17:69179527
|
C | T | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2769+2626G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179527 | ||||||
chr17:69179626
|
C | CA | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2769+2526dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69179626 | ||||||
chr17:69180233
|
T | C | 2 | a0006c0007t0004g0111a0006c0007t0004g0195 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2769+1920A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180233 | ||||||
chr17:69180321
|
A | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.2769+1832T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180321 | ||||||
chr17:69180600
|
T | TTA | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2769+1551_2769+155 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180600 | ||||||
chr17:69180667
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2769+1486A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180667 | ||||||
chr17:69180668
|
C | T | 1 | a0002c0002t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2769+1485G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180668 | ||||||
chr17:69180721
|
T | C | 4 | a0007c0008t0004g0196a0007c0008t0007g0334a0007c0008t0007g0336others(1): Show | 4 | HG02647.hp1 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769+1432A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69180721 | ||||||
chr17:69181060
|
A | G | 3 | a0002c0002t0001g0061a0002c0002t0001g0097a0002c0002t0001g0099 | 3 | HG03017.hp1 HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2769+1093T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181060 | ||||||
chr17:69181147
|
G | A | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2769+1006C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181147 | ||||||
chr17:69181151
|
A | C | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2769+1002T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181151 | ||||||
chr17:69181416
|
T | C | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2769+737A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181416 | ||||||
chr17:69181422
|
T | C | 4 | a0005c0013t0001g0039a0005c0013t0001g0049a0005c0014t0001g0139others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769+731A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181422 | ||||||
chr17:69181674
|
A | G | 1 | a0001c0001t0002g0307 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2769+479T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181674 | ||||||
chr17:69181735
|
A | G | 1 | a0004c0006t0003g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2769+418T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181735 | ||||||
chr17:69181788
|
T | C | 1 | a0005c0014t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2769+365A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181788 | ||||||
chr17:69181992
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2769+161C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | 69181992 | ||||||
chr17:69182330
|
T | C | 2 | a0004c0004t0003g0241a0004c0004t0003g0242 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2632-40A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182330 | ||||||
chr17:69182435
|
C | T | 1 | a0002c0002t0001g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2632-145G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182435 | ||||||
chr17:69182505
|
GA | G | 5 | a0003c0003t0001g0041a0003c0003t0001g0087a0003c0003t0001g0090others(2): Show | 5 | NA18953.hp1 NA18964.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2631+169delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182505 | ||||||
chr17:69182572
|
A | G | 143 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2631+103T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182572 | ||||||
chr17:69182641
|
A | C | 3 | a0002c0002t0001g0100a0004c0004t0003g0241a0004c0004t0003g0242 | 3 | HG02886.hp1 NA19030.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2631+34T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182641 | ||||||
chr17:69182642
|
C | A | 5 | a0005c0005t0004g0218a0006c0016t0004g0186a0012c0011t0002g0055others(2): Show | 5 | HG03453.hp2 NA18522.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2631+33G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182642 | ||||||
chr17:69182660
|
T | C | 1 | a0004c0004t0003g0234 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2631+15A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182660 | ||||||
chr17:69182672
|
T | C | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.2631+3A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 21/38 | chr17 | 69182672 | ||||||
chr17:69182813
|
C | T | 221 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
splice_region_variant&intron_variant | LOW | c.2498-5G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69182813 | ||||||
chr17:69182835
|
GA | G | 150 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(147): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2498-28delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69182835 | ||||||
chr17:69182835
|
GAA | G | 70 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(67): Show | 72 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.2498-29_2498-28del others(2): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69182835 | ||||||
chr17:69182835
|
GAAA | G | 8 | a0004c0004t0003g0232a0004c0004t0003g0233a0004c0004t0003g0234others(5): Show | 8 | HG01074.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2498-30_2498-28del others(3): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69182835 | ||||||
chr17:69182836
|
A | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2498-28T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69182836 | ||||||
chr17:69183288
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2498-480C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69183288 | ||||||
chr17:69183373
|
G | A | 1 | a0001c0001t0008g0326 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2498-565C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69183373 | ||||||
chr17:69183498
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2498-690C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69183498 | ||||||
chr17:69183556
|
G | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2498-748C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69183556 | ||||||
chr17:69183854
|
A | G | 2 | a0007c0008t0007g0006a0007c0008t0007g0337 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2498-1046T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69183854 | ||||||
chr17:69184117
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2498-1309G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184117 | ||||||
chr17:69184211
|
A | G | 14 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(11): Show | 14 | HG00609.hp1 HG02129.hp2 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.2497+1266T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184211 | ||||||
chr17:69184258
|
C | T | 5 | a0002c0002t0001g0002a0002c0002t0001g0031a0002c0002t0001g0096others(2): Show | 6 | HG02083.hp1 HG04228.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2497+1219G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184258 | ||||||
chr17:69184428
|
T | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2497+1049A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184428 | ||||||
chr17:69184598
|
G | A | 77 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(74): Show | 79 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.2497+879C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184598 | ||||||
chr17:69184654
|
A | T | 4 | a0001c0001t0002g0001a0001c0001t0002g0072a0001c0001t0002g0073others(1): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2497+823T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184654 | ||||||
chr17:69184661
|
T | G | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2497+816A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184661 | ||||||
chr17:69184751
|
A | G | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2497+726T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184751 | ||||||
chr17:69184779
|
T | C | 220 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(217): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2497+698A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184779 | ||||||
chr17:69184849
|
A | ATG | 7 | a0001c0001t0002g0028a0001c0001t0002g0030a0008c0009t0009g0004others(4): Show | 8 | HG02451.hp2 HG03098.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2497+626_2497+627d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184849 | ||||||
chr17:69184849
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2497+620_2497+627d others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184849 | ||||||
chr17:69184849
|
ATG | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0283a0001c0001t0008g0326 | 3 | HG02523.hp2 HG03654.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2497+626_2497+627d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184849 | ||||||
chr17:69184849
|
ATGTG | A | 128 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(125): Show | 130 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2497+624_2497+627d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184849 | ||||||
chr17:69184849
|
ATGTGTG | A | 15 | a0002c0002t0001g0183a0003c0003t0001g0056a0003c0003t0001g0071others(12): Show | 15 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2497+622_2497+627d others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184849 | ||||||
chr17:69184867
|
G | A | 1 | a0002c0002t0001g0119 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2497+610C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184867 | ||||||
chr17:69184869
|
G | A | 128 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(125): Show | 130 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2497+608C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184869 | ||||||
chr17:69184871
|
G | A | 181 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(178): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.2497+606C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184871 | ||||||
chr17:69184871
|
G | GTA | 37 | a0004c0004t0003g0074a0004c0004t0003g0208a0004c0004t0003g0209others(34): Show | 38 | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2497+604_2497+605d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184871 | ||||||
chr17:69184871
|
G | GTGTGTA | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2497+605_2497+606i others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184871 | ||||||
chr17:69184871
|
GTA | G | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0019c0037t0007g0331 | 3 | HG01346.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2497+604_2497+605d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184871 | ||||||
chr17:69184873
|
A | G | 12 | a0001c0001t0002g0040a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 13 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2497+604T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184873 | ||||||
chr17:69184875
|
A | G | 3 | a0013c0020t0006g0132a0013c0021t0006g0305a0019c0037t0007g0331 | 3 | HG01346.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2497+602T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184875 | ||||||
chr17:69184882
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2497+595G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184882 | ||||||
chr17:69184916
|
T | TAC | 23 | a0001c0001t0002g0166a0001c0001t0002g0257a0001c0001t0006g0224others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(20): Show |
intron_variant | MODIFIER | c.2497+559_2497+560d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
T | TACAC | 41 | a0001c0001t0002g0301a0003c0003t0001g0201a0003c0025t0001g0042others(38): Show | 43 | HG00280.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.2497+557_2497+560d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
T | TACACAC | 11 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.2497+555_2497+560d others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
TAC | T | 5 | a0003c0003t0001g0071a0003c0003t0005g0323a0003c0003t0005g0324others(2): Show | 5 | HG01243.hp1 HG01346.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.2497+559_2497+560d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
TACAC | T | 20 | a0001c0001t0002g0176a0002c0002t0001g0145a0003c0003t0001g0087others(17): Show | 21 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2497+557_2497+560d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
TACACACA others(1): Show |
T | 28 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(25): Show | 28 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2497+553_2497+560d others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69184916
|
TACACACA others(3): Show |
T | 2 | a0003c0003t0001g0127a0021c0023t0001g0211 | 2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2497+551_2497+560d others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69184916 | ||||||
chr17:69185002
|
C | A | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2497+475G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185002 | ||||||
chr17:69185075
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2497+402G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185075 | ||||||
chr17:69185184
|
C | T | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2497+293G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185184 | ||||||
chr17:69185192
|
G | A | 221 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2497+285C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185192 | ||||||
chr17:69185268
|
A | C | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2497+209T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185268 | ||||||
chr17:69185367
|
G | GGAGCAA | 3 | a0003c0003t0001g0127a0003c0003t0016g0308a0021c0023t0001g0211 | 3 | HG02723.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2497+104_2497+109d others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185367 | ||||||
chr17:69185399
|
C | A | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2497+78G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185399 | ||||||
chr17:69185407
|
T | G | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2497+70A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | 69185407 | ||||||
chr17:69185716
|
A | G | 9 | a0005c0005t0004g0218a0005c0005t0004g0219a0005c0005t0004g0220others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2331-73T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69185716 | ||||||
chr17:69186158
|
C | T | 1 | a0002c0002t0001g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2331-515G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69186158 | ||||||
chr17:69186606
|
C | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2331-963G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69186606 | ||||||
chr17:69186945
|
A | G | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2330+736T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69186945 | ||||||
chr17:69186994
|
C | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2330+687G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69186994 | ||||||
chr17:69187203
|
G | A | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2330+478C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69187203 | ||||||
chr17:69187427
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2330+254G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69187427 | ||||||
chr17:69187535
|
C | G | 194 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(191): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.2330+146G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 19/38 | chr17 | 69187535 | ||||||
chr17:69188016
|
C | A | 1 | a0002c0002t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2132-137G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188016 | ||||||
chr17:69188055
|
G | A | 234 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(231): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2132-176C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188055 | ||||||
chr17:69188110
|
A | T | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2132-231T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188110 | ||||||
chr17:69188150
|
G | C | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2132-271C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188150 | ||||||
chr17:69188271
|
T | C | 1 | a0002c0002t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2132-392A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188271 | ||||||
chr17:69188299
|
T | C | 1 | a0009c0018t0002g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2132-420A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188299 | ||||||
chr17:69188326
|
T | G | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2132-447A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188326 | ||||||
chr17:69188334
|
C | T | 3 | a0002c0002t0001g0064a0002c0002t0001g0101a0009c0018t0001g0102 | 3 | NA19007.hp1 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2132-455G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188334 | ||||||
chr17:69188431
|
T | G | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2132-552A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188431 | ||||||
chr17:69188696
|
C | T | 74 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(71): Show | 76 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.2132-817G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188696 | ||||||
chr17:69188768
|
G | A | 53 | a0003c0028t0006g0248a0004c0004t0003g0005a0004c0004t0003g0007others(50): Show | 55 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.2132-889C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188768 | ||||||
chr17:69188880
|
T | G | 1 | a0001c0001t0002g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2132-1001A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188880 | ||||||
chr17:69188959
|
T | C | 29 | a0005c0005t0004g0199a0005c0005t0004g0213a0005c0005t0004g0214others(26): Show | 30 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2132-1080A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69188959 | ||||||
chr17:69189441
|
T | A | 1 | a0023c0026t0001g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2131+917A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69189441 | ||||||
chr17:69189840
|
G | C | 143 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2131+518C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69189840 | ||||||
chr17:69189844
|
T | G | 6 | a0005c0005t0004g0184a0005c0005t0004g0218a0005c0005t0004g0219others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2131+514A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69189844 | ||||||
chr17:69189956
|
CTTA | C | 7 | a0003c0003t0001g0057a0003c0003t0001g0088a0003c0003t0001g0089others(4): Show | 7 | HG00323.hp1 HG00738.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2131+399_2131+401d others(5): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69189956 | ||||||
chr17:69189996
|
A | G | 27 | a0004c0004t0003g0105a0004c0004t0003g0141a0004c0004t0003g0232others(24): Show | 27 | HG00609.hp2 HG01074.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2131+362T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69189996 | ||||||
chr17:69190198
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2131+160C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69190198 | ||||||
chr17:69190302
|
A | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2131+56T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69190302 | ||||||
chr17:69190305
|
T | G | 11 | a0002c0002t0001g0183a0003c0003t0001g0056a0003c0003t0001g0071others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2131+53A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 18/38 | chr17 | 69190305 | ||||||
chr17:69190504
|
C | T | 1 | a0004c0004t0003g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2012-27G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190504 | ||||||
chr17:69190561
|
A | C | 1 | a0002c0002t0001g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2012-84T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190561 | ||||||
chr17:69190614
|
C | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2012-137G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190614 | ||||||
chr17:69190689
|
TA | T | 25 | a0002c0002t0001g0276a0003c0003t0001g0013a0003c0003t0001g0020others(22): Show | 25 | HG01952.hp2 HG01975.hp1 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.2012-213delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190689 | ||||||
chr17:69190732
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2012-255A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190732 | ||||||
chr17:69190865
|
A | G | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2011+311T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69190865 | ||||||
chr17:69191025
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2011+151C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69191025 | ||||||
chr17:69191163
|
C | T | 3 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130 | 3 | HG02717.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2011+13G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 17/38 | chr17 | 69191163 | ||||||
chr17:69191462
|
CACTTCAA others(12): Show |
C | 1 | a0001c0001t0002g0284 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1872-166_1872-148d others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69191462 | ||||||
chr17:69191464
|
CT | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1872-150delA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69191464 | ||||||
chr17:69191657
|
A | ATG | 240 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(237): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1872-344_1872-343d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69191657 | ||||||
chr17:69191800
|
G | C | 186 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(183): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1872-485C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69191800 | ||||||
chr17:69191878
|
C | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1872-563G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69191878 | ||||||
chr17:69192046
|
C | T | 5 | a0002c0002t0001g0032a0002c0002t0001g0082a0002c0002t0001g0229others(2): Show | 5 | NA18955.hp1 NA18975.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1871+517G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192046 | ||||||
chr17:69192192
|
C | T | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | HG01261.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1871+371G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192192 | ||||||
chr17:69192243
|
T | G | 47 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(44): Show | 49 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1871+320A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192243 | ||||||
chr17:69192259
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1871+304C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192259 | ||||||
chr17:69192312
|
A | AAAAC | 233 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(230): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1871+247_1871+250d others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192312 | ||||||
chr17:69192404
|
G | C | 84 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(81): Show | 87 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.1871+159C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192404 | ||||||
chr17:69192424
|
A | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1871+139T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192424 | ||||||
chr17:69192435
|
A | G | 320 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.1871+128T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192435 | ||||||
chr17:69192473
|
T | C | 1 | a0002c0002t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1871+90A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192473 | ||||||
chr17:69192527
|
T | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(338): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1871+36A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | 69192527 | ||||||
chr17:69192857
|
T | G | 1 | a0016c0032t0002g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1781-204A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 15/38 | chr17 | 69192857 | ||||||
chr17:69192892
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1780+218C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 15/38 | chr17 | 69192892 | ||||||
chr17:69193296
|
A | C | 1 | a0001c0001t0002g0275 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1642-48T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193296 | ||||||
chr17:69193310
|
C | T | 1 | a0002c0002t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1642-62G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193310 | ||||||
chr17:69193339
|
A | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1642-91T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193339 | ||||||
chr17:69193354
|
C | A | 1 | a0002c0002t0001g0051 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1642-106G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193354 | ||||||
chr17:69193354
|
C | T | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1642-106G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193354 | ||||||
chr17:69193455
|
A | G | 1 | a0003c0003t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1641+38T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193455 | ||||||
chr17:69193466
|
A | T | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1641+27T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 14/38 | chr17 | 69193466 | ||||||
chr17:69193746
|
G | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030 | 3 | NA19063.hp2 NA19082.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1521+68C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/38 | chr17 | 69193746 | ||||||
chr17:69193760
|
T | C | 1 | a0003c0003t0001g0052 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1521+54A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/38 | chr17 | 69193760 | ||||||
chr17:69193801
|
T | C | 1 | a0001c0001t0013g0158 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1521+13A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/38 | chr17 | 69193801 | ||||||
chr17:69193810
|
G | A | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.1521+4C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 13/38 | chr17 | 69193810 | ||||||
chr17:69194585
|
A | G | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1235-90T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69194585 | ||||||
chr17:69194789
|
T | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1235-294A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69194789 | ||||||
chr17:69194806
|
C | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1235-311G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69194806 | ||||||
chr17:69194950
|
T | C | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1235-455A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69194950 | ||||||
chr17:69194951
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1235-456T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69194951 | ||||||
chr17:69195002
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1235-507A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195002 | ||||||
chr17:69195008
|
A | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1235-513T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195008 | ||||||
chr17:69195030
|
G | A | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1235-535C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195030 | ||||||
chr17:69195129
|
C | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(77): Show | 81 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1235-634G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195129 | ||||||
chr17:69195131
|
G | A | 1 | a0008c0009t0009g0226 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1235-636C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195131 | ||||||
chr17:69195203
|
G | A | 1 | a0003c0003t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1235-708C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195203 | ||||||
chr17:69195307
|
T | G | 240 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(237): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1235-812A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195307 | ||||||
chr17:69195333
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1235-838C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195333 | ||||||
chr17:69195357
|
T | C | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1235-862A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195357 | ||||||
chr17:69195373
|
T | A | 1 | a0002c0002t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1235-878A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195373 | ||||||
chr17:69195385
|
T | C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1235-890A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195385 | ||||||
chr17:69195459
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1235-964A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195459 | ||||||
chr17:69195473
|
T | C | 1 | a0001c0034t0002g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1235-978A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195473 | ||||||
chr17:69195554
|
C | CT | 94 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1235-1060dupA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195554
|
C | CTT | 38 | a0001c0001t0006g0225a0004c0004t0003g0005a0004c0004t0003g0007others(35): Show | 39 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1235-1061_1235-106 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195554
|
C | CTTTTT | 12 | a0002c0002t0001g0014a0002c0002t0001g0043a0002c0002t0001g0098others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1235-1064_1235-106 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195554
|
C | CTTTTTT | 170 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0015others(167): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1235-1065_1235-106 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195554
|
C | CTTTTTTT | 9 | a0001c0001t0002g0153a0002c0002t0001g0266a0002c0002t0001g0279others(6): Show | 9 | HG01884.hp1 HG02040.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1235-1066_1235-106 others(11): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195554
|
C | CTTTTTTT others(5): Show |
1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1235-1071_1235-106 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195554 | ||||||
chr17:69195680
|
C | T | 77 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(74): Show | 79 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1235-1185G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195680 | ||||||
chr17:69195713
|
C | T | 36 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1235-1218G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195713 | ||||||
chr17:69195895
|
C | A | 77 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(74): Show | 79 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1234+1169G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69195895 | ||||||
chr17:69196052
|
C | T | 1 | a0007c0008t0007g0334 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1234+1012G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196052 | ||||||
chr17:69196111
|
C | G | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234+953G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196111 | ||||||
chr17:69196126
|
ACGGGGCG others(4): Show |
A | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1234+927_1234+937d others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196126 | ||||||
chr17:69196127
|
C | T | 44 | a0003c0003t0001g0056a0003c0003t0001g0071a0003c0003t0001g0118others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1234+937G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196127 | ||||||
chr17:69196132
|
C | T | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1234+932G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196132 | ||||||
chr17:69196133
|
G | A | 1 | a0004c0004t0003g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1234+931C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196133 | ||||||
chr17:69196138
|
C | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1234+926G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196138 | ||||||
chr17:69196218
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234+846C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196218 | ||||||
chr17:69196254
|
C | T | 1 | a0002c0002t0001g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1234+810G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196254 | ||||||
chr17:69196267
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1234+797C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196267 | ||||||
chr17:69196279
|
T | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234+785A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196279 | ||||||
chr17:69196295
|
G | A | 1 | a0023c0026t0001g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1234+769C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196295 | ||||||
chr17:69196347
|
C | G | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1234+717G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196347 | ||||||
chr17:69196431
|
G | A | 1 | a0007c0008t0007g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1234+633C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196431 | ||||||
chr17:69196433
|
G | A | 1 | a0003c0003t0001g0182 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1234+631C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196433 | ||||||
chr17:69196496
|
G | A | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1234+568C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196496 | ||||||
chr17:69196583
|
G | A | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1234+481C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196583 | ||||||
chr17:69196597
|
T | C | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1234+467A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196597 | ||||||
chr17:69196614
|
G | A | 143 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1234+450C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196614 | ||||||
chr17:69196652
|
C | G | 1 | a0001c0001t0002g0086 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1234+412G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196652 | ||||||
chr17:69196748
|
C | T | 1 | a0003c0003t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1234+316G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196748 | ||||||
chr17:69196770
|
C | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1234+294G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196770 | ||||||
chr17:69196873
|
C | T | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234+191G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196873 | ||||||
chr17:69196906
|
G | A | 1 | a0010c0010t0006g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1234+158C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196906 | ||||||
chr17:69196951
|
C | T | 1 | a0003c0003t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1234+113G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196951 | ||||||
chr17:69196965
|
T | C | 1 | a0003c0003t0001g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1234+99A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69196965 | ||||||
chr17:69197009
|
A | AGGGAGG | 127 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(124): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1234+49_1234+54dup others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69197009 | ||||||
chr17:69197009
|
A | AGGGAGGG others(5): Show |
13 | a0003c0003t0001g0057a0003c0003t0001g0088a0003c0003t0001g0089others(10): Show | 13 | HG00323.hp1 HG00738.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1234+43_1234+54dup others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69197009 | ||||||
chr17:69197009
|
A | G | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1234+55T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69197009 | ||||||
chr17:69197021
|
G | A | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1234+43C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69197021 | ||||||
chr17:69197027
|
A | G | 4 | a0003c0003t0001g0127a0003c0003t0001g0149a0003c0003t0016g0308others(1): Show | 4 | HG02723.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234+37T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | 69197027 | ||||||
chr17:69197449
|
C | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1176-327G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197449 | ||||||
chr17:69197567
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1176-445G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197567 | ||||||
chr17:69197722
|
C | T | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1176-600G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197722 | ||||||
chr17:69197740
|
G | C | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1176-618C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197740 | ||||||
chr17:69197781
|
A | AT | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176-660dupA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197781 | ||||||
chr17:69197839
|
T | C | 1 | a0005c0005t0004g0219 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1176-717A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197839 | ||||||
chr17:69197982
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1176-860C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69197982 | ||||||
chr17:69198086
|
A | ACT | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1176-966_1176-965d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198086 | ||||||
chr17:69198191
|
C | A | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1176-1069G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198191 | ||||||
chr17:69198440
|
G | T | 1 | a0001c0001t0002g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1176-1318C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198440 | ||||||
chr17:69198705
|
C | T | 1 | a0003c0003t0005g0309 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1176-1583G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198705 | ||||||
chr17:69198761
|
C | T | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1176-1639G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198761 | ||||||
chr17:69198976
|
G | C | 234 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(231): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1176-1854C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69198976 | ||||||
chr17:69199216
|
T | A | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1176-2094A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199216 | ||||||
chr17:69199244
|
T | A | 1 | a0002c0002t0001g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1176-2122A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199244 | ||||||
chr17:69199248
|
C | T | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1176-2126G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199248 | ||||||
chr17:69199266
|
C | CTTCTT | 233 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(230): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1176-2145_1176-214 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199266 | ||||||
chr17:69199379
|
A | G | 83 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(80): Show | 85 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1175+2121T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199379 | ||||||
chr17:69199442
|
C | G | 239 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(236): Show | 244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1175+2058G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199442 | ||||||
chr17:69199600
|
T | C | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175+1900A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199600 | ||||||
chr17:69199672
|
C | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1175+1828G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199672 | ||||||
chr17:69199691
|
A | C | 148 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(145): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1175+1809T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199691 | ||||||
chr17:69199760
|
G | A | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG02074.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1175+1740C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199760 | ||||||
chr17:69199771
|
C | T | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1175+1729G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199771 | ||||||
chr17:69199794
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1175+1706C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199794 | ||||||
chr17:69199889
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1175+1611C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199889 | ||||||
chr17:69199945
|
G | A | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1175+1555C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69199945 | ||||||
chr17:69200000
|
A | T | 2 | a0003c0003t0001g0127a0021c0023t0001g0211 | 2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1175+1500T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200000 | ||||||
chr17:69200002
|
T | C | 75 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1175+1498A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200002 | ||||||
chr17:69200113
|
C | T | 1 | a0003c0003t0005g0319 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175+1387G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200113 | ||||||
chr17:69200114
|
G | A | 1 | a0006c0007t0004g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175+1386C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200114 | ||||||
chr17:69200211
|
A | G | 240 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(237): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1175+1289T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200211 | ||||||
chr17:69200330
|
G | A | 45 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(42): Show | 47 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1175+1170C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200330 | ||||||
chr17:69200334
|
T | A | 1 | a0004c0004t0003g0272 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1175+1166A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200334 | ||||||
chr17:69200462
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1175+1038G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200462 | ||||||
chr17:69200619
|
T | C | 1 | a0002c0002t0001g0062 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1175+881A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200619 | ||||||
chr17:69200785
|
T | TCACTGCA others(5): Show |
4 | a0006c0007t0004g0185a0006c0007t0004g0187a0006c0007t0004g0190others(1): Show | 4 | HG01109.hp2 HG01361.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+703_1175+714d others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200785 | ||||||
chr17:69200816
|
C | T | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1175+684G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200816 | ||||||
chr17:69200818
|
T | A | 3 | a0003c0003t0001g0013a0003c0003t0001g0182a0003c0003t0001g0306 | 3 | NA19060.hp1 NA19082.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1175+682A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200818 | ||||||
chr17:69200866
|
C | T | 1 | a0001c0001t0002g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1175+634G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69200866 | ||||||
chr17:69201057
|
A | G | 1 | a0005c0014t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1175+443T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201057 | ||||||
chr17:69201137
|
T | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1175+363A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201137 | ||||||
chr17:69201197
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1175+303A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201197 | ||||||
chr17:69201333
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1175+167C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201333 | ||||||
chr17:69201334
|
T | C | 148 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(145): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1175+166A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201334 | ||||||
chr17:69201350
|
T | C | 144 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1175+150A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201350 | ||||||
chr17:69201477
|
T | C | 2 | a0004c0004t0003g0241a0004c0004t0003g0242 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1175+23A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | 69201477 | ||||||
chr17:69201713
|
A | G | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007-45T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201713 | ||||||
chr17:69201745
|
A | G | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1007-77T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201745 | ||||||
chr17:69201779
|
CATTTAT | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007-117_1007-112d others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201779 | ||||||
chr17:69201793
|
A | AT | 6 | a0002c0002t0001g0008a0002c0002t0001g0047a0002c0002t0001g0048others(3): Show | 6 | HG00323.hp2 HG01106.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-126dupA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201793 | ||||||
chr17:69201793
|
AT | A | 29 | a0001c0001t0002g0165a0004c0004t0003g0105a0004c0004t0003g0141others(26): Show | 29 | HG00609.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1007-126delA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201793 | ||||||
chr17:69201847
|
C | G | 1 | a0001c0001t0002g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1007-179G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201847 | ||||||
chr17:69201891
|
C | G | 1 | a0005c0005t0015g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1007-223G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201891 | ||||||
chr17:69201942
|
C | T | 1 | a0006c0007t0010g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1007-274G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201942 | ||||||
chr17:69201950
|
C | T | 77 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(74): Show | 79 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1007-282G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69201950 | ||||||
chr17:69202080
|
G | T | 1 | a0001c0001t0002g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1007-412C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202080 | ||||||
chr17:69202097
|
A | T | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1007-429T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202097 | ||||||
chr17:69202142
|
G | A | 1 | a0003c0003t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1007-474C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202142 | ||||||
chr17:69202266
|
T | C | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1007-598A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202266 | ||||||
chr17:69202419
|
G | A | 1 | a0005c0005t0004g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1007-751C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202419 | ||||||
chr17:69202444
|
G | C | 1 | a0010c0010t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-776C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202444 | ||||||
chr17:69202629
|
AT | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007-962delA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202629 | ||||||
chr17:69202778
|
C | CTT | 234 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(231): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1007-1111_1007-111 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202778 | ||||||
chr17:69202833
|
A | T | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1007-1165T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202833 | ||||||
chr17:69202866
|
T | C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1007-1198A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202866 | ||||||
chr17:69202909
|
T | C | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 48 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1007-1241A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202909 | ||||||
chr17:69202992
|
T | C | 9 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(6): Show | 10 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-1324A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69202992 | ||||||
chr17:69203044
|
A | T | 1 | a0008c0009t0009g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1007-1376T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203044 | ||||||
chr17:69203133
|
T | A | 2 | a0003c0003t0001g0092a0003c0003t0001g0093 | 2 | HG02027.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1007-1465A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203133 | ||||||
chr17:69203434
|
C | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1007-1766G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203434 | ||||||
chr17:69203455
|
A | G | 8 | a0003c0003t0005g0309a0003c0003t0005g0318a0003c0003t0005g0319others(5): Show | 8 | HG01952.hp2 HG01975.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-1787T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203455 | ||||||
chr17:69203505
|
C | T | 224 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(221): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1007-1837G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203505 | ||||||
chr17:69203507
|
T | A | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1007-1839A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203507 | ||||||
chr17:69203648
|
C | T | 2 | a0005c0005t0004g0215a0005c0005t0004g0216 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1007-1980G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203648 | ||||||
chr17:69203737
|
G | A | 1 | a0004c0004t0003g0304 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1007-2069C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203737 | ||||||
chr17:69203815
|
T | C | 3 | a0002c0002t0001g0064a0002c0002t0001g0101a0009c0018t0001g0102 | 3 | NA19007.hp1 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1007-2147A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69203815 | ||||||
chr17:69204376
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1007-2708A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204376 | ||||||
chr17:69204641
|
T | G | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007-2973A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204641 | ||||||
chr17:69204660
|
A | G | 233 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(230): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1007-2992T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204660 | ||||||
chr17:69204719
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1007-3051A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204719 | ||||||
chr17:69204794
|
T | A | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1007-3126A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204794 | ||||||
chr17:69204802
|
G | T | 1 | a0003c0003t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1007-3134C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204802 | ||||||
chr17:69204867
|
A | G | 234 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(231): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1007-3199T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204867 | ||||||
chr17:69204958
|
G | A | 3 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278 | 3 | NA18964.hp2 NA19056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1007-3290C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69204958 | ||||||
chr17:69205077
|
G | C | 145 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1007-3409C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205077 | ||||||
chr17:69205168
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1007-3500T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205168 | ||||||
chr17:69205460
|
A | C | 1 | a0001c0001t0002g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1007-3792T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205460 | ||||||
chr17:69205593
|
G | A | 2 | a0004c0004t0003g0208a0004c0004t0003g0209 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1007-3925C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205593 | ||||||
chr17:69205854
|
G | A | 28 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(25): Show | 28 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1007-4186C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205854 | ||||||
chr17:69205919
|
A | G | 28 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(25): Show | 28 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1007-4251T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69205919 | ||||||
chr17:69206155
|
GA | G | 38 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(35): Show | 39 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1007-4488delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206155 | ||||||
chr17:69206346
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1007-4678C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206346 | ||||||
chr17:69206390
|
T | C | 193 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(190): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1007-4722A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206390 | ||||||
chr17:69206412
|
C | A | 1 | a0003c0003t0001g0021 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1007-4744G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206412 | ||||||
chr17:69206434
|
C | G | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1007-4766G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206434 | ||||||
chr17:69206434
|
C | T | 1 | a0022c0024t0001g0303 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1007-4766G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206434 | ||||||
chr17:69206443
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1007-4775C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69206443 | ||||||
chr17:69207323
|
T | C | 193 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(190): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1007-5655A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207323 | ||||||
chr17:69207446
|
G | A | 1 | a0010c0010t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-5778C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207446 | ||||||
chr17:69207534
|
G | GAT | 6 | a0001c0001t0002g0026a0001c0001t0002g0068a0001c0001t0002g0264others(3): Show | 6 | HG02055.hp2 HG02129.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-5868_1007-586 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207534 | ||||||
chr17:69207766
|
G | A | 1 | a0002c0002t0001g0276 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1007-6098C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207766 | ||||||
chr17:69207809
|
G | C | 1 | a0003c0003t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1007-6141C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207809 | ||||||
chr17:69207856
|
T | C | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1007-6188A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207856 | ||||||
chr17:69207888
|
G | A | 1 | a0009c0018t0002g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007-6220C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207888 | ||||||
chr17:69207938
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1007-6270C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69207938 | ||||||
chr17:69208145
|
C | T | 31 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0258others(28): Show | 31 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1007-6477G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208145 | ||||||
chr17:69208230
|
A | C | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1006+6474T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208230 | ||||||
chr17:69208279
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1006+6425C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208279 | ||||||
chr17:69208338
|
A | C | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+6366T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208338 | ||||||
chr17:69208353
|
G | C | 8 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(5): Show | 9 | HG01346.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+6351C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208353 | ||||||
chr17:69208362
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1006+6342C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208362 | ||||||
chr17:69208417
|
C | CA | 8 | a0001c0001t0002g0040a0001c0001t0002g0144a0001c0001t0002g0169others(5): Show | 8 | HG01123.hp2 HG03130.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+6286dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
C | CAAAA | 8 | a0007c0008t0007g0335a0007c0008t0007g0337a0007c0008t0007g0338others(5): Show | 9 | HG01106.hp2 HG01346.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+6283_1006+628 others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
C | CAAAAAAA others(3): Show |
1 | a0010c0010t0006g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+6277_1006+628 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
C | CAAAAAAA others(4): Show |
1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1006+6276_1006+628 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
CAA | C | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0105others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006+6285_1006+628 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
CAAAA | C | 8 | a0002c0002t0001g0036a0002c0002t0001g0063a0002c0002t0001g0116others(5): Show | 8 | HG01361.hp2 HG02027.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+6283_1006+628 others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208417
|
CAAAAA | C | 156 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(153): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1006+6282_1006+628 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208417 | ||||||
chr17:69208500
|
A | G | 1 | a0001c0001t0008g0327 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1006+6204T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208500 | ||||||
chr17:69208568
|
A | C | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+6136T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208568 | ||||||
chr17:69208657
|
A | C | 1 | a0001c0001t0002g0147 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1006+6047T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208657 | ||||||
chr17:69208696
|
A | G | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+6008T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208696 | ||||||
chr17:69208720
|
A | C | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1006+5984T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208720 | ||||||
chr17:69208853
|
G | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+5851C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208853 | ||||||
chr17:69208881
|
T | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+5823A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208881 | ||||||
chr17:69208886
|
A | T | 7 | a0001c0001t0017g0332a0002c0002t0001g0276a0003c0028t0006g0248others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+5818T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208886 | ||||||
chr17:69208914
|
T | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+5790A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69208914 | ||||||
chr17:69209073
|
G | A | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+5631C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209073 | ||||||
chr17:69209122
|
G | A | 1 | a0003c0003t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1006+5582C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209122 | ||||||
chr17:69209192
|
A | G | 45 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(42): Show | 46 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1006+5512T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209192 | ||||||
chr17:69209324
|
GAATTC | G | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+5375_1006+537 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209324 | ||||||
chr17:69209379
|
T | G | 8 | a0001c0001t0002g0270a0001c0001t0002g0287a0001c0001t0002g0292others(5): Show | 8 | HG02015.hp1 NA18943.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+5325A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209379 | ||||||
chr17:69209479
|
C | T | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+5225G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209479 | ||||||
chr17:69209523
|
G | T | 1 | a0002c0002t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1006+5181C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209523 | ||||||
chr17:69209641
|
T | C | 188 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(185): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1006+5063A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209641 | ||||||
chr17:69209658
|
T | C | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+5046A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209658 | ||||||
chr17:69209687
|
C | T | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1006+5017G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209687 | ||||||
chr17:69209702
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1006+5002A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209702 | ||||||
chr17:69209718
|
G | GA | 188 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(185): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1006+4985dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209718 | ||||||
chr17:69209833
|
G | A | 1 | a0026c0019t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1006+4871C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209833 | ||||||
chr17:69209961
|
T | C | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+4743A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209961 | ||||||
chr17:69209981
|
C | T | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+4723G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69209981 | ||||||
chr17:69210062
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+4642C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210062 | ||||||
chr17:69210081
|
T | TTTA | 86 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1006+4620_1006+462 others(7): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTA | 9 | a0001c0001t0002g0068a0001c0001t0002g0162a0001c0001t0002g0176others(6): Show | 9 | HG00140.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+4617_1006+462 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTAT others(2): Show |
22 | a0001c0001t0002g0040a0001c0001t0002g0066a0001c0001t0002g0079others(19): Show | 22 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1006+4614_1006+462 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTAT others(5): Show |
6 | a0001c0001t0002g0163a0001c0001t0002g0177a0004c0004t0003g0239others(3): Show | 6 | HG00609.hp2 HG02040.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+4611_1006+462 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTAT others(8): Show |
24 | a0001c0001t0002g0258a0001c0001t0002g0275a0004c0004t0003g0005others(21): Show | 25 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006+4608_1006+462 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTAT others(11): Show |
8 | a0004c0004t0003g0233a0004c0004t0003g0235a0004c0006t0003g0033others(5): Show | 8 | HG01074.hp1 HG01433.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+4605_1006+462 others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
T | TTTATTAT others(14): Show |
4 | a0004c0004t0003g0141a0004c0006t0003g0104a0004c0006t0003g0121others(1): Show | 4 | HG04115.hp1 NA18945.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+4602_1006+462 others(25): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210081
|
TTTA | T | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+4620_1006+462 others(7): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210081 | ||||||
chr17:69210166
|
A | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1006+4538T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210166 | ||||||
chr17:69210170
|
C | CT | 73 | a0001c0001t0002g0001a0001c0001t0002g0030a0001c0001t0002g0035others(70): Show | 74 | HG00438.hp2 HG00642.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1006+4533dupA | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(7): Show |
1 | a0006c0007t0010g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1006+4520_1006+453 others(18): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(10): Show |
1 | a0006c0007t0004g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1006+4517_1006+453 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(12): Show |
1 | a0006c0007t0004g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1006+4515_1006+453 others(23): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(14): Show |
1 | a0006c0016t0004g0186 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1006+4513_1006+453 others(25): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(15): Show |
1 | a0006c0007t0004g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1006+4512_1006+453 others(26): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(17): Show |
3 | a0005c0005t0004g0199a0005c0005t0015g0217a0006c0007t0004g0185 | 3 | HG01109.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1006+4510_1006+453 others(28): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(21): Show |
2 | a0005c0005t0004g0213a0005c0005t0004g0214 | 2 | HG01099.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1006+4506_1006+453 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(22): Show |
1 | a0005c0005t0004g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1006+4505_1006+453 others(33): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(23): Show |
1 | a0005c0005t0004g0215 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1006+4504_1006+453 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(25): Show |
1 | a0005c0005t0004g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006+4533_1006+453 others(36): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | CTTTTTTT others(26): Show |
1 | a0005c0005t0004g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1006+4533_1006+453 others(37): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
C | T | 2 | a0003c0028t0006g0248a0005c0005t0004g0222 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1006+4534G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
CTTTTTT | C | 7 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+4528_1006+453 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
CTTTTTTT others(4): Show |
C | 8 | a0004c0004t0003g0241a0004c0004t0003g0242a0004c0004t0003g0280others(5): Show | 8 | HG02559.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+4523_1006+453 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210170
|
CTTTTTTT others(5): Show |
C | 37 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(34): Show | 38 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1006+4522_1006+453 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210170 | ||||||
chr17:69210205
|
C | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+4499G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210205 | ||||||
chr17:69210206
|
G | A | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1006+4498C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210206 | ||||||
chr17:69210222
|
G | A | 4 | a0002c0002t0001g0099a0002c0002t0001g0125a0002c0002t0001g0126others(1): Show | 4 | HG01256.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+4482C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210222 | ||||||
chr17:69210227
|
G | A | 1 | a0005c0005t0004g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1006+4477C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210227 | ||||||
chr17:69210238
|
G | A | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+4466C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210238 | ||||||
chr17:69210263
|
C | T | 167 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(164): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1006+4441G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210263 | ||||||
chr17:69210343
|
C | T | 3 | a0011c0012t0008g0325a0011c0012t0008g0328a0011c0012t0008g0329 | 3 | NA18943.hp2 NA18960.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1006+4361G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210343 | ||||||
chr17:69210345
|
G | A | 31 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(28): Show | 31 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1006+4359C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210345 | ||||||
chr17:69210347
|
G | A | 31 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(28): Show | 31 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1006+4357C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210347 | ||||||
chr17:69210440
|
C | T | 1 | a0003c0003t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1006+4264G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210440 | ||||||
chr17:69210469
|
G | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+4235C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210469 | ||||||
chr17:69210484
|
C | T | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+4220G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210484 | ||||||
chr17:69210551
|
T | C | 2 | a0002c0002t0001g0038a0003c0003t0001g0206 | 2 | HG00642.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1006+4153A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210551 | ||||||
chr17:69210558
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1006+4146A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210558 | ||||||
chr17:69210572
|
A | G | 176 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(173): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1006+4132T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210572 | ||||||
chr17:69210605
|
C | CATTAT | 192 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1006+4094_1006+409 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210605 | ||||||
chr17:69210616
|
T | C | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1006+4088A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210616 | ||||||
chr17:69210732
|
C | T | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1006+3972G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210732 | ||||||
chr17:69210828
|
ATGCCACA others(4): Show |
A | 1 | a0002c0002t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1006+3865_1006+387 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210828 | ||||||
chr17:69210832
|
CACATATT others(10): Show |
C | 27 | a0002c0002t0001g0150a0003c0003t0001g0056a0003c0003t0001g0071others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.1006+3855_1006+387 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210832 | ||||||
chr17:69210832
|
CACATATT others(12): Show |
C | 113 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(110): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1006+3853_1006+387 others(23): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210832 | ||||||
chr17:69210834
|
C | T | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1006+3870G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210834 | ||||||
chr17:69210839
|
T | A | 26 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(23): Show | 26 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3865A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210839 | ||||||
chr17:69210842
|
T | TATATATA others(2): Show |
9 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(6): Show | 9 | HG01099.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+3861_1006+386 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210842 | ||||||
chr17:69210842
|
T | TATATATA others(4): Show |
11 | a0005c0005t0004g0218a0005c0005t0004g0262a0005c0005t0015g0217others(8): Show | 11 | HG00639.hp1 HG01361.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+3861_1006+386 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210842 | ||||||
chr17:69210842
|
T | TATATATA others(6): Show |
2 | a0005c0005t0004g0215a0005c0005t0004g0216 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1006+3861_1006+386 others(17): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210842 | ||||||
chr17:69210843
|
G | T | 26 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(23): Show | 26 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3861C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210843 | ||||||
chr17:69210844
|
C | A | 26 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(23): Show | 26 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3860G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210844 | ||||||
chr17:69210845
|
C | T | 26 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(23): Show | 26 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3859G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210845 | ||||||
chr17:69210847
|
C | CACATATA others(3): Show |
4 | a0008c0009t0009g0004a0008c0009t0009g0226a0008c0009t0009g0244others(1): Show | 5 | HG02451.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CACATATA others(13): Show |
1 | a0008c0009t0009g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1006+3856_1006+385 others(24): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CACATATA others(29): Show |
1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1006+3856_1006+385 others(40): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CAT | 9 | a0001c0001t0002g0146a0001c0001t0002g0159a0001c0001t0002g0167others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+3855_1006+385 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(5): Show |
1 | a0004c0004t0003g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1006+3845_1006+385 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(7): Show |
1 | a0010c0010t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1006+3843_1006+385 others(18): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(11): Show |
1 | a0004c0004t0003g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1006+3839_1006+385 others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(13): Show |
7 | a0003c0028t0006g0248a0004c0004t0003g0005a0004c0004t0003g0074others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(24): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(15): Show |
1 | a0004c0004t0003g0247 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1006+3856_1006+385 others(26): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(17): Show |
6 | a0004c0004t0003g0207a0004c0004t0003g0242a0004c0004t0003g0256others(3): Show | 6 | HG02148.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(28): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(19): Show |
6 | a0004c0006t0003g0050a0004c0006t0003g0054a0005c0013t0001g0049others(3): Show | 6 | HG01891.hp1 HG02004.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(30): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(21): Show |
3 | a0004c0004t0003g0141a0004c0006t0011g0330a0010c0010t0006g0194 | 3 | HG02015.hp2 HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(23): Show |
5 | a0004c0004t0003g0235a0004c0004t0003g0241a0004c0004t0003g0255others(2): Show | 5 | HG01074.hp1 HG01243.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(25): Show |
6 | a0004c0004t0003g0232a0004c0004t0003g0237a0004c0004t0003g0238others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(36): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(27): Show |
5 | a0004c0004t0003g0234a0004c0004t0003g0236a0004c0004t0003g0271others(2): Show | 5 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(38): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(29): Show |
4 | a0004c0004t0003g0007a0004c0004t0003g0233a0004c0004t0003g0239others(1): Show | 4 | HG00609.hp2 HG00733.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(40): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(31): Show |
2 | a0004c0006t0003g0033a0004c0006t0003g0045 | 2 | NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1006+3856_1006+385 others(42): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | CATATATA others(33): Show |
1 | a0004c0006t0003g0044 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1006+3856_1006+385 others(44): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210847
|
C | T | 35 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(32): Show | 36 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1006+3857G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210847 | ||||||
chr17:69210865
|
T | TATATATA others(12): Show |
1 | a0007c0008t0004g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1006+3838_1006+383 others(23): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210865 | ||||||
chr17:69210865
|
T | TATATATA others(14): Show |
4 | a0007c0008t0007g0006a0007c0008t0007g0336a0007c0008t0007g0337others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+3838_1006+383 others(25): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210865 | ||||||
chr17:69210865
|
T | TATATATA others(16): Show |
1 | a0007c0008t0007g0335 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1006+3838_1006+383 others(27): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210865 | ||||||
chr17:69210865
|
T | TATATATA others(18): Show |
1 | a0007c0008t0007g0334 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1006+3838_1006+383 others(29): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210865 | ||||||
chr17:69210865
|
T | TATATATA others(20): Show |
1 | a0007c0008t0007g0333 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1006+3838_1006+383 others(31): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69210865 | ||||||
chr17:69211055
|
T | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+3649A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211055 | ||||||
chr17:69211068
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1006+3636C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211068 | ||||||
chr17:69211219
|
G | A | 3 | a0002c0002t0001g0046a0002c0002t0001g0250a0002c0002t0001g0251 | 3 | HG00733.hp1 HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1006+3485C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211219 | ||||||
chr17:69211247
|
C | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+3457G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211247 | ||||||
chr17:69211292
|
C | CATATATA others(25): Show |
1 | a0001c0001t0002g0283 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1006+3380_1006+341 others(36): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211292 | ||||||
chr17:69211293
|
A | T | 124 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(121): Show | 126 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1006+3411T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211293 | ||||||
chr17:69211302
|
CATCATAT others(21): Show |
C | 3 | a0005c0005t0004g0215a0005c0005t0004g0216a0005c0005t0004g0240 | 3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1006+3374_1006+340 others(32): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211302 | ||||||
chr17:69211302
|
CATCATAT others(23): Show |
C | 26 | a0005c0005t0004g0184a0005c0005t0004g0213a0005c0005t0004g0214others(23): Show | 26 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3372_1006+340 others(34): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211302 | ||||||
chr17:69211302
|
CATCATAT others(25): Show |
C | 1 | a0006c0007t0010g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1006+3370_1006+340 others(36): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211302 | ||||||
chr17:69211305
|
CATATATA others(10): Show |
C | 1 | a0021c0023t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006+3382_1006+339 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(12): Show |
C | 14 | a0002c0002t0001g0116a0003c0003t0001g0020a0003c0003t0001g0021others(11): Show | 14 | HG00642.hp2 HG00738.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006+3380_1006+339 others(23): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(14): Show |
C | 110 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(107): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1006+3378_1006+339 others(25): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(16): Show |
C | 15 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.1006+3376_1006+339 others(27): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(18): Show |
C | 9 | a0007c0008t0007g0006a0007c0008t0007g0333a0007c0008t0007g0334others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006+3374_1006+339 others(29): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(20): Show |
C | 5 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006+3372_1006+339 others(31): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211305
|
CATATATA others(24): Show |
C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1006+3368_1006+339 others(35): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211305 | ||||||
chr17:69211314
|
G | GAT | 4 | a0001c0001t0002g0035a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 4 | HG02040.hp1 NA18971.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+3388_1006+338 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
G | GATATATA others(3): Show |
1 | a0001c0001t0002g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1006+3380_1006+338 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GAT | G | 35 | a0001c0001t0002g0027a0001c0001t0002g0040a0001c0001t0002g0066others(32): Show | 35 | HG00140.hp1 HG00639.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1006+3388_1006+338 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATAT | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0030others(22): Show | 26 | HG00099.hp1 HG00280.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1006+3386_1006+338 others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATAT | G | 19 | a0001c0001t0002g0012a0001c0001t0002g0164a0001c0001t0002g0165others(16): Show | 20 | HG01346.hp2 HG02015.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1006+3384_1006+338 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATATA others(1): Show |
G | 9 | a0001c0001t0006g0011a0001c0034t0002g0109a0004c0006t0003g0033others(6): Show | 9 | HG02004.hp2 HG03471.hp2 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+3382_1006+338 others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATATA others(3): Show |
G | 4 | a0001c0001t0002g0297a0001c0001t0002g0298a0004c0006t0003g0269others(1): Show | 4 | HG01975.hp2 HG02015.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+3380_1006+338 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATATA others(5): Show |
G | 2 | a0001c0001t0002g0166a0008c0009t0009g0200 | 2 | HG02523.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1006+3378_1006+338 others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATATA others(7): Show |
G | 1 | a0004c0004t0003g0239 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1006+3376_1006+338 others(18): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211314
|
GATATATA others(11): Show |
G | 2 | a0004c0004t0003g0193a0004c0004t0003g0280 | 2 | HG03579.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1006+3372_1006+338 others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211314 | ||||||
chr17:69211321
|
A | G | 1 | a0005c0005t0004g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1006+3383T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211321 | ||||||
chr17:69211329
|
A | G | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1006+3375T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211329 | ||||||
chr17:69211331
|
A | G | 1 | a0015c0030t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1006+3373T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211331 | ||||||
chr17:69211334
|
TATATATA others(4): Show |
T | 8 | a0004c0004t0003g0005a0004c0004t0003g0074a0004c0004t0003g0207others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+3359_1006+336 others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211334 | ||||||
chr17:69211344
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1006+3342_1006+335 others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211344 | ||||||
chr17:69211346
|
T | C | 9 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(6): Show | 10 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006+3358A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211346 | ||||||
chr17:69211347
|
A | G | 1 | a0002c0002t0001g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1006+3357T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211347 | ||||||
chr17:69211348
|
T | G | 1 | a0004c0004t0003g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006+3356A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211348 | ||||||
chr17:69211349
|
A | G | 186 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1006+3355T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211349 | ||||||
chr17:69211351
|
A | G | 138 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1006+3353T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211351 | ||||||
chr17:69211352
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0006g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1006+3342_1006+335 others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211352 | ||||||
chr17:69211358
|
T | C | 2 | a0001c0001t0002g0299a0004c0004t0003g0247 | 2 | HG01934.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1006+3346A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211358 | ||||||
chr17:69211360
|
T | C | 31 | a0001c0001t0002g0170a0001c0001t0002g0178a0001c0001t0002g0181others(28): Show | 31 | HG00609.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1006+3344A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211360 | ||||||
chr17:69211360
|
T | TAC | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG01074.hp1 HG01192.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+3342_1006+334 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211360 | ||||||
chr17:69211362
|
C | T | 182 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(179): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1006+3342G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211362 | ||||||
chr17:69211370
|
C | T | 2 | a0002c0002t0001g0008a0002c0002t0001g0075 | 2 | HG00323.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1006+3334G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211370 | ||||||
chr17:69211528
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1006+3176G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211528 | ||||||
chr17:69211624
|
C | T | 5 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+3080G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211624 | ||||||
chr17:69211705
|
T | A | 234 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(231): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1006+2999A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211705 | ||||||
chr17:69211784
|
G | A | 1 | a0007c0008t0004g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1006+2920C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211784 | ||||||
chr17:69211891
|
C | T | 1 | a0010c0010t0006g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1006+2813G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69211891 | ||||||
chr17:69212061
|
T | A | 1 | a0010c0010t0006g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+2643A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212061 | ||||||
chr17:69212294
|
T | C | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+2410A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212294 | ||||||
chr17:69212503
|
T | C | 213 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(210): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1006+2201A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212503 | ||||||
chr17:69212519
|
T | C | 3 | a0005c0005t0004g0215a0005c0005t0004g0216a0005c0005t0004g0240 | 3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1006+2185A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212519 | ||||||
chr17:69212560
|
C | T | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+2144G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212560 | ||||||
chr17:69212592
|
A | G | 1 | a0003c0003t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1006+2112T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212592 | ||||||
chr17:69212858
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1006+1846G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212858 | ||||||
chr17:69212955
|
G | A | 1 | a0006c0007t0004g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1006+1749C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69212955 | ||||||
chr17:69213155
|
T | C | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1006+1549A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213155 | ||||||
chr17:69213322
|
A | C | 240 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(237): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1006+1382T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213322 | ||||||
chr17:69213374
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+1330C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213374 | ||||||
chr17:69213398
|
G | A | 1 | a0003c0003t0001g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1006+1306C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213398 | ||||||
chr17:69213400
|
C | G | 1 | a0021c0023t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006+1304G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213400 | ||||||
chr17:69213412
|
T | C | 232 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(229): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1006+1292A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213412 | ||||||
chr17:69213412
|
T | G | 1 | a0003c0003t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1006+1292A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213412 | ||||||
chr17:69213730
|
G | A | 41 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(38): Show | 42 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006+974C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213730 | ||||||
chr17:69213734
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+970C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213734 | ||||||
chr17:69213742
|
A | G | 1 | a0002c0002t0001g0101 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1006+962T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213742 | ||||||
chr17:69213904
|
T | C | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+800A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69213904 | ||||||
chr17:69214002
|
A | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1006+702T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214002 | ||||||
chr17:69214095
|
T | G | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+609A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214095 | ||||||
chr17:69214118
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG00639.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1006+586G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214118 | ||||||
chr17:69214126
|
A | C | 232 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(229): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1006+578T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214126 | ||||||
chr17:69214166
|
C | T | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+538G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214166 | ||||||
chr17:69214239
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+465C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214239 | ||||||
chr17:69214252
|
A | C | 139 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006+452T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214252 | ||||||
chr17:69214298
|
G | A | 1 | a0002c0002t0001g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1006+406C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214298 | ||||||
chr17:69214331
|
C | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+373G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214331 | ||||||
chr17:69214371
|
T | C | 187 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(184): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1006+333A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214371 | ||||||
chr17:69214390
|
C | CTG | 3 | a0005c0005t0004g0213a0005c0005t0004g0214a0005c0005t0004g0262 | 3 | HG01099.hp2 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1006+312_1006+313d others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214390 | ||||||
chr17:69214463
|
C | T | 5 | a0003c0028t0006g0248a0009c0022t0012g0136a0010c0010t0006g0135others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+241G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214463 | ||||||
chr17:69214471
|
C | T | 2 | a0004c0004t0003g0241a0004c0004t0003g0242 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1006+233G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214471 | ||||||
chr17:69214502
|
G | A | 1 | a0010c0010t0006g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+202C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214502 | ||||||
chr17:69214514
|
CA | C | 174 | a0001c0001t0002g0281a0002c0002t0001g0002a0002c0002t0001g0008others(171): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1006+189delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214514 | ||||||
chr17:69214536
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1006+168C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214536 | ||||||
chr17:69214578
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1006+126A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | 69214578 | ||||||
chr17:69214917
|
T | A | 162 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(159): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.859-66A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69214917 | ||||||
chr17:69214918
|
A | T | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859-67T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69214918 | ||||||
chr17:69214959
|
T | C | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.859-108A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69214959 | ||||||
chr17:69214977
|
T | C | 227 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.859-126A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69214977 | ||||||
chr17:69215106
|
C | T | 1 | a0009c0022t0012g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.859-255G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215106 | ||||||
chr17:69215143
|
T | C | 1 | a0003c0003t0001g0052 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.859-292A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215143 | ||||||
chr17:69215180
|
A | G | 31 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(28): Show | 31 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.859-329T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215180 | ||||||
chr17:69215258
|
C | T | 227 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.859-407G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215258 | ||||||
chr17:69215312
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.859-461C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215312 | ||||||
chr17:69215395
|
T | A | 186 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.858+420A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215395 | ||||||
chr17:69215452
|
A | T | 1 | a0013c0020t0006g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.858+363T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215452 | ||||||
chr17:69215543
|
T | C | 2 | a0002c0002t0001g0064a0002c0002t0001g0101 | 2 | NA19007.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.858+272A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215543 | ||||||
chr17:69215568
|
T | C | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.858+247A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215568 | ||||||
chr17:69215666
|
T | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.858+149A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215666 | ||||||
chr17:69215701
|
A | C | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.858+114T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 8/38 | chr17 | 69215701 | ||||||
chr17:69216004
|
A | T | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.673-4T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 7/38 | chr17 | 69216004 | ||||||
chr17:69216124
|
T | C | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672+93A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 7/38 | chr17 | 69216124 | ||||||
chr17:69216433
|
A | C | 213 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(210): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.531-75T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216433 | ||||||
chr17:69216454
|
G | A | 11 | a0002c0002t0001g0183a0003c0003t0001g0056a0003c0003t0001g0071others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-96C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216454 | ||||||
chr17:69216507
|
G | A | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.531-149C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216507 | ||||||
chr17:69216558
|
C | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.531-200G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216558 | ||||||
chr17:69216578
|
A | C | 1 | a0004c0004t0003g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.531-220T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216578 | ||||||
chr17:69216627
|
C | T | 227 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.531-269G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216627 | ||||||
chr17:69216743
|
AAAC | A | 7 | a0001c0001t0002g0027a0001c0001t0002g0172a0001c0001t0002g0173others(4): Show | 7 | HG01928.hp2 NA18962.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-388_531-386del others(3): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216743 | ||||||
chr17:69216810
|
A | G | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-452T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216810 | ||||||
chr17:69216917
|
A | T | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-559T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69216917 | ||||||
chr17:69217110
|
G | A | 1 | a0001c0001t0002g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.531-752C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217110 | ||||||
chr17:69217116
|
G | A | 12 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(9): Show | 13 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.531-758C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217116 | ||||||
chr17:69217234
|
C | T | 1 | a0003c0003t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.531-876G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217234 | ||||||
chr17:69217255
|
GA | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 47 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.531-898delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217255 | ||||||
chr17:69217301
|
T | G | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-943A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217301 | ||||||
chr17:69217357
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.531-999C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217357 | ||||||
chr17:69217383
|
C | T | 227 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.531-1025G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217383 | ||||||
chr17:69217405
|
T | C | 8 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(5): Show | 9 | HG01346.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-1047A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217405 | ||||||
chr17:69217455
|
A | G | 46 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(43): Show | 47 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.531-1097T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217455 | ||||||
chr17:69217542
|
C | T | 6 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-1184G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217542 | ||||||
chr17:69217643
|
G | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.531-1285C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217643 | ||||||
chr17:69217821
|
A | C | 11 | a0002c0002t0001g0183a0003c0003t0001g0056a0003c0003t0001g0071others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-1463T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69217821 | ||||||
chr17:69218305
|
G | T | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.530+1240C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218305 | ||||||
chr17:69218513
|
A | G | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.530+1032T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218513 | ||||||
chr17:69218527
|
T | C | 6 | a0008c0009t0009g0004a0008c0009t0009g0200a0008c0009t0009g0226others(3): Show | 7 | HG01346.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1018A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218527 | ||||||
chr17:69218618
|
TATATATA others(33): Show |
T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+887_530+926del others(40): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218618 | ||||||
chr17:69218664
|
T | C | 213 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(210): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.530+881A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218664 | ||||||
chr17:69218693
|
G | GCTCT | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+851_530+852ins others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218693 | ||||||
chr17:69218713
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.530+832G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218713 | ||||||
chr17:69218892
|
C | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.530+653G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218892 | ||||||
chr17:69218947
|
C | T | 40 | a0004c0004t0003g0005a0004c0004t0003g0007a0004c0004t0003g0074others(37): Show | 41 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.530+598G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69218947 | ||||||
chr17:69219314
|
C | T | 6 | a0003c0003t0001g0057a0003c0003t0001g0088a0003c0003t0001g0089others(3): Show | 6 | HG00323.hp1 HG00738.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+231G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69219314 | ||||||
chr17:69219344
|
C | T | 186 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.530+201G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69219344 | ||||||
chr17:69219445
|
C | T | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+100G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69219445 | ||||||
chr17:69219468
|
G | A | 8 | a0007c0008t0004g0196a0007c0008t0007g0006a0007c0008t0007g0333others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+77C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69219468 | ||||||
chr17:69219520
|
A | G | 1 | a0005c0005t0004g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.530+25T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 6/38 | chr17 | 69219520 | ||||||
chr17:69219836
|
A | G | 1 | a0002c0002t0001g0119 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.304-65T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69219836 | ||||||
chr17:69219852
|
T | A | 1 | a0003c0003t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.304-81A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69219852 | ||||||
chr17:69219924
|
T | C | 1 | a0001c0034t0002g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.304-153A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69219924 | ||||||
chr17:69220063
|
T | C | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.304-292A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220063 | ||||||
chr17:69220064
|
A | G | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.304-293T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220064 | ||||||
chr17:69220083
|
G | T | 27 | a0005c0005t0004g0184a0005c0005t0004g0199a0005c0005t0004g0213others(24): Show | 27 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.304-312C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220083 | ||||||
chr17:69220171
|
G | C | 141 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(138): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.304-400C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220171 | ||||||
chr17:69220495
|
G | A | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.304-724C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220495 | ||||||
chr17:69220501
|
A | T | 3 | a0003c0003t0001g0041a0003c0003t0001g0087a0003c0003t0001g0131 | 3 | NA18953.hp1 NA18964.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.304-730T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220501 | ||||||
chr17:69220632
|
T | C | 228 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(225): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.304-861A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220632 | ||||||
chr17:69220643
|
G | A | 1 | a0003c0003t0001g0103 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.304-872C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220643 | ||||||
chr17:69220797
|
C | T | 1 | a0003c0028t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.303+995G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69220797 | ||||||
chr17:69221094
|
T | A | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+698A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221094 | ||||||
chr17:69221292
|
T | C | 228 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.303+500A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221292 | ||||||
chr17:69221586
|
T | C | 233 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(230): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.303+206A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221586 | ||||||
chr17:69221607
|
G | A | 4 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+185C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221607 | ||||||
chr17:69221640
|
G | A | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.303+152C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221640 | ||||||
chr17:69221655
|
C | G | 224 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(221): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.303+137G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 5/38 | chr17 | 69221655 | ||||||
chr17:69222045
|
C | A | 1 | a0006c0007t0010g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.200-150G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222045 | ||||||
chr17:69222056
|
A | G | 140 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0014others(137): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.200-161T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222056 | ||||||
chr17:69222272
|
C | T | 2 | a0013c0020t0006g0132a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.199+261G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222272 | ||||||
chr17:69222273
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.199+260C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222273 | ||||||
chr17:69222290
|
A | T | 1 | a0011c0012t0008g0325 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.199+243T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222290 | ||||||
chr17:69222293
|
G | A | 3 | a0010c0010t0006g0135a0010c0010t0006g0140a0010c0010t0006g0194 | 3 | HG01891.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.199+240C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222293 | ||||||
chr17:69222337
|
C | CA | 7 | a0001c0001t0002g0177a0001c0001t0002g0300a0008c0009t0009g0004others(4): Show | 8 | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+195dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222337 | ||||||
chr17:69222337
|
CA | C | 181 | a0001c0001t0002g0178a0002c0002t0001g0002a0002c0002t0001g0008others(178): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.199+195delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222337 | ||||||
chr17:69222420
|
G | A | 1 | a0001c0001t0017g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199+113C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222420 | ||||||
chr17:69222498
|
C | A | 1 | a0003c0003t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.199+35G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222498 | ||||||
chr17:69222498
|
C | G | 1 | a0001c0001t0002g0275 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.199+35G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222498 | ||||||
chr17:69222531
|
A | G | 1 | a0025c0029t0014g0197 | 1 | HG01243.hp1 | splice_donor_variant&intron_variant | HIGH | c.199+2T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4/38 | chr17 | 69222531 | ||||||
chr17:69222873
|
C | T | 3 | a0009c0022t0012g0136a0010c0010t0006g0135a0010c0010t0006g0140 | 3 | HG01891.hp1 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35-176G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69222873 | ||||||
chr17:69223063
|
G | A | 1 | a0004c0004t0003g0247 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.35-366C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223063 | ||||||
chr17:69223225
|
C | G | 1 | a0008c0009t0009g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.35-528G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223225 | ||||||
chr17:69223276
|
A | ATATC | 70 | a0001c0001t0002g0257a0001c0001t0006g0009a0001c0001t0006g0010others(67): Show | 72 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.35-583_35-580dupGA others(2): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223276 | ||||||
chr17:69223319
|
A | G | 323 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.35-622T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223319 | ||||||
chr17:69223367
|
A | T | 4 | a0002c0002t0005g0312a0002c0002t0005g0313a0002c0002t0005g0314others(1): Show | 4 | NA18973.hp2 NA19002.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-670T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223367 | ||||||
chr17:69223469
|
T | A | 39 | a0001c0001t0002g0147a0001c0001t0002g0178a0001c0001t0002g0179others(36): Show | 39 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.35-772A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223469 | ||||||
chr17:69223506
|
A | G | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.35-809T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223506 | ||||||
chr17:69223562
|
G | A | 219 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0040others(216): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.35-865C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223562 | ||||||
chr17:69223627
|
C | T | 49 | a0001c0001t0006g0224a0001c0001t0006g0225a0002c0002t0001g0082others(46): Show | 49 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.35-930G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223627 | ||||||
chr17:69223780
|
T | G | 4 | a0003c0003t0001g0261a0005c0005t0004g0199a0013c0020t0006g0132others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-1083A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223780 | ||||||
chr17:69223919
|
T | G | 154 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(151): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.35-1222A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223919 | ||||||
chr17:69223949
|
C | T | 1 | a0010c0010t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35-1252G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223949 | ||||||
chr17:69223956
|
T | C | 71 | a0001c0001t0002g0252a0001c0001t0002g0257a0001c0001t0002g0258others(68): Show | 73 | HG00609.hp2 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.35-1259A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69223956 | ||||||
chr17:69224142
|
A | T | 11 | a0004c0004t0003g0193a0005c0005t0004g0184a0006c0007t0004g0185others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+1183T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224142 | ||||||
chr17:69224158
|
G | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.34+1167C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224158 | ||||||
chr17:69224225
|
G | A | 1 | a0003c0003t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.34+1100C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224225 | ||||||
chr17:69224268
|
T | C | 1 | a0003c0003t0016g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.34+1057A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224268 | ||||||
chr17:69224313
|
C | T | 201 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(198): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.34+1012G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224313 | ||||||
chr17:69224382
|
G | A | 128 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(125): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.34+943C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224382 | ||||||
chr17:69224459
|
C | A | 1 | a0019c0037t0007g0331 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.34+866G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224459 | ||||||
chr17:69224495
|
C | G | 115 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.34+830G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224495 | ||||||
chr17:69224538
|
A | G | 1 | a0003c0003t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.34+787T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224538 | ||||||
chr17:69224572
|
G | T | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.34+753C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224572 | ||||||
chr17:69224688
|
G | GA | 119 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(116): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.34+636dupT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224688 | ||||||
chr17:69224688
|
GA | G | 17 | a0001c0001t0002g0147a0001c0001t0006g0009a0001c0001t0006g0010others(14): Show | 17 | HG00733.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.34+636delT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224688 | ||||||
chr17:69224688
|
GAA | G | 12 | a0002c0002t0001g0138a0002c0015t0001g0003a0003c0003t0001g0133others(9): Show | 13 | HG00099.hp2 HG00738.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.34+635_34+636delTT | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224688 | ||||||
chr17:69224718
|
A | T | 232 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(229): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.34+607T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224718 | ||||||
chr17:69224727
|
G | A | 3 | a0003c0003t0001g0128a0003c0003t0001g0129a0003c0003t0001g0130 | 3 | HG02717.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.34+598C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224727 | ||||||
chr17:69224862
|
T | C | 118 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(115): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.34+463A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69224862 | ||||||
chr17:69225056
|
T | C | 1 | a0003c0003t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.34+269A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225056 | ||||||
chr17:69225114
|
T | C | 2 | a0003c0003t0001g0261a0005c0005t0004g0262 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.34+211A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225114 | ||||||
chr17:69225116
|
AAAAC | A | 117 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(114): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.34+205_34+208delGT others(2): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225116 | ||||||
chr17:69225161
|
C | T | 12 | a0004c0004t0003g0193a0005c0005t0004g0184a0006c0007t0004g0185others(9): Show | 12 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+164G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225161 | ||||||
chr17:69225165
|
C | A | 2 | a0001c0001t0018g0342a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.34+160G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225165 | ||||||
chr17:69225173
|
T | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0026others(338): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.34+152A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225173 | ||||||
chr17:69225191
|
C | T | 1 | a0003c0003t0005g0309 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.34+134G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225191 | ||||||
chr17:69225297
|
C | A | 9 | a0001c0001t0017g0332a0007c0008t0007g0006a0007c0008t0007g0333others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+28G>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 3/38 | chr17 | 69225297 | ||||||
chr17:69225543
|
A | G | 9 | a0001c0001t0017g0332a0007c0008t0007g0006a0007c0008t0007g0333others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-171-14T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225543 | ||||||
chr17:69225665
|
A | C | 2 | a0001c0001t0018g0342a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-171-136T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225665 | ||||||
chr17:69225679
|
C | T | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-171-150G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225679 | ||||||
chr17:69225692
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-171-163T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225692 | ||||||
chr17:69225727
|
A | G | 1 | a0013c0020t0006g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-171-198T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225727 | ||||||
chr17:69225769
|
C | G | 1 | a0001c0001t0002g0273 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-171-240G>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225769 | ||||||
chr17:69225894
|
A | G | 1 | a0002c0002t0001g0015 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-171-365T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69225894 | ||||||
chr17:69226020
|
G | A | 2 | a0003c0003t0001g0302a0022c0024t0001g0303 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-171-491C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226020 | ||||||
chr17:69226120
|
G | T | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-171-591C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226120 | ||||||
chr17:69226588
|
T | G | 1 | a0001c0001t0018g0342 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-172+557A>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226588 | ||||||
chr17:69226670
|
G | A | 231 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0035others(228): Show | 236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-172+475C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226670 | ||||||
chr17:69226680
|
C | T | 30 | a0001c0001t0002g0001a0001c0001t0002g0040a0001c0001t0002g0072others(27): Show | 31 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-172+465G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226680 | ||||||
chr17:69226722
|
C | T | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-172+423G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226722 | ||||||
chr17:69226736
|
A | G | 1 | a0023c0026t0001g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-172+409T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226736 | ||||||
chr17:69226872
|
T | C | 9 | a0001c0001t0002g0263a0001c0001t0002g0264a0002c0002t0001g0142others(6): Show | 9 | HG01123.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-172+273A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226872 | ||||||
chr17:69226903
|
G | T | 3 | a0001c0001t0002g0270a0004c0004t0003g0271a0004c0004t0003g0272 | 3 | NA18989.hp2 NA19000.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-172+242C>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226903 | ||||||
chr17:69226921
|
G | A | 38 | a0001c0001t0002g0012a0001c0001t0002g0028a0001c0001t0002g0029others(35): Show | 39 | HG01928.hp2 HG01934.hp2 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.-172+224C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69226921 | ||||||
chr17:69227114
|
G | GAT | 13 | a0001c0001t0002g0144a0001c0001t0017g0332a0002c0002t0001g0138others(10): Show | 14 | HG00099.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-172+29_-172+30dup others(2): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATAT | 4 | a0003c0003t0001g0133a0003c0003t0001g0134a0013c0020t0006g0132others(1): Show | 4 | HG00738.hp2 HG01346.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+27_-172+30dup others(4): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATAT | 5 | a0001c0001t0018g0342a0003c0003t0001g0128a0003c0003t0001g0129others(2): Show | 5 | HG02717.hp1 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+25_-172+30dup others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(3): Show |
5 | a0002c0002t0001g0124a0002c0002t0001g0125a0002c0002t0001g0126others(2): Show | 5 | HG02451.hp1 HG02723.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+21_-172+30dup others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(5): Show |
12 | a0001c0001t0002g0117a0002c0002t0001g0114a0002c0002t0001g0115others(9): Show | 12 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-172+19_-172+30dup others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(7): Show |
50 | a0001c0001t0002g0026a0001c0001t0002g0072a0001c0001t0002g0073others(47): Show | 51 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-172+17_-172+30dup others(14): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(9): Show |
21 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(18): Show | 21 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.-172+15_-172+30dup others(16): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(11): Show |
13 | a0001c0001t0002g0001a0002c0002t0001g0008a0002c0002t0001g0014others(10): Show | 14 | HG00323.hp2 HG00733.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.-172+13_-172+30dup others(18): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(13): Show |
8 | a0001c0001t0002g0040a0002c0002t0001g0038a0002c0002t0001g0043others(5): Show | 8 | HG01069.hp2 HG01169.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-172+30_-172+31ins others(20): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(15): Show |
3 | a0001c0001t0002g0035a0002c0002t0001g0036a0002c0002t0001g0037 | 3 | NA19010.hp2 NA19054.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-172+30_-172+31ins others(22): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227114
|
G | GATATATA others(17): Show |
3 | a0002c0002t0001g0032a0004c0006t0003g0033a0004c0006t0003g0034 | 3 | NA18974.hp2 NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-172+30_-172+31ins others(24): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227114 | ||||||
chr17:69227127
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-172+17_-172+18ins others(15): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 2/38 | chr17 | 69227127 | ||||||
chr17:69227343
|
A | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 4 | NA18984.hp2 NA19063.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.-312-58T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227343 | ||||||
chr17:69227517
|
A | T | 2 | a0001c0001t0018g0342a0013c0021t0006g0305 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-312-232T>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227517 | ||||||
chr17:69227559
|
A | G | 13 | a0001c0001t0002g0026a0002c0002t0001g0014a0002c0002t0001g0015others(10): Show | 13 | HG00609.hp1 HG02129.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.-312-274T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227559 | ||||||
chr17:69227667
|
G | C | 2 | a0003c0003t0001g0302a0022c0024t0001g0303 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-312-382C>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227667 | ||||||
chr17:69227685
|
T | A | 1 | a0004c0004t0003g0304 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-312-400A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227685 | ||||||
chr17:69227786
|
C | T | 1 | a0003c0003t0001g0013 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-312-501G>A | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227786 | ||||||
chr17:69227890
|
A | C | 1 | a0001c0001t0002g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-312-605T>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227890 | ||||||
chr17:69227967
|
G | A | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-313+614C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69227967 | ||||||
chr17:69228022
|
A | G | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02055.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-313+559T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228022 | ||||||
chr17:69228051
|
A | G | 1 | a0001c0001t0018g0342 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-313+530T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228051 | ||||||
chr17:69228160
|
T | C | 1 | a0001c0001t0018g0342 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-313+421A>G | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228160 | ||||||
chr17:69228307
|
G | A | 1 | a0013c0021t0006g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-313+274C>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228307 | ||||||
chr17:69228335
|
T | A | 2 | a0001c0001t0002g0307a0003c0003t0001g0306 | 2 | NA19081.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-313+246A>T | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228335 | ||||||
chr17:69228406
|
A | G | 1 | a0002c0002t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-313+175T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228406 | ||||||
chr17:69228474
|
AATAAT | A | 3 | a0006c0007t0010g0339a0006c0007t0010g0340a0006c0007t0010g0341 | 3 | HG02723.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-313+102_-313+106d others(7): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228474 | ||||||
chr17:69228524
|
A | G | 1 | a0004c0004t0003g0007 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-313+57T>C | ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1/38 | chr17 | 69228524 |