geneid | 10350 |
---|---|
ensemblid | ENSG00000154258.17 |
hgncid | 39 |
symbol | ABCA9 |
name | ATP binding cassette subfamily A member 9 |
refseq_nuc | NM_080283.4 |
refseq_prot | NP_525022.2 |
ensembl_nuc | ENST00000340001.9 |
ensembl_prot | ENSP00000342216.3 |
mane_status | MANE Select |
chr | chr17 |
start | 68974488 |
end | 69060927 |
strand | - |
ver | v1.2 |
region | chr17:68974488-69060927 |
region5000 | chr17:68969488-69065927 |
regionname0 | ABCA9_chr17_68974488_69060927 |
regionname5000 | ABCA9_chr17_68969488_69065927 |
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 | 0/0 | 1624 | 108 | 23 | 11 | 52 | 8 | 14 | 40 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002 | 0/1 | 1624 | 108 | 10 | 21 | 57 | 6 | 13 | 44 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003 | 1/0 | 1624 | 34 | 23 | 3 | 0 | 0 | 7 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0004 | 0/0 | 1624 | 18 | 16 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0005 | 0/0 | 1624 | 14 | 0 | 4 | 9 | 0 | 1 | 8 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0006 | 0/0 | 1624 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0007 | 0/0 | 1624 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0008 | 0/0 | 1624 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0009 | 0/0 | 1624 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0010 | 0/0 | 1049 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0011 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0012 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0013 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0014 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0015 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0016 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0017 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0018 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0019 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0020 | 0/0 | 1624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0021 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0022 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0023 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
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 | 0/0 | 4875 | 87 | 12 | 7 | 52 | 3 | 13 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0002 | 0/1 | 4875 | 86 | 10 | 21 | 40 | 4 | 10 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0003 | 1/0 | 4875 | 34 | 23 | 3 | 0 | 0 | 7 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0004 | 0/0 | 4875 | 19 | 0 | 0 | 16 | 1 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0005 | 0/0 | 4875 | 18 | 16 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0006 | 0/0 | 4875 | 14 | 0 | 4 | 9 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0007 | 0/0 | 4875 | 11 | 2 | 4 | 0 | 4 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0008 | 0/0 | 4875 | 8 | 8 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0009 | 0/0 | 4875 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0010 | 0/0 | 4875 | 5 | 0 | 5 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0011 | 0/0 | 4875 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0012 | 0/0 | 4875 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0013 | 0/0 | 4875 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0014 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0015 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0016 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0017 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0018 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0019 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0020 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0021 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0022 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0023 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0024 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0025 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0026 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0027 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0028 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0029 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0030 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0031 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
c0032 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
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 | 1/0 | 1503 | 125 | 22 | 15 | 60 | 8 | 19 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0002 | 0/1 | 1499 | 116 | 11 | 24 | 60 | 6 | 14 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0003 | 0/0 | 1499 | 41 | 35 | 5 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0004 | 0/0 | 1499 | 12 | 11 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0005 | 0/0 | 1497 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0006 | 0/0 | 1497 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0007 | 0/0 | 1499 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0008 | 0/0 | 1503 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0009 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0010 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0011 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0012 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0013 | 0/0 | 1499 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
t0014 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
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 | 5 | 4 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
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 | 0/0 | 4875 | 87 | 12 | 7 | 52 | 3 | 13 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0007 | 0/0 | 4875 | 11 | 2 | 4 | 0 | 4 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0008 | 0/0 | 4875 | 8 | 8 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0021 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0029 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0002 | 0/1 | 4875 | 86 | 10 | 21 | 40 | 4 | 10 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0004 | 0/0 | 4875 | 19 | 0 | 0 | 16 | 1 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0026 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0027 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0028 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003 | 1/0 | 4875 | 34 | 23 | 3 | 0 | 0 | 7 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0004c0005 | 0/0 | 4875 | 18 | 16 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0005c0006 | 0/0 | 4875 | 14 | 0 | 4 | 9 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0006c0010 | 0/0 | 4875 | 5 | 0 | 5 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0007c0009 | 0/0 | 4875 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0008c0013 | 0/0 | 4875 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0008c0020 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0009c0011 | 0/0 | 4875 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0010c0012 | 0/0 | 4875 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0011c0015 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0012c0014 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0013c0016 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0014c0031 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0015c0030 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0016c0017 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0017c0025 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0018c0022 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0019c0023 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0020c0024 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0021c0032 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0022c0018 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0023c0019 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6377 | 78 | 8 | 4 | 50 | 3 | 13 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0006 | 0/0 | 6371 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0008 | 0/0 | 6377 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0009 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0011 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0001t0012 | 0/0 | 6377 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0007t0001 | 0/0 | 6377 | 10 | 1 | 4 | 0 | 4 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0007t0004 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0008t0001 | 0/0 | 6377 | 8 | 8 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0021t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0001c0029t0001 | 0/0 | 6377 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0002t0002 | 0/1 | 6373 | 84 | 10 | 19 | 40 | 4 | 10 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0002t0007 | 0/0 | 6373 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0004t0002 | 0/0 | 6373 | 19 | 0 | 0 | 16 | 1 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0026t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0027t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0002c0028t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003t0001 | 1/0 | 6377 | 11 | 5 | 1 | 0 | 0 | 4 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003t0003 | 0/0 | 6373 | 10 | 7 | 2 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003t0004 | 0/0 | 6373 | 11 | 10 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003t0010 | 0/0 | 6377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0003c0003t0013 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0004c0005t0003 | 0/0 | 6373 | 18 | 16 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0005c0006t0001 | 0/0 | 6377 | 14 | 0 | 4 | 9 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0006c0010t0002 | 0/0 | 6373 | 5 | 0 | 5 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0007c0009t0005 | 0/0 | 6371 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0008c0013t0003 | 0/0 | 6373 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0008c0020t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0009c0011t0003 | 0/0 | 6373 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0010c0012t0001 | 0/0 | 6377 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0011c0015t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0012c0014t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0013c0016t0002 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0014c0031t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0015c0030t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0016c0017t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0017c0025t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0018c0022t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0019c0023t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0020c0024t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0021c0032t0001 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0022c0018t0014 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
a0023c0019t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | copy fasta | chr17 | 68969488 | 69065927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0012g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0021t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0029t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0026t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0027t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0028t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0013g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0010t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0010t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0010t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0010t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0010t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0009t0005g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0009t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0009t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0009t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0013t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0013t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0020t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0009c0011t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0009c0011t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0010c0012t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0010c0012t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0011c0015t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0012c0014t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0013c0016t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0014c0031t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0015c0030t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0016c0017t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0017c0025t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0018c0022t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0019c0023t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0020c0024t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0021c0032t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0022c0018t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0023c0019t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0029 | t0001 | g0200 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0068 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00140 | hp2 | a0001 | c0007 | t0001 | g0225 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00280 | hp1 | a0002 | c0004 | t0002 | g0262 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00280 | hp2 | a0001 | c0007 | t0001 | g0241 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00544 | hp2 | a0005 | c0006 | t0001 | g0293 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00639 | hp1 | a0002 | c0002 | t0007 | g0133 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00639 | hp2 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00642 | hp2 | a0001 | c0007 | t0001 | g0211 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00733 | hp1 | a0008 | c0013 | t0003 | g0057 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01069 | hp1 | a0007 | c0009 | t0005 | g0296 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01071 | hp1 | a0007 | c0009 | t0005 | g0010 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01074 | hp1 | a0005 | c0006 | t0001 | g0275 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01074 | hp2 | a0002 | c0002 | t0007 | g0132 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01106 | hp1 | a0007 | c0009 | t0005 | g0010 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0234 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01109 | hp2 | a0004 | c0005 | t0003 | g0290 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01167 | hp2 | a0010 | c0012 | t0001 | g0273 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0089 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01169 | hp2 | a0010 | c0012 | t0001 | g0282 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01257 | hp1 | a0006 | c0010 | t0002 | g0083 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0251 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01258 | hp1 | a0001 | c0007 | t0001 | g0116 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0250 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01346 | hp1 | a0004 | c0005 | t0003 | g0001 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0039 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01361 | hp2 | a0001 | c0007 | t0001 | g0141 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01496 | hp1 | a0001 | c0007 | t0001 | g0115 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01496 | hp2 | a0006 | c0010 | t0002 | g0120 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01516 | hp1 | a0001 | c0007 | t0001 | g0008 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01516 | hp2 | a0002 | c0027 | t0002 | g0069 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01517 | hp1 | a0001 | c0007 | t0001 | g0008 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0140 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01884 | hp1 | a0003 | c0003 | t0004 | g0023 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01891 | hp1 | a0001 | c0021 | t0003 | g0015 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0045 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01952 | hp2 | a0006 | c0010 | t0002 | g0145 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01975 | hp2 | a0005 | c0006 | t0001 | g0292 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01978 | hp1 | a0005 | c0006 | t0001 | g0276 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01978 | hp2 | a0006 | c0010 | t0002 | g0155 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02004 | hp2 | a0005 | c0006 | t0001 | g0277 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02055 | hp2 | a0007 | c0009 | t0005 | g0295 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02071 | hp2 | a0002 | c0004 | t0002 | g0267 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02074 | hp2 | a0002 | c0004 | t0002 | g0139 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02083 | hp2 | a0002 | c0004 | t0002 | g0108 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02132 | hp2 | a0001 | c0001 | t0011 | g0249 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02145 | hp1 | a0012 | c0014 | t0003 | g0048 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02155 | hp1 | a0002 | c0004 | t0002 | g0112 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02258 | hp2 | a0013 | c0016 | t0002 | g0050 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02273 | hp1 | a0006 | c0010 | t0002 | g0144 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02280 | hp2 | a0001 | c0007 | t0001 | g0090 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02451 | hp1 | a0018 | c0022 | t0003 | g0014 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02451 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02572 | hp2 | a0001 | c0008 | t0001 | g0167 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0028 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02622 | hp1 | a0011 | c0015 | t0003 | g0049 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0025 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02630 | hp1 | a0004 | c0005 | t0003 | g0288 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02630 | hp2 | a0003 | c0003 | t0003 | g0037 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02647 | hp1 | a0001 | c0008 | t0001 | g0193 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02647 | hp2 | a0004 | c0005 | t0003 | g0287 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0042 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02717 | hp1 | a0001 | c0008 | t0001 | g0196 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02717 | hp2 | a0003 | c0003 | t0004 | g0020 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02723 | hp2 | a0001 | c0008 | t0001 | g0181 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02735 | hp2 | a0020 | c0024 | t0002 | g0062 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02809 | hp1 | a0004 | c0005 | t0003 | g0285 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02809 | hp2 | a0016 | c0017 | t0003 | g0189 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02818 | hp1 | a0004 | c0005 | t0003 | g0270 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02818 | hp2 | a0003 | c0003 | t0004 | g0003 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02886 | hp1 | a0004 | c0005 | t0003 | g0274 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02886 | hp2 | a0001 | c0007 | t0004 | g0093 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02922 | hp1 | a0001 | c0008 | t0001 | g0191 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02922 | hp2 | a0004 | c0005 | t0003 | g0268 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02970 | hp1 | a0004 | c0005 | t0003 | g0286 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02976 | hp2 | a0003 | c0003 | t0004 | g0024 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0018 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03041 | hp2 | a0009 | c0011 | t0003 | g0046 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03098 | hp1 | a0008 | c0020 | t0003 | g0054 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03098 | hp2 | a0004 | c0005 | t0003 | g0271 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03130 | hp1 | a0003 | c0003 | t0004 | g0003 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03139 | hp1 | a0003 | c0003 | t0004 | g0021 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03195 | hp1 | a0001 | c0008 | t0001 | g0263 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03209 | hp1 | a0001 | c0008 | t0001 | g0190 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03209 | hp2 | a0003 | c0003 | t0003 | g0038 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03225 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03453 | hp1 | a0004 | c0005 | t0003 | g0272 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0031 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03486 | hp1 | a0004 | c0005 | t0003 | g0269 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0034 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03490 | hp2 | a0002 | c0028 | t0002 | g0081 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03491 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03516 | hp1 | a0023 | c0019 | t0003 | g0055 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03516 | hp2 | a0019 | c0023 | t0003 | g0013 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03579 | hp1 | a0003 | c0003 | t0003 | g0033 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03579 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03654 | hp1 | a0002 | c0004 | t0002 | g0265 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0138 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03834 | hp1 | a0003 | c0003 | t0004 | g0019 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0154 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03927 | hp2 | a0003 | c0003 | t0013 | g0022 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04115 | hp1 | a0005 | c0006 | t0001 | g0294 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0161 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0260 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04228 | hp2 | a0002 | c0004 | t0002 | g0085 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18522 | hp1 | a0003 | c0003 | t0003 | g0041 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18522 | hp2 | a0003 | c0003 | t0004 | g0017 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | CHB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0026 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18957 | hp1 | a0002 | c0004 | t0002 | g0109 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18962 | hp2 | a0002 | c0004 | t0002 | g0212 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18967 | hp2 | a0002 | c0004 | t0002 | g0156 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18969 | hp1 | a0002 | c0004 | t0002 | g0110 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18974 | hp2 | a0005 | c0006 | t0001 | g0009 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18979 | hp1 | a0002 | c0004 | t0002 | g0183 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18979 | hp2 | a0002 | c0004 | t0002 | g0148 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18980 | hp2 | a0005 | c0006 | t0001 | g0280 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18982 | hp2 | a0002 | c0004 | t0002 | g0111 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18985 | hp1 | a0005 | c0006 | t0001 | g0284 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18987 | hp2 | a0002 | c0004 | t0002 | g0197 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18989 | hp1 | a0005 | c0006 | t0001 | g0281 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18993 | hp1 | a0005 | c0006 | t0001 | g0009 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19002 | hp1 | a0002 | c0026 | t0002 | g0073 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19002 | hp2 | a0005 | c0006 | t0001 | g0279 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19009 | hp2 | a0015 | c0030 | t0002 | g0205 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19011 | hp2 | a0002 | c0004 | t0002 | g0247 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19043 | hp1 | a0008 | c0013 | t0003 | g0056 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19043 | hp2 | a0007 | c0009 | t0005 | g0297 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19054 | hp1 | a0021 | c0032 | t0001 | g0226 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19066 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19067 | hp1 | a0002 | c0004 | t0002 | g0157 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19068 | hp2 | a0002 | c0004 | t0002 | g0113 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19075 | hp2 | a0017 | c0025 | t0002 | g0058 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19083 | hp2 | a0002 | c0004 | t0002 | g0184 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19086 | hp1 | a0005 | c0006 | t0001 | g0283 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19087 | hp1 | a0014 | c0031 | t0002 | g0236 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19087 | hp2 | a0005 | c0006 | t0001 | g0278 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19240 | hp1 | a0009 | c0011 | t0003 | g0047 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19240 | hp2 | a0003 | c0003 | t0003 | g0036 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0192 | AFR | ASW | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ASW | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0135 | EUR | TSI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0027 | SAS | GIH | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02486 | hp2 | a0003 | c0003 | t0010 | g0030 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0043 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02559 | hp2 | a0004 | c0005 | t0003 | g0289 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03471 | hp2 | a0022 | c0018 | t0014 | g0298 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG06807 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0075 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20300 | hp2 | a0004 | c0005 | t0003 | g0291 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA21309 | hp1 | a0003 | c0003 | t0003 | g0040 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0065 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0118 | REF | REF | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0044 | REF | REF | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68986306
|
C | T | 4 | a0004a0012a0016others(1): Show | 21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
missense_variant | MODERATE | c.4066G>A | p.Gly1356Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/39 | 4141/6377 | 4066/4875 | 1356/1624 | chr17 | 68986306 | ||
chr17:68989851
|
T | G | 7 | a0002a0006a0013others(4): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
missense_variant | MODERATE | c.3917A>C | p.Lys1306Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/39 | 3992/6377 | 3917/4875 | 1306/1624 | chr17 | 68989851 | ||
chr17:68989875
|
T | C | 1 | a0019 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.3893A>G | p.Asn1298Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/39 | 3968/6377 | 3893/4875 | 1298/1624 | chr17 | 68989875 | ||
chr17:69008235
|
T | A | 1 | a0010 | 2 | HG01167.hp2 HG01169.hp2 |
stop_gained&splice_region_variant | HIGH | c.3148A>T | p.Lys1050* | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 24/39 | 3223/6377 | 3148/4875 | 1050/1624 | chr17 | 69008235 | ||
chr17:69016293
|
G | A | 1 | a0015 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.2999C>T | p.Ser1000Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/39 | 3074/6377 | 2999/4875 | 1000/1624 | chr17 | 69016293 | ||
chr17:69016309
|
G | A | 2 | a0008a0009 | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.2983C>T | p.Leu995Phe | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/39 | 3058/6377 | 2983/4875 | 995/1624 | chr17 | 69016309 | ||
chr17:69017778
|
C | T | 1 | a0017 | 1 | NA19075.hp2 | missense_variant | MODERATE | c.2779G>A | p.Asp927Asn | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/39 | 2854/6377 | 2779/4875 | 927/1624 | chr17 | 69017778 | ||
chr17:69018533
|
G | C | 3 | a0018a0019a0023 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.2647C>G | p.Leu883Val | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/39 | 2722/6377 | 2647/4875 | 883/1624 | chr17 | 69018533 | ||
chr17:69021789
|
T | C | 1 | a0006 | 5 | HG01257.hp1 HG01496.hp2 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.2354A>G | p.Asn785Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/39 | 2429/6377 | 2354/4875 | 785/1624 | chr17 | 69021789 | ||
chr17:69029202
|
C | T | 1 | a0020 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1471G>A | p.Ala491Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/39 | 1546/6377 | 1471/4875 | 491/1624 | chr17 | 69029202 | ||
chr17:69033857
|
T | C | 1 | a0014 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.1145A>G | p.Tyr382Cys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/39 | 1220/6377 | 1145/4875 | 382/1624 | chr17 | 69033857 | ||
chr17:69035316
|
C | T | 22 | a0001a0002a0004others(19): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
missense_variant | MODERATE | c.1058G>A | p.Arg353His | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/39 | 1133/6377 | 1058/4875 | 353/1624 | chr17 | 69035316 | ||
chr17:69035396
|
C | A | 1 | a0021 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.978G>T | p.Lys326Asn | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/39 | 1053/6377 | 978/4875 | 326/1624 | chr17 | 69035396 | ||
chr17:69035739
|
A | G | 4 | a0007a0008a0022others(1): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
missense_variant | MODERATE | c.863T>C | p.Ile288Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/39 | 938/6377 | 863/4875 | 288/1624 | chr17 | 69035739 | ||
chr17:69043504
|
C | T | 3 | a0004a0005a0010 | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
missense_variant | MODERATE | c.785G>A | p.Arg262Gln | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/39 | 860/6377 | 785/4875 | 262/1624 | chr17 | 69043504 | ||
chr17:69049311
|
G | T | 4 | a0009a0011a0012others(1): Show | 5 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
missense_variant | MODERATE | c.276C>A | p.Asn92Lys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/39 | 351/6377 | 276/4875 | 92/1624 | chr17 | 69049311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68985116
|
C | A | 2 | a0018c0022a0023c0019 | 2 | HG02451.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.4221G>T | p.Ala1407Ala | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 33/39 | 4296/6377 | 4221/4875 | 1407/1624 | chr17 | 68985116 | ||
chr17:68986286
|
G | A | 1 | a0002c0028 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.4086C>T | p.Gly1362Gly | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/39 | 4161/6377 | 4086/4875 | 1362/1624 | chr17 | 68986286 | ||
chr17:68989101
|
A | G | 1 | a0019c0023 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.3973T>C | p.Leu1325Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/39 | 4048/6377 | 3973/4875 | 1325/1624 | chr17 | 68989101 | ||
chr17:69007825
|
A | G | 1 | a0002c0027 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.3369T>C | p.Tyr1123Tyr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/39 | 3444/6377 | 3369/4875 | 1123/1624 | chr17 | 69007825 | ||
chr17:69007870
|
G | A | 1 | a0001c0029 | 1 | HG00099.hp1 | splice_region_variant&synonymous_variant | LOW | c.3324C>T | p.Ile1108Ile | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/39 | 3399/6377 | 3324/4875 | 1108/1624 | chr17 | 69007870 | ||
chr17:69017776
|
A | G | 1 | a0002c0026 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.2781T>C | p.Asp927Asp | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/39 | 2856/6377 | 2781/4875 | 927/1624 | chr17 | 69017776 | ||
chr17:69018501
|
C | T | 1 | a0001c0021 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2679G>A | p.Pro893Pro | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/39 | 2754/6377 | 2679/4875 | 893/1624 | chr17 | 69018501 | ||
chr17:69020504
|
G | A | 1 | a0008c0020 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2484C>T | p.Ser828Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/39 | 2559/6377 | 2484/4875 | 828/1624 | chr17 | 69020504 | ||
chr17:69032119
|
T | C | 11 | a0001c0007a0001c0029a0002c0002others(8): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
synonymous_variant | LOW | c.1434A>G | p.Lys478Lys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/39 | 1509/6377 | 1434/4875 | 478/1624 | chr17 | 69032119 | ||
chr17:69035741
|
A | G | 2 | a0001c0008a0016c0017 | 9 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.861T>C | p.Leu287Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/39 | 936/6377 | 861/4875 | 287/1624 | chr17 | 69035741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68974507
|
T | G | 1 | a0007c0009t0005 | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1408 | chr17 | 68974507 | |||||
chr17:68974717
|
G | A | 2 | a0001c0001t0006a0007c0009t0005 | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1198 | chr17 | 68974717 | |||||
chr17:68974782
|
CAG | C | 2 | a0001c0001t0006a0007c0009t0005 | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1131_*1132delCT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1131 | chr17 | 68974782 | |||||
chr17:68974804
|
G | A | 31 | a0001c0001t0003a0001c0001t0006a0001c0007t0004others(28): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1111 | chr17 | 68974804 | |||||
chr17:68975001
|
C | A | 1 | a0003c0003t0010 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 914 | chr17 | 68975001 | |||||
chr17:68975016
|
C | T | 1 | a0002c0002t0007 | 2 | HG00639.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*899G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 899 | chr17 | 68975016 | |||||
chr17:68975100
|
G | A | 3 | a0001c0001t0006a0003c0003t0013a0007c0009t0005 | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 815 | chr17 | 68975100 | |||||
chr17:68975108
|
G | T | 1 | a0001c0001t0008 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 807 | chr17 | 68975108 | |||||
chr17:68975434
|
G | C | 12 | a0002c0002t0002a0002c0002t0007a0002c0004t0002others(9): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*481C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 481 | chr17 | 68975434 | |||||
chr17:68975523
|
A | G | 3 | a0001c0007t0004a0003c0003t0004a0003c0003t0013 | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*392T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 392 | chr17 | 68975523 | |||||
chr17:68975554
|
AAAAT | A | 31 | a0001c0001t0003a0001c0001t0006a0001c0007t0004others(28): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*357_*360delATTT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 357 | chr17 | 68975554 | |||||
chr17:68975629
|
A | G | 1 | a0001c0001t0009 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 286 | chr17 | 68975629 | |||||
chr17:68975738
|
T | C | 13 | a0001c0001t0011a0002c0002t0002a0002c0002t0007others(10): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 177 | chr17 | 68975738 | |||||
chr17:68975757
|
C | T | 12 | a0002c0002t0002a0002c0002t0007a0002c0004t0002others(9): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 158 | chr17 | 68975757 | |||||
chr17:68975847
|
T | G | 1 | a0001c0001t0012 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 68 | chr17 | 68975847 | |||||
chr17:68975914
|
T | G | 3 | a0001c0007t0004a0003c0003t0004a0003c0003t0013 | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1 | chr17 | 68975914 | |||||
chr17:69060910
|
T | C | 2 | a0007c0009t0005a0022c0018t0014 | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-58A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/39 | 9784 | chr17 | 69060910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68976109
|
A | T | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4776+26T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 38/38 | chr17 | 68976109 | ||||||
chr17:68976223
|
A | ATT | 18 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(15): Show | 22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4721-35_4721-34dup others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976223 | ||||||
chr17:68976416
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.4721-226T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976416 | ||||||
chr17:68976479
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.4721-289C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976479 | ||||||
chr17:68976487
|
C | T | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4721-297G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976487 | ||||||
chr17:68976505
|
C | T | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-315G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976505 | ||||||
chr17:68976908
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4721-718C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976908 | ||||||
chr17:68976977
|
C | A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4721-787G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976977 | ||||||
chr17:68977003
|
T | C | 6 | a0001c0008t0001g0190a0001c0008t0001g0191a0001c0008t0001g0192others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4721-813A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977003 | ||||||
chr17:68977005
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4721-815C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977005 | ||||||
chr17:68977037
|
TGAA | T | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4721-850_4721-848d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977037 | ||||||
chr17:68977257
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4721-1067C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977257 | ||||||
chr17:68977297
|
A | C | 15 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4721-1107T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977297 | ||||||
chr17:68977338
|
G | A | 17 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(14): Show | 21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4721-1148C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977338 | ||||||
chr17:68977365
|
G | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4721-1175C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977365 | ||||||
chr17:68977477
|
T | C | 1 | a0002c0002t0002g0079 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4721-1287A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977477 | ||||||
chr17:68977555
|
C | T | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4721-1365G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977555 | ||||||
chr17:68977599
|
G | A | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-1409C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977599 | ||||||
chr17:68977697
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4721-1507G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977697 | ||||||
chr17:68977744
|
T | C | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-1554A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977744 | ||||||
chr17:68977842
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4721-1652A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977842 | ||||||
chr17:68977931
|
T | C | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4721-1741A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977931 | ||||||
chr17:68978238
|
T | C | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-2048A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978238 | ||||||
chr17:68978333
|
C | T | 1 | a0001c0001t0006g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4721-2143G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978333 | ||||||
chr17:68978443
|
T | C | 2 | a0001c0001t0003g0165a0008c0020t0003g0054 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4721-2253A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978443 | ||||||
chr17:68978484
|
G | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4721-2294C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978484 | ||||||
chr17:68978488
|
T | C | 1 | a0007c0009t0005g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4721-2298A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978488 | ||||||
chr17:68978570
|
C | A | 1 | a0009c0011t0003g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4721-2380G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978570 | ||||||
chr17:68978606
|
C | T | 17 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(14): Show | 21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4721-2416G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978606 | ||||||
chr17:68978611
|
G | A | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-2421C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978611 | ||||||
chr17:68978680
|
C | T | 1 | a0002c0002t0002g0067 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4721-2490G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978680 | ||||||
chr17:68978692
|
G | A | 1 | a0002c0002t0002g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4721-2502C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978692 | ||||||
chr17:68978719
|
A | G | 5 | a0002c0002t0002g0089a0002c0002t0002g0118a0002c0002t0002g0124others(2): Show | 5 | HG01081.hp1 HG01169.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.4721-2529T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978719 | ||||||
chr17:68978737
|
G | A | 2 | a0003c0003t0004g0017a0003c0003t0004g0018 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4721-2547C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978737 | ||||||
chr17:68978890
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4721-2700G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978890 | ||||||
chr17:68978934
|
C | A | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4721-2744G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978934 | ||||||
chr17:68979000
|
C | T | 1 | a0001c0008t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4721-2810G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979000 | ||||||
chr17:68979025
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-2835A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979025 | ||||||
chr17:68979120
|
A | G | 1 | a0001c0007t0001g0116 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4721-2930T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979120 | ||||||
chr17:68979141
|
T | C | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4721-2951A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979141 | ||||||
chr17:68979194
|
T | G | 3 | a0002c0002t0002g0063a0002c0004t0002g0110a0002c0004t0002g0111 | 3 | HG02738.hp2 NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.4721-3004A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979194 | ||||||
chr17:68979302
|
G | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-3112C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979302 | ||||||
chr17:68979306
|
G | A | 297 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(294): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.4721-3116C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979306 | ||||||
chr17:68979308
|
TC | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4721-3119delG | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979308 | ||||||
chr17:68979436
|
T | C | 2 | a0002c0002t0002g0086a0002c0004t0002g0265 | 2 | HG03139.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4720+3126A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979436 | ||||||
chr17:68979463
|
C | T | 1 | a0002c0002t0002g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4720+3099G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979463 | ||||||
chr17:68979486
|
G | A | 170 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(167): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.4720+3076C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979486 | ||||||
chr17:68979525
|
T | TTTTTGAT others(43): Show |
4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+3036_4720+303 others(54): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979525 | ||||||
chr17:68979625
|
T | C | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2937A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979625 | ||||||
chr17:68979626
|
G | A | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2936C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979626 | ||||||
chr17:68979629
|
A | G | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2933T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979629 | ||||||
chr17:68979632
|
T | C | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2930A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979632 | ||||||
chr17:68979851
|
T | C | 2 | a0018c0022t0003g0014a0023c0019t0003g0055 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4720+2711A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979851 | ||||||
chr17:68980005
|
G | A | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+2557C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980005 | ||||||
chr17:68980006
|
A | C | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+2556T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980006 | ||||||
chr17:68980262
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4720+2300C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980262 | ||||||
chr17:68980359
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2203A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980359 | ||||||
chr17:68980364
|
A | G | 171 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(168): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.4720+2198T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980364 | ||||||
chr17:68980365
|
G | A | 13 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(10): Show | 14 | HG00733.hp1 HG01884.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.4720+2197C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980365 | ||||||
chr17:68980377
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2185A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980377 | ||||||
chr17:68980387
|
G | A | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2175C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980387 | ||||||
chr17:68980388
|
T | G | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2174A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980388 | ||||||
chr17:68980394
|
T | A | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2168A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980394 | ||||||
chr17:68980397
|
C | A | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2165G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980397 | ||||||
chr17:68980398
|
G | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2164C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980398 | ||||||
chr17:68980416
|
C | T | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4720+2146G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980416 | ||||||
chr17:68980421
|
A | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2141T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980421 | ||||||
chr17:68980425
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2137A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980425 | ||||||
chr17:68980434
|
G | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2128C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980434 | ||||||
chr17:68980435
|
G | A | 10 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(7): Show | 10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.4720+2127C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980435 | ||||||
chr17:68980451
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2111A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980451 | ||||||
chr17:68980467
|
T | G | 14 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(11): Show | 14 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4720+2095A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980467 | ||||||
chr17:68980493
|
T | C | 18 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(15): Show | 22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4720+2069A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980493 | ||||||
chr17:68980498
|
C | T | 1 | a0002c0002t0002g0129 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4720+2064G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980498 | ||||||
chr17:68980499
|
G | A | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2063C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980499 | ||||||
chr17:68980758
|
C | T | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1804G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980758 | ||||||
chr17:68980883
|
G | A | 1 | a0002c0004t0002g0267 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4720+1679C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980883 | ||||||
chr17:68980928
|
T | TA | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4720+1633dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980928 | ||||||
chr17:68980928
|
TA | T | 24 | a0001c0001t0001g0176a0001c0001t0001g0221a0001c0001t0001g0252others(21): Show | 25 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.4720+1633delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980928 | ||||||
chr17:68980953
|
C | T | 1 | a0002c0002t0002g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4720+1609G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980953 | ||||||
chr17:68981127
|
C | G | 225 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0164others(222): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.4720+1435G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981127 | ||||||
chr17:68981173
|
C | T | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1389G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981173 | ||||||
chr17:68981196
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4720+1366T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981196 | ||||||
chr17:68981210
|
T | C | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4720+1352A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981210 | ||||||
chr17:68981337
|
GAAAA | G | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+1221_4720+122 others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981337 | ||||||
chr17:68981426
|
A | G | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1136T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981426 | ||||||
chr17:68981456
|
C | T | 2 | a0001c0001t0003g0165a0008c0020t0003g0054 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4720+1106G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981456 | ||||||
chr17:68981835
|
C | CA | 124 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0001g0219others(121): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.4720+726dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | ||||||
chr17:68981835
|
C | CAA | 25 | a0001c0007t0004g0093a0002c0002t0002g0059a0002c0002t0002g0065others(22): Show | 26 | HG00733.hp2 HG01192.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.4720+725_4720+726d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | ||||||
chr17:68981835
|
CA | C | 9 | a0001c0001t0001g0174a0001c0001t0001g0209a0001c0001t0001g0215others(6): Show | 9 | HG00323.hp2 HG00733.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.4720+726delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | ||||||
chr17:68981870
|
C | T | 1 | a0005c0006t0001g0280 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4720+692G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981870 | ||||||
chr17:68981909
|
T | C | 4 | a0005c0006t0001g0009a0005c0006t0001g0278a0005c0006t0001g0283others(1): Show | 5 | NA18974.hp2 NA18985.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.4720+653A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981909 | ||||||
chr17:68981921
|
A | C | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4720+641T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981921 | ||||||
chr17:68981928
|
TG | T | 18 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(15): Show | 22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4720+633delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981928 | ||||||
chr17:68982031
|
G | T | 4 | a0001c0001t0001g0012a0003c0003t0001g0032a0003c0003t0001g0043others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+531C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982031 | ||||||
chr17:68982178
|
G | A | 14 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(11): Show | 14 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4720+384C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982178 | ||||||
chr17:68982199
|
T | C | 3 | a0003c0003t0003g0037a0003c0003t0003g0038a0003c0003t0003g0039 | 3 | HG01361.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4720+363A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982199 | ||||||
chr17:68982866
|
A | C | 56 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(53): Show | 62 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4641-225T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982866 | ||||||
chr17:68982882
|
T | C | 3 | a0001c0007t0004g0093a0003c0003t0004g0021a0003c0003t0004g0025 | 3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4641-241A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982882 | ||||||
chr17:68982906
|
T | C | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4641-265A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982906 | ||||||
chr17:68982954
|
G | A | 7 | a0002c0004t0002g0113a0002c0004t0002g0183a0002c0004t0002g0184others(4): Show | 7 | HG02818.hp1 NA18962.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.4641-313C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982954 | ||||||
chr17:68983046
|
G | A | 52 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(49): Show | 58 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.4641-405C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983046 | ||||||
chr17:68983078
|
C | T | 56 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(53): Show | 62 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4641-437G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983078 | ||||||
chr17:68983131
|
A | G | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4641-490T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983131 | ||||||
chr17:68983350
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4640+359A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983350 | ||||||
chr17:68983537
|
T | C | 1 | a0006c0010t0002g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4640+172A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983537 | ||||||
chr17:68983558
|
T | G | 171 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(168): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.4640+151A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983558 | ||||||
chr17:68983973
|
G | A | 1 | a0001c0007t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4499+83C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 35/38 | chr17 | 68983973 | ||||||
chr17:68984226
|
T | G | 1 | a0002c0002t0002g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4380-51A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984226 | ||||||
chr17:68984272
|
C | A | 1 | a0002c0002t0002g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4380-97G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984272 | ||||||
chr17:68984402
|
T | C | 2 | a0001c0001t0003g0165a0008c0020t0003g0054 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4380-227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984402 | ||||||
chr17:68984498
|
C | T | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4380-323G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984498 | ||||||
chr17:68984567
|
T | C | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4379+318A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984567 | ||||||
chr17:68984581
|
G | A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4379+304C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984581 | ||||||
chr17:68984661
|
A | T | 1 | a0019c0023t0003g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4379+224T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984661 | ||||||
chr17:68984878
|
A | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | NA19009.hp1 NA19067.hp2 |
splice_region_variant&intron_variant | LOW | c.4379+7T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984878 | ||||||
chr17:68985338
|
G | C | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4209-210C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985338 | ||||||
chr17:68985345
|
C | T | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4209-217G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985345 | ||||||
chr17:68985379
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4209-251A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985379 | ||||||
chr17:68985457
|
A | G | 7 | a0001c0001t0001g0012a0003c0003t0001g0016a0003c0003t0001g0029others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4209-329T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985457 | ||||||
chr17:68985491
|
G | A | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4209-363C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985491 | ||||||
chr17:68985504
|
C | G | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4209-376G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985504 | ||||||
chr17:68985511
|
A | G | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4209-383T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985511 | ||||||
chr17:68985615
|
C | T | 1 | a0001c0029t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4209-487G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985615 | ||||||
chr17:68985826
|
G | A | 3 | a0001c0007t0004g0093a0003c0003t0004g0021a0003c0003t0004g0025 | 3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4208+338C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985826 | ||||||
chr17:68985919
|
G | A | 1 | a0012c0014t0003g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4208+245C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985919 | ||||||
chr17:68985932
|
T | C | 2 | a0001c0008t0001g0167a0001c0008t0001g0181 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4208+232A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985932 | ||||||
chr17:68985955
|
G | GA | 12 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(9): Show | 12 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.4208+208dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985955 | ||||||
chr17:68985982
|
T | C | 2 | a0003c0003t0004g0017a0003c0003t0004g0018 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4208+182A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985982 | ||||||
chr17:68985998
|
C | T | 17 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(14): Show | 21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4208+166G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985998 | ||||||
chr17:68986489
|
C | T | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4048-165G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986489 | ||||||
chr17:68986850
|
T | C | 12 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(9): Show | 12 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.4048-526A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986850 | ||||||
chr17:68986906
|
G | A | 2 | a0018c0022t0003g0014a0023c0019t0003g0055 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4048-582C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986906 | ||||||
chr17:68987160
|
T | G | 1 | a0002c0004t0002g0112 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4048-836A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987160 | ||||||
chr17:68987295
|
C | T | 1 | a0002c0002t0002g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4048-971G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987295 | ||||||
chr17:68987369
|
T | A | 1 | a0003c0003t0004g0021 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4048-1045A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987369 | ||||||
chr17:68987612
|
A | G | 172 | a0001c0001t0001g0253a0001c0001t0003g0165a0001c0001t0006g0051others(169): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.4048-1288T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987612 | ||||||
chr17:68987736
|
G | A | 6 | a0002c0002t0002g0005a0002c0002t0002g0095a0002c0002t0002g0103others(3): Show | 7 | HG00544.hp1 HG02165.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4047+1291C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987736 | ||||||
chr17:68987736
|
G | GT | 15 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0248others(12): Show | 17 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.4047+1290dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987736 | ||||||
chr17:68987739
|
TTTTTTTG others(20): Show |
T | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4047+1261_4047+128 others(31): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987739 | ||||||
chr17:68987745
|
TG | T | 10 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(7): Show | 10 | HG01361.hp1 HG02630.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.4047+1281delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987745 | ||||||
chr17:68987746
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4047+1281C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987746 | ||||||
chr17:68987758
|
G | T | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4047+1269C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987758 | ||||||
chr17:68987758
|
GTTTGTTT others(5): Show |
G | 5 | a0001c0001t0001g0170a0001c0001t0001g0240a0001c0001t0001g0245others(2): Show | 5 | HG00323.hp2 HG01081.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4047+1257_4047+126 others(16): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987758 | ||||||
chr17:68987761
|
TG | T | 67 | a0001c0007t0004g0093a0002c0002t0002g0005a0002c0002t0002g0011others(64): Show | 69 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.4047+1265delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987761 | ||||||
chr17:68987761
|
TGTTTG | T | 51 | a0001c0001t0001g0253a0002c0002t0002g0002a0002c0002t0002g0006others(48): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.4047+1261_4047+126 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987761 | ||||||
chr17:68987762
|
G | T | 18 | a0001c0001t0003g0165a0001c0021t0003g0015a0002c0002t0002g0101others(15): Show | 18 | HG00639.hp2 HG01361.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.4047+1265C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987762 | ||||||
chr17:68987762
|
GTTTGT | G | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4047+1260_4047+126 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987762 | ||||||
chr17:68987764
|
T | G | 2 | a0001c0021t0003g0015a0003c0003t0004g0017 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4047+1263A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987764 | ||||||
chr17:68987765
|
T | G | 11 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0018others(8): Show | 12 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.4047+1262A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987765 | ||||||
chr17:68987766
|
G | T | 90 | a0001c0001t0003g0165a0001c0007t0004g0093a0001c0021t0003g0015others(87): Show | 92 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4047+1261C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987766 | ||||||
chr17:68987767
|
T | G | 1 | a0008c0020t0003g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4047+1260A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987767 | ||||||
chr17:68987774
|
G | T | 153 | a0001c0001t0001g0253a0001c0001t0003g0165a0001c0001t0006g0051others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.4047+1253C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987774 | ||||||
chr17:68987822
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4047+1205C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987822 | ||||||
chr17:68987860
|
G | A | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4047+1167C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987860 | ||||||
chr17:68987953
|
G | A | 1 | a0002c0002t0002g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4047+1074C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987953 | ||||||
chr17:68987991
|
T | C | 50 | a0001c0001t0003g0165a0001c0007t0004g0093a0001c0021t0003g0015others(47): Show | 55 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.4047+1036A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987991 | ||||||
chr17:68988039
|
C | T | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4047+988G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988039 | ||||||
chr17:68988083
|
A | G | 17 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(14): Show | 21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4047+944T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988083 | ||||||
chr17:68988119
|
G | T | 2 | a0003c0003t0001g0004a0003c0003t0001g0027 | 3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4047+908C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988119 | ||||||
chr17:68988236
|
G | GT | 16 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(13): Show | 20 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.4047+790dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988236 | ||||||
chr17:68988288
|
T | C | 50 | a0001c0001t0003g0165a0001c0007t0004g0093a0001c0021t0003g0015others(47): Show | 55 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.4047+739A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988288 | ||||||
chr17:68988347
|
T | C | 31 | a0001c0007t0004g0093a0001c0021t0003g0015a0003c0003t0004g0003others(28): Show | 36 | HG01109.hp2 HG01346.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.4047+680A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988347 | ||||||
chr17:68988597
|
A | G | 2 | a0001c0001t0008g0250a0001c0001t0008g0251 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4047+430T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988597 | ||||||
chr17:68988670
|
C | T | 1 | a0007c0009t0005g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4047+357G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988670 | ||||||
chr17:68988744
|
G | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4047+283C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988744 | ||||||
chr17:68988869
|
A | G | 1 | a0019c0023t0003g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4047+158T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988869 | ||||||
chr17:68989199
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0208 | 3 | HG00323.hp1 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3956-81G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989199 | ||||||
chr17:68989225
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3956-107T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989225 | ||||||
chr17:68989242
|
C | CCT | 6 | a0001c0001t0001g0266a0002c0002t0002g0159a0003c0003t0003g0042others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3956-126_3956-125d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989242 | ||||||
chr17:68989242
|
C | CCTCT | 6 | a0002c0002t0002g0070a0002c0002t0002g0103a0002c0002t0002g0160others(3): Show | 6 | HG00544.hp1 HG02074.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3956-128_3956-125d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989242 | ||||||
chr17:68989256
|
T | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0182a0001c0001t0001g0202 | 3 | HG02071.hp1 HG03831.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3956-138A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCA | 7 | a0001c0001t0001g0061a0001c0001t0001g0166a0001c0001t0001g0207others(4): Show | 7 | HG00099.hp1 HG02004.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.3956-140_3956-139d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCACA | 3 | a0001c0001t0001g0186a0001c0008t0001g0192a0017c0025t0002g0058 | 3 | HG04204.hp2 NA19075.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3956-142_3956-139d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCA | 3 | a0001c0001t0003g0165a0003c0003t0003g0040a0008c0020t0003g0054 | 3 | HG03098.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCACA | 9 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(6): Show | 9 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCTCA | 41 | a0002c0002t0002g0011a0002c0002t0002g0064a0002c0002t0002g0065others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCTCAC others(1): Show |
46 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0059others(43): Show | 49 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCTCAC others(3): Show |
9 | a0002c0002t0002g0078a0002c0002t0002g0104a0002c0002t0002g0125others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCTCAC others(5): Show |
2 | a0002c0002t0002g0134a0002c0002t0002g0149 | 2 | HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
T | TCTCTCAC others(9): Show |
2 | a0002c0002t0002g0119a0002c0002t0002g0151 | 2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
TCA | T | 38 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(35): Show | 44 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.3956-140_3956-139d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
TCACA | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0248others(1): Show | 4 | HG01884.hp2 HG01891.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.3956-142_3956-139d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
TCACACA | T | 15 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(12): Show | 16 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.3956-144_3956-139d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989256
|
TCACACAC others(3): Show |
T | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3956-148_3956-139d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | ||||||
chr17:68989258
|
A | T | 10 | a0002c0002t0002g0005a0002c0002t0002g0095a0002c0002t0002g0124others(7): Show | 11 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3956-140T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989258 | ||||||
chr17:68989260
|
A | T | 21 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(18): Show | 26 | HG01109.hp2 HG01346.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3956-142T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989260 | ||||||
chr17:68989262
|
A | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0021t0003g0015others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3956-144T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989262 | ||||||
chr17:68989264
|
A | T | 14 | a0001c0007t0004g0093a0001c0021t0003g0015a0003c0003t0004g0003others(11): Show | 15 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.3956-146T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989264 | ||||||
chr17:68989266
|
A | T | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.3956-148T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989266 | ||||||
chr17:68989268
|
A | T | 5 | a0001c0007t0004g0093a0003c0003t0004g0021a0003c0003t0004g0025others(2): Show | 5 | HG00733.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3956-150T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989268 | ||||||
chr17:68989295
|
C | CA | 4 | a0002c0002t0002g0079a0002c0002t0002g0150a0002c0004t0002g0267others(1): Show | 4 | HG02071.hp2 HG04115.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.3956-178_3956-177i others(3): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989295 | ||||||
chr17:68989418
|
A | T | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3956-300T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989418 | ||||||
chr17:68989525
|
G | A | 1 | a0001c0007t0001g0090 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3955+288C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989525 | ||||||
chr17:68989550
|
A | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0229a0001c0001t0012g0234 | 3 | HG01109.hp1 HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3955+263T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989550 | ||||||
chr17:68989672
|
A | G | 15 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3955+141T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989672 | ||||||
chr17:68989706
|
C | T | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3955+107G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989706 | ||||||
chr17:68989796
|
G | A | 2 | a0002c0002t0002g0119a0002c0002t0002g0151 | 2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3955+17C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989796 | ||||||
chr17:68990015
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0215 | 3 | NA18946.hp1 NA18957.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.3838-85G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990015 | ||||||
chr17:68990021
|
A | C | 297 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(294): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3838-91T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990021 | ||||||
chr17:68990223
|
C | G | 1 | a0002c0002t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3838-293G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990223 | ||||||
chr17:68990244
|
C | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(2): Show | 5 | HG00408.hp1 HG02132.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.3838-314G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990244 | ||||||
chr17:68990488
|
C | G | 1 | a0002c0004t0002g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3837+349G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990488 | ||||||
chr17:68990562
|
A | C | 57 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(54): Show | 63 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.3837+275T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990562 | ||||||
chr17:68991061
|
A | T | 171 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(168): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.3717-104T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991061 | ||||||
chr17:68991088
|
A | G | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3717-131T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991088 | ||||||
chr17:68991113
|
C | G | 171 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(168): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.3717-156G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991113 | ||||||
chr17:68991275
|
A | C | 114 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.3717-318T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991275 | ||||||
chr17:68991405
|
C | A | 1 | a0002c0002t0002g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3717-448G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991405 | ||||||
chr17:68991480
|
G | A | 1 | a0002c0002t0002g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3717-523C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991480 | ||||||
chr17:68991705
|
C | A | 15 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3716+470G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991705 | ||||||
chr17:68992375
|
T | C | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3625-109A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992375 | ||||||
chr17:68992493
|
T | C | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3625-227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992493 | ||||||
chr17:68992525
|
A | G | 57 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(54): Show | 63 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.3625-259T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992525 | ||||||
chr17:68992604
|
G | A | 18 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(15): Show | 22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3625-338C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992604 | ||||||
chr17:68992786
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3624+230G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992786 | ||||||
chr17:68992808
|
T | C | 4 | a0001c0001t0001g0012a0003c0003t0001g0032a0003c0003t0001g0043others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3624+208A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992808 | ||||||
chr17:68992825
|
AG | A | 148 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(145): Show | 154 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.3624+190delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992825 | ||||||
chr17:68992825
|
AGG | A | 16 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(13): Show | 20 | HG01109.hp2 HG01346.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.3624+189_3624+190d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992825 | ||||||
chr17:68992826
|
G | A | 5 | a0002c0002t0002g0068a0002c0002t0002g0122a0002c0002t0002g0123others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.3624+190C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992826 | ||||||
chr17:68992852
|
C | CGT | 26 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(23): Show | 31 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.3624+162_3624+163d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992852 | ||||||
chr17:68992852
|
C | T | 2 | a0018c0022t0003g0014a0023c0019t0003g0055 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3624+164G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992852 | ||||||
chr17:68992861
|
G | GTGTGTGT others(23): Show |
11 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(8): Show | 12 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.3624+154_3624+155i others(32): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992861 | ||||||
chr17:68992863
|
GTGTGTGC others(19): Show |
G | 1 | a0004c0005t0003g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3624+127_3624+152d others(28): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992863 | ||||||
chr17:68992965
|
C | T | 1 | a0002c0002t0002g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3624+51G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992965 | ||||||
chr17:68993231
|
C | T | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3556-147G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993231 | ||||||
chr17:68993349
|
C | A | 15 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3556-265G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993349 | ||||||
chr17:68993519
|
A | G | 7 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3556-435T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993519 | ||||||
chr17:68993679
|
C | T | 1 | a0002c0004t0002g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3556-595G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993679 | ||||||
chr17:68993826
|
C | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3556-742G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993826 | ||||||
chr17:68993949
|
C | T | 11 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0096others(8): Show | 14 | HG02040.hp2 HG02080.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.3556-865G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993949 | ||||||
chr17:68994003
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0008g0250a0001c0001t0008g0251 | 3 | HG00323.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3556-919C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994003 | ||||||
chr17:68994096
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206 | 3 | HG02074.hp1 HG02135.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3556-1012C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994096 | ||||||
chr17:68994370
|
C | A | 1 | a0005c0006t0001g0280 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3556-1286G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994370 | ||||||
chr17:68994381
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0214 | 2 | NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3556-1297G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994381 | ||||||
chr17:68994417
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0229a0001c0001t0012g0234 | 3 | HG01109.hp1 HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3556-1333G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994417 | ||||||
chr17:68994490
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0168 | 3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3555+1405G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994490 | ||||||
chr17:68994516
|
C | T | 1 | a0017c0025t0002g0058 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3555+1379G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994516 | ||||||
chr17:68994715
|
C | A | 12 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0096others(9): Show | 15 | HG02040.hp2 HG02080.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.3555+1180G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994715 | ||||||
chr17:68994764
|
G | C | 15 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3555+1131C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994764 | ||||||
chr17:68994794
|
G | C | 2 | a0010c0012t0001g0273a0010c0012t0001g0282 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3555+1101C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994794 | ||||||
chr17:68994816
|
T | G | 1 | a0008c0013t0003g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3555+1079A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994816 | ||||||
chr17:68994862
|
G | A | 3 | a0002c0002t0002g0101a0002c0002t0002g0118a0002c0002t0002g0124 | 3 | HG02145.hp2 HG03540.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3555+1033C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994862 | ||||||
chr17:68994882
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0239 | 2 | HG02165.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.3555+1013C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994882 | ||||||
chr17:68994889
|
C | T | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0009c0011t0003g0046others(1): Show | 4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3555+1006G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994889 | ||||||
chr17:68995075
|
T | C | 12 | a0001c0007t0004g0093a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.3555+820A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995075 | ||||||
chr17:68995079
|
A | G | 5 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0271others(2): Show | 9 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3555+816T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995079 | ||||||
chr17:68995433
|
C | T | 1 | a0001c0007t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3555+462G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995433 | ||||||
chr17:68995451
|
C | T | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3555+444G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995451 | ||||||
chr17:68995489
|
C | T | 4 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3555+406G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995489 | ||||||
chr17:68995541
|
T | G | 1 | a0001c0001t0001g0194 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3555+354A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995541 | ||||||
chr17:68995655
|
T | C | 1 | a0019c0023t0003g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3555+240A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995655 | ||||||
chr17:68995698
|
TG | T | 168 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(165): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.3555+196delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995698 | ||||||
chr17:68995886
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0240 | 2 | HG01081.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3555+9T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995886 | ||||||
chr17:68996156
|
T | A | 1 | a0013c0016t0002g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3436-142A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996156 | ||||||
chr17:68996376
|
G | T | 2 | a0018c0022t0003g0014a0023c0019t0003g0055 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3436-362C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996376 | ||||||
chr17:68996566
|
C | T | 31 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(28): Show | 36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-552G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996566 | ||||||
chr17:68996575
|
T | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-561A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996575 | ||||||
chr17:68996584
|
G | A | 31 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(28): Show | 36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-570C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996584 | ||||||
chr17:68996664
|
A | T | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-650T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996664 | ||||||
chr17:68996684
|
T | C | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-670A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996684 | ||||||
chr17:68996763
|
G | A | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-749C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996763 | ||||||
chr17:68997034
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-1020C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997034 | ||||||
chr17:68997157
|
C | G | 2 | a0001c0008t0001g0191a0003c0003t0001g0031 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3436-1143G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997157 | ||||||
chr17:68997182
|
C | T | 21 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(18): Show | 22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.3436-1168G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997182 | ||||||
chr17:68997190
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-1176G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997190 | ||||||
chr17:68997594
|
C | CT | 10 | a0001c0001t0001g0229a0001c0001t0001g0255a0001c0001t0012g0234others(7): Show | 12 | HG00280.hp1 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.3436-1581dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | ||||||
chr17:68997594
|
CT | C | 80 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0195others(77): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.3436-1581delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | ||||||
chr17:68997594
|
CTTT | C | 25 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(22): Show | 30 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.3436-1583_3436-158 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | ||||||
chr17:68997602
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-1588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997602 | ||||||
chr17:68997707
|
A | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3436-1693T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997707 | ||||||
chr17:68997814
|
C | T | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3436-1800G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997814 | ||||||
chr17:68997828
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3436-1814T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997828 | ||||||
chr17:68997988
|
T | C | 10 | a0001c0008t0001g0167a0001c0008t0001g0181a0001c0008t0001g0190others(7): Show | 10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-1974A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997988 | ||||||
chr17:68997999
|
G | A | 22 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(19): Show | 23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-1985C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997999 | ||||||
chr17:68998021
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3436-2007C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998021 | ||||||
chr17:68998050
|
A | G | 1 | a0008c0020t0003g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3436-2036T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998050 | ||||||
chr17:68998103
|
C | T | 4 | a0008c0013t0003g0056a0008c0020t0003g0054a0009c0011t0003g0046others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3436-2089G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998103 | ||||||
chr17:68998157
|
G | A | 6 | a0001c0008t0001g0190a0001c0008t0001g0191a0001c0008t0001g0192others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-2143C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998157 | ||||||
chr17:68998266
|
A | G | 31 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(28): Show | 36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-2252T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998266 | ||||||
chr17:68998309
|
A | G | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3436-2295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998309 | ||||||
chr17:68998366
|
T | C | 1 | a0003c0003t0003g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3436-2352A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998366 | ||||||
chr17:68998417
|
C | A | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3436-2403G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998417 | ||||||
chr17:68998419
|
T | A | 22 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(19): Show | 23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-2405A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998419 | ||||||
chr17:68998479
|
A | G | 10 | a0001c0008t0001g0167a0001c0008t0001g0181a0001c0008t0001g0190others(7): Show | 10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-2465T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998479 | ||||||
chr17:68998508
|
G | A | 8 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(5): Show | 8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-2494C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998508 | ||||||
chr17:68998646
|
A | C | 120 | a0001c0007t0001g0090a0001c0007t0001g0115a0001c0007t0001g0116others(117): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.3436-2632T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998646 | ||||||
chr17:68998647
|
TATTA | T | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-2637_3436-263 others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998647 | ||||||
chr17:68998828
|
A | C | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-2814T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998828 | ||||||
chr17:68998832
|
C | CT | 8 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(5): Show | 8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-2819dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998832 | ||||||
chr17:68998832
|
CT | C | 13 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(10): Show | 13 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3436-2819delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998832 | ||||||
chr17:68998835
|
T | C | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-2821A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998835 | ||||||
chr17:68998981
|
C | G | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-2967G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998981 | ||||||
chr17:68999102
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3436-3088C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999102 | ||||||
chr17:68999123
|
T | TATC | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3436-3110_3436-310 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999123 | ||||||
chr17:68999192
|
C | T | 6 | a0001c0007t0001g0090a0006c0010t0002g0083a0006c0010t0002g0120others(3): Show | 6 | HG01257.hp1 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3436-3178G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999192 | ||||||
chr17:68999232
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3436-3218G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999232 | ||||||
chr17:68999238
|
C | T | 8 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(5): Show | 8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-3224G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999238 | ||||||
chr17:68999271
|
T | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3436-3257A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999271 | ||||||
chr17:68999437
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3436-3423G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999437 | ||||||
chr17:68999498
|
T | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-3484A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999498 | ||||||
chr17:68999543
|
T | C | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-3529A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999543 | ||||||
chr17:68999575
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3436-3561G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999575 | ||||||
chr17:68999605
|
A | C | 2 | a0008c0013t0003g0057a0011c0015t0003g0049 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3436-3591T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999605 | ||||||
chr17:68999640
|
G | C | 1 | a0021c0032t0001g0226 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3436-3626C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999640 | ||||||
chr17:68999696
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3436-3682G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999696 | ||||||
chr17:68999773
|
T | A | 1 | a0002c0002t0002g0134 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3436-3759A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999773 | ||||||
chr17:68999845
|
T | A | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-3831A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999845 | ||||||
chr17:68999987
|
C | T | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3436-3973G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999987 | ||||||
chr17:68999999
|
G | T | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-3985C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999999 | ||||||
chr17:69000056
|
T | G | 7 | a0001c0001t0001g0012a0003c0003t0001g0016a0003c0003t0001g0029others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3436-4042A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000056 | ||||||
chr17:69000159
|
G | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0208 | 3 | HG00323.hp1 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3436-4145C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000159 | ||||||
chr17:69000200
|
C | T | 1 | a0013c0016t0002g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3436-4186G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000200 | ||||||
chr17:69000251
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-4237G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000251 | ||||||
chr17:69000386
|
C | T | 1 | a0002c0002t0002g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3436-4372G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000386 | ||||||
chr17:69000602
|
T | C | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3436-4588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000602 | ||||||
chr17:69000607
|
T | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3436-4593A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000607 | ||||||
chr17:69000608
|
G | A | 1 | a0007c0009t0005g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3436-4594C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000608 | ||||||
chr17:69000694
|
T | C | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3436-4680A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000694 | ||||||
chr17:69000735
|
A | G | 1 | a0003c0003t0003g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3436-4721T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000735 | ||||||
chr17:69000755
|
A | G | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-4741T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000755 | ||||||
chr17:69000757
|
G | A | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3436-4743C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000757 | ||||||
chr17:69000763
|
G | A | 4 | a0001c0021t0003g0015a0008c0013t0003g0056a0008c0013t0003g0057others(1): Show | 4 | HG00733.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3436-4749C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000763 | ||||||
chr17:69000782
|
A | G | 1 | a0003c0003t0003g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3436-4768T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000782 | ||||||
chr17:69000803
|
CAGTGGTT others(3): Show |
C | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-4799_3436-479 others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000803 | ||||||
chr17:69000816
|
T | G | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-4802A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000816 | ||||||
chr17:69000856
|
T | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3436-4842A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000856 | ||||||
chr17:69000871
|
T | C | 21 | a0001c0021t0003g0015a0004c0005t0003g0001a0004c0005t0003g0268others(18): Show | 25 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3436-4857A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000871 | ||||||
chr17:69000933
|
T | TTGG | 53 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(50): Show | 59 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.3436-4920_3436-491 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000933 | ||||||
chr17:69001130
|
G | A | 1 | a0004c0005t0003g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3436-5116C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001130 | ||||||
chr17:69001147
|
T | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3436-5133A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001147 | ||||||
chr17:69001215
|
C | T | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-5201G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001215 | ||||||
chr17:69001477
|
A | G | 22 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(19): Show | 23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-5463T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001477 | ||||||
chr17:69001578
|
C | T | 1 | a0008c0013t0003g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3436-5564G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001578 | ||||||
chr17:69001841
|
C | G | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-5827G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001841 | ||||||
chr17:69001954
|
G | A | 22 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(19): Show | 23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3435+5805C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001954 | ||||||
chr17:69001975
|
A | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+5784T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001975 | ||||||
chr17:69002033
|
G | A | 1 | a0002c0002t0002g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3435+5726C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002033 | ||||||
chr17:69002081
|
T | C | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5678A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002081 | ||||||
chr17:69002083
|
A | G | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5676T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002083 | ||||||
chr17:69002101
|
T | C | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5658A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002101 | ||||||
chr17:69002171
|
T | C | 1 | a0002c0002t0002g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3435+5588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002171 | ||||||
chr17:69002220
|
A | G | 1 | a0002c0004t0002g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3435+5539T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002220 | ||||||
chr17:69002260
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+5499G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002260 | ||||||
chr17:69002277
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3435+5482G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002277 | ||||||
chr17:69002294
|
G | A | 12 | a0001c0001t0001g0255a0001c0001t0001g0256a0003c0003t0004g0003others(9): Show | 13 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.3435+5465C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002294 | ||||||
chr17:69002425
|
G | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3435+5334C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002425 | ||||||
chr17:69002438
|
A | T | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3435+5321T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002438 | ||||||
chr17:69002563
|
TGTG | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+5193_3435+519 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002563 | ||||||
chr17:69002603
|
G | A | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+5156C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002603 | ||||||
chr17:69002604
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+5155C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002604 | ||||||
chr17:69002604
|
G | C | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+5155C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002604 | ||||||
chr17:69002634
|
C | T | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3435+5125G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002634 | ||||||
chr17:69002712
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3435+5047A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002712 | ||||||
chr17:69002793
|
G | A | 1 | a0003c0003t0003g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3435+4966C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002793 | ||||||
chr17:69002942
|
C | A | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3435+4817G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002942 | ||||||
chr17:69003008
|
G | T | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3435+4751C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003008 | ||||||
chr17:69003026
|
A | G | 5 | a0002c0002t0002g0005a0002c0002t0002g0095a0002c0002t0002g0159others(2): Show | 6 | HG00544.hp1 NA18954.hp1 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+4733T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003026 | ||||||
chr17:69003045
|
C | A | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+4714G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003045 | ||||||
chr17:69003061
|
C | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4698G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003061 | ||||||
chr17:69003070
|
C | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4689G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003070 | ||||||
chr17:69003072
|
G | A | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4687C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003072 | ||||||
chr17:69003484
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+4275A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003484 | ||||||
chr17:69003487
|
A | G | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3435+4272T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003487 | ||||||
chr17:69003524
|
G | A | 1 | a0003c0003t0004g0021 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3435+4235C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003524 | ||||||
chr17:69003613
|
G | A | 2 | a0005c0006t0001g0279a0005c0006t0001g0281 | 2 | NA18989.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3435+4146C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003613 | ||||||
chr17:69003624
|
T | G | 1 | a0002c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3435+4135A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003624 | ||||||
chr17:69003656
|
C | T | 23 | a0001c0001t0012g0234a0001c0021t0003g0015a0003c0003t0003g0033others(20): Show | 24 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+4103G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003656 | ||||||
chr17:69003740
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+4019G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003740 | ||||||
chr17:69003757
|
A | G | 1 | a0022c0018t0014g0298 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3435+4002T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003757 | ||||||
chr17:69003826
|
C | G | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+3933G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003826 | ||||||
chr17:69003947
|
G | A | 2 | a0001c0001t0001g0186a0006c0010t0002g0120 | 2 | HG01496.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3435+3812C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003947 | ||||||
chr17:69003954
|
G | C | 1 | a0002c0002t0002g0140 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3435+3805C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003954 | ||||||
chr17:69004006
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3435+3753C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004006 | ||||||
chr17:69004077
|
C | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+3682G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004077 | ||||||
chr17:69004149
|
C | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+3610G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004149 | ||||||
chr17:69004207
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3435+3552A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004207 | ||||||
chr17:69004466
|
C | T | 120 | a0001c0007t0001g0090a0001c0007t0001g0115a0001c0007t0001g0116others(117): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.3435+3293G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004466 | ||||||
chr17:69004697
|
G | T | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+3062C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004697 | ||||||
chr17:69004774
|
C | T | 1 | a0003c0003t0003g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3435+2985G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004774 | ||||||
chr17:69004786
|
T | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3435+2973A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004786 | ||||||
chr17:69004793
|
G | T | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+2966C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004793 | ||||||
chr17:69004825
|
T | C | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+2934A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004825 | ||||||
chr17:69004854
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+2905C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004854 | ||||||
chr17:69004893
|
G | A | 1 | a0006c0010t0002g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3435+2866C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004893 | ||||||
chr17:69004896
|
T | C | 174 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3435+2863A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004896 | ||||||
chr17:69004942
|
C | T | 10 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(7): Show | 10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3435+2817G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004942 | ||||||
chr17:69004992
|
C | T | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435+2767G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004992 | ||||||
chr17:69005078
|
T | C | 10 | a0003c0003t0004g0003a0003c0003t0004g0017a0003c0003t0004g0018others(7): Show | 11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.3435+2681A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005078 | ||||||
chr17:69005108
|
G | T | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+2651C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005108 | ||||||
chr17:69005141
|
C | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+2618G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005141 | ||||||
chr17:69005173
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3435+2586T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005173 | ||||||
chr17:69005190
|
C | A | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+2569G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005190 | ||||||
chr17:69005377
|
A | G | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+2382T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005377 | ||||||
chr17:69005427
|
A | G | 223 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0164others(220): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.3435+2332T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005427 | ||||||
chr17:69005579
|
T | C | 1 | a0002c0002t0002g0119 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3435+2180A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005579 | ||||||
chr17:69005597
|
C | T | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3435+2162G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005597 | ||||||
chr17:69005612
|
G | A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+2147C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005612 | ||||||
chr17:69005623
|
A | G | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+2136T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005623 | ||||||
chr17:69006042
|
C | A | 173 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(170): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435+1717G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006042 | ||||||
chr17:69006069
|
A | T | 1 | a0017c0025t0002g0058 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3435+1690T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006069 | ||||||
chr17:69006169
|
C | G | 20 | a0002c0002t0002g0011a0002c0002t0002g0088a0002c0002t0002g0091others(17): Show | 20 | HG00408.hp2 HG00438.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.3435+1590G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006169 | ||||||
chr17:69006517
|
G | A | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3435+1242C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006517 | ||||||
chr17:69006717
|
A | C | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+1042T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006717 | ||||||
chr17:69006905
|
T | C | 2 | a0008c0013t0003g0056a0008c0013t0003g0057 | 2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+854A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006905 | ||||||
chr17:69006913
|
G | T | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+846C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006913 | ||||||
chr17:69007084
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3435+675A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007084 | ||||||
chr17:69007108
|
A | T | 2 | a0003c0003t0003g0040a0003c0003t0003g0042 | 2 | HG02698.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3435+651T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007108 | ||||||
chr17:69007144
|
G | A | 119 | a0001c0007t0001g0090a0001c0007t0001g0115a0001c0007t0001g0116others(116): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.3435+615C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007144 | ||||||
chr17:69007200
|
T | C | 297 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(294): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3435+559A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007200 | ||||||
chr17:69007204
|
C | T | 24 | a0001c0007t0001g0161a0002c0002t0002g0002a0002c0002t0002g0006others(21): Show | 27 | HG02040.hp2 HG02074.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.3435+555G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007204 | ||||||
chr17:69007293
|
C | T | 3 | a0001c0007t0001g0115a0001c0007t0001g0116a0001c0007t0001g0141 | 3 | HG01258.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3435+466G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007293 | ||||||
chr17:69007332
|
C | T | 2 | a0002c0002t0002g0114a0002c0002t0002g0224 | 2 | HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3435+427G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007332 | ||||||
chr17:69007333
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3435+426C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007333 | ||||||
chr17:69007387
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3435+372G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007387 | ||||||
chr17:69007518
|
T | C | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+241A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007518 | ||||||
chr17:69007645
|
A | G | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435+114T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007645 | ||||||
chr17:69007683
|
T | C | 1 | a0001c0007t0001g0008 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3435+76A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007683 | ||||||
chr17:69007727
|
G | A | 2 | a0001c0001t0008g0250a0001c0001t0008g0251 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3435+32C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007727 | ||||||
chr17:69007931
|
T | C | 23 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(20): Show | 27 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.3322-59A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 24/38 | chr17 | 69007931 | ||||||
chr17:69008245
|
A | G | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3148-10T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008245 | ||||||
chr17:69008342
|
ATAT | A | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3148-110_3148-108d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008342 | ||||||
chr17:69008352
|
G | A | 1 | a0001c0008t0001g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3148-117C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008352 | ||||||
chr17:69008352
|
G | C | 2 | a0002c0002t0002g0102a0002c0002t0002g0126 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3148-117C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008352 | ||||||
chr17:69008368
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3148-133G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008368 | ||||||
chr17:69008436
|
T | G | 1 | a0002c0002t0002g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3148-201A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008436 | ||||||
chr17:69008448
|
G | A | 2 | a0002c0002t0002g0128a0002c0002t0002g0129 | 2 | HG02132.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3148-213C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008448 | ||||||
chr17:69008633
|
G | A | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-398C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008633 | ||||||
chr17:69008902
|
G | T | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-667C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008902 | ||||||
chr17:69009053
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3148-818G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009053 | ||||||
chr17:69009118
|
TA | T | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3148-884delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009118 | ||||||
chr17:69009120
|
T | C | 1 | a0002c0004t0002g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3148-885A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009120 | ||||||
chr17:69009262
|
G | A | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-1027C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009262 | ||||||
chr17:69009358
|
G | T | 2 | a0007c0009t0005g0010a0007c0009t0005g0296 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3148-1123C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009358 | ||||||
chr17:69009403
|
CTTCCGTG others(11): Show |
C | 13 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(10): Show | 14 | HG01175.hp2 HG02572.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.3148-1186_3148-116 others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009403 | ||||||
chr17:69009554
|
C | T | 22 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(19): Show | 23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3148-1319G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009554 | ||||||
chr17:69009567
|
T | C | 4 | a0001c0001t0001g0210a0001c0001t0001g0227a0001c0001t0001g0238others(1): Show | 4 | HG02080.hp1 NA18967.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.3148-1332A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009567 | ||||||
chr17:69009617
|
C | T | 1 | a0002c0002t0002g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3148-1382G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009617 | ||||||
chr17:69009893
|
A | G | 1 | a0002c0002t0002g0147 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3148-1658T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009893 | ||||||
chr17:69009916
|
T | C | 1 | a0002c0002t0002g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3148-1681A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009916 | ||||||
chr17:69009991
|
C | T | 22 | a0002c0002t0002g0059a0002c0002t0002g0060a0002c0002t0002g0063others(19): Show | 22 | HG00099.hp2 HG01192.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.3148-1756G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009991 | ||||||
chr17:69010097
|
C | A | 4 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0271others(1): Show | 8 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3148-1862G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010097 | ||||||
chr17:69010175
|
T | TA | 134 | a0001c0001t0001g0185a0001c0007t0001g0090a0001c0007t0001g0116others(131): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.3147+1800dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010175 | ||||||
chr17:69010175
|
TA | T | 6 | a0001c0001t0001g0259a0003c0003t0004g0020a0005c0006t0001g0009others(3): Show | 7 | HG02717.hp2 NA18974.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.3147+1800delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010175 | ||||||
chr17:69010319
|
G | A | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3147+1657C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010319 | ||||||
chr17:69010399
|
A | G | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3147+1577T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010399 | ||||||
chr17:69010415
|
T | C | 1 | a0002c0002t0002g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3147+1561A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010415 | ||||||
chr17:69010527
|
A | T | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3147+1449T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010527 | ||||||
chr17:69010705
|
A | G | 12 | a0001c0021t0003g0015a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3147+1271T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010705 | ||||||
chr17:69010722
|
G | A | 2 | a0003c0003t0004g0017a0003c0003t0004g0018 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3147+1254C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010722 | ||||||
chr17:69010873
|
C | T | 173 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(170): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3147+1103G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010873 | ||||||
chr17:69011044
|
C | T | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3147+932G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011044 | ||||||
chr17:69011197
|
G | T | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3147+779C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011197 | ||||||
chr17:69011553
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3147+423G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011553 | ||||||
chr17:69011652
|
T | G | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3147+324A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011652 | ||||||
chr17:69012095
|
T | C | 1 | a0002c0002t0002g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3040-12A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012095 | ||||||
chr17:69012116
|
C | T | 2 | a0018c0022t0003g0014a0023c0019t0003g0055 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3040-33G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012116 | ||||||
chr17:69012119
|
T | C | 2 | a0001c0021t0003g0015a0011c0015t0003g0049 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3040-36A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012119 | ||||||
chr17:69012241
|
C | T | 1 | a0001c0007t0001g0090 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3040-158G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012241 | ||||||
chr17:69012318
|
G | A | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3040-235C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012318 | ||||||
chr17:69012355
|
T | C | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3040-272A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012355 | ||||||
chr17:69012412
|
T | C | 2 | a0001c0001t0003g0165a0003c0003t0003g0037 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3040-329A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012412 | ||||||
chr17:69012574
|
C | G | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3040-491G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012574 | ||||||
chr17:69012597
|
A | T | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3040-514T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012597 | ||||||
chr17:69012665
|
A | G | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3040-582T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012665 | ||||||
chr17:69012667
|
T | C | 11 | a0001c0001t0001g0244a0003c0003t0003g0033a0003c0003t0003g0034others(8): Show | 11 | HG00639.hp2 HG01361.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3040-584A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012667 | ||||||
chr17:69012772
|
T | A | 1 | a0002c0002t0002g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3040-689A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012772 | ||||||
chr17:69012824
|
T | C | 174 | a0001c0001t0001g0244a0001c0001t0003g0165a0001c0001t0006g0051others(171): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.3040-741A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012824 | ||||||
chr17:69012911
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3040-828G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012911 | ||||||
chr17:69012912
|
G | A | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3040-829C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012912 | ||||||
chr17:69012916
|
A | G | 2 | a0001c0008t0001g0263a0016c0017t0003g0189 | 2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3040-833T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012916 | ||||||
chr17:69012927
|
T | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3040-844A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012927 | ||||||
chr17:69013007
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3040-924T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013007 | ||||||
chr17:69013029
|
G | A | 1 | a0002c0002t0002g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3040-946C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013029 | ||||||
chr17:69013180
|
T | G | 1 | a0002c0002t0002g0131 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3040-1097A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013180 | ||||||
chr17:69013447
|
A | AG | 6 | a0001c0008t0001g0190a0001c0008t0001g0191a0001c0008t0001g0192others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3040-1365dupC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013447 | ||||||
chr17:69013689
|
AGACACTG others(11): Show |
A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3040-1624_3040-160 others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013689 | ||||||
chr17:69013768
|
C | T | 11 | a0001c0001t0001g0188a0003c0003t0004g0003a0003c0003t0004g0017others(8): Show | 12 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.3040-1685G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013768 | ||||||
chr17:69013829
|
G | GTACTT | 4 | a0003c0003t0004g0019a0018c0022t0003g0014a0019c0023t0003g0013others(1): Show | 4 | HG02451.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3040-1751_3040-174 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013829 | ||||||
chr17:69013884
|
C | G | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3040-1801G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013884 | ||||||
chr17:69014323
|
A | AAAT | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3039+1927_3039+192 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014323 | ||||||
chr17:69014384
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3039+1869A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014384 | ||||||
chr17:69014400
|
T | C | 1 | a0002c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3039+1853A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014400 | ||||||
chr17:69014474
|
C | G | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+1779G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014474 | ||||||
chr17:69014716
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0008g0250a0001c0001t0008g0251 | 3 | HG00323.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3039+1537C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014716 | ||||||
chr17:69014958
|
A | G | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+1295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014958 | ||||||
chr17:69015027
|
C | G | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3039+1226G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015027 | ||||||
chr17:69015121
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0168 | 3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3039+1132C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015121 | ||||||
chr17:69015159
|
C | CA | 20 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(17): Show | 24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3039+1093dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015159 | ||||||
chr17:69015345
|
G | A | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3039+908C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015345 | ||||||
chr17:69015363
|
C | T | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3039+890G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015363 | ||||||
chr17:69015383
|
C | T | 1 | a0003c0003t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3039+870G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015383 | ||||||
chr17:69015593
|
T | C | 1 | a0001c0008t0001g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3039+660A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015593 | ||||||
chr17:69015613
|
A | ATAATT | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+635_3039+639d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015613 | ||||||
chr17:69015726
|
A | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+527T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015726 | ||||||
chr17:69015863
|
T | C | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+390A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015863 | ||||||
chr17:69015969
|
TTG | T | 127 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(124): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.3039+282_3039+283d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | ||||||
chr17:69015969
|
TTGTG | T | 31 | a0001c0021t0003g0015a0003c0003t0001g0004a0003c0003t0001g0027others(28): Show | 34 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.3039+280_3039+283d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | ||||||
chr17:69015969
|
TTGTGTG | T | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+278_3039+283d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | ||||||
chr17:69015983
|
G | A | 1 | a0003c0003t0001g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3039+270C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015983 | ||||||
chr17:69016094
|
G | A | 19 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(16): Show | 23 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3039+159C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016094 | ||||||
chr17:69016100
|
G | A | 1 | a0020c0024t0002g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3039+153C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016100 | ||||||
chr17:69016102
|
G | A | 1 | a0020c0024t0002g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3039+151C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | ||||||
chr17:69016102
|
GTA | G | 21 | a0001c0001t0001g0182a0001c0001t0001g0202a0001c0001t0001g0240others(18): Show | 25 | HG01081.hp2 HG01099.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3039+149_3039+150d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | ||||||
chr17:69016102
|
GTATA | G | 27 | a0001c0001t0001g0012a0001c0021t0003g0015a0003c0003t0001g0016others(24): Show | 28 | HG00639.hp2 HG01361.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.3039+147_3039+150d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | ||||||
chr17:69016104
|
A | G | 120 | a0001c0001t0003g0165a0001c0007t0001g0090a0001c0007t0001g0115others(117): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3039+149T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016104 | ||||||
chr17:69016106
|
A | G | 15 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(12): Show | 19 | HG01346.hp1 HG02055.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3039+147T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016106 | ||||||
chr17:69016108
|
A | G | 4 | a0006c0010t0002g0120a0006c0010t0002g0144a0006c0010t0002g0145others(1): Show | 4 | HG01496.hp2 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3039+145T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016108 | ||||||
chr17:69016113
|
T | C | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3039+140A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016113 | ||||||
chr17:69016119
|
T | C | 3 | a0001c0001t0003g0165a0018c0022t0003g0014a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3039+134A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | ||||||
chr17:69016119
|
T | TAC | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3039+133_3039+134i others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | ||||||
chr17:69016119
|
TATATAC | T | 7 | a0001c0007t0001g0161a0002c0002t0002g0005a0002c0002t0002g0078others(4): Show | 8 | HG00140.hp1 HG00544.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.3039+128_3039+133d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | ||||||
chr17:69016121
|
T | C | 17 | a0001c0001t0003g0165a0003c0003t0003g0033a0003c0003t0003g0034others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.3039+132A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016121 | ||||||
chr17:69016121
|
TATAC | T | 95 | a0001c0007t0001g0090a0001c0007t0001g0115a0001c0007t0001g0116others(92): Show | 98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.3039+128_3039+131d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016121 | ||||||
chr17:69016123
|
T | C | 32 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0231others(29): Show | 34 | HG00544.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.3039+130A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | ||||||
chr17:69016123
|
T | TAC | 18 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0210others(15): Show | 18 | HG00408.hp1 HG02040.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+128_3039+129d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | ||||||
chr17:69016123
|
TAC | T | 9 | a0001c0001t0001g0177a0002c0002t0002g0079a0002c0002t0002g0140others(6): Show | 9 | HG01517.hp2 HG02074.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.3039+128_3039+129d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | ||||||
chr17:69016123
|
TACAC | T | 14 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(11): Show | 15 | HG01167.hp1 HG01175.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.3039+126_3039+129d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | ||||||
chr17:69016125
|
C | T | 5 | a0001c0001t0001g0186a0001c0008t0001g0167a0001c0029t0001g0200others(2): Show | 5 | HG00099.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+128G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016125 | ||||||
chr17:69016127
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3039+126G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016127 | ||||||
chr17:69016137
|
C | T | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3039+116G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016137 | ||||||
chr17:69016148
|
T | A | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+105A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016148 | ||||||
chr17:69016173
|
TATAAC | T | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+75_3039+79del others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016173 | ||||||
chr17:69016455
|
A | G | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2902-65T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016455 | ||||||
chr17:69016489
|
A | G | 1 | a0003c0003t0003g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2902-99T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016489 | ||||||
chr17:69016493
|
G | C | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2902-103C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016493 | ||||||
chr17:69016532
|
T | C | 1 | a0003c0003t0003g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2902-142A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016532 | ||||||
chr17:69016853
|
C | CGT | 12 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(9): Show | 12 | HG00733.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2902-465_2902-464d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016853 | ||||||
chr17:69016947
|
T | G | 1 | a0002c0002t0002g0137 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2902-557A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016947 | ||||||
chr17:69016953
|
C | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2902-563G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016953 | ||||||
chr17:69017032
|
C | G | 1 | a0002c0004t0002g0108 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2901+624G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017032 | ||||||
chr17:69017257
|
A | C | 10 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(7): Show | 10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2901+399T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017257 | ||||||
chr17:69017561
|
G | A | 5 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(2): Show | 5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901+95C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017561 | ||||||
chr17:69018065
|
G | GTCTA | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2768-280_2768-277d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/38 | chr17 | 69018065 | ||||||
chr17:69018155
|
A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2767+258T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/38 | chr17 | 69018155 | ||||||
chr17:69018661
|
A | G | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2601-82T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018661 | ||||||
chr17:69018700
|
A | G | 2 | a0003c0003t0001g0004a0003c0003t0001g0027 | 3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2601-121T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018700 | ||||||
chr17:69018805
|
G | A | 1 | a0004c0005t0003g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2601-226C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018805 | ||||||
chr17:69018823
|
G | A | 1 | a0019c0023t0003g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2601-244C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018823 | ||||||
chr17:69018828
|
T | C | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2601-249A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018828 | ||||||
chr17:69019138
|
T | C | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2601-559A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019138 | ||||||
chr17:69019387
|
C | T | 12 | a0001c0021t0003g0015a0003c0003t0004g0003a0003c0003t0004g0017others(9): Show | 13 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2601-808G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019387 | ||||||
chr17:69019516
|
A | G | 2 | a0003c0003t0003g0033a0003c0003t0003g0034 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2600+872T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019516 | ||||||
chr17:69019787
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0168 | 3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2600+601G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019787 | ||||||
chr17:69020676
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2402-90T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020676 | ||||||
chr17:69020713
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2402-127A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020713 | ||||||
chr17:69020825
|
T | G | 2 | a0008c0013t0003g0056a0008c0020t0003g0054 | 2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2402-239A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020825 | ||||||
chr17:69021133
|
A | G | 2 | a0003c0003t0004g0017a0003c0003t0004g0018 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2402-547T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021133 | ||||||
chr17:69021176
|
G | A | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2401+566C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021176 | ||||||
chr17:69021296
|
C | G | 1 | a0002c0002t0002g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2401+446G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021296 | ||||||
chr17:69021313
|
A | G | 2 | a0008c0013t0003g0057a0011c0015t0003g0049 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2401+429T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021313 | ||||||
chr17:69021430
|
A | G | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2401+312T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021430 | ||||||
chr17:69021678
|
G | GTCCT | 33 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(30): Show | 35 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.2401+60_2401+63dup others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | ||||||
chr17:69021678
|
G | GTCCTTCC others(5): Show |
1 | a0003c0003t0003g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2401+52_2401+63dup others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | ||||||
chr17:69021678
|
GTCCT | G | 18 | a0001c0001t0001g0252a0001c0021t0003g0015a0004c0005t0003g0001others(15): Show | 22 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2401+60_2401+63del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | ||||||
chr17:69021697
|
C | CTTCCT | 3 | a0018c0022t0003g0014a0019c0023t0003g0013a0023c0019t0003g0055 | 3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2401+44_2401+45ins others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021697 | ||||||
chr17:69021900
|
T | A | 1 | a0001c0007t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2282-39A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69021900 | ||||||
chr17:69022074
|
C | T | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2282-213G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022074 | ||||||
chr17:69022291
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2282-430T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022291 | ||||||
chr17:69022292
|
T | C | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2282-431A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022292 | ||||||
chr17:69022315
|
C | G | 3 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0271 | 7 | HG01346.hp1 HG02451.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2282-454G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022315 | ||||||
chr17:69022329
|
A | AT | 16 | a0001c0001t0001g0186a0003c0003t0003g0033a0003c0003t0003g0034others(13): Show | 17 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2282-469dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022329 | ||||||
chr17:69022350
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2282-489T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022350 | ||||||
chr17:69022431
|
C | T | 26 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(23): Show | 30 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2282-570G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022431 | ||||||
chr17:69022455
|
G | C | 1 | a0002c0002t0002g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2282-594C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022455 | ||||||
chr17:69022494
|
T | TTG | 10 | a0001c0001t0001g0232a0001c0007t0001g0090a0002c0002t0002g0072others(7): Show | 10 | HG00733.hp1 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2282-635_2282-634d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | ||||||
chr17:69022494
|
TTG | T | 12 | a0001c0001t0001g0254a0001c0001t0003g0165a0001c0021t0003g0015others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2282-635_2282-634d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | ||||||
chr17:69022494
|
TTGTGTGT others(21): Show |
T | 1 | a0004c0005t0003g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2282-661_2282-634d others(30): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | ||||||
chr17:69022518
|
G | A | 3 | a0001c0001t0006g0053a0018c0022t0003g0014a0023c0019t0003g0055 | 3 | HG02055.hp1 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2282-657C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022518 | ||||||
chr17:69022518
|
G | GTGTA | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2282-658_2282-657i others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022518 | ||||||
chr17:69022520
|
A | ATG | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0019c0023t0003g0013 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2282-661_2282-660d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | ||||||
chr17:69022520
|
A | G | 8 | a0001c0001t0006g0053a0007c0009t0005g0010a0007c0009t0005g0295others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2282-659T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | ||||||
chr17:69022520
|
ATGTGTGT others(1): Show |
A | 3 | a0008c0013t0003g0056a0008c0020t0003g0054a0009c0011t0003g0046 | 3 | HG03041.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2282-667_2282-660d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | ||||||
chr17:69022528
|
G | A | 1 | a0009c0011t0003g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2282-667C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022528 | ||||||
chr17:69022647
|
C | T | 8 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(5): Show | 8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2282-786G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022647 | ||||||
chr17:69022660
|
G | A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2282-799C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022660 | ||||||
chr17:69022721
|
C | CCT | 26 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(23): Show | 30 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2282-862_2282-861d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022721 | ||||||
chr17:69022771
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2282-910C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022771 | ||||||
chr17:69022780
|
G | T | 1 | a0003c0003t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2282-919C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022780 | ||||||
chr17:69022997
|
T | A | 1 | a0004c0005t0003g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2282-1136A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022997 | ||||||
chr17:69023006
|
T | C | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2282-1145A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023006 | ||||||
chr17:69023564
|
C | T | 4 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0271others(1): Show | 8 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2281+650G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023564 | ||||||
chr17:69023638
|
C | T | 2 | a0001c0007t0004g0093a0002c0002t0002g0094 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2281+576G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023638 | ||||||
chr17:69023788
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0240 | 2 | HG01081.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2281+426T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023788 | ||||||
chr17:69023836
|
ATTCTTTC others(24): Show |
A | 4 | a0008c0013t0003g0056a0008c0020t0003g0054a0009c0011t0003g0046others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+347_2281+377d others(33): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023836 | ||||||
chr17:69023868
|
T | C | 4 | a0008c0013t0003g0056a0008c0020t0003g0054a0009c0011t0003g0046others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+346A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023868 | ||||||
chr17:69023869
|
G | C | 4 | a0008c0013t0003g0056a0008c0020t0003g0054a0009c0011t0003g0046others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+345C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023869 | ||||||
chr17:69023886
|
C | T | 1 | a0002c0002t0002g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2281+328G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023886 | ||||||
chr17:69023924
|
A | G | 1 | a0001c0007t0001g0225 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2281+290T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023924 | ||||||
chr17:69023997
|
AT | A | 21 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(18): Show | 22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2281+216delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023997 | ||||||
chr17:69024089
|
T | C | 2 | a0002c0002t0002g0119a0002c0002t0002g0158 | 2 | NA18953.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2281+125A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69024089 | ||||||
chr17:69024187
|
C | T | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2281+27G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69024187 | ||||||
chr17:69024385
|
A | G | 43 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(40): Show | 48 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2142-32T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024385 | ||||||
chr17:69024635
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2142-282C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024635 | ||||||
chr17:69024639
|
T | C | 1 | a0004c0005t0003g0287 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2142-286A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024639 | ||||||
chr17:69024693
|
T | G | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2142-340A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024693 | ||||||
chr17:69024697
|
G | A | 221 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0164others(218): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2142-344C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024697 | ||||||
chr17:69024849
|
G | C | 3 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0271 | 7 | HG01346.hp1 HG02451.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142-496C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024849 | ||||||
chr17:69024994
|
T | C | 120 | a0001c0007t0001g0090a0001c0007t0001g0115a0001c0007t0001g0116others(117): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.2142-641A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024994 | ||||||
chr17:69025015
|
A | G | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2142-662T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025015 | ||||||
chr17:69025071
|
T | G | 11 | a0001c0021t0003g0015a0003c0003t0004g0003a0003c0003t0004g0017others(8): Show | 12 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2142-718A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025071 | ||||||
chr17:69025073
|
C | T | 1 | a0003c0003t0003g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2142-720G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025073 | ||||||
chr17:69025214
|
C | T | 4 | a0001c0001t0001g0012a0003c0003t0001g0032a0003c0003t0001g0043others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142-861G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025214 | ||||||
chr17:69025228
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2142-875G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025228 | ||||||
chr17:69025232
|
A | G | 10 | a0003c0003t0004g0003a0003c0003t0004g0017a0003c0003t0004g0018others(7): Show | 11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2142-879T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025232 | ||||||
chr17:69025353
|
G | A | 2 | a0009c0011t0003g0046a0009c0011t0003g0047 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2142-1000C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025353 | ||||||
chr17:69025419
|
T | G | 1 | a0002c0002t0002g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2141+958A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025419 | ||||||
chr17:69025700
|
T | C | 6 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2141+677A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025700 | ||||||
chr17:69025773
|
G | A | 1 | a0002c0002t0002g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2141+604C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025773 | ||||||
chr17:69025994
|
C | A | 130 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2141+383G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025994 | ||||||
chr17:69026134
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2141+243C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69026134 | ||||||
chr17:69026600
|
C | T | 1 | a0002c0002t0002g0142 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2051-133G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026600 | ||||||
chr17:69026627
|
C | T | 2 | a0001c0001t0003g0165a0003c0003t0004g0020 | 2 | HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2051-160G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026627 | ||||||
chr17:69026644
|
A | G | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2051-177T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026644 | ||||||
chr17:69026669
|
G | A | 11 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2051-202C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026669 | ||||||
chr17:69026759
|
T | C | 21 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(18): Show | 22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2050+217A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026759 | ||||||
chr17:69027138
|
G | A | 1 | a0001c0007t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1912-24C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027138 | ||||||
chr17:69027154
|
G | A | 14 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(11): Show | 18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1912-40C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027154 | ||||||
chr17:69027232
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1911+98T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027232 | ||||||
chr17:69027244
|
C | G | 10 | a0003c0003t0003g0033a0003c0003t0003g0034a0003c0003t0003g0035others(7): Show | 10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1911+86G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027244 | ||||||
chr17:69027558
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1791+82T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 13/38 | chr17 | 69027558 | ||||||
chr17:69027614
|
A | G | 173 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(170): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1791+26T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 13/38 | chr17 | 69027614 | ||||||
chr17:69028043
|
T | G | 11 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1616-228A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028043 | ||||||
chr17:69028126
|
A | G | 2 | a0003c0003t0004g0021a0003c0003t0004g0025 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1616-311T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028126 | ||||||
chr17:69028384
|
C | T | 2 | a0002c0002t0002g0102a0002c0002t0002g0126 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615+151G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028384 | ||||||
chr17:69028413
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1615+122G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028413 | ||||||
chr17:69028444
|
T | C | 173 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(170): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1615+91A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028444 | ||||||
chr17:69028658
|
T | A | 173 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(170): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1505-13A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028658 | ||||||
chr17:69028742
|
C | T | 1 | a0003c0003t0004g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1505-97G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028742 | ||||||
chr17:69028794
|
A | G | 10 | a0003c0003t0004g0003a0003c0003t0004g0017a0003c0003t0004g0018others(7): Show | 11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1505-149T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028794 | ||||||
chr17:69028798
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1505-153G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028798 | ||||||
chr17:69028807
|
G | A | 8 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505-162C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028807 | ||||||
chr17:69028814
|
T | C | 2 | a0002c0002t0002g0130a0002c0002t0002g0131 | 2 | NA18946.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1505-169A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028814 | ||||||
chr17:69029019
|
G | GT | 15 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(12): Show | 19 | HG01109.hp2 HG01346.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1504+149dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029019 | ||||||
chr17:69029089
|
T | C | 3 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054 | 3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1504+80A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029089 | ||||||
chr17:69029100
|
C | G | 1 | a0002c0002t0002g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1504+69G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029100 | ||||||
chr17:69029282
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1446-55T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029282 | ||||||
chr17:69029423
|
G | A | 1 | a0007c0009t0005g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446-196C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029423 | ||||||
chr17:69029423
|
G | T | 10 | a0001c0008t0001g0167a0001c0008t0001g0181a0001c0008t0001g0190others(7): Show | 10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1446-196C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029423 | ||||||
chr17:69029465
|
G | A | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1446-238C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029465 | ||||||
chr17:69029549
|
G | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-322C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029549 | ||||||
chr17:69029563
|
A | G | 1 | a0001c0008t0001g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1446-336T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029563 | ||||||
chr17:69029614
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1446-387A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029614 | ||||||
chr17:69029710
|
G | A | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-483C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029710 | ||||||
chr17:69029714
|
A | G | 1 | a0007c0009t0005g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446-487T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029714 | ||||||
chr17:69029790
|
G | A | 5 | a0001c0001t0001g0242a0001c0001t0006g0051a0001c0001t0006g0052others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446-563C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029790 | ||||||
chr17:69029900
|
G | T | 26 | a0001c0021t0003g0015a0003c0003t0003g0033a0003c0003t0003g0034others(23): Show | 27 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1446-673C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029900 | ||||||
chr17:69030090
|
A | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-863T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030090 | ||||||
chr17:69030272
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA18939.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1446-1045A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030272 | ||||||
chr17:69030412
|
G | T | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1446-1185C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030412 | ||||||
chr17:69030485
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1446-1258C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030485 | ||||||
chr17:69031061
|
A | C | 1 | a0002c0004t0002g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1445+1047T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031061 | ||||||
chr17:69031095
|
C | G | 1 | a0003c0003t0004g0020 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1445+1013G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031095 | ||||||
chr17:69031202
|
T | G | 2 | a0007c0009t0005g0010a0007c0009t0005g0296 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1445+906A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031202 | ||||||
chr17:69031729
|
A | G | 139 | a0001c0001t0001g0240a0001c0007t0001g0090a0001c0007t0001g0115others(136): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1445+379T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031729 | ||||||
chr17:69032071
|
G | C | 19 | a0001c0001t0003g0165a0001c0001t0006g0051a0001c0001t0006g0052others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1445+37C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69032071 | ||||||
chr17:69032079
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1445+29A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69032079 | ||||||
chr17:69032280
|
T | C | 1 | a0002c0002t0002g0149 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1277-4A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032280 | ||||||
chr17:69032511
|
A | T | 1 | a0003c0003t0001g0043 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1277-235T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032511 | ||||||
chr17:69032765
|
G | T | 3 | a0001c0001t0001g0012a0018c0022t0003g0014a0019c0023t0003g0013 | 3 | HG02451.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1277-489C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032765 | ||||||
chr17:69033303
|
C | CAA | 16 | a0001c0001t0001g0012a0007c0009t0005g0010a0007c0009t0005g0295others(13): Show | 17 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1276+421_1276+422d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | ||||||
chr17:69033303
|
C | CAAA | 8 | a0001c0001t0001g0061a0001c0001t0001g0213a0001c0001t0006g0051others(5): Show | 8 | HG01074.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+420_1276+422d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | ||||||
chr17:69033303
|
C | CAAAA | 229 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(226): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1276+419_1276+422d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | ||||||
chr17:69033303
|
C | CAAAAA | 13 | a0001c0001t0001g0084a0001c0001t0001g0254a0001c0001t0001g0264others(10): Show | 13 | HG01952.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+418_1276+422d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | ||||||
chr17:69033324
|
G | C | 47 | a0001c0001t0001g0084a0001c0007t0001g0090a0001c0007t0001g0115others(44): Show | 47 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1276+402C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033324 | ||||||
chr17:69033682
|
C | G | 7 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0031others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+44G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033682 | ||||||
chr17:69034131
|
T | A | 3 | a0001c0001t0001g0012a0018c0022t0003g0014a0019c0023t0003g0013 | 3 | HG02451.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1129-258A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034131 | ||||||
chr17:69034460
|
T | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(136): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1129-587A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034460 | ||||||
chr17:69034530
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1129-657G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034530 | ||||||
chr17:69034604
|
T | C | 1 | a0006c0010t0002g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1128+642A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034604 | ||||||
chr17:69034605
|
T | C | 1 | a0006c0010t0002g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1128+641A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034605 | ||||||
chr17:69034781
|
C | T | 1 | a0008c0013t0003g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1128+465G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034781 | ||||||
chr17:69034936
|
G | A | 2 | a0018c0022t0003g0014a0019c0023t0003g0013 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1128+310C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034936 | ||||||
chr17:69035228
|
T | C | 288 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(285): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1128+18A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69035228 | ||||||
chr17:69035622
|
A | G | 2 | a0001c0007t0004g0093a0002c0002t0002g0094 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.942+38T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/38 | chr17 | 69035622 | ||||||
chr17:69035974
|
G | A | 2 | a0002c0002t0002g0121a0002c0002t0002g0138 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.801-173C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69035974 | ||||||
chr17:69036071
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.801-270C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036071 | ||||||
chr17:69036128
|
G | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.801-327C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036128 | ||||||
chr17:69036147
|
T | C | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.801-346A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036147 | ||||||
chr17:69036372
|
T | C | 1 | a0018c0022t0003g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.801-571A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036372 | ||||||
chr17:69036493
|
C | T | 2 | a0003c0003t0001g0004a0003c0003t0001g0027 | 3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.801-692G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036493 | ||||||
chr17:69036871
|
C | CA | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG01071.hp1 HG01099.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.801-1071dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
C | CAAAA | 65 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(62): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.801-1074_801-1071d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
C | CAAAAA | 42 | a0001c0001t0001g0171a0001c0001t0001g0186a0001c0001t0001g0198others(39): Show | 43 | HG00438.hp2 HG00544.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.801-1075_801-1071d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
C | CAAAAAA | 19 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0180others(16): Show | 19 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.801-1076_801-1071d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
CA | C | 79 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(76): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.801-1071delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
CAA | C | 8 | a0002c0002t0002g0005a0002c0002t0002g0059a0002c0002t0002g0060others(5): Show | 9 | HG00733.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-1072_801-1071d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036871
|
CAAAAAAA others(3): Show |
C | 1 | a0018c0022t0003g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.801-1080_801-1071d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | ||||||
chr17:69036925
|
TA | T | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.801-1125delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036925 | ||||||
chr17:69036934
|
C | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0162others(139): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.801-1133G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036934 | ||||||
chr17:69037345
|
C | T | 107 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(104): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.801-1544G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037345 | ||||||
chr17:69037614
|
G | T | 3 | a0002c0002t0002g0104a0002c0002t0007g0132a0002c0002t0007g0133 | 3 | HG00639.hp1 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.801-1813C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037614 | ||||||
chr17:69037696
|
G | A | 1 | a0019c0023t0003g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.801-1895C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037696 | ||||||
chr17:69037754
|
G | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0162others(139): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.801-1953C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037754 | ||||||
chr17:69037975
|
A | G | 280 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(277): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.801-2174T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037975 | ||||||
chr17:69038305
|
G | A | 1 | a0002c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.801-2504C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038305 | ||||||
chr17:69038370
|
T | C | 1 | a0002c0002t0002g0103 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.801-2569A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038370 | ||||||
chr17:69038371
|
G | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.801-2570C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038371 | ||||||
chr17:69038426
|
T | C | 47 | a0001c0001t0001g0084a0001c0007t0001g0090a0001c0007t0001g0115others(44): Show | 47 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.801-2625A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038426 | ||||||
chr17:69038630
|
A | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.801-2829T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038630 | ||||||
chr17:69038695
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.801-2894A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038695 | ||||||
chr17:69038822
|
C | T | 1 | a0001c0007t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.801-3021G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038822 | ||||||
chr17:69038934
|
G | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(134): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.801-3133C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038934 | ||||||
chr17:69039137
|
T | A | 1 | a0003c0003t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.801-3336A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039137 | ||||||
chr17:69039158
|
A | G | 1 | a0003c0003t0003g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801-3357T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039158 | ||||||
chr17:69039247
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.801-3446G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039247 | ||||||
chr17:69039737
|
T | G | 248 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(245): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.800+3752A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039737 | ||||||
chr17:69039750
|
C | T | 280 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(277): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.800+3739G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039750 | ||||||
chr17:69039944
|
CAT | C | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(1): Show | 4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+3543_800+3544d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039944 | ||||||
chr17:69040256
|
C | T | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.800+3233G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040256 | ||||||
chr17:69040385
|
T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.800+3104A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040385 | ||||||
chr17:69040445
|
A | G | 1 | a0007c0009t0005g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.800+3044T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040445 | ||||||
chr17:69040450
|
A | G | 7 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0031others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+3039T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040450 | ||||||
chr17:69040514
|
T | C | 1 | a0001c0007t0001g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.800+2975A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040514 | ||||||
chr17:69040717
|
A | T | 1 | a0002c0028t0002g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.800+2772T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040717 | ||||||
chr17:69040845
|
TAC | T | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.800+2642_800+2643d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040845 | ||||||
chr17:69040862
|
A | C | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.800+2627T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040862 | ||||||
chr17:69040894
|
C | T | 1 | a0004c0005t0003g0285 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800+2595G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040894 | ||||||
chr17:69041184
|
G | T | 295 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(292): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.800+2305C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041184 | ||||||
chr17:69041215
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.800+2274T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041215 | ||||||
chr17:69041226
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.800+2263G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041226 | ||||||
chr17:69041339
|
T | G | 106 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.800+2150A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041339 | ||||||
chr17:69041452
|
A | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.800+2037T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041452 | ||||||
chr17:69041635
|
G | C | 32 | a0001c0001t0001g0012a0004c0005t0003g0001a0004c0005t0003g0268others(29): Show | 37 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.800+1854C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041635 | ||||||
chr17:69041711
|
TA | T | 294 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(291): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.800+1777delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041711 | ||||||
chr17:69041727
|
A | T | 1 | a0001c0001t0009g0199 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.800+1762T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041727 | ||||||
chr17:69041729
|
T | TCTATTAT others(5): Show |
1 | a0001c0001t0009g0199 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.800+1759_800+1760i others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041729
|
T | TTATC | 10 | a0001c0001t0001g0012a0001c0001t0001g0182a0001c0001t0001g0207others(7): Show | 10 | HG00408.hp1 HG00408.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.800+1756_800+1759d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041729
|
T | TTATCTAT others(1): Show |
83 | a0001c0001t0001g0084a0001c0001t0001g0201a0001c0001t0001g0208others(80): Show | 89 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.800+1752_800+1759d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041729
|
T | TTATCTAT others(5): Show |
161 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0162others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.800+1748_800+1759d others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041729
|
T | TTATCTAT others(9): Show |
9 | a0001c0001t0001g0172a0001c0001t0001g0206a0001c0001t0001g0243others(6): Show | 9 | HG01517.hp2 HG01975.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.800+1744_800+1759d others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041729
|
T | TTATCTAT others(13): Show |
2 | a0001c0001t0001g0238a0002c0028t0002g0081 | 2 | HG02080.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.800+1740_800+1759d others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | ||||||
chr17:69041879
|
A | G | 295 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(292): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.800+1610T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041879 | ||||||
chr17:69041982
|
T | G | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.800+1507A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041982 | ||||||
chr17:69041993
|
C | T | 7 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(4): Show | 7 | HG01175.hp2 HG02572.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+1496G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041993 | ||||||
chr17:69042059
|
T | G | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(1): Show | 4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+1430A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042059 | ||||||
chr17:69042107
|
A | G | 9 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(6): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.800+1382T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042107 | ||||||
chr17:69042178
|
CTA | C | 107 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(104): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.800+1309_800+1310d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042178 | ||||||
chr17:69042182
|
T | C | 9 | a0001c0008t0001g0167a0001c0008t0001g0181a0001c0008t0001g0190others(6): Show | 9 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.800+1307A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042182 | ||||||
chr17:69042186
|
A | G | 138 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(135): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.800+1303T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042186 | ||||||
chr17:69042409
|
C | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.800+1080G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042409 | ||||||
chr17:69042513
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.800+976A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042513 | ||||||
chr17:69042791
|
A | G | 1 | a0009c0011t0003g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.800+698T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042791 | ||||||
chr17:69042837
|
A | G | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG02071.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.800+652T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042837 | ||||||
chr17:69042930
|
T | C | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+559A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042930 | ||||||
chr17:69043008
|
C | G | 1 | a0001c0029t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.800+481G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043008 | ||||||
chr17:69043080
|
CAGTGACA others(50): Show |
C | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+352_800+408del others(57): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043080 | ||||||
chr17:69043094
|
C | A | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+395G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043094 | ||||||
chr17:69043133
|
T | C | 1 | a0001c0008t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.800+356A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043133 | ||||||
chr17:69043316
|
G | A | 9 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(6): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.800+173C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043316 | ||||||
chr17:69043458
|
C | T | 7 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0031others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+31G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043458 | ||||||
chr17:69043798
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-83G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043798 | ||||||
chr17:69043923
|
G | A | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-208C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043923 | ||||||
chr17:69043970
|
T | A | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-255A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043970 | ||||||
chr17:69044203
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.573+294G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044203 | ||||||
chr17:69044240
|
T | A | 1 | a0001c0007t0001g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573+257A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044240 | ||||||
chr17:69044270
|
T | C | 12 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(9): Show | 13 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.573+227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044270 | ||||||
chr17:69044468
|
T | G | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.573+29A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044468 | ||||||
chr17:69044630
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.470-30C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044630 | ||||||
chr17:69044919
|
G | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.469+253C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044919 | ||||||
chr17:69044941
|
T | TG | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.469+230_469+231ins others(1): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044941 | ||||||
chr17:69044981
|
T | G | 1 | a0001c0001t0001g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.469+191A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044981 | ||||||
chr17:69045014
|
C | G | 1 | a0002c0002t0002g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.469+158G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045014 | ||||||
chr17:69045079
|
T | C | 1 | a0002c0002t0002g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.469+93A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045079 | ||||||
chr17:69045126
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.469+46A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045126 | ||||||
chr17:69045430
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.305-94A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045430 | ||||||
chr17:69045467
|
T | C | 88 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(85): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.305-131A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045467 | ||||||
chr17:69045867
|
C | G | 7 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0031others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.305-531G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045867 | ||||||
chr17:69046055
|
G | C | 1 | a0003c0003t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.305-719C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046055 | ||||||
chr17:69046316
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.305-980A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046316 | ||||||
chr17:69046567
|
C | T | 1 | a0001c0001t0009g0199 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.305-1231G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046567 | ||||||
chr17:69046599
|
T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.305-1263A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046599 | ||||||
chr17:69046621
|
T | G | 108 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.305-1285A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046621 | ||||||
chr17:69046718
|
C | T | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.305-1382G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046718 | ||||||
chr17:69046719
|
A | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.305-1383T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046719 | ||||||
chr17:69046804
|
C | G | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-1468G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046804 | ||||||
chr17:69046875
|
C | CTA | 4 | a0001c0001t0011g0249a0002c0004t0002g0183a0003c0003t0001g0004others(1): Show | 5 | HG02132.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1541_305-1540d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
C | CTATA | 5 | a0001c0001t0008g0250a0001c0001t0008g0251a0003c0003t0001g0016others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-1543_305-1540d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTA | C | 25 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0170others(22): Show | 26 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.305-1541_305-1540d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATA | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0171others(64): Show | 69 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.305-1543_305-1540d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATA | C | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG00639.hp2 HG02717.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.305-1545_305-1540d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(1): Show |
C | 12 | a0001c0001t0001g0173a0001c0001t0001g0194a0001c0001t0001g0195others(9): Show | 12 | HG02572.hp2 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-1547_305-1540d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(3): Show |
C | 8 | a0001c0001t0001g0162a0001c0007t0001g0090a0002c0002t0002g0006others(5): Show | 9 | HG02155.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.305-1549_305-1540d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(5): Show |
C | 16 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0003g0165others(13): Show | 16 | HG00438.hp1 HG00642.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.305-1551_305-1540d others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(7): Show |
C | 91 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0115others(88): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.305-1553_305-1540d others(16): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(9): Show |
C | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.305-1555_305-1540d others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046875
|
CTATATAT others(11): Show |
C | 29 | a0001c0001t0001g0012a0004c0005t0003g0001a0004c0005t0003g0268others(26): Show | 34 | HG01074.hp1 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-1557_305-1540d others(20): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | ||||||
chr17:69046894
|
TATATATA others(29): Show |
T | 1 | a0004c0005t0003g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.305-1594_305-1559d others(38): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046894 | ||||||
chr17:69046901
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.305-1566_305-1565i others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046901 | ||||||
chr17:69046926
|
T | A | 1 | a0001c0001t0006g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.305-1590A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046926 | ||||||
chr17:69046930
|
G | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.305-1594C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046930 | ||||||
chr17:69046937
|
T | TTA | 9 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(6): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-1603_305-1602d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046937 | ||||||
chr17:69046937
|
TTA | T | 108 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.305-1603_305-1602d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046937 | ||||||
chr17:69047122
|
C | G | 2 | a0003c0003t0004g0017a0003c0003t0004g0018 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.305-1786G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047122 | ||||||
chr17:69047209
|
A | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.305-1873T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047209 | ||||||
chr17:69047256
|
T | C | 1 | a0002c0002t0002g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.305-1920A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047256 | ||||||
chr17:69047357
|
G | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.304+1926C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047357 | ||||||
chr17:69047459
|
A | G | 1 | a0008c0020t0003g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+1824T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047459 | ||||||
chr17:69047495
|
G | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.304+1788C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047495 | ||||||
chr17:69047515
|
A | G | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.304+1768T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047515 | ||||||
chr17:69047713
|
A | G | 3 | a0001c0021t0003g0015a0018c0022t0003g0014a0019c0023t0003g0013 | 3 | HG01891.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.304+1570T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047713 | ||||||
chr17:69047770
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.304+1513C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047770 | ||||||
chr17:69048075
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.304+1208A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048075 | ||||||
chr17:69048215
|
T | A | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304+1068A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048215 | ||||||
chr17:69048275
|
C | T | 5 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1008G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048275 | ||||||
chr17:69048420
|
T | C | 108 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.304+863A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048420 | ||||||
chr17:69048426
|
T | TA | 137 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(134): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.304+856dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048426 | ||||||
chr17:69048428
|
C | T | 1 | a0003c0003t0003g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.304+855G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048428 | ||||||
chr17:69048462
|
C | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.304+821G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048462 | ||||||
chr17:69048654
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.304+629C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048654 | ||||||
chr17:69048721
|
C | A | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+562G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048721 | ||||||
chr17:69048753
|
T | C | 6 | a0002c0002t0002g0006a0002c0002t0002g0150a0002c0002t0002g0151others(3): Show | 7 | NA18980.hp1 NA18992.hp1 NA19058.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+530A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048753 | ||||||
chr17:69048827
|
C | A | 25 | a0001c0001t0001g0061a0002c0002t0002g0059a0002c0002t0002g0060others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.304+456G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048827 | ||||||
chr17:69048830
|
C | T | 19 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(16): Show | 20 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.304+453G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048830 | ||||||
chr17:69049569
|
T | A | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-79A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049569 | ||||||
chr17:69049762
|
T | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.97-272A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049762 | ||||||
chr17:69049776
|
T | C | 1 | a0002c0002t0002g0260 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97-286A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049776 | ||||||
chr17:69049796
|
G | A | 1 | a0011c0015t0003g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.97-306C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049796 | ||||||
chr17:69049946
|
AC | A | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-457delG | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049946 | ||||||
chr17:69049984
|
G | A | 1 | a0013c0016t0002g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97-494C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049984 | ||||||
chr17:69050101
|
T | C | 2 | a0018c0022t0003g0014a0019c0023t0003g0013 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.97-611A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050101 | ||||||
chr17:69050221
|
G | T | 2 | a0003c0003t0001g0016a0003c0003t0001g0029 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.97-731C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050221 | ||||||
chr17:69050323
|
A | AAC | 7 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0031others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+706_96+707dupGT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050323 | ||||||
chr17:69050343
|
AAC | A | 103 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0007t0001g0115others(100): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.96+686_96+687delGT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050343
|
AACAC | A | 14 | a0001c0021t0003g0015a0002c0002t0002g0154a0003c0003t0001g0004others(11): Show | 15 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+684_96+687delGT others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050343
|
AACACAC | A | 9 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0185others(6): Show | 9 | HG01175.hp2 HG01978.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+682_96+687delGT others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050343
|
AACACACA others(1): Show |
A | 103 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(100): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.96+680_96+687delGT others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050343
|
AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.96+676_96+687delGT others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050343
|
AACACACA others(7): Show |
A | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+674_96+687delGT others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | ||||||
chr17:69050525
|
A | T | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.96+506T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050525 | ||||||
chr17:69050706
|
G | A | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+325C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050706 | ||||||
chr17:69050826
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.96+205G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050826 | ||||||
chr17:69050906
|
AT | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0166others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.96+124delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050906 | ||||||
chr17:69051004
|
T | C | 1 | a0002c0002t0002g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+27A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69051004 | ||||||
chr17:69051185
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-13-46C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051185 | ||||||
chr17:69051287
|
G | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0162others(138): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-13-148C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051287 | ||||||
chr17:69051372
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13-233T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051372 | ||||||
chr17:69052235
|
C | T | 1 | a0009c0011t0003g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-1096G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052235 | ||||||
chr17:69052434
|
A | G | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052434 | ||||||
chr17:69052668
|
G | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-13-1529C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052668 | ||||||
chr17:69052844
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0185a0001c0021t0003g0015others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-1705G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052844 | ||||||
chr17:69053067
|
CTCCTTCA others(10): Show |
C | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-1945_-13-1929d others(19): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053067 | ||||||
chr17:69053717
|
C | A | 3 | a0004c0005t0003g0001a0004c0005t0003g0270a0004c0005t0003g0271 | 7 | HG01346.hp1 HG02451.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-2578G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053717 | ||||||
chr17:69053780
|
CTG | C | 83 | a0001c0001t0001g0084a0001c0007t0001g0090a0001c0007t0001g0115others(80): Show | 87 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-13-2643_-13-2642d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053780 | ||||||
chr17:69054246
|
A | G | 141 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0162others(138): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-13-3107T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054246 | ||||||
chr17:69054386
|
G | A | 4 | a0001c0001t0001g0012a0001c0021t0003g0015a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-3247C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054386 | ||||||
chr17:69054526
|
CA | C | 6 | a0001c0001t0001g0012a0001c0021t0003g0015a0002c0004t0002g0184others(3): Show | 6 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-3388delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054526 | ||||||
chr17:69054726
|
T | C | 1 | a0001c0021t0003g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-13-3587A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054726 | ||||||
chr17:69054810
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | NA18953.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-13-3671C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054810 | ||||||
chr17:69054908
|
C | A | 1 | a0005c0006t0001g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3769G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054908 | ||||||
chr17:69054920
|
A | G | 1 | a0002c0004t0002g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-13-3781T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054920 | ||||||
chr17:69054965
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-13-3826T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054965 | ||||||
chr17:69055105
|
C | T | 1 | a0004c0005t0003g0272 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13-3966G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055105 | ||||||
chr17:69055113
|
A | G | 1 | a0009c0011t0003g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-3974T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055113 | ||||||
chr17:69055196
|
A | T | 108 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-13-4057T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055196 | ||||||
chr17:69055207
|
T | C | 1 | a0002c0002t0002g0260 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13-4068A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055207 | ||||||
chr17:69055448
|
G | C | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-4309C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055448 | ||||||
chr17:69055505
|
AAC | A | 3 | a0001c0021t0003g0015a0018c0022t0003g0014a0019c0023t0003g0013 | 3 | HG01891.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13-4368_-13-4367d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055505 | ||||||
chr17:69055788
|
T | A | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-4649A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055788 | ||||||
chr17:69055842
|
A | T | 1 | a0001c0008t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-13-4703T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055842 | ||||||
chr17:69055885
|
A | G | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-13-4746T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055885 | ||||||
chr17:69055910
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-13-4771T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055910 | ||||||
chr17:69055934
|
C | G | 4 | a0004c0005t0003g0001a0004c0005t0003g0269a0004c0005t0003g0270others(1): Show | 8 | HG01346.hp1 HG02451.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-4795G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055934 | ||||||
chr17:69056077
|
C | T | 267 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(264): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-14+4789G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056077 | ||||||
chr17:69056081
|
C | A | 1 | a0002c0002t0002g0158 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-14+4785G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056081 | ||||||
chr17:69056095
|
A | T | 9 | a0007c0009t0005g0010a0007c0009t0005g0295a0007c0009t0005g0296others(6): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+4771T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056095 | ||||||
chr17:69056331
|
G | T | 8 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01175.hp2 HG02572.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+4535C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056331 | ||||||
chr17:69056720
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-14+4146T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056720 | ||||||
chr17:69056976
|
T | G | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-14+3890A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056976 | ||||||
chr17:69056986
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+3880G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056986 | ||||||
chr17:69057141
|
G | A | 1 | a0003c0003t0003g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-14+3725C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057141 | ||||||
chr17:69057152
|
T | C | 34 | a0001c0001t0001g0012a0001c0021t0003g0015a0003c0003t0001g0045others(31): Show | 39 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+3714A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057152 | ||||||
chr17:69057378
|
C | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+3488G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057378 | ||||||
chr17:69057441
|
G | C | 18 | a0001c0001t0001g0012a0001c0001t0006g0051a0001c0001t0006g0052others(15): Show | 19 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+3425C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057441 | ||||||
chr17:69057507
|
CTAGGCTT others(13): Show |
C | 14 | a0003c0003t0001g0004a0003c0003t0001g0027a0003c0003t0001g0028others(11): Show | 16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14+3339_-14+3358d others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057507 | ||||||
chr17:69057574
|
A | C | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+3292T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057574 | ||||||
chr17:69057824
|
T | G | 1 | a0002c0004t0002g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14+3042A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057824 | ||||||
chr17:69057840
|
TTCTTG | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+3021_-14+3025d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057840 | ||||||
chr17:69057997
|
G | A | 4 | a0008c0013t0003g0056a0008c0013t0003g0057a0008c0020t0003g0054others(1): Show | 4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2869C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057997 | ||||||
chr17:69058007
|
G | C | 281 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(278): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-14+2859C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058007 | ||||||
chr17:69058049
|
A | T | 1 | a0017c0025t0002g0058 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-14+2817T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058049 | ||||||
chr17:69058066
|
T | C | 1 | a0018c0022t0003g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-14+2800A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058066 | ||||||
chr17:69058148
|
G | A | 1 | a0002c0002t0002g0159 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-14+2718C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058148 | ||||||
chr17:69058413
|
C | T | 4 | a0001c0021t0003g0015a0003c0003t0001g0045a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2453G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058413 | ||||||
chr17:69058437
|
G | C | 5 | a0001c0001t0001g0012a0001c0021t0003g0015a0003c0003t0001g0045others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2429C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058437 | ||||||
chr17:69058439
|
G | T | 1 | a0004c0005t0003g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14+2427C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058439 | ||||||
chr17:69058441
|
T | C | 4 | a0001c0021t0003g0015a0003c0003t0001g0045a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2425A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058441 | ||||||
chr17:69058568
|
C | G | 238 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(235): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-14+2298G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058568 | ||||||
chr17:69058568
|
C | T | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+2298G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058568 | ||||||
chr17:69058589
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-14+2277G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058589 | ||||||
chr17:69058653
|
C | A | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+2213G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058653 | ||||||
chr17:69058794
|
C | G | 281 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(278): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-14+2072G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058794 | ||||||
chr17:69058836
|
C | CA | 107 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-14+2029dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058836 | ||||||
chr17:69058836
|
CA | C | 34 | a0001c0001t0001g0012a0003c0003t0001g0016a0003c0003t0001g0045others(31): Show | 39 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+2029delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058836 | ||||||
chr17:69058856
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-14+2010T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058856 | ||||||
chr17:69059172
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0003g0165 | 3 | HG01884.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-14+1694G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059172 | ||||||
chr17:69059404
|
A | G | 267 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(264): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-14+1462T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059404 | ||||||
chr17:69059424
|
G | A | 1 | a0003c0003t0001g0043 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14+1442C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059424 | ||||||
chr17:69059448
|
C | T | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+1418G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059448 | ||||||
chr17:69059573
|
C | A | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+1293G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059573 | ||||||
chr17:69059624
|
T | C | 5 | a0001c0001t0001g0012a0001c0021t0003g0015a0003c0003t0001g0045others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+1242A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059624 | ||||||
chr17:69059643
|
T | C | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+1223A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059643 | ||||||
chr17:69059669
|
A | AT | 168 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(165): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-14+1196dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059669 | ||||||
chr17:69059677
|
T | A | 4 | a0001c0021t0003g0015a0003c0003t0001g0045a0018c0022t0003g0014others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1189A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059677 | ||||||
chr17:69059712
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-14+1154C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059712 | ||||||
chr17:69059760
|
A | G | 267 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0061others(264): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-14+1106T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059760 | ||||||
chr17:69059783
|
T | C | 1 | a0003c0003t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-14+1083A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059783 | ||||||
chr17:69060027
|
GTTCT | G | 17 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0053others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+835_-14+838del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060027 | ||||||
chr17:69060142
|
T | G | 108 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0007t0001g0090others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-14+724A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060142 | ||||||
chr17:69060207
|
T | C | 1 | a0002c0004t0002g0267 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-14+659A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060207 | ||||||
chr17:69060521
|
AAAAC | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-14+341_-14+344del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060521 | ||||||
chr17:69060599
|
ATT | A | 29 | a0004c0005t0003g0001a0004c0005t0003g0268a0004c0005t0003g0269others(26): Show | 34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+265_-14+266del others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060599 | ||||||
chr17:69060765
|
C | T | 1 | a0002c0002t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-14+101G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060765 |