geneid | 81616 |
---|---|
ensemblid | ENSG00000130377.14 |
hgncid | 24174 |
symbol | ACSBG2 |
name | acyl-CoA synthetase bubblegum family member 2 |
refseq_nuc | NM_030924.5 |
refseq_prot | NP_112186.3 |
ensembl_nuc | ENST00000588485.6 |
ensembl_prot | ENSP00000466336.2 |
mane_status | MANE Select |
chr | chr19 |
start | 6135667 |
end | 6193091 |
strand | + |
ver | v1.2 |
region | chr19:6135667-6193091 |
region5000 | chr19:6130667-6198091 |
regionname0 | ACSBG2_chr19_6135667_6193091 |
regionname5000 | ACSBG2_chr19_6130667_6198091 |
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 | 0/1 | 666 | 124 | 36 | 25 | 40 | 8 | 14 | 26 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002 | 1/0 | 666 | 76 | 19 | 15 | 31 | 1 | 9 | 21 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003 | 0/0 | 666 | 20 | 12 | 1 | 6 | 0 | 1 | 6 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004 | 0/0 | 666 | 12 | 2 | 2 | 6 | 0 | 2 | 2 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0005 | 0/0 | 666 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0006 | 0/0 | 666 | 6 | 0 | 3 | 0 | 3 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0007 | 0/0 | 666 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0008 | 0/0 | 666 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0009 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0010 | 0/0 | 666 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0011 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0012 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0013 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0014 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0015 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0016 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0017 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0018 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
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 | 0/1 | 2001 | 121 | 34 | 25 | 39 | 8 | 14 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0002 | 1/0 | 2001 | 76 | 19 | 15 | 31 | 1 | 9 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0003 | 0/0 | 2001 | 11 | 1 | 2 | 6 | 0 | 2 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0004 | 0/0 | 2001 | 9 | 9 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0005 | 0/0 | 2001 | 7 | 0 | 1 | 6 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0006 | 0/0 | 2001 | 6 | 6 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0007 | 0/0 | 2001 | 6 | 0 | 3 | 0 | 3 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0008 | 0/0 | 2001 | 3 | 3 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0009 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0010 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0011 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0012 | 0/0 | 2001 | 2 | 1 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0013 | 0/0 | 2001 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0014 | 0/0 | 2001 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0015 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0016 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0017 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0018 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0019 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0020 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0021 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0022 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0023 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0024 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
c0025 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
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 | 1/1 | 734 | 226 | 62 | 46 | 81 | 12 | 23 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
t0002 | 0/0 | 734 | 26 | 19 | 0 | 6 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
t0003 | 0/0 | 734 | 5 | 5 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
t0004 | 0/0 | 734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
t0005 | 0/0 | 734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
t0006 | 0/0 | 734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
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 | 0/1 | 2001 | 121 | 34 | 25 | 39 | 8 | 14 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0017 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0020 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0024 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002c0002 | 1/0 | 2001 | 76 | 19 | 15 | 31 | 1 | 9 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0004 | 0/0 | 2001 | 9 | 9 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0005 | 0/0 | 2001 | 7 | 0 | 1 | 6 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0011 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0012 | 0/0 | 2001 | 2 | 1 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004c0003 | 0/0 | 2001 | 11 | 1 | 2 | 6 | 0 | 2 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004c0019 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0005c0006 | 0/0 | 2001 | 6 | 6 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0006c0007 | 0/0 | 2001 | 6 | 0 | 3 | 0 | 3 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0007c0008 | 0/0 | 2001 | 3 | 3 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0008c0014 | 0/0 | 2001 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0009c0010 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0010c0013 | 0/0 | 2001 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0011c0009 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0012c0021 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0013c0016 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0014c0023 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0015c0025 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0016c0022 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0017c0018 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0018c0015 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2734 | 116 | 29 | 25 | 39 | 8 | 14 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0001t0003 | 0/0 | 2734 | 5 | 5 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0017t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0020t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0001c0024t0001 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002c0002t0001 | 1/0 | 2734 | 71 | 19 | 15 | 30 | 1 | 5 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002c0002t0004 | 0/0 | 2734 | 3 | 0 | 0 | 0 | 0 | 3 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002c0002t0005 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0002c0002t0006 | 0/0 | 2734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0004t0002 | 0/0 | 2734 | 9 | 9 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0005t0001 | 0/0 | 2734 | 7 | 0 | 1 | 6 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0011t0001 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0003c0012t0002 | 0/0 | 2734 | 2 | 1 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004c0003t0001 | 0/0 | 2734 | 6 | 0 | 2 | 2 | 0 | 2 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004c0003t0002 | 0/0 | 2734 | 5 | 1 | 0 | 4 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0004c0019t0002 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0005c0006t0001 | 0/0 | 2734 | 6 | 6 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0006c0007t0001 | 0/0 | 2734 | 6 | 0 | 3 | 0 | 3 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0007c0008t0002 | 0/0 | 2734 | 3 | 3 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0008c0014t0001 | 0/0 | 2734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0009c0010t0002 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0010c0013t0002 | 0/0 | 2734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0011c0009t0002 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0012c0021t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0013c0016t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0014c0023t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0015c0025t0001 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0016c0022t0001 | 0/0 | 2734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0017c0018t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
a0018c0015t0001 | 0/0 | 2734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | copy fasta | chr19 | 6130667 | 6198091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0017t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0020t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0001c0024t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0002c0002t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0004t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0011t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0011t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0012t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0003c0012t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0004c0019t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0005c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0006c0007t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0007c0008t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0007c0008t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0007c0008t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0008c0014t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0008c0014t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0009c0010t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0009c0010t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0010c0013t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0010c0013t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0011c0009t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0011c0009t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0012c0021t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0013c0016t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0014c0023t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0015c0025t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0016c0022t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0017c0018t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
a0018c0015t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00099 | hp2 | a0006 | c0007 | t0001 | g0060 | EUR | GBR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00140 | hp1 | a0006 | c0007 | t0001 | g0064 | EUR | GBR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00597 | hp1 | a0015 | c0025 | t0001 | g0061 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00673 | hp2 | a0001 | c0024 | t0001 | g0036 | EAS | CHS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01069 | hp1 | a0004 | c0003 | t0001 | g0048 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01071 | hp2 | a0004 | c0003 | t0001 | g0047 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01074 | hp1 | a0006 | c0007 | t0001 | g0059 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01168 | hp1 | a0006 | c0007 | t0001 | g0058 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01169 | hp2 | a0006 | c0007 | t0001 | g0065 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01433 | hp1 | a0003 | c0005 | t0001 | g0133 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0092 | EUR | IBS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01884 | hp1 | a0001 | c0017 | t0001 | g0239 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01884 | hp2 | a0011 | c0009 | t0002 | g0147 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01891 | hp1 | a0013 | c0016 | t0001 | g0014 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02027 | hp1 | a0004 | c0003 | t0002 | g0137 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02055 | hp2 | a0003 | c0004 | t0002 | g0009 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02080 | hp1 | a0010 | c0013 | t0002 | g0110 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02129 | hp1 | a0004 | c0003 | t0002 | g0134 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02145 | hp1 | a0005 | c0006 | t0001 | g0018 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | CDX | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | CDX | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02258 | hp1 | a0003 | c0004 | t0002 | g0011 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02572 | hp2 | a0014 | c0023 | t0001 | g0201 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02602 | hp1 | a0002 | c0002 | t0004 | g0097 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02622 | hp2 | a0007 | c0008 | t0002 | g0161 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02630 | hp1 | a0007 | c0008 | t0002 | g0145 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02630 | hp2 | a0003 | c0004 | t0002 | g0006 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02647 | hp2 | a0005 | c0006 | t0001 | g0028 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02723 | hp1 | a0012 | c0021 | t0001 | g0100 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02723 | hp2 | a0017 | c0018 | t0001 | g0148 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02886 | hp2 | a0005 | c0006 | t0001 | g0027 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02895 | hp2 | a0004 | c0003 | t0002 | g0138 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02897 | hp1 | a0003 | c0004 | t0002 | g0013 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03017 | hp2 | a0002 | c0002 | t0006 | g0069 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03098 | hp1 | a0005 | c0006 | t0001 | g0025 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03130 | hp2 | a0001 | c0020 | t0001 | g0051 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03139 | hp1 | a0005 | c0006 | t0001 | g0026 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03139 | hp2 | a0003 | c0004 | t0002 | g0012 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03195 | hp2 | a0009 | c0010 | t0002 | g0052 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03209 | hp1 | a0011 | c0009 | t0002 | g0164 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03209 | hp2 | a0009 | c0010 | t0002 | g0054 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03453 | hp1 | a0003 | c0012 | t0002 | g0197 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03453 | hp2 | a0003 | c0011 | t0001 | g0144 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03486 | hp1 | a0003 | c0004 | t0002 | g0010 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03492 | hp2 | a0018 | c0015 | t0001 | g0257 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03516 | hp2 | a0003 | c0004 | t0002 | g0007 | AFR | ESN | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03579 | hp1 | a0005 | c0006 | t0001 | g0023 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03654 | hp2 | a0002 | c0002 | t0004 | g0106 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03669 | hp1 | a0004 | c0003 | t0001 | g0044 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03834 | hp2 | a0003 | c0012 | t0002 | g0046 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04199 | hp1 | a0004 | c0003 | t0001 | g0049 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04199 | hp2 | a0002 | c0002 | t0004 | g0247 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04228 | hp1 | a0016 | c0022 | t0001 | g0075 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18522 | hp1 | a0004 | c0019 | t0002 | g0050 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18612 | hp2 | a0004 | c0003 | t0002 | g0135 | EAS | CHB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18747 | hp1 | a0004 | c0003 | t0001 | g0043 | EAS | CHB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18945 | hp2 | a0008 | c0014 | t0001 | g0119 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18973 | hp2 | a0003 | c0005 | t0001 | g0243 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18974 | hp2 | a0008 | c0014 | t0001 | g0246 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18975 | hp2 | a0003 | c0005 | t0001 | g0242 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18980 | hp2 | a0010 | c0013 | t0002 | g0114 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18981 | hp1 | a0002 | c0002 | t0005 | g0116 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18983 | hp2 | a0003 | c0005 | t0001 | g0244 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19000 | hp1 | a0004 | c0003 | t0002 | g0136 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19012 | hp2 | a0004 | c0003 | t0001 | g0045 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19030 | hp2 | a0003 | c0011 | t0001 | g0160 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19066 | hp2 | a0003 | c0005 | t0001 | g0241 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19077 | hp2 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19085 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | YRI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20752 | hp1 | a0006 | c0007 | t0001 | g0057 | EUR | TSI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | GIH | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02109 | hp1 | a0003 | c0004 | t0002 | g0008 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02486 | hp2 | a0007 | c0008 | t0002 | g0162 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02559 | hp1 | a0003 | c0004 | t0002 | g0131 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | USA | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | USA | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | LWK | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0255 | REF | REF | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0080 | REF | REF | ACSBG2_chr19_6130667_6198091 | ACSBG2 | chr19 | 6130667 | 6198091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:6141562
|
A | G | 1 | a0008 | 2 | NA18945.hp2 NA18974.hp2 |
missense_variant | MODERATE | c.19A>G | p.Thr7Ala | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/15 | 293/2734 | 19/2001 | 7/666 | chr19 | 6141562 | ||
chr19:6141582
|
T | A | 1 | a0018 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.39T>A | p.Asp13Glu | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/15 | 313/2734 | 39/2001 | 13/666 | chr19 | 6141582 | ||
chr19:6147665
|
C | A | 3 | a0007a0011a0017 | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.287C>A | p.Ser96Tyr | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/15 | 561/2734 | 287/2001 | 96/666 | chr19 | 6147665 | ||
chr19:6151720
|
G | A | 1 | a0012 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.311G>A | p.Arg104His | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/15 | 585/2734 | 311/2001 | 104/666 | chr19 | 6151720 | ||
chr19:6151766
|
T | A | 1 | a0016 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.357T>A | p.Phe119Leu | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/15 | 631/2734 | 357/2001 | 119/666 | chr19 | 6151766 | ||
chr19:6151788
|
C | A | 1 | a0013 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.379C>A | p.Leu127Ile | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/15 | 653/2734 | 379/2001 | 127/666 | chr19 | 6151788 | ||
chr19:6156472
|
T | C | 10 | a0001a0003a0004others(7): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
missense_variant | MODERATE | c.428T>C | p.Val143Ala | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/15 | 702/2734 | 428/2001 | 143/666 | chr19 | 6156472 | ||
chr19:6156499
|
A | G | 1 | a0006 | 6 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(3): Show |
missense_variant | MODERATE | c.455A>G | p.Lys152Arg | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/15 | 729/2734 | 455/2001 | 152/666 | chr19 | 6156499 | ||
chr19:6165891
|
G | A | 1 | a0011 | 2 | HG01884.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.614G>A | p.Arg205Lys | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/15 | 888/2734 | 614/2001 | 205/666 | chr19 | 6165891 | ||
chr19:6165983
|
A | T | 1 | a0015 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.706A>T | p.Ile236Leu | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/15 | 980/2734 | 706/2001 | 236/666 | chr19 | 6165983 | ||
chr19:6187666
|
G | A | 1 | a0009 | 2 | HG03195.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.1748G>A | p.Arg583Gln | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2022/2734 | 1748/2001 | 583/666 | chr19 | 6187666 | ||
chr19:6187669
|
G | A | 4 | a0004a0007a0010others(1): Show | 19 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
missense_variant | MODERATE | c.1751G>A | p.Gly584Asp | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2025/2734 | 1751/2001 | 584/666 | chr19 | 6187669 | ||
chr19:6187675
|
G | A | 4 | a0004a0007a0010others(1): Show | 19 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
missense_variant | MODERATE | c.1757G>A | p.Gly586Asp | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2031/2734 | 1757/2001 | 586/666 | chr19 | 6187675 | ||
chr19:6187720
|
C | G | 2 | a0005a0014 | 7 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.1802C>G | p.Pro601Arg | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2076/2734 | 1802/2001 | 601/666 | chr19 | 6187720 | ||
chr19:6187789
|
G | A | 7 | a0003a0004a0007others(4): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
missense_variant | MODERATE | c.1871G>A | p.Arg624Lys | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2145/2734 | 1871/2001 | 624/666 | chr19 | 6187789 | ||
chr19:6187794
|
G | C | 7 | a0003a0004a0007others(4): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
missense_variant | MODERATE | c.1876G>C | p.Glu626Gln | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2150/2734 | 1876/2001 | 626/666 | chr19 | 6187794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:6147459
|
G | A | 1 | a0013c0016 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.81G>A | p.Leu27Leu | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/15 | 355/2734 | 81/2001 | 27/666 | chr19 | 6147459 | ||
chr19:6147471
|
T | C | 1 | a0001c0017 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.93T>C | p.Cys31Cys | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/15 | 367/2734 | 93/2001 | 31/666 | chr19 | 6147471 | ||
chr19:6151712
|
T | C | 6 | a0001c0020a0003c0004a0003c0005others(3): Show | 21 | HG01433.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
synonymous_variant | LOW | c.303T>C | p.Gly101Gly | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/15 | 577/2734 | 303/2001 | 101/666 | chr19 | 6151712 | ||
chr19:6165982
|
C | T | 1 | a0001c0024 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.705C>T | p.Gly235Gly | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/15 | 979/2734 | 705/2001 | 235/666 | chr19 | 6165982 | ||
chr19:6183222
|
G | A | 11 | a0003c0004a0003c0005a0003c0011others(8): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
synonymous_variant | LOW | c.1272G>A | p.Glu424Glu | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/15 | 1546/2734 | 1272/2001 | 424/666 | chr19 | 6183222 | ||
chr19:6187646
|
C | T | 11 | a0003c0004a0003c0005a0003c0011others(8): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
synonymous_variant | LOW | c.1728C>T | p.Phe576Phe | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/15 | 2002/2734 | 1728/2001 | 576/666 | chr19 | 6187646 | ||
chr19:6190588
|
A | G | 3 | a0003c0004a0003c0012a0009c0010 | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.1932A>G | p.Pro644Pro | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/15 | 2206/2734 | 1932/2001 | 644/666 | chr19 | 6190588 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:6135676
|
A | G | 1 | a0002c0002t0004 | 3 | HG02602.hp1 HG03654.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-265A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/15 | 5868 | chr19 | 6135676 | |||||
chr19:6141523
|
C | A | 1 | a0002c0002t0005 | 1 | NA18981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-21C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/15 | 21 | chr19 | 6141523 | |||||
chr19:6192725
|
C | A | 1 | a0001c0001t0003 | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*93C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2068 | chr19 | 6192725 | |||||
chr19:6192807
|
C | T | 8 | a0003c0004t0002a0003c0012t0002a0004c0003t0002others(5): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2150 | chr19 | 6192807 | |||||
chr19:6192842
|
T | G | 8 | a0003c0004t0002a0003c0012t0002a0004c0003t0002others(5): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*210T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2185 | chr19 | 6192842 | |||||
chr19:6192894
|
C | T | 1 | a0002c0002t0006 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2237 | chr19 | 6192894 | |||||
chr19:6192916
|
C | G | 8 | a0003c0004t0002a0003c0012t0002a0004c0003t0002others(5): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2259 | chr19 | 6192916 | |||||
chr19:6192971
|
C | T | 8 | a0003c0004t0002a0003c0012t0002a0004c0003t0002others(5): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 15/15 | 2314 | chr19 | 6192971 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:6136107
|
A | AT | 16 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(13): Show | 16 | HG00280.hp2 HG00741.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.-32+214dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6136107 | |||||
chr19:6136107
|
AT | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 40 | HG00673.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-32+214delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6136107 | |||||
chr19:6136137
|
G | A | 13 | a0001c0001t0001g0053a0001c0020t0001g0051a0002c0002t0001g0042others(10): Show | 13 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+228G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136137 | ||||||
chr19:6136138
|
C | A | 13 | a0001c0001t0001g0053a0001c0020t0001g0051a0002c0002t0001g0042others(10): Show | 13 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+229C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136138 | ||||||
chr19:6136144
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00642.hp2 HG01070.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+235T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136144 | ||||||
chr19:6136145
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00642.hp2 HG01070.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+236G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136145 | ||||||
chr19:6136149
|
A | AGGCTGGA others(7): Show |
180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-32+243_-32+244ins others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6136149 | |||||
chr19:6136149
|
A | AGGCTGGA others(7): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG02559.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-32+243_-32+244ins others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6136149 | |||||
chr19:6136216
|
T | C | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32+307T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136216 | ||||||
chr19:6136248
|
T | C | 1 | a0003c0005t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-32+339T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136248 | ||||||
chr19:6136400
|
A | G | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32+491A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136400 | ||||||
chr19:6136431
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32+522C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136431 | ||||||
chr19:6136477
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-32+568C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136477 | ||||||
chr19:6136503
|
T | C | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 31 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.-32+594T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136503 | ||||||
chr19:6136508
|
ACG | A | 4 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(1): Show | 4 | HG02027.hp1 HG02129.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+603_-32+604del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6136508 | |||||
chr19:6136509
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+600C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136509 | ||||||
chr19:6136512
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-32+603G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136512 | ||||||
chr19:6136523
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+614C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136523 | ||||||
chr19:6136606
|
A | G | 14 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(11): Show | 14 | HG01934.hp1 HG02647.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32+697A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136606 | ||||||
chr19:6136609
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-32+700C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6136609 | ||||||
chr19:6137156
|
T | C | 26 | a0001c0001t0001g0015a0002c0002t0001g0019a0002c0002t0001g0020others(23): Show | 26 | HG01891.hp1 HG01934.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-32+1247T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137156 | ||||||
chr19:6137208
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-32+1299T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137208 | ||||||
chr19:6137209
|
T | TG | 49 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0038others(46): Show | 49 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-32+1316dupG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6137209 | |||||
chr19:6137209
|
TG | T | 63 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0034others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-32+1316delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6137209 | |||||
chr19:6137209
|
TGG | T | 34 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+1315_-32+1316d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6137209 | |||||
chr19:6137209
|
TGGG | T | 24 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(21): Show | 24 | HG01934.hp1 HG02129.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32+1314_-32+1316d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6137209 | |||||
chr19:6137211
|
G | A | 1 | a0004c0003t0002g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-32+1302G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137211 | ||||||
chr19:6137211
|
G | GC | 3 | a0001c0020t0001g0051a0004c0019t0002g0050a0009c0010t0002g0052 | 3 | HG03130.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-32+1302_-32+1303i others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137211 | ||||||
chr19:6137211
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-32+1302G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137211 | ||||||
chr19:6137212
|
G | C | 3 | a0004c0003t0001g0047a0004c0003t0001g0048a0004c0003t0001g0049 | 3 | HG01069.hp1 HG01071.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-32+1303G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137212 | ||||||
chr19:6137213
|
G | C | 5 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(2): Show | 5 | HG03669.hp1 HG03834.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+1304G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137213 | ||||||
chr19:6137218
|
G | A | 1 | a0006c0007t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-32+1309G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137218 | ||||||
chr19:6137218
|
G | T | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32+1309G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137218 | ||||||
chr19:6137220
|
G | T | 4 | a0003c0005t0001g0001a0003c0005t0001g0242a0003c0005t0001g0243others(1): Show | 5 | NA18973.hp2 NA18975.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+1311G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137220 | ||||||
chr19:6137222
|
G | A | 9 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32+1313G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137222 | ||||||
chr19:6137455
|
G | A | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+1546G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137455 | ||||||
chr19:6137613
|
T | A | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32+1704T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137613 | ||||||
chr19:6137743
|
G | A | 8 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+1834G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137743 | ||||||
chr19:6137791
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+1882G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137791 | ||||||
chr19:6137799
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-32+1890C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137799 | ||||||
chr19:6137847
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+1938C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137847 | ||||||
chr19:6137944
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-32+2035A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6137944 | ||||||
chr19:6138016
|
A | G | 49 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(46): Show | 50 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-32+2107A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138016 | ||||||
chr19:6138032
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-32+2123G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138032 | ||||||
chr19:6138041
|
C | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-32+2132C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138041 | ||||||
chr19:6138095
|
C | T | 1 | a0002c0002t0001g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-32+2186C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138095 | ||||||
chr19:6138099
|
G | GGTAGTTT others(7): Show |
1 | a0002c0002t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-32+2191_-32+2204d others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138099 | |||||
chr19:6138460
|
A | AAG | 3 | a0001c0001t0001g0132a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG02922.hp2 NA18906.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-32+2558_-32+2559d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138460 | |||||
chr19:6138469
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-32+2560G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138469 | ||||||
chr19:6138479
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-32+2570A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138479 | ||||||
chr19:6138493
|
G | A | 1 | a0002c0002t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-32+2584G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138493 | ||||||
chr19:6138536
|
GGGGA | G | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+2642_-32+2645d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138536 | |||||
chr19:6138543
|
GAGGGAGG others(17): Show |
G | 8 | a0002c0002t0001g0072a0002c0002t0001g0099a0002c0002t0001g0101others(5): Show | 8 | HG02004.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32+2646_-32+2669d others(26): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138543 | |||||
chr19:6138551
|
GAGGAAGG others(1): Show |
G | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+2648_-32+2655d others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138551 | |||||
chr19:6138553
|
GGAA | G | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32+2646_-32+2648d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138553 | |||||
chr19:6138585
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-32+2676A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138585 | ||||||
chr19:6138593
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-32+2684A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138593 | ||||||
chr19:6138602
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-32+2693G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138602 | ||||||
chr19:6138602
|
G | GAGGA | 26 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(23): Show | 26 | HG01884.hp1 HG01884.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-32+2709_-32+2712d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138602 | |||||
chr19:6138602
|
G | GAGGAAGG others(1): Show |
126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-32+2705_-32+2712d others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138602 | |||||
chr19:6138606
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+2697A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138606 | ||||||
chr19:6138610
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+2701A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138610 | ||||||
chr19:6138618
|
AAGGGG | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+2713_-32+2717d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138618 | |||||
chr19:6138625
|
G | A | 1 | a0002c0002t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-32+2716G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138625 | ||||||
chr19:6138630
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+2721A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138630 | ||||||
chr19:6138633
|
GAAAGGAA others(23): Show |
G | 14 | a0002c0002t0001g0042a0003c0005t0001g0001a0003c0005t0001g0133others(11): Show | 15 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32+2730_-32+2759d others(32): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138633 | |||||
chr19:6138634
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+2725A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138634 | ||||||
chr19:6138642
|
GGAAGGGA others(1): Show |
G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+2739_-32+2746d others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138642 | |||||
chr19:6138650
|
AGAAGGAA others(26): Show |
A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-32+2751_-32+2783d others(35): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138650 | |||||
chr19:6138652
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+2743A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138652 | ||||||
chr19:6138662
|
GA | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+2757delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6138662 | |||||
chr19:6138669
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32+2760C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138669 | ||||||
chr19:6138673
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+2764G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138673 | ||||||
chr19:6138683
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32+2774G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138683 | ||||||
chr19:6138690
|
A | G | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-32+2781A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138690 | ||||||
chr19:6138705
|
G | A | 1 | a0002c0002t0001g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-32+2796G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138705 | ||||||
chr19:6138716
|
A | G | 14 | a0002c0002t0001g0042a0003c0005t0001g0001a0003c0005t0001g0133others(11): Show | 15 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31-2797A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138716 | ||||||
chr19:6138931
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-2582T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138931 | ||||||
chr19:6138950
|
C | A | 1 | a0003c0004t0002g0006 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-31-2563C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6138950 | ||||||
chr19:6139047
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-2466G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139047 | ||||||
chr19:6139089
|
C | T | 30 | a0001c0001t0001g0053a0001c0020t0001g0051a0002c0002t0001g0019others(27): Show | 30 | HG00741.hp2 HG01891.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.-31-2424C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139089 | ||||||
chr19:6139091
|
T | A | 30 | a0001c0001t0001g0053a0001c0020t0001g0051a0002c0002t0001g0019others(27): Show | 30 | HG00741.hp2 HG01891.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.-31-2422T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139091 | ||||||
chr19:6139092
|
A | AT | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-31-2408dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6139092 | |||||
chr19:6139092
|
ATT | A | 30 | a0001c0001t0001g0053a0001c0020t0001g0051a0002c0002t0001g0019others(27): Show | 30 | HG00741.hp2 HG01891.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.-31-2409_-31-2408d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6139092 | |||||
chr19:6139094
|
T | TA | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-2419_-31-2418i others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139094 | ||||||
chr19:6139118
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0199 | 3 | HG01952.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-31-2395T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139118 | ||||||
chr19:6139133
|
G | C | 1 | a0002c0002t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-31-2380G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139133 | ||||||
chr19:6139134
|
C | G | 1 | a0002c0002t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-31-2379C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139134 | ||||||
chr19:6139165
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-31-2348A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139165 | ||||||
chr19:6139186
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31-2327C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139186 | ||||||
chr19:6139389
|
C | T | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31-2124C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139389 | ||||||
chr19:6139420
|
GCCACCTG others(27): Show |
G | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-31-2092_-31-2059d others(36): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139420 | ||||||
chr19:6139471
|
A | G | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-2042A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139471 | ||||||
chr19:6139612
|
G | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-31-1901G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139612 | ||||||
chr19:6139614
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-31-1899G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139614 | ||||||
chr19:6139624
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-31-1889C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139624 | ||||||
chr19:6139644
|
C | T | 1 | a0003c0011t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-31-1869C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139644 | ||||||
chr19:6139660
|
C | T | 14 | a0002c0002t0001g0042a0003c0005t0001g0001a0003c0005t0001g0133others(11): Show | 15 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31-1853C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139660 | ||||||
chr19:6139791
|
A | G | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-1722A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139791 | ||||||
chr19:6139907
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-31-1606T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139907 | ||||||
chr19:6139938
|
C | A | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-31-1575C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139938 | ||||||
chr19:6139952
|
G | A | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-1561G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139952 | ||||||
chr19:6139989
|
C | T | 1 | a0006c0007t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-31-1524C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6139989 | ||||||
chr19:6140005
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31-1508C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140005 | ||||||
chr19:6140179
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-31-1334C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140179 | ||||||
chr19:6140224
|
C | CA | 21 | a0001c0001t0001g0139a0001c0001t0001g0140a0002c0002t0001g0063others(18): Show | 22 | HG01433.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-1274dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6140224 | |||||
chr19:6140224
|
C | CAA | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-31-1275_-31-1274d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6140224 | |||||
chr19:6140548
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-31-965C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140548 | ||||||
chr19:6140571
|
T | C | 1 | a0002c0002t0001g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-31-942T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140571 | ||||||
chr19:6140640
|
A | T | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-873A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140640 | ||||||
chr19:6140711
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-31-802T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140711 | ||||||
chr19:6140723
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-31-790G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140723 | ||||||
chr19:6140743
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-31-770G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140743 | ||||||
chr19:6140784
|
C | A | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-729C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140784 | ||||||
chr19:6140796
|
C | CT | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-711dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 6140796 | |||||
chr19:6140846
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-31-667G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140846 | ||||||
chr19:6140905
|
C | T | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-608C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140905 | ||||||
chr19:6140941
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-31-572G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6140941 | ||||||
chr19:6141019
|
C | T | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-494C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141019 | ||||||
chr19:6141089
|
G | T | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-424G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141089 | ||||||
chr19:6141126
|
C | T | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-387C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141126 | ||||||
chr19:6141308
|
A | T | 1 | a0002c0002t0001g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-31-205A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141308 | ||||||
chr19:6141362
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01981.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-31-151C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141362 | ||||||
chr19:6141460
|
C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-31-53C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141460 | ||||||
chr19:6141497
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-31-16C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | chr19 | 6141497 | ||||||
chr19:6141743
|
T | G | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.67+133T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6141743 | ||||||
chr19:6141747
|
G | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.67+137G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6141747 | ||||||
chr19:6141798
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.67+188G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6141798 | ||||||
chr19:6141927
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.67+317C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6141927 | ||||||
chr19:6142032
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.67+422A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142032 | ||||||
chr19:6142119
|
A | G | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+509A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142119 | ||||||
chr19:6142366
|
G | C | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+756G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142366 | ||||||
chr19:6142524
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.67+914A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142524 | ||||||
chr19:6142709
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.67+1099T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142709 | ||||||
chr19:6142752
|
C | CA | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0192others(3): Show | 6 | HG00558.hp2 HG02132.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1158dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6142752 | |||||
chr19:6142752
|
C | CAA | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.67+1157_67+1158dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6142752 | |||||
chr19:6142752
|
C | CAAA | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1156_67+1158dup others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6142752 | |||||
chr19:6142752
|
CA | C | 16 | a0002c0002t0001g0042a0002c0002t0001g0062a0002c0002t0001g0098others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+1158delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6142752 | |||||
chr19:6142759
|
A | C | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.67+1149A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142759 | ||||||
chr19:6142796
|
A | C | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+1186A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142796 | ||||||
chr19:6142837
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.67+1227G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142837 | ||||||
chr19:6142890
|
T | C | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+1280T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142890 | ||||||
chr19:6142973
|
A | G | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+1363A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142973 | ||||||
chr19:6142991
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.67+1381G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142991 | ||||||
chr19:6142998
|
T | C | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+1388T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6142998 | ||||||
chr19:6143085
|
T | C | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+1475T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143085 | ||||||
chr19:6143087
|
G | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+1477G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143087 | ||||||
chr19:6143120
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.67+1510T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143120 | ||||||
chr19:6143126
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1516C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143126 | ||||||
chr19:6143158
|
C | A | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1548C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143158 | ||||||
chr19:6143188
|
T | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.67+1578T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143188 | ||||||
chr19:6143211
|
AT | A | 25 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+1613delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143211 | |||||
chr19:6143383
|
C | CA | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+1780dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143383 | |||||
chr19:6143385
|
AAAAAAC | A | 15 | a0001c0001t0003g0146a0002c0002t0001g0019a0002c0002t0001g0020others(12): Show | 15 | HG01934.hp1 HG02615.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+1803_67+1808del others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143385 | |||||
chr19:6143410
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.67+1800A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143410 | ||||||
chr19:6143581
|
CTACAGTC others(2): Show |
C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1974_67+1982del others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143581 | |||||
chr19:6143621
|
C | G | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2011C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143621 | ||||||
chr19:6143647
|
A | T | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.67+2037A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143647 | ||||||
chr19:6143950
|
G | A | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+2340G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143950 | ||||||
chr19:6143972
|
TTTG | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+2371_67+2373del others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143972 | |||||
chr19:6143991
|
T | C | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+2381T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6143991 | ||||||
chr19:6143996
|
AGTTT | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2396_67+2399del others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6143996 | |||||
chr19:6144074
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.67+2464T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144074 | ||||||
chr19:6144081
|
T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2471T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144081 | ||||||
chr19:6144090
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.67+2480C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144090 | ||||||
chr19:6144182
|
G | T | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2572G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144182 | ||||||
chr19:6144199
|
T | C | 1 | a0004c0003t0002g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.67+2589T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144199 | ||||||
chr19:6144206
|
G | A | 7 | a0001c0001t0001g0171a0003c0005t0001g0001a0003c0005t0001g0133others(4): Show | 8 | HG00140.hp2 HG01433.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+2596G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144206 | ||||||
chr19:6144347
|
A | G | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2737A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144347 | ||||||
chr19:6144399
|
G | A | 1 | a0006c0007t0001g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67+2789G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144399 | ||||||
chr19:6144439
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+2829T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144439 | ||||||
chr19:6144721
|
G | A | 15 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(12): Show | 15 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-2725G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144721 | ||||||
chr19:6144744
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.68-2702G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144744 | ||||||
chr19:6144757
|
C | A | 1 | a0002c0002t0001g0076 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.68-2689C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144757 | ||||||
chr19:6144896
|
A | G | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-2550A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144896 | ||||||
chr19:6144997
|
T | C | 3 | a0006c0007t0001g0058a0006c0007t0001g0059a0006c0007t0001g0065 | 3 | HG01074.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.68-2449T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6144997 | ||||||
chr19:6145020
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.68-2426C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145020 | ||||||
chr19:6145047
|
A | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.68-2399A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145047 | ||||||
chr19:6145121
|
G | A | 14 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(11): Show | 14 | HG01934.hp1 HG02647.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-2325G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145121 | ||||||
chr19:6145138
|
C | A | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-2308C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145138 | ||||||
chr19:6145165
|
G | A | 4 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(1): Show | 4 | HG02027.hp1 HG02129.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2281G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145165 | ||||||
chr19:6145173
|
C | T | 1 | a0005c0006t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-2273C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145173 | ||||||
chr19:6145279
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-2167C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145279 | ||||||
chr19:6145281
|
C | T | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-2165C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145281 | ||||||
chr19:6145345
|
C | T | 15 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(12): Show | 15 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-2101C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145345 | ||||||
chr19:6145363
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68-2083G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145363 | ||||||
chr19:6145429
|
C | CA | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0040others(3): Show | 6 | HG01891.hp2 HG01934.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-2000dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6145429 | |||||
chr19:6145429
|
CA | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.68-2000delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6145429 | |||||
chr19:6145429
|
CAA | C | 8 | a0002c0002t0001g0072a0002c0002t0001g0099a0002c0002t0001g0101others(5): Show | 8 | HG02004.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-2001_68-2000del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6145429 | |||||
chr19:6145448
|
T | G | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68-1998T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145448 | ||||||
chr19:6145461
|
T | C | 5 | a0001c0001t0001g0053a0001c0020t0001g0051a0004c0019t0002g0050others(2): Show | 5 | HG00741.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1985T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145461 | ||||||
chr19:6145553
|
G | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.68-1893G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145553 | ||||||
chr19:6145975
|
T | C | 1 | a0004c0003t0002g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.68-1471T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145975 | ||||||
chr19:6145990
|
C | A | 1 | a0002c0002t0001g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.68-1456C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6145990 | ||||||
chr19:6146196
|
G | A | 3 | a0001c0001t0001g0150a0003c0012t0002g0197a0014c0023t0001g0201 | 3 | HG02257.hp2 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68-1250G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146196 | ||||||
chr19:6146198
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1248G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146198 | ||||||
chr19:6146247
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.68-1199A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146247 | ||||||
chr19:6146257
|
G | A | 6 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-1189G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146257 | ||||||
chr19:6146341
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-1105G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146341 | ||||||
chr19:6146473
|
A | AAAT | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.68-965_68-963dupAT others(1): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6146473 | |||||
chr19:6146492
|
G | A | 3 | a0006c0007t0001g0058a0006c0007t0001g0059a0006c0007t0001g0065 | 3 | HG01074.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.68-954G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146492 | ||||||
chr19:6146564
|
G | A | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-882G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146564 | ||||||
chr19:6146570
|
A | C | 1 | a0006c0007t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.68-876A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146570 | ||||||
chr19:6146620
|
C | T | 1 | a0003c0005t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-826C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146620 | ||||||
chr19:6146777
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-669C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146777 | ||||||
chr19:6146798
|
T | TA | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-640dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 6146798 | |||||
chr19:6146907
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 76 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.68-539G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6146907 | ||||||
chr19:6147180
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.68-266C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6147180 | ||||||
chr19:6147254
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-192G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6147254 | ||||||
chr19:6147271
|
A | C | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68-175A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6147271 | ||||||
chr19:6147331
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.68-115A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6147331 | ||||||
chr19:6147442
|
G | C | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.68-4G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | chr19 | 6147442 | ||||||
chr19:6147732
|
G | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.297+57G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6147732 | ||||||
chr19:6147919
|
T | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0172others(2): Show | 5 | NA18747.hp2 NA18963.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+244T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6147919 | ||||||
chr19:6147928
|
A | T | 14 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(11): Show | 14 | HG01934.hp1 HG02647.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+253A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6147928 | ||||||
chr19:6147928
|
AT | A | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+259delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6147928 | |||||
chr19:6148132
|
C | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+457C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148132 | ||||||
chr19:6148321
|
C | T | 10 | a0001c0001t0001g0132a0001c0001t0001g0166a0001c0001t0001g0200others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+646C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148321 | ||||||
chr19:6148388
|
G | A | 3 | a0002c0002t0004g0097a0002c0002t0004g0106a0002c0002t0004g0247 | 3 | HG02602.hp1 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.297+713G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148388 | ||||||
chr19:6148411
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.297+736C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148411 | ||||||
chr19:6148427
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.297+752C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148427 | ||||||
chr19:6148428
|
T | C | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.297+753T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148428 | ||||||
chr19:6148439
|
G | A | 2 | a0001c0020t0001g0051a0004c0019t0002g0050 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.297+764G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148439 | ||||||
chr19:6148571
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+896G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148571 | ||||||
chr19:6148618
|
T | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+943T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148618 | ||||||
chr19:6148647
|
G | GA | 12 | a0002c0002t0001g0042a0002c0002t0001g0107a0003c0012t0002g0046others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+987dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6148647 | |||||
chr19:6148647
|
GA | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+987delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6148647 | |||||
chr19:6148647
|
GAAAA | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.297+984_297+987del others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6148647 | |||||
chr19:6148777
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.297+1102C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148777 | ||||||
chr19:6148789
|
G | A | 1 | a0004c0003t0001g0047 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.297+1114G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148789 | ||||||
chr19:6148802
|
C | A | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.297+1127C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148802 | ||||||
chr19:6148803
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.297+1128C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6148803 | ||||||
chr19:6149031
|
C | T | 11 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(8): Show | 11 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+1356C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149031 | ||||||
chr19:6149195
|
G | T | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+1520G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149195 | ||||||
chr19:6149338
|
A | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG01884.hp2 HG02027.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+1663A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149338 | ||||||
chr19:6149493
|
T | G | 1 | a0002c0002t0001g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+1818T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149493 | ||||||
chr19:6149504
|
C | CT | 22 | a0002c0002t0001g0019a0002c0002t0001g0021a0002c0002t0001g0022others(19): Show | 22 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.297+1851dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6149504 | |||||
chr19:6149504
|
CT | C | 20 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(17): Show | 21 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+1851delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6149504 | |||||
chr19:6149504
|
CTTT | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.297+1849_297+1851d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6149504 | |||||
chr19:6149504
|
CTTTTTT | C | 7 | a0002c0002t0001g0042a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+1846_297+1851d others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6149504 | |||||
chr19:6149663
|
C | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+1988C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149663 | ||||||
chr19:6149663
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.297+1988C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149663 | ||||||
chr19:6149667
|
C | G | 8 | a0002c0002t0001g0042a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+1992C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149667 | ||||||
chr19:6149684
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.297+2009A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149684 | ||||||
chr19:6149706
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.298-2001T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149706 | ||||||
chr19:6149727
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1980C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149727 | ||||||
chr19:6149759
|
TGGCCTCC others(129): Show |
T | 21 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(18): Show | 22 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.298-1920_298-1785d others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6149759 | |||||
chr19:6149781
|
T | G | 1 | a0002c0002t0006g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.298-1926T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149781 | ||||||
chr19:6149884
|
T | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.298-1823T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149884 | ||||||
chr19:6149926
|
G | A | 15 | a0001c0001t0001g0053a0001c0020t0001g0051a0003c0004t0002g0006others(12): Show | 15 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.298-1781G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149926 | ||||||
chr19:6149936
|
G | A | 12 | a0002c0002t0001g0063a0002c0002t0001g0074a0002c0002t0001g0077others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.298-1771G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6149936 | ||||||
chr19:6150103
|
T | TAATAA | 2 | a0004c0003t0002g0134a0004c0003t0002g0137 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.298-1582_298-1578d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6150103 | |||||
chr19:6150340
|
C | CA | 33 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(30): Show | 33 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.298-1349dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6150340 | |||||
chr19:6150340
|
C | CAAAA | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1352_298-1349d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6150340 | |||||
chr19:6150567
|
T | A | 1 | a0011c0009t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298-1140T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150567 | ||||||
chr19:6150607
|
C | T | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298-1100C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150607 | ||||||
chr19:6150663
|
AG | A | 5 | a0002c0002t0001g0067a0002c0002t0001g0094a0002c0002t0001g0096others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-1043delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150663 | ||||||
chr19:6150842
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.298-865C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150842 | ||||||
chr19:6150931
|
T | G | 3 | a0001c0001t0001g0150a0003c0012t0002g0197a0014c0023t0001g0201 | 3 | HG02257.hp2 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298-776T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150931 | ||||||
chr19:6150969
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-738C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6150969 | ||||||
chr19:6151095
|
C | G | 6 | a0002c0002t0001g0063a0002c0002t0001g0074a0002c0002t0001g0077others(3): Show | 6 | HG00544.hp1 HG02027.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-612C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151095 | ||||||
chr19:6151097
|
G | A | 6 | a0002c0002t0001g0063a0002c0002t0001g0074a0002c0002t0001g0077others(3): Show | 6 | HG00544.hp1 HG02027.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-610G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151097 | ||||||
chr19:6151113
|
CA | C | 15 | a0001c0001t0001g0140a0001c0020t0001g0051a0002c0002t0001g0072others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.298-578delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 6151113 | |||||
chr19:6151468
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.298-239C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151468 | ||||||
chr19:6151538
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.298-169T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151538 | ||||||
chr19:6151637
|
G | A | 7 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-70G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151637 | ||||||
chr19:6151692
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-15C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | chr19 | 6151692 | ||||||
chr19:6152094
|
G | A | 3 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022 | 3 | HG01934.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.386+299G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152094 | ||||||
chr19:6152136
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.386+341G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152136 | ||||||
chr19:6152279
|
A | AT | 22 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(19): Show | 22 | HG00642.hp1 HG01515.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+506dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152279 | |||||
chr19:6152279
|
ATTTTTTT others(267): Show |
A | 3 | a0001c0001t0001g0150a0003c0012t0002g0197a0014c0023t0001g0201 | 3 | HG02257.hp2 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.386+502_386+775del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152279 | |||||
chr19:6152281
|
TTTTTTTT others(263): Show |
T | 1 | a0004c0003t0001g0048 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.386+506_386+775del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152281 | |||||
chr19:6152282
|
TTTTTTTT others(262): Show |
T | 6 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(3): Show | 6 | HG01071.hp2 HG03669.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+508_386+776del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152282 | |||||
chr19:6152283
|
TTTTTTTT others(261): Show |
T | 3 | a0001c0001t0001g0196a0001c0001t0001g0224a0001c0001t0001g0254 | 3 | HG00558.hp1 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.386+507_386+774del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152283 | |||||
chr19:6152284
|
TTTTTTTT others(260): Show |
T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.386+507_386+773del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152284 | |||||
chr19:6152285
|
TTTTTTTT others(259): Show |
T | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(13): Show | 16 | HG00544.hp2 HG00673.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.386+507_386+772del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152285 | |||||
chr19:6152286
|
TTTTTTTT others(258): Show |
T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0003c0004t0002g0006others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.386+507_386+771del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152286 | |||||
chr19:6152287
|
T | TG | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+492_386+493ins others(1): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152287 | ||||||
chr19:6152288
|
TTTTTTTT others(256): Show |
T | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.386+507_386+769del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152288 | |||||
chr19:6152291
|
TTTTTTTT others(253): Show |
T | 5 | a0003c0005t0001g0001a0003c0005t0001g0241a0003c0005t0001g0242others(2): Show | 6 | NA18973.hp2 NA18975.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+507_386+766del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152291 | |||||
chr19:6152292
|
TTTTTTTT others(252): Show |
T | 1 | a0003c0005t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.386+507_386+765del | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152292 | |||||
chr19:6152306
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+511C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152306 | ||||||
chr19:6152315
|
G | A | 6 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+520G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152315 | ||||||
chr19:6152332
|
G | A | 2 | a0002c0002t0001g0103a0012c0021t0001g0100 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.386+537G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152332 | ||||||
chr19:6152351
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+556C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152351 | ||||||
chr19:6152376
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+581C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152376 | ||||||
chr19:6152435
|
C | T | 20 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140others(17): Show | 20 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.386+640C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152435 | ||||||
chr19:6152439
|
C | T | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+644C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152439 | ||||||
chr19:6152456
|
A | G | 15 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.386+661A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152456 | ||||||
chr19:6152551
|
A | AT | 19 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(16): Show | 19 | HG00741.hp2 HG01884.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.386+775dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152551 | |||||
chr19:6152551
|
A | ATT | 5 | a0004c0003t0002g0136a0007c0008t0002g0161a0007c0008t0002g0162others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+774_386+775dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6152551 | |||||
chr19:6152641
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.386+846G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152641 | ||||||
chr19:6152724
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.386+929G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152724 | ||||||
chr19:6152826
|
G | T | 14 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.386+1031G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152826 | ||||||
chr19:6152886
|
T | C | 1 | a0002c0002t0001g0111 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.386+1091T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152886 | ||||||
chr19:6152913
|
A | C | 3 | a0003c0005t0001g0001a0003c0005t0001g0243a0003c0005t0001g0244 | 4 | NA18973.hp2 NA18983.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+1118A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152913 | ||||||
chr19:6152965
|
C | T | 2 | a0002c0002t0001g0103a0012c0021t0001g0100 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.386+1170C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152965 | ||||||
chr19:6152981
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+1186C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152981 | ||||||
chr19:6152983
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0259 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.386+1188C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6152983 | ||||||
chr19:6153138
|
C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.386+1343C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153138 | ||||||
chr19:6153178
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+1383C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153178 | ||||||
chr19:6153190
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.386+1395G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153190 | ||||||
chr19:6153476
|
C | T | 7 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+1681C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153476 | ||||||
chr19:6153584
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.386+1789T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153584 | ||||||
chr19:6153675
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.386+1880A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153675 | ||||||
chr19:6153859
|
TAAAGA | T | 54 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 55 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.386+2084_386+2088d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6153859 | |||||
chr19:6153878
|
G | GGAAAAGA others(9): Show |
112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.386+2083_386+2084i others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153878 | ||||||
chr19:6153880
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.386+2085A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6153880 | ||||||
chr19:6153889
|
GA | G | 49 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(46): Show | 50 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.386+2100delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6153889 | |||||
chr19:6154019
|
T | C | 1 | a0006c0007t0001g0060 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.386+2224T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154019 | ||||||
chr19:6154093
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.386+2298C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154093 | ||||||
chr19:6154178
|
AG | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG00741.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387-2251delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154178 | |||||
chr19:6154244
|
A | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.387-2187A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154244 | ||||||
chr19:6154323
|
G | A | 5 | a0003c0005t0001g0001a0003c0005t0001g0241a0003c0005t0001g0242others(2): Show | 6 | NA18973.hp2 NA18975.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-2108G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154323 | ||||||
chr19:6154328
|
G | A | 2 | a0001c0001t0001g0173a0002c0002t0001g0063 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.387-2103G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154328 | ||||||
chr19:6154402
|
A | AAG | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-1999_387-1998d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
A | AAGAG | 33 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(30): Show | 34 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.387-2001_387-1998d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
A | AAGAGAG | 3 | a0003c0004t0002g0131a0003c0005t0001g0133a0005c0006t0001g0023 | 3 | HG01433.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387-2003_387-1998d others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
A | AAGAGAGA others(1): Show |
56 | a0002c0002t0001g0005a0002c0002t0001g0042a0002c0002t0001g0062others(53): Show | 56 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.387-2005_387-1998d others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
A | AAGAGAGA others(3): Show |
10 | a0002c0002t0001g0073a0002c0002t0001g0088a0002c0002t0001g0099others(7): Show | 10 | HG00099.hp2 HG02055.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-2007_387-1998d others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
A | AAGAGAGA others(5): Show |
1 | a0003c0004t0002g0013 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387-2009_387-1998d others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154402
|
AAG | A | 8 | a0002c0002t0001g0079a0003c0012t0002g0046a0004c0003t0001g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-1999_387-1998d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154402 | |||||
chr19:6154432
|
GA | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.387-1995delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6154432 | |||||
chr19:6154433
|
A | AG | 4 | a0001c0001t0001g0173a0001c0001t0001g0216a0001c0001t0001g0253others(1): Show | 4 | HG00544.hp2 HG00741.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1998_387-1997i others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154433 | ||||||
chr19:6154434
|
A | G | 9 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.387-1997A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154434 | ||||||
chr19:6154434
|
A | T | 45 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(42): Show | 46 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1997A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154434 | ||||||
chr19:6154435
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.387-1996A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154435 | ||||||
chr19:6154438
|
T | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.387-1993T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154438 | ||||||
chr19:6154489
|
C | T | 4 | a0001c0020t0001g0051a0004c0019t0002g0050a0009c0010t0002g0052others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.387-1942C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154489 | ||||||
chr19:6154654
|
G | A | 3 | a0002c0002t0004g0097a0002c0002t0004g0106a0002c0002t0004g0247 | 3 | HG02602.hp1 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.387-1777G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154654 | ||||||
chr19:6154660
|
C | T | 2 | a0002c0002t0001g0090a0014c0023t0001g0201 | 2 | HG02572.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.387-1771C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6154660 | ||||||
chr19:6155000
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.387-1431T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155000 | ||||||
chr19:6155089
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.387-1342T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155089 | ||||||
chr19:6155269
|
C | A | 7 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.387-1162C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155269 | ||||||
chr19:6155285
|
T | C | 1 | a0003c0005t0001g0242 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.387-1146T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155285 | ||||||
chr19:6155362
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0215 | 2 | HG01515.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.387-1069C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155362 | ||||||
chr19:6155427
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.387-1004A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155427 | ||||||
chr19:6155454
|
T | C | 49 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(46): Show | 50 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.387-977T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155454 | ||||||
chr19:6155511
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.387-920C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155511 | ||||||
chr19:6155652
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.387-779T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155652 | ||||||
chr19:6155722
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.387-709T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155722 | ||||||
chr19:6155756
|
G | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.387-675G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155756 | ||||||
chr19:6155784
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.387-647T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155784 | ||||||
chr19:6155789
|
C | CA | 116 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.387-623dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155789 | |||||
chr19:6155789
|
C | CAA | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(15): Show | 18 | HG00642.hp2 HG01255.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.387-624_387-623dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155789 | |||||
chr19:6155789
|
CA | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0020t0001g0051others(11): Show | 14 | HG01074.hp1 HG02155.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.387-623delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155789 | |||||
chr19:6155789
|
CAA | C | 34 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(31): Show | 34 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.387-624_387-623del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155789 | |||||
chr19:6155789
|
CAAA | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-625_387-623del others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155789 | |||||
chr19:6155856
|
G | A | 3 | a0006c0007t0001g0058a0006c0007t0001g0059a0006c0007t0001g0065 | 3 | HG01074.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.387-575G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155856 | ||||||
chr19:6155910
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.387-521G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155910 | ||||||
chr19:6155922
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.387-495dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155922 | |||||
chr19:6155922
|
C | CAA | 8 | a0001c0001t0001g0255a0002c0002t0001g0029a0005c0006t0001g0018others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-496_387-495dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155922 | |||||
chr19:6155922
|
CA | C | 55 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(52): Show | 56 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.387-495delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 6155922 | |||||
chr19:6155937
|
T | A | 1 | a0001c0001t0001g0237 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.387-494T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6155937 | ||||||
chr19:6156003
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.387-428G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6156003 | ||||||
chr19:6156008
|
C | T | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.387-423C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6156008 | ||||||
chr19:6156195
|
C | T | 49 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(46): Show | 50 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.387-236C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6156195 | ||||||
chr19:6156262
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.387-169G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6156262 | ||||||
chr19:6156394
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.387-37G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | chr19 | 6156394 | ||||||
chr19:6156665
|
T | C | 49 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(46): Show | 50 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.507+114T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6156665 | ||||||
chr19:6156785
|
CA | C | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.507+235delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6156785 | ||||||
chr19:6156786
|
AT | A | 32 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0056others(29): Show | 32 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.507+250delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6156786 | |||||
chr19:6156786
|
ATT | A | 20 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(17): Show | 21 | HG01433.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+249_507+250del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6156786 | |||||
chr19:6156787
|
T | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.507+236T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6156787 | ||||||
chr19:6156821
|
G | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+270G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6156821 | ||||||
chr19:6156951
|
CT | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(20): Show | 23 | HG00741.hp2 HG01884.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.507+411delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6156951 | |||||
chr19:6156977
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.507+426C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6156977 | ||||||
chr19:6157032
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.507+481T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157032 | ||||||
chr19:6157150
|
G | A | 1 | a0002c0002t0006g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.507+599G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157150 | ||||||
chr19:6157155
|
A | G | 2 | a0004c0003t0001g0047a0004c0003t0001g0048 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.507+604A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157155 | ||||||
chr19:6157195
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(23): Show | 26 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.507+644G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157195 | ||||||
chr19:6157243
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.507+692G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157243 | ||||||
chr19:6157244
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.507+693A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157244 | ||||||
chr19:6157414
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.507+863G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157414 | ||||||
chr19:6157441
|
C | T | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.507+890C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157441 | ||||||
chr19:6157527
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(19): Show | 22 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.507+976C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6157527 | ||||||
chr19:6158060
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507+1509C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158060 | ||||||
chr19:6158060
|
CT | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.507+1522delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6158060 | |||||
chr19:6158061
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507+1510T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158061 | ||||||
chr19:6158086
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.507+1535C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158086 | ||||||
chr19:6158156
|
C | T | 1 | a0003c0012t0002g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.507+1605C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158156 | ||||||
chr19:6158181
|
G | A | 28 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(25): Show | 29 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+1630G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158181 | ||||||
chr19:6158224
|
T | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(20): Show | 23 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.507+1673T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158224 | ||||||
chr19:6158226
|
T | G | 4 | a0001c0020t0001g0051a0004c0019t0002g0050a0009c0010t0002g0052others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+1675T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158226 | ||||||
chr19:6158259
|
A | G | 52 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(49): Show | 53 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.507+1708A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158259 | ||||||
chr19:6158303
|
C | T | 28 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(25): Show | 29 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+1752C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158303 | ||||||
chr19:6158371
|
C | G | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.507+1820C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158371 | ||||||
chr19:6158411
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.507+1860T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158411 | ||||||
chr19:6158440
|
G | GT | 55 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0053others(52): Show | 55 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.507+1904dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6158440 | |||||
chr19:6158481
|
T | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(48): Show | 52 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.507+1930T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158481 | ||||||
chr19:6158530
|
T | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.507+1979T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158530 | ||||||
chr19:6158797
|
A | G | 1 | a0003c0012t0002g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.507+2246A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158797 | ||||||
chr19:6158896
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0172others(2): Show | 5 | NA18747.hp2 NA18963.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-2319C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158896 | ||||||
chr19:6158899
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0206 | 2 | HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.508-2316C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6158899 | ||||||
chr19:6159003
|
T | G | 51 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0139others(48): Show | 52 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.508-2212T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159003 | ||||||
chr19:6159122
|
T | C | 1 | a0003c0011t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-2093T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159122 | ||||||
chr19:6159158
|
A | G | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.508-2057A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159158 | ||||||
chr19:6159208
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.508-2007T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159208 | ||||||
chr19:6159242
|
A | T | 1 | a0003c0012t0002g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.508-1973A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159242 | ||||||
chr19:6159353
|
G | A | 7 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(4): Show | 8 | HG01433.hp1 HG02723.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.508-1862G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159353 | ||||||
chr19:6159440
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0259 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.508-1775C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159440 | ||||||
chr19:6159731
|
A | G | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-1484A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159731 | ||||||
chr19:6159771
|
G | A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-1444G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159771 | ||||||
chr19:6159876
|
C | G | 1 | a0002c0002t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.508-1339C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159876 | ||||||
chr19:6159948
|
C | T | 7 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(4): Show | 8 | HG01433.hp1 HG02723.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.508-1267C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6159948 | ||||||
chr19:6160067
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.508-1148C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160067 | ||||||
chr19:6160186
|
C | T | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-1029C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160186 | ||||||
chr19:6160282
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.508-933C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160282 | ||||||
chr19:6160285
|
G | C | 3 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.508-930G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160285 | ||||||
chr19:6160330
|
G | A | 2 | a0002c0002t0001g0062a0002c0002t0001g0068 | 2 | HG01175.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.508-885G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160330 | ||||||
chr19:6160389
|
C | CA | 21 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0166others(18): Show | 22 | HG00099.hp2 HG01433.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-811dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6160389 | |||||
chr19:6160404
|
AG | A | 34 | a0001c0001t0001g0184a0001c0001t0001g0206a0001c0001t0001g0250others(31): Show | 34 | HG00280.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.508-810delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160404 | ||||||
chr19:6160405
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.508-810G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160405 | ||||||
chr19:6160511
|
G | T | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-704G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160511 | ||||||
chr19:6160575
|
G | C | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-640G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160575 | ||||||
chr19:6160865
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.508-350C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160865 | ||||||
chr19:6160918
|
G | A | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-297G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160918 | ||||||
chr19:6160928
|
C | T | 2 | a0011c0009t0002g0147a0011c0009t0002g0164 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.508-287C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6160928 | ||||||
chr19:6161049
|
G | A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-166G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6161049 | ||||||
chr19:6161078
|
C | T | 8 | a0002c0002t0001g0072a0002c0002t0001g0099a0002c0002t0001g0101others(5): Show | 8 | HG02004.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.508-137C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6161078 | ||||||
chr19:6161099
|
C | CA | 22 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(19): Show | 22 | HG01934.hp1 HG02145.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-103dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6161099 | |||||
chr19:6161099
|
C | CAA | 8 | a0001c0001t0001g0215a0001c0001t0001g0232a0003c0005t0001g0001others(5): Show | 9 | HG00323.hp1 HG01433.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-104_508-103dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6161099 | |||||
chr19:6161099
|
C | CAAA | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.508-105_508-103dup others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6161099 | |||||
chr19:6161099
|
C | CAAAA | 6 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0186others(3): Show | 6 | HG00280.hp1 HG00673.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-106_508-103dup others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 6161099 | |||||
chr19:6161150
|
C | G | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-65C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6161150 | ||||||
chr19:6161208
|
C | T | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.508-7C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | chr19 | 6161208 | ||||||
chr19:6161329
|
AG | A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.588+37delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6161329 | |||||
chr19:6161392
|
C | G | 22 | a0001c0001t0001g0015a0003c0005t0001g0001a0003c0005t0001g0133others(19): Show | 23 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.588+97C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161392 | ||||||
chr19:6161427
|
AGGTGGGG others(36): Show |
A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.588+140_588+182del others(43): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6161427 | |||||
chr19:6161487
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.588+192G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161487 | ||||||
chr19:6161494
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.588+199G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161494 | ||||||
chr19:6161498
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.588+203T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161498 | ||||||
chr19:6161643
|
A | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+348A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161643 | ||||||
chr19:6161696
|
A | G | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+401A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161696 | ||||||
chr19:6161719
|
G | C | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.588+424G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161719 | ||||||
chr19:6161766
|
C | G | 9 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+471C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6161766 | ||||||
chr19:6162036
|
A | G | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.588+741A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162036 | ||||||
chr19:6162090
|
A | T | 5 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+795A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162090 | ||||||
chr19:6162111
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+816C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162111 | ||||||
chr19:6162192
|
G | A | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.588+897G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162192 | ||||||
chr19:6162205
|
C | G | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+910C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162205 | ||||||
chr19:6162245
|
AC | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+951delC | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162245 | ||||||
chr19:6162264
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.588+988dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162264 | |||||
chr19:6162264
|
C | CAA | 12 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0001g0173others(9): Show | 12 | HG00673.hp2 HG00741.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+987_588+988dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162264 | |||||
chr19:6162357
|
A | G | 43 | a0001c0001t0001g0015a0001c0020t0001g0051a0003c0004t0002g0006others(40): Show | 44 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(41): Show |
intron_variant | MODIFIER | c.588+1062A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162357 | ||||||
chr19:6162382
|
C | T | 1 | a0004c0003t0001g0045 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.588+1087C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162382 | ||||||
chr19:6162390
|
C | A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.588+1095C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162390 | ||||||
chr19:6162428
|
G | A | 3 | a0002c0002t0004g0097a0002c0002t0004g0106a0002c0002t0004g0247 | 3 | HG02602.hp1 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.588+1133G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162428 | ||||||
chr19:6162460
|
G | A | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.588+1165G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162460 | ||||||
chr19:6162524
|
G | A | 6 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255others(3): Show | 6 | HG00280.hp2 HG01981.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+1229G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162524 | ||||||
chr19:6162554
|
A | G | 21 | a0001c0001t0001g0015a0003c0005t0001g0001a0003c0005t0001g0133others(18): Show | 22 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.588+1259A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162554 | ||||||
chr19:6162566
|
C | CA | 9 | a0001c0001t0003g0163a0002c0002t0001g0042a0002c0002t0001g0076others(6): Show | 9 | HG00140.hp1 HG01978.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+1293dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162566 | |||||
chr19:6162566
|
C | CAA | 13 | a0001c0001t0001g0039a0001c0001t0001g0181a0001c0001t0001g0192others(10): Show | 14 | HG00323.hp1 HG01069.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+1292_588+1293d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162566 | |||||
chr19:6162566
|
C | CAAA | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.588+1291_588+1293d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162566 | |||||
chr19:6162566
|
C | CAAAA | 12 | a0001c0001t0001g0055a0001c0001t0001g0132a0001c0001t0001g0150others(9): Show | 12 | HG00544.hp2 HG00642.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.588+1290_588+1293d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162566 | |||||
chr19:6162566
|
CAAA | C | 19 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(16): Show | 19 | HG01071.hp2 HG02055.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.588+1291_588+1293d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162566 | |||||
chr19:6162638
|
GTC | G | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1346_588+1347d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6162638 | |||||
chr19:6162747
|
G | T | 43 | a0001c0001t0001g0015a0001c0020t0001g0051a0003c0004t0002g0006others(40): Show | 44 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(41): Show |
intron_variant | MODIFIER | c.588+1452G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162747 | ||||||
chr19:6162976
|
G | T | 4 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1681G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6162976 | ||||||
chr19:6163010
|
C | T | 10 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+1715C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163010 | ||||||
chr19:6163038
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0191others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1743G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163038 | ||||||
chr19:6163073
|
G | A | 1 | a0004c0003t0001g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.588+1778G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163073 | ||||||
chr19:6163121
|
A | AAAT | 18 | a0001c0001t0001g0017a0001c0001t0001g0132a0001c0001t0001g0171others(15): Show | 18 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.588+1869_588+1871d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163121 | |||||
chr19:6163121
|
AAAT | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.588+1869_588+1871d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163121 | |||||
chr19:6163121
|
AAATAAT | A | 29 | a0001c0001t0001g0159a0001c0001t0001g0174a0001c0001t0001g0196others(26): Show | 29 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+1866_588+1871d others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163121 | |||||
chr19:6163121
|
AAATAATA others(5): Show |
A | 4 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0112others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1860_588+1871d others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163121 | |||||
chr19:6163137
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+1842A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163137 | ||||||
chr19:6163171
|
C | A | 1 | a0001c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.588+1876C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163171 | ||||||
chr19:6163188
|
ACCTGTAA others(284): Show |
A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.588+1917_588+2207d others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163188 | |||||
chr19:6163243
|
G | A | 1 | a0003c0011t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+1948G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163243 | ||||||
chr19:6163447
|
T | TAA | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+2162_588+2163d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163447 | |||||
chr19:6163521
|
A | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+2226A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163521 | ||||||
chr19:6163597
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0199 | 3 | HG01952.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.589-2269C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163597 | ||||||
chr19:6163680
|
G | C | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.589-2186G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163680 | ||||||
chr19:6163735
|
A | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0029 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.589-2131A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163735 | ||||||
chr19:6163783
|
C | CA | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0038others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.589-2065dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163783 | |||||
chr19:6163783
|
CA | C | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(21): Show | 24 | HG01891.hp2 HG01934.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.589-2065delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163783 | |||||
chr19:6163783
|
CAA | C | 21 | a0002c0002t0001g0032a0003c0004t0002g0006a0003c0004t0002g0007others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.589-2066_589-2065d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163783 | |||||
chr19:6163783
|
CAAA | C | 22 | a0001c0001t0001g0015a0001c0020t0001g0051a0003c0005t0001g0001others(19): Show | 23 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.589-2067_589-2065d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6163783 | |||||
chr19:6163797
|
A | C | 1 | a0007c0008t0002g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.589-2069A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163797 | ||||||
chr19:6163808
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0258 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.589-2058G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163808 | ||||||
chr19:6163994
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.589-1872A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6163994 | ||||||
chr19:6164025
|
G | A | 43 | a0001c0001t0001g0015a0001c0020t0001g0051a0003c0004t0002g0006others(40): Show | 44 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(41): Show |
intron_variant | MODIFIER | c.589-1841G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164025 | ||||||
chr19:6164434
|
C | CT | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0155others(24): Show | 27 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.589-1416dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6164434 | |||||
chr19:6164434
|
C | CTTT | 20 | a0001c0001t0001g0015a0003c0005t0001g0001a0003c0005t0001g0133others(17): Show | 21 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.589-1418_589-1416d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6164434 | |||||
chr19:6164577
|
C | A | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.589-1289C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164577 | ||||||
chr19:6164577
|
C | T | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.589-1289C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164577 | ||||||
chr19:6164731
|
G | T | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.589-1135G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164731 | ||||||
chr19:6164778
|
T | C | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.589-1088T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164778 | ||||||
chr19:6164826
|
C | T | 1 | a0002c0002t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.589-1040C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164826 | ||||||
chr19:6164858
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0191others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-1008G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164858 | ||||||
chr19:6164913
|
C | CT | 5 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-952dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 6164913 | |||||
chr19:6164999
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-867G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6164999 | ||||||
chr19:6165082
|
C | G | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.589-784C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165082 | ||||||
chr19:6165177
|
C | T | 1 | a0018c0015t0001g0257 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.589-689C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165177 | ||||||
chr19:6165207
|
C | T | 1 | a0004c0003t0002g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.589-659C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165207 | ||||||
chr19:6165255
|
C | T | 21 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.589-611C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165255 | ||||||
chr19:6165396
|
C | T | 21 | a0001c0001t0001g0015a0003c0005t0001g0001a0003c0005t0001g0133others(18): Show | 22 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.589-470C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165396 | ||||||
chr19:6165439
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.589-427G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165439 | ||||||
chr19:6165567
|
A | T | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-299A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165567 | ||||||
chr19:6165796
|
G | A | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-70G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165796 | ||||||
chr19:6165818
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-48G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165818 | ||||||
chr19:6165826
|
G | A | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-40G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | chr19 | 6165826 | ||||||
chr19:6166040
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+25G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166040 | ||||||
chr19:6166085
|
G | T | 1 | a0001c0017t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.738+70G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166085 | ||||||
chr19:6166125
|
A | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0166a0001c0001t0001g0200others(6): Show | 10 | HG01433.hp1 HG02451.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.738+110A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166125 | ||||||
chr19:6166148
|
G | T | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738+133G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166148 | ||||||
chr19:6166277
|
A | AGCTTGTG others(3): Show |
1 | a0010c0013t0002g0114 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738+263_738+264ins others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166277 | |||||
chr19:6166279
|
G | C | 14 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.738+264G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166279 | ||||||
chr19:6166279
|
G | T | 1 | a0010c0013t0002g0114 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738+264G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166279 | ||||||
chr19:6166280
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738+265_738+266ins others(23): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166280 | ||||||
chr19:6166280
|
T | TGTGTGTG others(20): Show |
1 | a0003c0004t0002g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.738+265_738+266ins others(27): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166280 | ||||||
chr19:6166280
|
T | TTG | 15 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0209others(12): Show | 15 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.738+315_738+316dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTG | 14 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0221others(11): Show | 14 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+313_738+316dup others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTG | 20 | a0001c0001t0001g0225a0001c0017t0001g0239a0002c0002t0001g0042others(17): Show | 20 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.738+311_738+316dup others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(1): Show |
14 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0067others(11): Show | 14 | HG00597.hp1 HG01074.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+309_738+316dup others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0171a0002c0002t0001g0029a0002c0002t0001g0101others(7): Show | 10 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.738+307_738+316dup others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(5): Show |
7 | a0002c0002t0001g0021a0002c0002t0001g0091a0002c0002t0001g0103others(4): Show | 7 | HG00099.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+305_738+316dup others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(7): Show |
10 | a0001c0001t0001g0039a0002c0002t0001g0019a0002c0002t0001g0030others(7): Show | 10 | HG02055.hp2 HG02976.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.738+303_738+316dup others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(9): Show |
6 | a0001c0001t0003g0141a0001c0001t0003g0142a0002c0002t0001g0024others(3): Show | 6 | HG02615.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+301_738+316dup others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(11): Show |
3 | a0005c0006t0001g0025a0005c0006t0001g0026a0012c0021t0001g0100 | 3 | HG02723.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.738+299_738+316dup others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0003g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.738+297_738+316dup others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(15): Show |
5 | a0001c0001t0003g0146a0003c0004t0002g0008a0003c0004t0002g0012others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+295_738+316dup others(22): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(17): Show |
4 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0011others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+293_738+316dup others(24): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(5): Show |
2 | a0004c0003t0002g0134a0004c0003t0002g0135 | 2 | HG02129.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.738+274_738+275ins others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(9): Show |
2 | a0003c0011t0001g0160a0004c0003t0002g0136 | 2 | NA19000.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.738+274_738+275ins others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(11): Show |
3 | a0004c0003t0002g0138a0011c0009t0002g0164a0013c0016t0001g0014 | 3 | HG01891.hp1 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.738+274_738+275ins others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(13): Show |
1 | a0011c0009t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.738+274_738+275ins others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(17): Show |
2 | a0001c0001t0001g0015a0007c0008t0002g0161 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.738+274_738+275ins others(24): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTGTGTGT others(19): Show |
3 | a0003c0011t0001g0144a0007c0008t0002g0145a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.738+274_738+275ins others(26): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTTTGTGT others(3): Show |
1 | a0003c0005t0001g0001 | 2 | NA19077.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.738+266_738+267ins others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTTTGTGT others(5): Show |
1 | a0003c0005t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.738+266_738+267ins others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
T | TTTTGTGT others(9): Show |
1 | a0003c0005t0001g0243 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.738+266_738+267ins others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
TTG | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(24): Show | 27 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.738+315_738+316del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
TTGTG | T | 56 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.738+313_738+316del others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
TTGTGTG | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0224a0001c0020t0001g0051others(2): Show | 5 | HG00558.hp1 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.738+311_738+316del others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166280
|
TTGTGTGT others(1): Show |
T | 6 | a0001c0001t0001g0196a0001c0001t0001g0216a0001c0001t0001g0235others(3): Show | 6 | HG00544.hp2 HG01256.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+309_738+316del others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166280 | |||||
chr19:6166328
|
GTGT | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0179others(1): Show | 4 | HG01433.hp2 HG01496.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+315_738+317del others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6166328 | |||||
chr19:6166331
|
T | TGTGTGTG others(4): Show |
1 | a0002c0002t0001g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.738+316_738+317ins others(11): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166331 | ||||||
chr19:6166331
|
T | TGTGTGTG others(8): Show |
2 | a0002c0002t0004g0106a0005c0006t0001g0028 | 2 | HG02647.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.738+316_738+317ins others(15): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166331 | ||||||
chr19:6166331
|
T | TGTGTGTG others(12): Show |
2 | a0002c0002t0001g0121a0003c0004t0002g0013 | 2 | HG02897.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.738+316_738+317ins others(19): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166331 | ||||||
chr19:6166331
|
T | TGTGTGTG others(20): Show |
1 | a0003c0012t0002g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.738+316_738+317ins others(27): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166331 | ||||||
chr19:6166490
|
G | T | 2 | a0002c0002t0001g0083a0002c0002t0001g0084 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.738+475G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166490 | ||||||
chr19:6166567
|
C | A | 22 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.738+552C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166567 | ||||||
chr19:6166654
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.738+639C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166654 | ||||||
chr19:6166796
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.738+781T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166796 | ||||||
chr19:6166804
|
A | T | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.738+789A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166804 | ||||||
chr19:6166810
|
T | G | 7 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+795T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166810 | ||||||
chr19:6166996
|
G | T | 7 | a0003c0012t0002g0046a0004c0003t0001g0043a0004c0003t0001g0044others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+981G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6166996 | ||||||
chr19:6167158
|
T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+1143T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167158 | ||||||
chr19:6167373
|
C | T | 15 | a0001c0001t0001g0015a0003c0011t0001g0144a0003c0011t0001g0160others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.738+1358C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167373 | ||||||
chr19:6167403
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.738+1388A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167403 | ||||||
chr19:6167420
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738+1405T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167420 | ||||||
chr19:6167662
|
T | C | 6 | a0004c0003t0001g0043a0004c0003t0001g0044a0004c0003t0001g0045others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+1647T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167662 | ||||||
chr19:6167750
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738+1735A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167750 | ||||||
chr19:6167983
|
A | C | 36 | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(33): Show | 36 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.738+1968A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6167983 | ||||||
chr19:6167984
|
C | CCA | 14 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.738+1970_738+1971i others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6167984 | |||||
chr19:6167988
|
C | CA | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+1974dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6167988 | |||||
chr19:6168153
|
C | T | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.738+2138C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168153 | ||||||
chr19:6168154
|
T | C | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.738+2139T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168154 | ||||||
chr19:6168164
|
T | C | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.738+2149T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168164 | ||||||
chr19:6168165
|
C | T | 1 | a0008c0014t0001g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.738+2150C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168165 | ||||||
chr19:6168409
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.738+2394C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168409 | ||||||
chr19:6168541
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0207others(1): Show | 4 | NA18950.hp1 NA18983.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+2526G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168541 | ||||||
chr19:6168657
|
G | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+2642G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168657 | ||||||
chr19:6168675
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.738+2660C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168675 | ||||||
chr19:6168830
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.738+2815G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168830 | ||||||
chr19:6168858
|
A | G | 1 | a0018c0015t0001g0257 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.738+2843A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6168858 | ||||||
chr19:6169070
|
C | T | 1 | a0002c0002t0001g0082 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.738+3055C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169070 | ||||||
chr19:6169272
|
T | C | 7 | a0002c0002t0001g0076a0002c0002t0001g0081a0002c0002t0001g0082others(4): Show | 7 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+3257T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169272 | ||||||
chr19:6169332
|
C | T | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.738+3317C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169332 | ||||||
chr19:6169664
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+3649C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169664 | ||||||
chr19:6169747
|
T | C | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.738+3732T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169747 | ||||||
chr19:6169780
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.738+3765G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169780 | ||||||
chr19:6169920
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738+3905C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6169920 | ||||||
chr19:6170092
|
T | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.738+4077T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6170092 | ||||||
chr19:6170631
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.738+4616A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6170631 | ||||||
chr19:6170729
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+4714A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6170729 | ||||||
chr19:6170846
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.738+4831A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6170846 | ||||||
chr19:6170847
|
T | C | 10 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.738+4832T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6170847 | ||||||
chr19:6170975
|
CT | C | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.738+4971delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6170975 | |||||
chr19:6171132
|
T | A | 2 | a0004c0003t0002g0135a0004c0003t0002g0136 | 2 | NA18612.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.738+5117T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171132 | ||||||
chr19:6171208
|
T | G | 6 | a0004c0003t0001g0043a0004c0003t0001g0044a0004c0003t0001g0045others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+5193T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171208 | ||||||
chr19:6171315
|
G | A | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.738+5300G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171315 | ||||||
chr19:6171400
|
G | A | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.738+5385G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171400 | ||||||
chr19:6171578
|
T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+5563T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171578 | ||||||
chr19:6171587
|
C | T | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.738+5572C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171587 | ||||||
chr19:6171662
|
T | A | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-5567T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171662 | ||||||
chr19:6171682
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.739-5547A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171682 | ||||||
chr19:6171691
|
G | A | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-5538G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171691 | ||||||
chr19:6171824
|
TTTC | T | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-5399_739-5397d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6171824 | |||||
chr19:6171933
|
T | A | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.739-5296T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6171933 | ||||||
chr19:6172295
|
T | G | 1 | a0002c0002t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.739-4934T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172295 | ||||||
chr19:6172448
|
C | T | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-4781C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172448 | ||||||
chr19:6172470
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.739-4759C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172470 | ||||||
chr19:6172509
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.739-4720C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172509 | ||||||
chr19:6172851
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.739-4378G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172851 | ||||||
chr19:6172926
|
C | T | 1 | a0002c0002t0001g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.739-4303C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6172926 | ||||||
chr19:6173135
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.739-4094A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173135 | ||||||
chr19:6173156
|
T | C | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-4073T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173156 | ||||||
chr19:6173354
|
A | G | 1 | a0004c0003t0002g0136 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.739-3875A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173354 | ||||||
chr19:6173610
|
C | T | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-3619C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173610 | ||||||
chr19:6173611
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.739-3618G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173611 | ||||||
chr19:6173679
|
T | A | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-3550T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173679 | ||||||
chr19:6173751
|
A | G | 1 | a0002c0002t0001g0248 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.739-3478A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6173751 | ||||||
chr19:6173937
|
A | AT | 18 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0056others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.739-3274dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6173937 | |||||
chr19:6173937
|
A | ATTTTT | 20 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.739-3278_739-3274d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6173937 | |||||
chr19:6173937
|
AT | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0194others(5): Show | 8 | HG00741.hp1 HG01256.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-3274delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6173937 | |||||
chr19:6173937
|
ATTTTT | A | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-3278_739-3274d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6173937 | |||||
chr19:6174018
|
C | A | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-3211C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174018 | ||||||
chr19:6174121
|
G | A | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739-3108G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174121 | ||||||
chr19:6174125
|
T | C | 55 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(52): Show | 56 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.739-3104T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174125 | ||||||
chr19:6174139
|
G | T | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739-3090G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174139 | ||||||
chr19:6174148
|
G | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.739-3081G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174148 | ||||||
chr19:6174209
|
C | T | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-3020C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174209 | ||||||
chr19:6174275
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2954C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174275 | ||||||
chr19:6174276
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2953A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174276 | ||||||
chr19:6174278
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2951C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174278 | ||||||
chr19:6174280
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2949G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174280 | ||||||
chr19:6174281
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2948C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174281 | ||||||
chr19:6174284
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2945G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174284 | ||||||
chr19:6174291
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2938C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174291 | ||||||
chr19:6174294
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2935A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174294 | ||||||
chr19:6174297
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2932T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174297 | ||||||
chr19:6174298
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2931T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174298 | ||||||
chr19:6174299
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2930T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174299 | ||||||
chr19:6174300
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2929G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174300 | ||||||
chr19:6174302
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2927C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174302 | ||||||
chr19:6174305
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2924T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174305 | ||||||
chr19:6174306
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2923C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174306 | ||||||
chr19:6174307
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2922C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174307 | ||||||
chr19:6174320
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2909A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174320 | ||||||
chr19:6174322
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2907C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174322 | ||||||
chr19:6174325
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2904C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174325 | ||||||
chr19:6174330
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2899C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174330 | ||||||
chr19:6174333
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2896C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174333 | ||||||
chr19:6174334
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2895T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174334 | ||||||
chr19:6174335
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2894C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174335 | ||||||
chr19:6174336
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2893C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174336 | ||||||
chr19:6174339
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2890T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174339 | ||||||
chr19:6174340
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2889C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174340 | ||||||
chr19:6174341
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2888T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174341 | ||||||
chr19:6174343
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2886T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174343 | ||||||
chr19:6174344
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2885C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174344 | ||||||
chr19:6174346
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2883G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174346 | ||||||
chr19:6174351
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2878A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174351 | ||||||
chr19:6174359
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2870A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174359 | ||||||
chr19:6174360
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2869C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174360 | ||||||
chr19:6174367
|
A | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2862A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174367 | ||||||
chr19:6174370
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2859T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174370 | ||||||
chr19:6174374
|
TCTCAAAG others(99): Show |
T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2854_739-2749d others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174374 | ||||||
chr19:6174484
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2745C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174484 | ||||||
chr19:6174486
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2743T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174486 | ||||||
chr19:6174488
|
C | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.739-2741C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174488 | ||||||
chr19:6174491
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2738G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174491 | ||||||
chr19:6174492
|
A | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2737A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174492 | ||||||
chr19:6174493
|
A | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2736A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174493 | ||||||
chr19:6174494
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2735G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174494 | ||||||
chr19:6174498
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2731T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174498 | ||||||
chr19:6174501
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2728C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174501 | ||||||
chr19:6174505
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2724G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174505 | ||||||
chr19:6174511
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2718T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174511 | ||||||
chr19:6174512
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2717A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174512 | ||||||
chr19:6174514
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2715T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174514 | ||||||
chr19:6174517
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2712T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174517 | ||||||
chr19:6174519
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2710T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174519 | ||||||
chr19:6174525
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2704T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174525 | ||||||
chr19:6174530
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2699T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174530 | ||||||
chr19:6174531
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2698G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174531 | ||||||
chr19:6174532
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2697G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174532 | ||||||
chr19:6174534
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2695T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174534 | ||||||
chr19:6174536
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2693C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174536 | ||||||
chr19:6174537
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2692A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174537 | ||||||
chr19:6174544
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2685T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174544 | ||||||
chr19:6174549
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2680A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174549 | ||||||
chr19:6174554
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2675A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174554 | ||||||
chr19:6174578
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2651A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174578 | ||||||
chr19:6174580
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2649A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174580 | ||||||
chr19:6174583
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2646A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174583 | ||||||
chr19:6174588
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2641T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174588 | ||||||
chr19:6174589
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2640G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174589 | ||||||
chr19:6174591
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2638T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174591 | ||||||
chr19:6174595
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2634A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174595 | ||||||
chr19:6174597
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2632C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174597 | ||||||
chr19:6174608
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2621T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174608 | ||||||
chr19:6174613
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2616G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174613 | ||||||
chr19:6174614
|
A | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2615A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174614 | ||||||
chr19:6174617
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2612G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174617 | ||||||
chr19:6174622
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2607G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174622 | ||||||
chr19:6174623
|
A | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2606A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174623 | ||||||
chr19:6174627
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2602A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174627 | ||||||
chr19:6174628
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2601C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174628 | ||||||
chr19:6174629
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2600A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174629 | ||||||
chr19:6174631
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2598C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174631 | ||||||
chr19:6174634
|
G | A | 1 | a0018c0015t0001g0257 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.739-2595G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174634 | ||||||
chr19:6174634
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2595G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174634 | ||||||
chr19:6174638
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2591T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174638 | ||||||
chr19:6174639
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2590C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174639 | ||||||
chr19:6174640
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2589A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174640 | ||||||
chr19:6174641
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2588T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174641 | ||||||
chr19:6174648
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2581A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174648 | ||||||
chr19:6174651
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2578A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174651 | ||||||
chr19:6174654
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2575G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174654 | ||||||
chr19:6174655
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2574T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174655 | ||||||
chr19:6174657
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2572T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174657 | ||||||
chr19:6174658
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2571T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174658 | ||||||
chr19:6174673
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2556C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174673 | ||||||
chr19:6174674
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2555A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174674 | ||||||
chr19:6174677
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2552G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174677 | ||||||
chr19:6174685
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2544T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174685 | ||||||
chr19:6174687
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2542C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174687 | ||||||
chr19:6174693
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2536G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174693 | ||||||
chr19:6174698
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2531A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174698 | ||||||
chr19:6174706
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2523G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174706 | ||||||
chr19:6174718
|
T | G | 1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-2511T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174718 | ||||||
chr19:6174723
|
C | A | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-2506C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174723 | ||||||
chr19:6174810
|
CTCA | C | 15 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-2410_739-2408d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6174810 | |||||
chr19:6174841
|
G | C | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.739-2388G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174841 | ||||||
chr19:6174914
|
A | C | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-2315A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174914 | ||||||
chr19:6174939
|
C | A | 1 | a0011c0009t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.739-2290C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6174939 | ||||||
chr19:6175373
|
G | A | 2 | a0002c0002t0004g0097a0002c0002t0004g0247 | 2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.739-1856G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175373 | ||||||
chr19:6175427
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.739-1802A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175427 | ||||||
chr19:6175594
|
G | A | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-1635G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175594 | ||||||
chr19:6175878
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00741.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.739-1351T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175878 | ||||||
chr19:6175882
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0056 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.739-1347A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175882 | ||||||
chr19:6175925
|
A | G | 36 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(33): Show | 36 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.739-1304A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6175925 | ||||||
chr19:6176303
|
T | C | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739-926T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176303 | ||||||
chr19:6176357
|
A | G | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-872A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176357 | ||||||
chr19:6176427
|
C | T | 21 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(18): Show | 22 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.739-802C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176427 | ||||||
chr19:6176442
|
A | C | 21 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(18): Show | 22 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.739-787A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176442 | ||||||
chr19:6176512
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.739-717G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176512 | ||||||
chr19:6176538
|
A | G | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-691A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176538 | ||||||
chr19:6176583
|
T | C | 21 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-646T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176583 | ||||||
chr19:6176684
|
C | T | 21 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(18): Show | 22 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.739-545C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176684 | ||||||
chr19:6176771
|
G | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0217 | 3 | HG01167.hp2 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.739-458G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176771 | ||||||
chr19:6176867
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.739-362G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6176867 | ||||||
chr19:6177040
|
A | T | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739-189A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6177040 | ||||||
chr19:6177159
|
A | AATAAAAA others(50): Show |
1 | a0001c0001t0003g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-44_739-43insCT others(55): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 6177159 | |||||
chr19:6177163
|
A | C | 16 | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.739-66A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | chr19 | 6177163 | ||||||
chr19:6177482
|
T | A | 1 | a0003c0011t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.906+86T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177482 | ||||||
chr19:6177508
|
G | A | 1 | a0013c0016t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.906+112G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177508 | ||||||
chr19:6177612
|
G | A | 1 | a0004c0019t0002g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.906+216G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177612 | ||||||
chr19:6177739
|
CT | C | 121 | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0001g0140others(118): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.906+357delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177739 | |||||
chr19:6177739
|
CTT | C | 27 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 27 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.906+356_906+357del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177739 | |||||
chr19:6177739
|
CTTT | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.906+355_906+357del others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177739 | |||||
chr19:6177853
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0192 | 2 | HG00423.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.906+457G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177853 | ||||||
chr19:6177863
|
C | G | 2 | a0002c0002t0001g0079a0002c0002t0001g0090 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.906+467C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177863 | ||||||
chr19:6177875
|
A | AGT | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0182others(14): Show | 17 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.906+518_906+519dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177875
|
A | AGTGT | 4 | a0001c0001t0001g0240a0002c0002t0001g0085a0002c0002t0001g0121others(1): Show | 4 | HG02723.hp2 HG06807.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+516_906+519dup others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177875
|
AGT | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 28 | HG00558.hp2 HG00642.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.906+518_906+519del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177875
|
AGTGT | A | 27 | a0001c0001t0001g0151a0001c0001t0001g0172a0001c0001t0001g0177others(24): Show | 27 | HG02109.hp1 HG02145.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.906+516_906+519del others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177875
|
AGTGTGT | A | 78 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.906+514_906+519del others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177875
|
AGTGTGTG others(1): Show |
A | 22 | a0001c0001t0001g0132a0001c0001t0001g0152a0001c0001t0001g0153others(19): Show | 22 | HG00423.hp2 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.906+512_906+519del others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6177875 | |||||
chr19:6177957
|
A | G | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.906+561A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6177957 | ||||||
chr19:6178066
|
C | T | 1 | a0003c0004t0002g0013 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.906+670C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178066 | ||||||
chr19:6178229
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0172others(2): Show | 5 | NA18747.hp2 NA18963.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+833C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178229 | ||||||
chr19:6178261
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.906+865A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178261 | ||||||
chr19:6178373
|
C | CATT | 4 | a0001c0001t0001g0039a0001c0001t0001g0189a0001c0001t0001g0225others(1): Show | 4 | HG02976.hp1 HG04184.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+999_906+1001du others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6178373 | |||||
chr19:6178373
|
CATT | C | 39 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(36): Show | 40 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.906+999_906+1001de others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6178373 | |||||
chr19:6178404
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1008A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178404 | ||||||
chr19:6178435
|
A | G | 55 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(52): Show | 56 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.906+1039A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178435 | ||||||
chr19:6178448
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00741.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.906+1052C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178448 | ||||||
chr19:6178678
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.906+1282T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178678 | ||||||
chr19:6178766
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+1370G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178766 | ||||||
chr19:6178806
|
G | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1410G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178806 | ||||||
chr19:6178867
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1471A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178867 | ||||||
chr19:6178868
|
C | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1472C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6178868 | ||||||
chr19:6179007
|
G | C | 2 | a0009c0010t0002g0052a0009c0010t0002g0054 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.906+1611G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179007 | ||||||
chr19:6179082
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1686T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179082 | ||||||
chr19:6179288
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.906+1892T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179288 | ||||||
chr19:6179293
|
A | AT | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.906+1920dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6179293 | |||||
chr19:6179293
|
A | ATT | 9 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0202others(6): Show | 9 | HG01167.hp2 HG01884.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.906+1919_906+1920d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6179293 | |||||
chr19:6179293
|
AT | A | 7 | a0001c0001t0003g0141a0002c0002t0001g0062a0002c0002t0001g0072others(4): Show | 7 | HG01256.hp1 HG01515.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+1920delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6179293 | |||||
chr19:6179293
|
ATTT | A | 18 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(15): Show | 19 | HG01433.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+1918_906+1920d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6179293 | |||||
chr19:6179295
|
T | A | 20 | a0003c0011t0001g0160a0004c0003t0001g0044a0004c0003t0001g0045others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.906+1899T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179295 | ||||||
chr19:6179296
|
T | A | 2 | a0003c0011t0001g0144a0004c0003t0001g0043 | 2 | HG03453.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.906+1900T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179296 | ||||||
chr19:6179298
|
T | A | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+1902T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179298 | ||||||
chr19:6179338
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+1942T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179338 | ||||||
chr19:6179579
|
A | G | 28 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(25): Show | 29 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.906+2183A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179579 | ||||||
chr19:6179595
|
T | G | 1 | a0002c0002t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.906+2199T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179595 | ||||||
chr19:6179758
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.906+2362G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179758 | ||||||
chr19:6179769
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0206 | 2 | HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.906+2373C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179769 | ||||||
chr19:6179947
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.906+2551T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6179947 | ||||||
chr19:6180059
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.906+2663G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180059 | ||||||
chr19:6180103
|
C | CCTCTCTG others(7): Show |
41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-2643_907-2642i others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6180103 | |||||
chr19:6180333
|
C | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-2418C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180333 | ||||||
chr19:6180346
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.907-2405A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180346 | ||||||
chr19:6180359
|
T | C | 1 | a0005c0006t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.907-2392T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180359 | ||||||
chr19:6180386
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-2365T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180386 | ||||||
chr19:6180444
|
C | T | 1 | a0002c0002t0005g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.907-2307C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180444 | ||||||
chr19:6180478
|
A | G | 29 | a0001c0001t0001g0173a0003c0005t0001g0001a0003c0005t0001g0133others(26): Show | 30 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.907-2273A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180478 | ||||||
chr19:6180545
|
C | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-2206C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180545 | ||||||
chr19:6180873
|
T | A | 3 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.907-1878T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180873 | ||||||
chr19:6180907
|
A | G | 1 | a0002c0002t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.907-1844A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180907 | ||||||
chr19:6180928
|
C | T | 1 | a0005c0006t0001g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.907-1823C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180928 | ||||||
chr19:6180936
|
G | A | 2 | a0012c0021t0001g0100a0017c0018t0001g0148 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.907-1815G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6180936 | ||||||
chr19:6181044
|
TA | T | 37 | a0002c0002t0001g0074a0002c0002t0005g0116a0003c0004t0002g0006others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.907-1689delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181044 | |||||
chr19:6181044
|
TAA | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.907-1690_907-1689d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181044 | |||||
chr19:6181058
|
A | G | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-1693A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181058 | ||||||
chr19:6181106
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-1645C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181106 | ||||||
chr19:6181221
|
C | CA | 8 | a0001c0001t0001g0002a0001c0001t0001g0189a0001c0001t0001g0193others(5): Show | 8 | HG01175.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-1511dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181221
|
C | CAAA | 7 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(4): Show | 8 | HG01433.hp1 NA18522.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-1513_907-1511d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181221
|
C | CAAAA | 8 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-1514_907-1511d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181221
|
C | CAAAAA | 5 | a0003c0004t0002g0009a0003c0004t0002g0013a0003c0004t0002g0131others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.907-1515_907-1511d others(7): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181221
|
C | CAAAAAAA | 14 | a0004c0003t0001g0043a0004c0003t0001g0045a0004c0003t0001g0047others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.907-1517_907-1511d others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181221
|
C | CAAAAAAA others(1): Show |
6 | a0003c0011t0001g0160a0004c0003t0001g0044a0007c0008t0002g0162others(3): Show | 6 | HG01884.hp2 HG02080.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-1518_907-1511d others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181221 | |||||
chr19:6181241
|
G | A | 1 | a0004c0019t0002g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907-1510G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181241 | ||||||
chr19:6181242
|
G | A | 1 | a0004c0019t0002g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907-1509G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181242 | ||||||
chr19:6181358
|
A | AAAAG | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-1384_907-1381d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181358 | |||||
chr19:6181376
|
AG | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0207others(1): Show | 4 | NA18950.hp1 NA18983.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-1373delG | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181376 | |||||
chr19:6181449
|
T | C | 3 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.907-1302T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181449 | ||||||
chr19:6181571
|
G | A | 1 | a0003c0011t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.907-1180G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181571 | ||||||
chr19:6181751
|
C | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG01496.hp1 HG01978.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-1000C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181751 | ||||||
chr19:6181756
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-995A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181756 | ||||||
chr19:6181813
|
G | GCC | 29 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0040others(26): Show | 29 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.907-928_907-927dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181813 | |||||
chr19:6181813
|
G | GCCC | 68 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.907-929_907-927dup others(3): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181813 | |||||
chr19:6181813
|
G | GCCCC | 25 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0001t0001g0165others(22): Show | 25 | HG00280.hp2 HG00544.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.907-930_907-927dup others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181813 | |||||
chr19:6181813
|
GC | G | 56 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0130others(53): Show | 56 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.907-927delC | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181813 | |||||
chr19:6181816
|
C | CCCCCA | 28 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.907-931_907-930ins others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6181816 | |||||
chr19:6181871
|
T | G | 55 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(52): Show | 56 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.907-880T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181871 | ||||||
chr19:6181929
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.907-822C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181929 | ||||||
chr19:6181983
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.907-768T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6181983 | ||||||
chr19:6182146
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.907-605T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182146 | ||||||
chr19:6182207
|
AT | A | 5 | a0002c0002t0001g0111a0002c0002t0001g0122a0002c0002t0001g0125others(2): Show | 5 | HG00408.hp1 HG00558.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-541delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6182207 | |||||
chr19:6182210
|
T | A | 5 | a0002c0002t0001g0111a0002c0002t0001g0122a0002c0002t0001g0125others(2): Show | 5 | HG00408.hp1 HG00558.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-541T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182210 | ||||||
chr19:6182210
|
T | TA | 21 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(18): Show | 21 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.907-528dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6182210 | |||||
chr19:6182281
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.907-470C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182281 | ||||||
chr19:6182289
|
CT | C | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.907-456delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 6182289 | |||||
chr19:6182398
|
T | C | 19 | a0004c0003t0001g0043a0004c0003t0001g0044a0004c0003t0001g0045others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.907-353T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182398 | ||||||
chr19:6182400
|
G | C | 3 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.907-351G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182400 | ||||||
chr19:6182487
|
T | C | 1 | a0004c0003t0001g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.907-264T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182487 | ||||||
chr19:6182572
|
A | G | 5 | a0005c0006t0001g0023a0005c0006t0001g0025a0005c0006t0001g0026others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.907-179A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182572 | ||||||
chr19:6182604
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.907-147T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182604 | ||||||
chr19:6182629
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.907-122T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182629 | ||||||
chr19:6182745
|
A | C | 3 | a0003c0011t0001g0144a0003c0011t0001g0160a0013c0016t0001g0014 | 3 | HG01891.hp1 HG03453.hp2 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.907-6A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | chr19 | 6182745 | ||||||
chr19:6183017
|
T | C | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1089-22T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 9/14 | chr19 | 6183017 | ||||||
chr19:6183037
|
A | G | 2 | a0002c0002t0001g0103a0012c0021t0001g0100 | 2 | HG02055.hp1 HG02723.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.1089-2A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 9/14 | chr19 | 6183037 | ||||||
chr19:6183324
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1322+52G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183324 | ||||||
chr19:6183377
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1322+105G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183377 | ||||||
chr19:6183457
|
C | T | 19 | a0004c0003t0001g0043a0004c0003t0001g0044a0004c0003t0001g0045others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1322+185C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183457 | ||||||
chr19:6183478
|
T | A | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1322+206T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183478 | ||||||
chr19:6183641
|
G | A | 10 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1322+369G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183641 | ||||||
chr19:6183690
|
A | C | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1322+418A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183690 | ||||||
chr19:6183731
|
G | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1322+459G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183731 | ||||||
chr19:6183779
|
A | G | 3 | a0003c0011t0001g0144a0003c0011t0001g0160a0013c0016t0001g0014 | 3 | HG01891.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1322+507A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183779 | ||||||
chr19:6183933
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1322+661A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183933 | ||||||
chr19:6183942
|
C | T | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1322+670C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6183942 | ||||||
chr19:6184063
|
T | C | 2 | a0009c0010t0002g0052a0009c0010t0002g0054 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1322+791T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184063 | ||||||
chr19:6184114
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1322+842T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184114 | ||||||
chr19:6184268
|
C | A | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1322+996C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184268 | ||||||
chr19:6184282
|
T | C | 2 | a0009c0010t0002g0052a0009c0010t0002g0054 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1322+1010T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184282 | ||||||
chr19:6184326
|
T | C | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1322+1054T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184326 | ||||||
chr19:6184351
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322+1079G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184351 | ||||||
chr19:6184427
|
G | C | 6 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(3): Show | 6 | HG02027.hp1 HG02080.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323-1009G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184427 | ||||||
chr19:6184614
|
G | GA | 8 | a0001c0001t0001g0002a0001c0001t0001g0165a0001c0001t0001g0180others(5): Show | 8 | HG01255.hp1 HG01255.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1323-807dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184614 | |||||
chr19:6184656
|
G | A | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1323-780G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184656 | ||||||
chr19:6184832
|
G | GA | 50 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0153others(47): Show | 50 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1323-564dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
G | GAA | 23 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0168others(20): Show | 23 | HG00408.hp2 HG00673.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1323-565_1323-564d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
G | GAAA | 17 | a0001c0001t0001g0002a0001c0001t0001g0156a0001c0001t0001g0178others(14): Show | 17 | HG00544.hp2 HG00673.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323-566_1323-564d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
G | GAAAAAAA others(3): Show |
3 | a0001c0001t0001g0261a0002c0002t0004g0097a0002c0002t0004g0247 | 3 | HG02602.hp1 HG04199.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1323-573_1323-564d others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GA | G | 15 | a0001c0001t0001g0038a0001c0001t0001g0171a0001c0001t0001g0174others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1323-564delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAA | G | 8 | a0001c0001t0001g0183a0002c0002t0001g0005a0002c0002t0001g0074others(5): Show | 8 | HG00099.hp2 HG02027.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1323-565_1323-564d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAA | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0182a0001c0001t0003g0141others(3): Show | 6 | HG01074.hp1 HG01168.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323-566_1323-564d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAA | G | 6 | a0001c0001t0001g0015a0001c0001t0003g0142a0001c0001t0003g0143others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323-567_1323-564d others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(3): Show |
G | 9 | a0001c0001t0001g0071a0002c0002t0001g0084a0004c0003t0001g0044others(6): Show | 9 | HG01169.hp1 HG01169.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1323-573_1323-564d others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(4): Show |
G | 11 | a0002c0002t0001g0112a0004c0003t0001g0047a0004c0003t0001g0048others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1323-574_1323-564d others(13): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(5): Show |
G | 10 | a0001c0001t0001g0055a0002c0002t0001g0083a0003c0011t0001g0144others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1323-575_1323-564d others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1323-576_1323-564d others(15): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(7): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1323-577_1323-564d others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(9): Show |
G | 2 | a0001c0001t0001g0034a0001c0001t0001g0169 | 2 | HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1323-579_1323-564d others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1323-580_1323-564d others(19): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(12): Show |
G | 2 | a0003c0004t0002g0009a0003c0004t0002g0013 | 2 | HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1323-582_1323-564d others(21): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(13): Show |
G | 14 | a0001c0020t0001g0051a0002c0002t0001g0101a0002c0002t0001g0102others(11): Show | 14 | HG02004.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1323-583_1323-564d others(22): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184832
|
GAAAAAAA others(14): Show |
G | 4 | a0002c0002t0001g0072a0002c0002t0001g0103a0012c0021t0001g0100others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323-584_1323-564d others(23): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184832 | |||||
chr19:6184836
|
A | G | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1323-600A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184836 | ||||||
chr19:6184837
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323-599A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184837 | ||||||
chr19:6184838
|
A | G | 1 | a0005c0006t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1323-598A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184838 | ||||||
chr19:6184839
|
A | G | 1 | a0005c0006t0001g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1323-597A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184839 | ||||||
chr19:6184840
|
A | G | 4 | a0005c0006t0001g0025a0005c0006t0001g0026a0005c0006t0001g0027others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323-596A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184840 | ||||||
chr19:6184845
|
A | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323-591A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184845 | ||||||
chr19:6184854
|
A | G | 1 | a0014c0023t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1323-582A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184854 | ||||||
chr19:6184856
|
A | AAAACAAA others(11): Show |
1 | a0003c0005t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1323-577_1323-576i others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184856 | |||||
chr19:6184856
|
A | AAACAAAA others(10): Show |
5 | a0003c0005t0001g0001a0003c0005t0001g0241a0003c0005t0001g0242others(2): Show | 6 | NA18973.hp2 NA18975.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323-578_1323-577i others(19): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184856 | |||||
chr19:6184860
|
A | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323-576A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184860 | ||||||
chr19:6184862
|
A | C | 2 | a0002c0002t0001g0126a0017c0018t0001g0148 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1323-574A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184862 | ||||||
chr19:6184865
|
A | C | 1 | a0005c0006t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1323-571A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184865 | ||||||
chr19:6184866
|
A | C | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323-570A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6184866 | ||||||
chr19:6184910
|
TTTTTTGT others(5): Show |
T | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1323-508_1323-497d others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 6184910 | |||||
chr19:6185157
|
G | A | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1323-279G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6185157 | ||||||
chr19:6185233
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1323-203A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6185233 | ||||||
chr19:6185389
|
T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323-47T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | chr19 | 6185389 | ||||||
chr19:6185732
|
G | A | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540+79G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6185732 | ||||||
chr19:6185986
|
C | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0074 | 2 | NA18982.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1540+333C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6185986 | ||||||
chr19:6186058
|
C | CT | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0034others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1540+419dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6186058 | |||||
chr19:6186058
|
CT | C | 12 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(9): Show | 13 | HG01433.hp1 HG01891.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540+419delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6186058 | |||||
chr19:6186123
|
A | ATCT | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1540+474_1540+476d others(5): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6186123 | |||||
chr19:6186285
|
T | C | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1540+632T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186285 | ||||||
chr19:6186337
|
G | A | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1540+684G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186337 | ||||||
chr19:6186431
|
T | C | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540+778T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186431 | ||||||
chr19:6186503
|
C | T | 2 | a0009c0010t0002g0052a0009c0010t0002g0054 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1541-780C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186503 | ||||||
chr19:6186555
|
G | GA | 8 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(5): Show | 9 | HG01433.hp1 HG01891.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541-721dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6186555 | |||||
chr19:6186563
|
T | A | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541-720T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186563 | ||||||
chr19:6186588
|
G | C | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1541-695G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186588 | ||||||
chr19:6186600
|
G | A | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1541-683G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186600 | ||||||
chr19:6186738
|
T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541-545T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186738 | ||||||
chr19:6186849
|
C | T | 7 | a0005c0006t0001g0018a0005c0006t0001g0023a0005c0006t0001g0025others(4): Show | 7 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541-434C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186849 | ||||||
chr19:6186866
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1541-417G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186866 | ||||||
chr19:6186867
|
G | A | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541-416G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186867 | ||||||
chr19:6186889
|
A | G | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541-394A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186889 | ||||||
chr19:6186974
|
G | GGT | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541-305_1541-304d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6186974 | |||||
chr19:6186988
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1541-295T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186988 | ||||||
chr19:6186989
|
G | A | 9 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(6): Show | 10 | HG01433.hp1 HG01891.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541-294G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6186989 | ||||||
chr19:6187002
|
G | GT | 14 | a0001c0001t0001g0157a0001c0001t0001g0165a0001c0001t0001g0166others(11): Show | 14 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1541-262dupT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6187002 | |||||
chr19:6187002
|
G | GTT | 28 | a0001c0001t0001g0167a0003c0004t0002g0006a0003c0004t0002g0007others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1541-263_1541-262d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6187002 | |||||
chr19:6187002
|
GT | G | 19 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(16): Show | 20 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1541-262delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 6187002 | |||||
chr19:6187028
|
G | T | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541-255G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6187028 | ||||||
chr19:6187123
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1541-160A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6187123 | ||||||
chr19:6187194
|
G | A | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1541-89G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | chr19 | 6187194 | ||||||
chr19:6187464
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0215 | 2 | HG01515.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1680+42G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 12/14 | chr19 | 6187464 | ||||||
chr19:6187507
|
T | C | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1680+85T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 12/14 | chr19 | 6187507 | ||||||
chr19:6187892
|
G | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0066 | 2 | NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1927+47G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6187892 | ||||||
chr19:6187947
|
A | G | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1927+102A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6187947 | ||||||
chr19:6187984
|
C | T | 22 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(19): Show | 23 | HG01433.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1927+139C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6187984 | ||||||
chr19:6188111
|
C | A | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1927+266C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188111 | ||||||
chr19:6188142
|
G | A | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1927+297G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188142 | ||||||
chr19:6188160
|
G | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1927+315G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188160 | ||||||
chr19:6188223
|
C | T | 32 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(29): Show | 32 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1927+378C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188223 | ||||||
chr19:6188250
|
C | T | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1927+405C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188250 | ||||||
chr19:6188345
|
C | CAA | 41 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(38): Show | 42 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1927+501_1927+502i others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 6188345 | |||||
chr19:6188415
|
C | T | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1927+570C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188415 | ||||||
chr19:6188487
|
A | G | 1 | a0002c0002t0004g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1927+642A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188487 | ||||||
chr19:6188510
|
G | A | 42 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(39): Show | 43 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.1927+665G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188510 | ||||||
chr19:6188798
|
A | G | 55 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(52): Show | 56 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.1927+953A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188798 | ||||||
chr19:6188888
|
G | C | 21 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(18): Show | 22 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1927+1043G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188888 | ||||||
chr19:6188936
|
G | A | 15 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(12): Show | 15 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1927+1091G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6188936 | ||||||
chr19:6189061
|
T | C | 55 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(52): Show | 56 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.1927+1216T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189061 | ||||||
chr19:6189101
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(18): Show | 22 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1927+1256G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189101 | ||||||
chr19:6189124
|
G | C | 21 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(18): Show | 22 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1927+1279G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189124 | ||||||
chr19:6189181
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(18): Show | 22 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1927+1336C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189181 | ||||||
chr19:6189278
|
A | C | 1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1928-1306A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189278 | ||||||
chr19:6189377
|
A | C | 13 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(10): Show | 13 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-1207A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189377 | ||||||
chr19:6189403
|
G | A | 36 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(33): Show | 37 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1928-1181G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189403 | ||||||
chr19:6189512
|
G | T | 1 | a0002c0002t0001g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1928-1072G>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189512 | ||||||
chr19:6189527
|
GT | G | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-1047delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 6189527 | |||||
chr19:6189709
|
TTC | T | 3 | a0003c0004t0002g0131a0009c0010t0002g0052a0009c0010t0002g0054 | 3 | HG02559.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1928-873_1928-872d others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 6189709 | |||||
chr19:6189710
|
TC | T | 8 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0009others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1928-873delC | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189710 | ||||||
chr19:6189711
|
C | T | 2 | a0003c0004t0002g0008a0003c0012t0002g0046 | 2 | HG02109.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1928-873C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189711 | ||||||
chr19:6189715
|
C | T | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-869C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189715 | ||||||
chr19:6189999
|
T | C | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-585T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6189999 | ||||||
chr19:6190062
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1928-522T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190062 | ||||||
chr19:6190174
|
C | G | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-410C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190174 | ||||||
chr19:6190214
|
G | A | 14 | a0001c0001t0001g0167a0003c0004t0002g0006a0003c0004t0002g0007others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1928-370G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190214 | ||||||
chr19:6190292
|
T | C | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-292T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190292 | ||||||
chr19:6190357
|
C | G | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-227C>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190357 | ||||||
chr19:6190565
|
A | T | 13 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1928-19A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 13/14 | chr19 | 6190565 | ||||||
chr19:6190790
|
A | AACACAC | 11 | a0001c0001t0001g0196a0001c0001t0001g0211a0001c0001t0001g0214others(8): Show | 11 | HG00558.hp1 HG02083.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.*35+102_*35+107dup others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190790 | |||||
chr19:6190798
|
C | CACACACA others(5): Show |
1 | a0004c0003t0001g0045 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.*35+107_*35+108ins others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190798 | |||||
chr19:6190798
|
CAT | C | 25 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0132others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.*35+108_*35+109del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190798 | |||||
chr19:6190800
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.*35+108T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190800 | ||||||
chr19:6190804
|
C | CAT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(69): Show | 72 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.*35+113_*35+114ins others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190804 | |||||
chr19:6190804
|
C | T | 11 | a0001c0001t0001g0196a0001c0001t0001g0211a0001c0001t0001g0214others(8): Show | 11 | HG00558.hp1 HG02083.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.*35+112C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190804 | ||||||
chr19:6190806
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.*35+114C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190806 | ||||||
chr19:6190808
|
T | C | 15 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0196others(12): Show | 15 | HG00558.hp1 HG00597.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.*35+116T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190808 | ||||||
chr19:6190808
|
T | TAC | 11 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0206others(8): Show | 11 | HG02083.hp2 HG02886.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.*35+118_*35+119dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190808 | |||||
chr19:6190812
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.*35+120T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190812 | ||||||
chr19:6190812
|
T | TAC | 38 | a0001c0001t0001g0132a0001c0001t0001g0152a0001c0001t0001g0155others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.*35+159_*35+160dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
T | TACAC | 33 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0139others(30): Show | 33 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*35+157_*35+160dup others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
T | TACACAC | 3 | a0002c0002t0001g0076a0002c0002t0001g0081a0002c0002t0001g0115 | 3 | HG00423.hp1 HG00673.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.*35+155_*35+160dup others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0170a0003c0012t0002g0046 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.*35+151_*35+160dup others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
T | TACACACA others(7): Show |
1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*35+147_*35+160dup others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
T | TACACACA others(13): Show |
1 | a0015c0025t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.*35+141_*35+160dup others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TAC | T | 31 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0037others(28): Show | 32 | HG00735.hp2 HG01891.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.*35+159_*35+160del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TACAC | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0261a0002c0002t0001g0092others(6): Show | 9 | HG01433.hp1 HG01515.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+157_*35+160del others(4): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TACACAC | T | 7 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.*35+155_*35+160del others(6): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TACACACA others(1): Show |
T | 16 | a0001c0001t0001g0221a0001c0001t0001g0240a0001c0017t0001g0239others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.*35+153_*35+160del others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TACACACA others(3): Show |
T | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*35+151_*35+160del others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190812
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0003g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*35+147_*35+160del others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6190812 | |||||
chr19:6190820
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.*35+128C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190820 | ||||||
chr19:6190966
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*35+274T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6190966 | ||||||
chr19:6191058
|
A | G | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*35+366A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191058 | ||||||
chr19:6191171
|
C | T | 2 | a0003c0011t0001g0160a0013c0016t0001g0014 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*35+479C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191171 | ||||||
chr19:6191182
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.*35+490C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191182 | ||||||
chr19:6191241
|
GT | G | 10 | a0001c0001t0001g0219a0002c0002t0001g0103a0003c0005t0001g0001others(7): Show | 11 | HG01433.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.*35+563delT | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6191241 | |||||
chr19:6191290
|
A | C | 13 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(10): Show | 13 | HG01884.hp2 HG02027.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.*35+598A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191290 | ||||||
chr19:6191316
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*35+624G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191316 | ||||||
chr19:6191317
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*35+625C>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191317 | ||||||
chr19:6191404
|
G | C | 3 | a0007c0008t0002g0145a0007c0008t0002g0161a0007c0008t0002g0162 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.*35+712G>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191404 | ||||||
chr19:6191481
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0029 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*35+789G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191481 | ||||||
chr19:6191576
|
A | G | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*35+884A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191576 | ||||||
chr19:6191650
|
T | A | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*35+958T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191650 | ||||||
chr19:6191650
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*35+958T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191650 | ||||||
chr19:6191681
|
A | T | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-987A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191681 | ||||||
chr19:6191716
|
G | A | 13 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(10): Show | 13 | HG01884.hp2 HG02027.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.*36-952G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191716 | ||||||
chr19:6191996
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.*36-672T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6191996 | ||||||
chr19:6192043
|
A | AAC | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-620_*36-619dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192043 | |||||
chr19:6192064
|
A | G | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-604A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192064 | ||||||
chr19:6192071
|
C | CA | 15 | a0001c0001t0001g0203a0002c0002t0001g0079a0002c0002t0001g0081others(12): Show | 15 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.*36-572dupA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAA | 7 | a0002c0002t0006g0069a0003c0005t0001g0001a0003c0005t0001g0133others(4): Show | 8 | HG01433.hp1 HG03017.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.*36-573_*36-572dup others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0015a0001c0001t0003g0142a0001c0001t0003g0163others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.*36-579_*36-572dup others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(3): Show |
2 | a0005c0006t0001g0027a0005c0006t0001g0028 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.*36-581_*36-572dup others(10): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(6): Show |
1 | a0003c0004t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*36-584_*36-572dup others(13): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(7): Show |
1 | a0009c0010t0002g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*36-585_*36-572dup others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(8): Show |
2 | a0003c0012t0002g0046a0009c0010t0002g0054 | 2 | HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.*36-586_*36-572dup others(15): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
C | CAAAAAAA others(9): Show |
8 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.*36-587_*36-572dup others(16): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
CA | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.*36-572delA | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192071
|
CAA | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0166a0001c0001t0001g0181others(6): Show | 9 | HG01069.hp2 HG01884.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-573_*36-572del others(2): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 6192071 | |||||
chr19:6192097
|
T | A | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*36-571T>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192097 | ||||||
chr19:6192101
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A | C | 13 | a0004c0003t0002g0134a0004c0003t0002g0135a0004c0003t0002g0136others(10): Show | 13 | HG01884.hp2 HG02027.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.*36-567A>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192101 | ||||||
chr19:6192144
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T | G | 14 | a0001c0001t0001g0015a0001c0001t0003g0141a0001c0001t0003g0142others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.*36-524T>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192144 | ||||||
chr19:6192172
|
C | T | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-496C>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192172 | ||||||
chr19:6192272
|
G | A | 2 | a0009c0010t0002g0052a0009c0010t0002g0054 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*36-396G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192272 | ||||||
chr19:6192281
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T | C | 6 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.*36-387T>C | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192281 | ||||||
chr19:6192437
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A | T | 1 | a0017c0018t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*36-231A>T | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192437 | ||||||
chr19:6192510
|
A | G | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-158A>G | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192510 | ||||||
chr19:6192560
|
G | A | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-108G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192560 | ||||||
chr19:6192569
|
G | A | 26 | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(23): Show | 26 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.*36-99G>A | ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | chr19 | 6192569 |