geneid | 55326 |
---|---|
ensemblid | ENSG00000155189.12 |
hgncid | 20886 |
symbol | AGPAT5 |
name | 1-acylglycerol-3-phosphate O-acyltransferase 5 |
refseq_nuc | NM_018361.5 |
refseq_prot | NP_060831.2 |
ensembl_nuc | ENST00000285518.11 |
ensembl_prot | ENSP00000285518.6 |
mane_status | MANE Select |
chr | chr8 |
start | 6708642 |
end | 6761503 |
strand | + |
ver | v1.2 |
region | chr8:6708642-6761503 |
region5000 | chr8:6703642-6766503 |
regionname0 | AGPAT5_chr8_6708642_6761503 |
regionname5000 | AGPAT5_chr8_6703642_6766503 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 364 | 398 | 83 | 75 | 180 | 15 | 43 | 140 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0002 | 0/0 | 364 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0003 | 0/0 | 364 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0004 | 0/0 | 364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1095 | 316 | 67 | 67 | 129 | 15 | 36 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0002 | 0/0 | 1095 | 60 | 0 | 6 | 48 | 0 | 6 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0003 | 0/0 | 1095 | 16 | 13 | 2 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0004 | 0/0 | 1095 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0005 | 0/0 | 1095 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0006 | 0/0 | 1095 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0007 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0008 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
c0009 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4143 | 150 | 17 | 37 | 77 | 10 | 9 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0002 | 0/0 | 4143 | 75 | 3 | 12 | 44 | 1 | 15 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0003 | 0/0 | 4143 | 64 | 5 | 17 | 26 | 2 | 14 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0004 | 0/0 | 4144 | 21 | 3 | 1 | 17 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0005 | 0/0 | 4144 | 8 | 8 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0006 | 0/0 | 4141 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0007 | 0/0 | 4145 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0008 | 1/0 | 4143 | 4 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0009 | 0/0 | 4143 | 4 | 0 | 0 | 3 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0010 | 0/0 | 4143 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0011 | 0/0 | 4144 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0012 | 0/0 | 4141 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0013 | 0/0 | 4143 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0014 | 0/0 | 4143 | 3 | 1 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0015 | 0/0 | 4143 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0016 | 0/0 | 4143 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0017 | 0/1 | 4143 | 2 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0018 | 0/0 | 4143 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0019 | 0/0 | 4143 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0020 | 0/0 | 4143 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0021 | 0/0 | 4143 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0022 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0023 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0024 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0025 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0026 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0027 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0028 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0029 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0030 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0031 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0032 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0033 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0034 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0035 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0036 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0037 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0038 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0039 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0040 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0041 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0042 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0043 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0044 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0045 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0046 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0047 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0048 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0049 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0050 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0051 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0052 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0053 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0054 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
t0055 | 0/0 | 4144 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
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 | 9 | 0 | 1 | 3 | 2 | 3 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0002 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1095 | 316 | 67 | 67 | 129 | 15 | 36 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002 | 0/0 | 1095 | 60 | 0 | 6 | 48 | 0 | 6 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003 | 0/0 | 1095 | 16 | 13 | 2 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0005 | 0/0 | 1095 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0006 | 0/0 | 1095 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0008 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0002c0004 | 0/0 | 1095 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0003c0009 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0004c0007 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5237 | 91 | 17 | 31 | 32 | 9 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0002 | 0/0 | 5237 | 71 | 1 | 12 | 42 | 1 | 15 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0003 | 0/0 | 5237 | 59 | 4 | 16 | 25 | 2 | 12 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0004 | 0/0 | 5238 | 21 | 3 | 1 | 17 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0005 | 0/0 | 5238 | 7 | 7 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0007 | 0/0 | 5239 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0008 | 1/0 | 5237 | 4 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0009 | 0/0 | 5237 | 4 | 0 | 0 | 3 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0010 | 0/0 | 5237 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0011 | 0/0 | 5238 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0014 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0015 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0016 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0017 | 0/1 | 5237 | 2 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0018 | 0/0 | 5237 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0019 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0020 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0021 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0022 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0023 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0024 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0025 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0026 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0027 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0028 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0029 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0030 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0031 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0033 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0034 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0035 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0036 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0037 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0038 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0039 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0040 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0042 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0043 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0045 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0046 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0047 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0048 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0050 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0051 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0053 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0054 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0001t0055 | 0/0 | 5238 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0001 | 0/0 | 5237 | 55 | 0 | 6 | 44 | 0 | 5 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0002 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0003 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0032 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0044 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0002t0052 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0002 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0006 | 0/0 | 5235 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0012 | 0/0 | 5235 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0013 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0014 | 0/0 | 5237 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0003t0041 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0005t0005 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0005t0013 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0006t0002 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0006t0049 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0001c0008t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0002c0004t0003 | 0/0 | 5237 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0003c0009t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
a0004c0007t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | copy fasta | chr8 | 6703642 | 6766503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0008g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0010g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0015g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0016g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0017g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0017g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0018g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0019g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0019g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0020g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0021g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0021g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0022g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0023g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0024g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0025g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0026g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0027g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0028g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0029g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0030g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0031g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0033g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0034g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0035g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0036g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0037g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0038g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0039g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0040g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0042g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0043g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0045g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0046g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0047g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0048g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0050g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0051g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0053g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0054g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0001t0055g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0032g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0044g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0002t0052g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0006g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0012g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0014g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0003t0041g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0005t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0005t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0005t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0006t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0006t0049g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0001c0008t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0002c0004t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0002c0004t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0003c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
a0004c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00280 | hp2 | a0003 | c0009 | t0001 | g0185 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0252 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00408 | hp1 | a0001 | c0002 | t0032 | g0229 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0273 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01070 | hp2 | a0001 | c0003 | t0014 | g0027 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01099 | hp1 | a0001 | c0003 | t0014 | g0027 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01106 | hp2 | a0002 | c0004 | t0003 | g0026 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01109 | hp2 | a0001 | c0001 | t0023 | g0020 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01175 | hp2 | a0001 | c0001 | t0043 | g0001 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01243 | hp1 | a0001 | c0001 | t0021 | g0131 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01261 | hp2 | a0001 | c0001 | t0040 | g0146 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01358 | hp1 | a0001 | c0001 | t0019 | g0274 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01496 | hp1 | a0001 | c0001 | t0017 | g0020 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0267 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01884 | hp1 | a0001 | c0001 | t0042 | g0222 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0204 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02055 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02055 | hp2 | a0002 | c0004 | t0003 | g0026 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02145 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02145 | hp2 | a0001 | c0001 | t0031 | g0118 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0203 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02280 | hp2 | a0001 | c0001 | t0038 | g0178 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02698 | hp1 | a0001 | c0001 | t0009 | g0251 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02738 | hp1 | a0001 | c0001 | t0045 | g0227 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0069 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0065 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02886 | hp2 | a0001 | c0001 | t0033 | g0125 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0048 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0232 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02922 | hp2 | a0001 | c0001 | t0053 | g0043 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0304 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0231 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03139 | hp1 | a0001 | c0001 | t0039 | g0044 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03139 | hp2 | a0001 | c0003 | t0012 | g0018 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03195 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0205 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03453 | hp1 | a0001 | c0001 | t0029 | g0109 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0068 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03486 | hp1 | a0001 | c0005 | t0005 | g0130 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03486 | hp2 | a0001 | c0005 | t0013 | g0073 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03490 | hp2 | a0002 | c0004 | t0003 | g0025 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03492 | hp2 | a0002 | c0004 | t0003 | g0025 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03516 | hp1 | a0001 | c0003 | t0041 | g0107 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03516 | hp2 | a0001 | c0003 | t0013 | g0064 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03540 | hp1 | a0001 | c0001 | t0048 | g0061 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0303 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0139 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03669 | hp2 | a0001 | c0002 | t0044 | g0220 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03704 | hp1 | a0004 | c0007 | t0001 | g0193 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03834 | hp1 | a0001 | c0001 | t0025 | g0021 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03927 | hp2 | a0001 | c0001 | t0027 | g0133 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04184 | hp1 | a0001 | c0001 | t0026 | g0021 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0152 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04199 | hp2 | a0001 | c0001 | t0054 | g0017 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18522 | hp1 | a0001 | c0001 | t0022 | g0045 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18906 | hp1 | a0001 | c0003 | t0012 | g0018 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18939 | hp2 | a0001 | c0001 | t0034 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18956 | hp1 | a0001 | c0001 | t0018 | g0014 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18957 | hp2 | a0001 | c0001 | t0009 | g0108 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18970 | hp1 | a0001 | c0001 | t0008 | g0257 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18975 | hp1 | a0001 | c0001 | t0046 | g0100 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18975 | hp2 | a0001 | c0006 | t0049 | g0292 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18987 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18993 | hp2 | a0001 | c0001 | t0009 | g0234 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19009 | hp2 | a0001 | c0001 | t0018 | g0241 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19010 | hp1 | a0001 | c0001 | t0030 | g0096 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19030 | hp1 | a0001 | c0001 | t0050 | g0075 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19043 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19054 | hp1 | a0001 | c0008 | t0001 | g0225 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19055 | hp1 | a0001 | c0002 | t0052 | g0158 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19064 | hp1 | a0001 | c0001 | t0055 | g0313 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19081 | hp1 | a0001 | c0001 | t0035 | g0297 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19082 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19089 | hp1 | a0001 | c0006 | t0002 | g0290 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA19240 | hp2 | a0001 | c0003 | t0012 | g0018 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20752 | hp2 | a0001 | c0001 | t0051 | g0135 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20805 | hp2 | a0001 | c0001 | t0036 | g0268 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20905 | hp1 | a0001 | c0001 | t0037 | g0269 | SAS | GIH | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | GIH | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0076 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02109 | hp2 | a0001 | c0005 | t0013 | g0072 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02486 | hp1 | a0001 | c0001 | t0016 | g0074 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02486 | hp2 | a0001 | c0003 | t0006 | g0305 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG02559 | hp2 | a0001 | c0003 | t0006 | g0306 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG03471 | hp2 | a0001 | c0001 | t0047 | g0189 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG06807 | hp1 | a0001 | c0001 | t0021 | g0042 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20300 | hp1 | a0001 | c0001 | t0015 | g0067 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
NA21309 | hp2 | a0001 | c0001 | t0024 | g0062 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0017 | g0047 | REF | REF | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0258 | REF | REF | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:6708766
|
G | C | 1 | a0002 | 4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
missense_variant | MODERATE | c.98G>C | p.Gly33Ala | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 125/5237 | 98/1095 | 33/364 | chr8 | 6708766 | ||
chr8:6730761
|
C | A | 1 | a0004 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.340C>A | p.His114Asn | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/8 | 367/5237 | 340/1095 | 114/364 | chr8 | 6730761 | ||
chr8:6757164
|
A | G | 1 | a0003 | 1 | HG00280.hp2 | missense_variant&splice_region_variant | MODERATE | c.871A>G | p.Met291Val | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 898/5237 | 871/1095 | 291/364 | chr8 | 6757164 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:6708830
|
C | G | 2 | a0001c0002a0003c0009 | 61 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(58): Show |
synonymous_variant | LOW | c.162C>G | p.Leu54Leu | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 189/5237 | 162/1095 | 54/364 | chr8 | 6708830 | ||
chr8:6708839
|
C | T | 1 | a0001c0006 | 2 | NA18975.hp2 NA19089.hp1 |
synonymous_variant | LOW | c.171C>T | p.Val57Val | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 198/5237 | 171/1095 | 57/364 | chr8 | 6708839 | ||
chr8:6730802
|
A | G | 1 | a0001c0005 | 3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.381A>G | p.Pro127Pro | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/8 | 408/5237 | 381/1095 | 127/364 | chr8 | 6730802 | ||
chr8:6732605
|
A | G | 1 | a0001c0003 | 16 | HG01070.hp2 HG01099.hp1 HG02055.hp1 others(13): Show |
synonymous_variant | LOW | c.450A>G | p.Lys150Lys | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/8 | 477/5237 | 450/1095 | 150/364 | chr8 | 6732605 | ||
chr8:6732632
|
C | T | 1 | a0001c0008 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.477C>T | p.Tyr159Tyr | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/8 | 504/5237 | 477/1095 | 159/364 | chr8 | 6732632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:6708653
|
C | A | 1 | a0001c0001t0022 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 16 | chr8 | 6708653 | |||||
chr8:6708665
|
G | A | 3 | a0001c0001t0011a0001c0001t0017a0001c0001t0023 | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 4 | chr8 | 6708665 | |||||
chr8:6757546
|
A | G | 2 | a0001c0001t0010a0001c0001t0016 | 7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*158A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 158 | chr8 | 6757546 | |||||
chr8:6757637
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*249A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 249 | chr8 | 6757637 | |||||
chr8:6757642
|
C | T | 1 | a0001c0001t0054 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 254 | chr8 | 6757642 | |||||
chr8:6757644
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*256A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 256 | chr8 | 6757644 | |||||
chr8:6757729
|
G | A | 4 | a0001c0001t0010a0001c0001t0016a0001c0001t0024others(1): Show | 11 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 341 | chr8 | 6757729 | |||||
chr8:6757730
|
T | C | 3 | a0001c0001t0025a0001c0001t0026a0001c0001t0027 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 342 | chr8 | 6757730 | |||||
chr8:6757754
|
A | G | 1 | a0001c0001t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 366 | chr8 | 6757754 | |||||
chr8:6757905
|
A | G | 1 | a0001c0002t0052 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 517 | chr8 | 6757905 | |||||
chr8:6758042
|
C | A | 1 | a0001c0001t0028 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 654 | chr8 | 6758042 | |||||
chr8:6758087
|
C | G | 2 | a0001c0001t0023a0001c0001t0051 | 2 | HG01109.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*699C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 699 | chr8 | 6758087 | |||||
chr8:6758142
|
A | G | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
3_prime_UTR_variant | MODIFIER | c.*754A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 754 | chr8 | 6758142 | |||||
chr8:6758233
|
G | A | 7 | a0001c0001t0003a0001c0001t0022a0001c0001t0029others(4): Show | 68 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*845G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 845 | chr8 | 6758233 | |||||
chr8:6758317
|
G | A | 2 | a0001c0003t0013a0001c0005t0013 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 929 | chr8 | 6758317 | |||||
chr8:6758326
|
G | A | 1 | a0001c0001t0018 | 2 | NA18956.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*938G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 938 | chr8 | 6758326 | |||||
chr8:6758331
|
C | G | 2 | a0001c0001t0015a0001c0001t0050 | 4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 943 | chr8 | 6758331 | |||||
chr8:6758360
|
C | T | 1 | a0001c0001t0031 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 972 | chr8 | 6758360 | |||||
chr8:6758368
|
G | A | 1 | a0001c0001t0010 | 4 | HG02572.hp1 HG02895.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*980G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 980 | chr8 | 6758368 | |||||
chr8:6758369
|
C | T | 1 | a0001c0006t0049 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 981 | chr8 | 6758369 | |||||
chr8:6758380
|
T | C | 1 | a0001c0002t0032 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 992 | chr8 | 6758380 | |||||
chr8:6758452
|
C | T | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1064C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1064 | chr8 | 6758452 | |||||
chr8:6758463
|
G | A | 1 | a0001c0001t0020 | 2 | HG01981.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1075 | chr8 | 6758463 | |||||
chr8:6758499
|
C | G | 2 | a0001c0001t0005a0001c0005t0005 | 8 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1111 | chr8 | 6758499 | |||||
chr8:6758517
|
G | A | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG03834.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1129 | chr8 | 6758517 | |||||
chr8:6758545
|
T | C | 1 | a0001c0001t0038 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1157T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1157 | chr8 | 6758545 | |||||
chr8:6758550
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1162A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1162 | chr8 | 6758550 | |||||
chr8:6758616
|
T | C | 54 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(51): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1228T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1228 | chr8 | 6758616 | |||||
chr8:6758629
|
C | T | 1 | a0001c0001t0037 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1241 | chr8 | 6758629 | |||||
chr8:6758646
|
C | T | 1 | a0001c0001t0036 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1258 | chr8 | 6758646 | |||||
chr8:6758650
|
A | C | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1262A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1262 | chr8 | 6758650 | |||||
chr8:6758690
|
G | C | 1 | a0001c0001t0020 | 2 | HG01981.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1302G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1302 | chr8 | 6758690 | |||||
chr8:6758719
|
C | T | 2 | a0001c0001t0021a0001c0001t0053 | 3 | HG01243.hp1 HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1331C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1331 | chr8 | 6758719 | |||||
chr8:6759000
|
A | G | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(5): Show | 42 | HG01934.hp1 HG02080.hp2 HG02109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1612A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1612 | chr8 | 6759000 | |||||
chr8:6759080
|
T | C | 2 | a0001c0003t0013a0001c0005t0013 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1692T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1692 | chr8 | 6759080 | |||||
chr8:6759116
|
T | C | 1 | a0001c0001t0034 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1728T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1728 | chr8 | 6759116 | |||||
chr8:6759135
|
A | T | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1747A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1747 | chr8 | 6759135 | |||||
chr8:6759171
|
G | T | 1 | a0001c0001t0048 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1783G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1783 | chr8 | 6759171 | |||||
chr8:6759197
|
C | T | 1 | a0001c0001t0055 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1809C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1809 | chr8 | 6759197 | |||||
chr8:6759266
|
G | A | 2 | a0001c0003t0006a0001c0003t0012 | 9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1878 | chr8 | 6759266 | |||||
chr8:6759319
|
C | A | 1 | a0001c0001t0035 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1931 | chr8 | 6759319 | |||||
chr8:6759332
|
G | A | 3 | a0001c0001t0039a0001c0003t0006a0001c0003t0012 | 10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1944G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1944 | chr8 | 6759332 | |||||
chr8:6759395
|
T | A | 1 | a0001c0001t0040 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2007 | chr8 | 6759395 | |||||
chr8:6759508
|
T | C | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2120T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2120 | chr8 | 6759508 | |||||
chr8:6759749
|
C | T | 1 | a0001c0001t0055 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2361 | chr8 | 6759749 | |||||
chr8:6759768
|
C | G | 1 | a0001c0001t0034 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2380C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2380 | chr8 | 6759768 | |||||
chr8:6759844
|
T | C | 7 | a0001c0001t0010a0001c0001t0016a0001c0001t0024others(4): Show | 12 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2456T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2456 | chr8 | 6759844 | |||||
chr8:6759956
|
T | C | 1 | a0001c0001t0042 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2568T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2568 | chr8 | 6759956 | |||||
chr8:6760076
|
G | A | 1 | a0001c0001t0043 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2688G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2688 | chr8 | 6760076 | |||||
chr8:6760232
|
A | C | 1 | a0001c0001t0026 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2844A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2844 | chr8 | 6760232 | |||||
chr8:6760233
|
A | G | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2845A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2845 | chr8 | 6760233 | |||||
chr8:6760256
|
G | C | 1 | a0001c0001t0019 | 2 | HG00323.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2868G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2868 | chr8 | 6760256 | |||||
chr8:6760271
|
G | A | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2883G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2883 | chr8 | 6760271 | |||||
chr8:6760451
|
C | G | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3063C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3063 | chr8 | 6760451 | |||||
chr8:6760461
|
C | G | 1 | a0001c0001t0030 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3073C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3073 | chr8 | 6760461 | |||||
chr8:6760474
|
C | CA | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3092dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3093 | INFO_REALIGN_3_PRIME | chr8 | 6760474 | ||||
chr8:6760557
|
A | G | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3169A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3169 | chr8 | 6760557 | |||||
chr8:6760584
|
G | C | 4 | a0001c0001t0014a0001c0001t0017a0001c0001t0023others(1): Show | 6 | HG01070.hp2 HG01099.hp1 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3196G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3196 | chr8 | 6760584 | |||||
chr8:6760626
|
A | G | 2 | a0001c0001t0015a0001c0001t0050 | 4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3238A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3238 | chr8 | 6760626 | |||||
chr8:6760649
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3261A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3261 | chr8 | 6760649 | |||||
chr8:6760735
|
A | G | 1 | a0001c0001t0046 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3347 | chr8 | 6760735 | |||||
chr8:6760797
|
CTA | C | 2 | a0001c0003t0006a0001c0003t0012 | 9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3411_*3412delAT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3411 | INFO_REALIGN_3_PRIME | chr8 | 6760797 | ||||
chr8:6760983
|
A | C | 1 | a0001c0001t0045 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3595A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3595 | chr8 | 6760983 | |||||
chr8:6761335
|
C | CT | 2 | a0001c0001t0007a0001c0001t0011 | 9 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3954dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3955 | INFO_REALIGN_3_PRIME | chr8 | 6761335 | ||||
chr8:6761342
|
T | TA | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0055others(1): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3960dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3961 | INFO_REALIGN_3_PRIME | chr8 | 6761342 | ||||
chr8:6761451
|
G | T | 1 | a0001c0002t0044 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4063G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 4063 | chr8 | 6761451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:6708928
|
G | A | 2 | a0001c0001t0021g0042a0001c0001t0053g0043 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+41G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6708928 | ||||||
chr8:6709114
|
C | T | 15 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(12): Show | 20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.219+227C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709114 | ||||||
chr8:6709150
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+263G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709150 | ||||||
chr8:6709167
|
G | C | 1 | a0001c0001t0022g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+280G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709167 | ||||||
chr8:6709231
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.219+344G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709231 | ||||||
chr8:6709235
|
G | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+348G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709235 | ||||||
chr8:6709294
|
T | C | 6 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+407T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709294 | ||||||
chr8:6709399
|
T | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(208): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+512T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709399 | ||||||
chr8:6709444
|
G | C | 6 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0052others(3): Show | 8 | HG00438.hp2 HG01109.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+557G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709444 | ||||||
chr8:6709485
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219+598T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709485 | ||||||
chr8:6709525
|
G | A | 10 | a0001c0001t0003g0230a0001c0001t0007g0034a0001c0001t0007g0231others(7): Show | 11 | HG01109.hp2 HG01496.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+638G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709525 | ||||||
chr8:6709562
|
T | TA | 30 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(27): Show | 38 | HG01346.hp1 HG01934.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.219+689dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | |||||
chr8:6709562
|
TA | T | 55 | a0001c0001t0001g0063a0001c0001t0001g0282a0001c0001t0001g0294others(52): Show | 64 | HG00597.hp2 HG00621.hp2 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.219+689delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | |||||
chr8:6709562
|
TAA | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 249 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.219+688_219+689del others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | |||||
chr8:6709567
|
A | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+680A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709567 | ||||||
chr8:6709709
|
G | C | 10 | a0001c0001t0001g0071a0001c0001t0004g0070a0001c0001t0010g0005others(7): Show | 13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+822G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709709 | ||||||
chr8:6709832
|
T | C | 1 | a0001c0002t0001g0022 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.219+945T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709832 | ||||||
chr8:6709901
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(209): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.219+1014A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709901 | ||||||
chr8:6709959
|
C | G | 36 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(33): Show | 49 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.219+1072C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709959 | ||||||
chr8:6710028
|
A | G | 2 | a0001c0003t0002g0303a0001c0003t0002g0304 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219+1141A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710028 | ||||||
chr8:6710036
|
G | T | 1 | a0001c0001t0002g0243 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.219+1149G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710036 | ||||||
chr8:6710066
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219+1179A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710066 | ||||||
chr8:6710123
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0275 | 3 | HG00323.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.219+1236C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710123 | ||||||
chr8:6710126
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(208): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+1239C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710126 | ||||||
chr8:6710128
|
T | TA | 37 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(34): Show | 50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+1248dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6710128 | |||||
chr8:6710186
|
A | T | 6 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+1299A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710186 | ||||||
chr8:6710300
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.219+1413G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710300 | ||||||
chr8:6710369
|
G | A | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+1482G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710369 | ||||||
chr8:6710378
|
A | C | 1 | a0001c0001t0011g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219+1491A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710378 | ||||||
chr8:6710419
|
A | G | 7 | a0001c0001t0004g0066a0001c0001t0015g0065a0001c0001t0015g0067others(4): Show | 7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+1532A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710419 | ||||||
chr8:6710429
|
G | A | 1 | a0001c0001t0004g0019 | 3 | NA18972.hp1 NA18983.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.219+1542G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710429 | ||||||
chr8:6710476
|
C | T | 1 | a0001c0001t0045g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.219+1589C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710476 | ||||||
chr8:6710553
|
T | A | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG00621.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.219+1666T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710553 | ||||||
chr8:6710614
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.219+1727C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710614 | ||||||
chr8:6710680
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(208): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+1793A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710680 | ||||||
chr8:6710708
|
C | G | 3 | a0001c0001t0001g0056a0001c0001t0002g0077a0001c0008t0001g0225 | 3 | NA18986.hp1 NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.219+1821C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710708 | ||||||
chr8:6710974
|
T | C | 31 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(28): Show | 39 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.219+2087T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710974 | ||||||
chr8:6711020
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+2133T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711020 | ||||||
chr8:6711021
|
T | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0081others(32): Show | 49 | HG00099.hp2 HG00438.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.219+2134T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711021 | ||||||
chr8:6711046
|
A | G | 37 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(34): Show | 50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+2159A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711046 | ||||||
chr8:6711100
|
T | A | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2213T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711100 | ||||||
chr8:6711125
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(136): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.219+2238C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711125 | ||||||
chr8:6711128
|
T | C | 1 | a0001c0001t0016g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219+2241T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711128 | ||||||
chr8:6711214
|
A | G | 2 | a0001c0002t0001g0033a0001c0002t0001g0224 | 3 | HG02129.hp1 NA18961.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.219+2327A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711214 | ||||||
chr8:6711319
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(220): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.219+2432A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711319 | ||||||
chr8:6711394
|
A | G | 1 | a0001c0001t0019g0274 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.219+2507A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711394 | ||||||
chr8:6711409
|
T | C | 6 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0052others(3): Show | 8 | HG00438.hp2 HG01109.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+2522T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711409 | ||||||
chr8:6711412
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+2525T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711412 | ||||||
chr8:6711466
|
A | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2579A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711466 | ||||||
chr8:6711501
|
T | C | 14 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(11): Show | 19 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.219+2614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711501 | ||||||
chr8:6711534
|
C | G | 1 | a0001c0001t0015g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219+2647C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711534 | ||||||
chr8:6711653
|
A | T | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+2766A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711653 | ||||||
chr8:6711665
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0051g0135 | 2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.219+2778G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711665 | ||||||
chr8:6711697
|
G | C | 1 | a0001c0002t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.219+2810G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711697 | ||||||
chr8:6711741
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(215): Show | 273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.219+2854C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711741 | ||||||
chr8:6711749
|
T | G | 72 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0081others(69): Show | 90 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.219+2862T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711749 | ||||||
chr8:6711804
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(256): Show | 328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.219+2917T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711804 | ||||||
chr8:6711826
|
G | T | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+2939G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711826 | ||||||
chr8:6711912
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+3025C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711912 | ||||||
chr8:6711985
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+3098C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711985 | ||||||
chr8:6712093
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.219+3206G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712093 | ||||||
chr8:6712127
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.219+3240C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712127 | ||||||
chr8:6712228
|
A | G | 1 | a0001c0001t0002g0318 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.219+3341A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712228 | ||||||
chr8:6712345
|
T | C | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219+3458T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712345 | ||||||
chr8:6712372
|
TTA | T | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0071others(126): Show | 164 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(161): Show |
intron_variant | MODIFIER | c.219+3501_219+3502d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6712372 | |||||
chr8:6712406
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(246): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.219+3519C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712406 | ||||||
chr8:6712449
|
G | A | 1 | a0001c0003t0006g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+3562G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712449 | ||||||
chr8:6712475
|
T | G | 1 | a0001c0001t0003g0080 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.219+3588T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712475 | ||||||
chr8:6712551
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219+3664G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712551 | ||||||
chr8:6712571
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.219+3684C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712571 | ||||||
chr8:6712632
|
G | A | 1 | a0001c0001t0029g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219+3745G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712632 | ||||||
chr8:6712637
|
T | G | 31 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(28): Show | 39 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.219+3750T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712637 | ||||||
chr8:6712640
|
G | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(215): Show | 273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.219+3753G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712640 | ||||||
chr8:6712713
|
G | C | 37 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(34): Show | 50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+3826G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712713 | ||||||
chr8:6712796
|
C | A | 1 | a0001c0001t0004g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219+3909C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712796 | ||||||
chr8:6712833
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(247): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.219+3946C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712833 | ||||||
chr8:6712848
|
A | G | 1 | a0001c0001t0015g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219+3961A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712848 | ||||||
chr8:6712854
|
A | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+3967A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712854 | ||||||
chr8:6712878
|
TTC | T | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+3993_219+3994d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6712878 | |||||
chr8:6712881
|
T | C | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+3994T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712881 | ||||||
chr8:6712911
|
C | A | 1 | a0001c0001t0002g0281 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219+4024C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712911 | ||||||
chr8:6712921
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+4034A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712921 | ||||||
chr8:6712937
|
C | G | 2 | a0001c0001t0001g0223a0001c0001t0042g0222 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.219+4050C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712937 | ||||||
chr8:6713053
|
C | T | 10 | a0001c0001t0001g0071a0001c0001t0004g0070a0001c0001t0010g0005others(7): Show | 13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+4166C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713053 | ||||||
chr8:6713062
|
T | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(248): Show | 314 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.219+4175T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713062 | ||||||
chr8:6713095
|
T | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.219+4208T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713095 | ||||||
chr8:6713108
|
T | C | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4221T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713108 | ||||||
chr8:6713121
|
A | G | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4234A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713121 | ||||||
chr8:6713175
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+4288G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713175 | ||||||
chr8:6713266
|
A | G | 1 | a0001c0001t0003g0221 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.219+4379A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713266 | ||||||
chr8:6713292
|
G | T | 1 | a0001c0001t0003g0106 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.219+4405G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713292 | ||||||
chr8:6713349
|
A | T | 1 | a0001c0002t0044g0220 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.219+4462A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713349 | ||||||
chr8:6713375
|
C | T | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4488C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713375 | ||||||
chr8:6713514
|
A | G | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+4627A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713514 | ||||||
chr8:6713521
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219+4634C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713521 | ||||||
chr8:6713595
|
C | A | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4708C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713595 | ||||||
chr8:6713646
|
C | T | 10 | a0001c0001t0001g0071a0001c0001t0004g0070a0001c0001t0010g0005others(7): Show | 13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+4759C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713646 | ||||||
chr8:6713656
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.219+4769C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713656 | ||||||
chr8:6713657
|
G | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+4770G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713657 | ||||||
chr8:6713688
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+4801G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713688 | ||||||
chr8:6713707
|
C | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(68): Show | 89 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.219+4820C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713707 | ||||||
chr8:6713720
|
A | AT | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(216): Show | 274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.219+4843dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6713720 | |||||
chr8:6713721
|
T | C | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4834T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713721 | ||||||
chr8:6713748
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0002g0248 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.219+4861G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713748 | ||||||
chr8:6713827
|
C | G | 4 | a0001c0001t0002g0279a0001c0001t0002g0280a0001c0001t0002g0299others(1): Show | 4 | HG00621.hp2 HG02135.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4940C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713827 | ||||||
chr8:6713856
|
A | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(53): Show | 74 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.219+4969A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713856 | ||||||
chr8:6713857
|
T | C | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+4970T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713857 | ||||||
chr8:6713882
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.219+4995C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713882 | ||||||
chr8:6713940
|
C | A | 15 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(12): Show | 20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.219+5053C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713940 | ||||||
chr8:6713952
|
C | G | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.219+5065C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713952 | ||||||
chr8:6714004
|
C | G | 2 | a0002c0004t0003g0025a0002c0004t0003g0026 | 4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+5117C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714004 | ||||||
chr8:6714067
|
C | G | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+5180C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714067 | ||||||
chr8:6714069
|
A | T | 1 | a0001c0001t0037g0269 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.219+5182A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714069 | ||||||
chr8:6714072
|
C | G | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+5185C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714072 | ||||||
chr8:6714113
|
A | C | 2 | a0001c0001t0021g0042a0001c0001t0053g0043 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+5226A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714113 | ||||||
chr8:6714151
|
A | G | 38 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(35): Show | 51 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.219+5264A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714151 | ||||||
chr8:6714189
|
C | G | 6 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+5302C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714189 | ||||||
chr8:6714268
|
C | T | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+5381C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714268 | ||||||
chr8:6714371
|
C | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.219+5484C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714371 | ||||||
chr8:6714434
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.219+5547A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714434 | ||||||
chr8:6714488
|
G | C | 5 | a0001c0001t0003g0023a0001c0001t0003g0083a0001c0001t0003g0084others(2): Show | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+5601G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714488 | ||||||
chr8:6714568
|
A | C | 2 | a0002c0004t0003g0025a0002c0004t0003g0026 | 4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+5681A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714568 | ||||||
chr8:6714588
|
C | T | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.219+5701C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714588 | ||||||
chr8:6714616
|
C | T | 7 | a0001c0001t0004g0066a0001c0001t0015g0065a0001c0001t0015g0067others(4): Show | 7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+5729C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714616 | ||||||
chr8:6714631
|
T | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0221 | 2 | HG01361.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.219+5744T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714631 | ||||||
chr8:6714644
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0029others(72): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.219+5757C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714644 | ||||||
chr8:6714676
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0208others(10): Show | 21 | HG00423.hp2 HG00544.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.219+5789A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714676 | ||||||
chr8:6714747
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(246): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.219+5860C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714747 | ||||||
chr8:6714760
|
T | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(41): Show | 57 | HG00408.hp1 HG00673.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.219+5873T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714760 | ||||||
chr8:6714761
|
A | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+5874A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714761 | ||||||
chr8:6714782
|
C | T | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+5895C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714782 | ||||||
chr8:6714841
|
C | T | 4 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0002g0298others(1): Show | 4 | HG00597.hp2 NA18960.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+5954C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714841 | ||||||
chr8:6714907
|
C | G | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.219+6020C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714907 | ||||||
chr8:6714924
|
G | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+6037G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714924 | ||||||
chr8:6714988
|
G | A | 35 | a0001c0001t0001g0071a0001c0001t0002g0014a0001c0001t0002g0035others(32): Show | 43 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+6101G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714988 | ||||||
chr8:6715070
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.219+6183G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715070 | ||||||
chr8:6715100
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0003g0087 | 2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219+6213G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715100 | ||||||
chr8:6715104
|
C | G | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+6217C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715104 | ||||||
chr8:6715110
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(278): Show | 352 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.219+6223G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715110 | ||||||
chr8:6715121
|
G | A | 1 | a0001c0001t0040g0146 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.219+6234G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715121 | ||||||
chr8:6715126
|
A | G | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+6239A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715126 | ||||||
chr8:6715198
|
A | G | 1 | a0001c0001t0036g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.219+6311A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715198 | ||||||
chr8:6715222
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.219+6335C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715222 | ||||||
chr8:6715265
|
A | G | 7 | a0001c0001t0004g0070a0001c0001t0010g0005a0001c0001t0016g0069others(4): Show | 10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+6378A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715265 | ||||||
chr8:6715321
|
C | A | 1 | a0001c0001t0003g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.219+6434C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715321 | ||||||
chr8:6715458
|
C | G | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+6571C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715458 | ||||||
chr8:6715659
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+6772A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715659 | ||||||
chr8:6715684
|
T | C | 37 | a0001c0001t0001g0071a0001c0001t0002g0014a0001c0001t0002g0035others(34): Show | 46 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.219+6797T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715684 | ||||||
chr8:6715735
|
A | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+6848A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715735 | ||||||
chr8:6715818
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.219+6931T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715818 | ||||||
chr8:6715962
|
G | T | 2 | a0001c0001t0001g0247a0001c0001t0002g0248 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.219+7075G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715962 | ||||||
chr8:6715966
|
C | T | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+7079C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715966 | ||||||
chr8:6716006
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0047g0189a0001c0003t0041g0107others(2): Show | 5 | HG02109.hp2 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+7119T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716006 | ||||||
chr8:6716011
|
C | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+7124C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716011 | ||||||
chr8:6716022
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7135C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716022 | ||||||
chr8:6716030
|
C | A | 3 | a0001c0001t0017g0020a0001c0001t0017g0047a0001c0001t0023g0020 | 3 | HG01109.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.219+7143C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716030 | ||||||
chr8:6716040
|
C | T | 3 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0076 | 6 | HG02109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+7153C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716040 | ||||||
chr8:6716044
|
C | G | 2 | a0001c0002t0001g0188a0001c0002t0001g0218 | 2 | HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.219+7157C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716044 | ||||||
chr8:6716176
|
A | G | 35 | a0001c0001t0001g0071a0001c0001t0002g0014a0001c0001t0002g0035others(32): Show | 43 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+7289A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716176 | ||||||
chr8:6716245
|
A | G | 2 | a0001c0003t0013g0064a0001c0003t0041g0107 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.219+7358A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716245 | ||||||
chr8:6716285
|
G | A | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7398G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716285 | ||||||
chr8:6716292
|
C | G | 1 | a0001c0001t0003g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219+7405C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716292 | ||||||
chr8:6716499
|
T | G | 1 | a0001c0001t0002g0270 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.219+7612T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716499 | ||||||
chr8:6716511
|
G | A | 4 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(1): Show | 7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+7624G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716511 | ||||||
chr8:6716547
|
T | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+7660T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716547 | ||||||
chr8:6716563
|
G | A | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+7676G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716563 | ||||||
chr8:6716572
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7685C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716572 | ||||||
chr8:6716583
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219+7696C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716583 | ||||||
chr8:6716688
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7801C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716688 | ||||||
chr8:6716690
|
G | A | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+7803G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716690 | ||||||
chr8:6716696
|
G | A | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+7809G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716696 | ||||||
chr8:6716706
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+7819G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716706 | ||||||
chr8:6716717
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0029others(70): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.219+7830C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716717 | ||||||
chr8:6716754
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(247): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.219+7867G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716754 | ||||||
chr8:6716777
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(216): Show | 274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.219+7890A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716777 | ||||||
chr8:6716803
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(245): Show | 311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.219+7916A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716803 | ||||||
chr8:6716834
|
AAAAC | A | 11 | a0001c0001t0004g0070a0001c0001t0009g0251a0001c0001t0010g0005others(8): Show | 14 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.219+7963_219+7966d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6716834 | |||||
chr8:6716861
|
A | G | 1 | a0003c0009t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.219+7974A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716861 | ||||||
chr8:6716872
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+7985G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716872 | ||||||
chr8:6716915
|
G | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7955G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716915 | ||||||
chr8:6716983
|
A | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7887A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716983 | ||||||
chr8:6716999
|
C | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7871C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716999 | ||||||
chr8:6717009
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220-7861C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717009 | ||||||
chr8:6717036
|
A | C | 1 | a0002c0004t0003g0026 | 2 | HG01106.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.220-7834A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717036 | ||||||
chr8:6717086
|
G | T | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7784G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717086 | ||||||
chr8:6717089
|
A | G | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7781A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717089 | ||||||
chr8:6717109
|
C | G | 2 | a0001c0001t0003g0121a0001c0001t0008g0273 | 2 | HG00558.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.220-7761C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717109 | ||||||
chr8:6717113
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-7757C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717113 | ||||||
chr8:6717216
|
T | C | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7654T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717216 | ||||||
chr8:6717220
|
G | A | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7650G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717220 | ||||||
chr8:6717269
|
T | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-7601T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717269 | ||||||
chr8:6717312
|
A | G | 5 | a0001c0001t0002g0291a0001c0001t0002g0293a0001c0001t0009g0108others(2): Show | 5 | NA18957.hp2 NA18975.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-7558A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717312 | ||||||
chr8:6717317
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG01884.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.220-7553G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717317 | ||||||
chr8:6717334
|
G | A | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-7536G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717334 | ||||||
chr8:6717373
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-7497A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717373 | ||||||
chr8:6717373
|
A | T | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-7497A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717373 | ||||||
chr8:6717387
|
G | A | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-7483G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717387 | ||||||
chr8:6717460
|
A | G | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-7410A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717460 | ||||||
chr8:6717508
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.220-7362A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717508 | ||||||
chr8:6717509
|
A | T | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7361A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717509 | ||||||
chr8:6717580
|
A | C | 1 | a0001c0001t0051g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.220-7290A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717580 | ||||||
chr8:6717618
|
A | G | 1 | a0001c0001t0053g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.220-7252A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717618 | ||||||
chr8:6717633
|
A | G | 1 | a0001c0001t0051g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.220-7237A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717633 | ||||||
chr8:6717708
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7162C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717708 | ||||||
chr8:6717734
|
C | T | 1 | a0001c0001t0003g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-7136C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717734 | ||||||
chr8:6717797
|
C | CTTTACGG others(2): Show |
9 | a0001c0001t0001g0071a0001c0003t0002g0303a0001c0003t0002g0304others(6): Show | 14 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-7072_220-7071i others(11): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6717797 | |||||
chr8:6717813
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(259): Show | 331 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.220-7057A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717813 | ||||||
chr8:6717909
|
T | C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-6961T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717909 | ||||||
chr8:6717981
|
C | G | 1 | a0001c0001t0015g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-6889C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717981 | ||||||
chr8:6717997
|
T | G | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-6873T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717997 | ||||||
chr8:6718143
|
C | G | 74 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(71): Show | 92 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220-6727C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718143 | ||||||
chr8:6718162
|
A | G | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-6708A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718162 | ||||||
chr8:6718284
|
G | C | 5 | a0001c0001t0003g0023a0001c0001t0003g0083a0001c0001t0003g0084others(2): Show | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-6586G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718284 | ||||||
chr8:6718292
|
T | C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-6578T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718292 | ||||||
chr8:6718317
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-6553G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718317 | ||||||
chr8:6718480
|
A | G | 1 | a0001c0001t0037g0269 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-6390A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718480 | ||||||
chr8:6718511
|
CTG | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(209): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.220-6355_220-6354d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6718511 | |||||
chr8:6718545
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.220-6325G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718545 | ||||||
chr8:6718567
|
G | A | 1 | a0001c0001t0019g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.220-6303G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718567 | ||||||
chr8:6718575
|
G | C | 6 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-6295G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718575 | ||||||
chr8:6718655
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(192): Show | 248 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.220-6215T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718655 | ||||||
chr8:6718668
|
A | T | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.220-6202A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718668 | ||||||
chr8:6718752
|
G | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(258): Show | 330 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.220-6118G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718752 | ||||||
chr8:6718893
|
A | G | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-5977A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718893 | ||||||
chr8:6718936
|
G | C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5934G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718936 | ||||||
chr8:6719043
|
T | G | 1 | a0001c0001t0003g0111 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220-5827T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719043 | ||||||
chr8:6719248
|
A | T | 10 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(7): Show | 12 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-5622A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719248 | ||||||
chr8:6719293
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5577G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719293 | ||||||
chr8:6719393
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5477G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719393 | ||||||
chr8:6719405
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.220-5465A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719405 | ||||||
chr8:6719557
|
C | G | 1 | a0001c0001t0007g0031 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.220-5313C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719557 | ||||||
chr8:6719619
|
G | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(255): Show | 327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.220-5251G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719619 | ||||||
chr8:6719674
|
A | T | 1 | a0001c0002t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.220-5196A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719674 | ||||||
chr8:6719717
|
T | C | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-5153T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719717 | ||||||
chr8:6719758
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.220-5112G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719758 | ||||||
chr8:6719785
|
T | A | 1 | a0001c0001t0002g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.220-5085T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719785 | ||||||
chr8:6719794
|
A | G | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-5076A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719794 | ||||||
chr8:6719819
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(256): Show | 327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.220-5051A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719819 | ||||||
chr8:6719845
|
A | T | 1 | a0001c0001t0003g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.220-5025A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719845 | ||||||
chr8:6719864
|
C | T | 1 | a0001c0001t0007g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.220-5006C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719864 | ||||||
chr8:6719866
|
A | G | 1 | a0001c0001t0003g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.220-5004A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719866 | ||||||
chr8:6719899
|
G | T | 1 | a0001c0001t0048g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.220-4971G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719899 | ||||||
chr8:6719982
|
G | C | 3 | a0001c0001t0017g0020a0001c0001t0017g0047a0001c0001t0023g0020 | 3 | HG01109.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.220-4888G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719982 | ||||||
chr8:6720014
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.220-4856A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720014 | ||||||
chr8:6720039
|
G | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(33): Show | 50 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.220-4831G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720039 | ||||||
chr8:6720098
|
T | A | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-4772T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720098 | ||||||
chr8:6720109
|
C | G | 1 | a0001c0001t0002g0289 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.220-4761C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720109 | ||||||
chr8:6720165
|
C | G | 32 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(29): Show | 40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-4705C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720165 | ||||||
chr8:6720257
|
CA | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.220-4603delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6720257 | |||||
chr8:6720267
|
A | G | 1 | a0001c0001t0004g0317 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.220-4603A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720267 | ||||||
chr8:6720282
|
T | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4588T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720282 | ||||||
chr8:6720353
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(135): Show | 175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.220-4517G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720353 | ||||||
chr8:6720429
|
G | A | 2 | a0001c0001t0021g0042a0001c0001t0053g0043 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.220-4441G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720429 | ||||||
chr8:6720449
|
A | C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4421A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720449 | ||||||
chr8:6720476
|
G | C | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220-4394G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720476 | ||||||
chr8:6720533
|
C | G | 1 | a0001c0001t0022g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-4337C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720533 | ||||||
chr8:6720575
|
G | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0071others(56): Show | 75 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.220-4295G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720575 | ||||||
chr8:6720578
|
A | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4292A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720578 | ||||||
chr8:6720625
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-4245A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720625 | ||||||
chr8:6720657
|
A | C | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-4213A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720657 | ||||||
chr8:6720670
|
A | T | 1 | a0001c0001t0004g0019 | 3 | NA18972.hp1 NA18983.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.220-4200A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720670 | ||||||
chr8:6720676
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-4194C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720676 | ||||||
chr8:6720682
|
G | A | 3 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0289 | 3 | NA18971.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.220-4188G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720682 | ||||||
chr8:6720713
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-4157G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720713 | ||||||
chr8:6720861
|
T | C | 1 | a0001c0001t0004g0307 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.220-4009T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720861 | ||||||
chr8:6720911
|
CAAT | C | 15 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(12): Show | 20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-3958_220-3956d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720911 | ||||||
chr8:6720966
|
G | A | 15 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(12): Show | 20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-3904G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720966 | ||||||
chr8:6721099
|
G | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3771G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721099 | ||||||
chr8:6721225
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-3645C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721225 | ||||||
chr8:6721230
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3640A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721230 | ||||||
chr8:6721240
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0024g0062a0001c0001t0025g0021others(2): Show | 5 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-3630G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721240 | ||||||
chr8:6721282
|
A | G | 1 | a0001c0001t0007g0031 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.220-3588A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721282 | ||||||
chr8:6721327
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3543A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721327 | ||||||
chr8:6721339
|
G | C | 1 | a0001c0001t0002g0301 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220-3531G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721339 | ||||||
chr8:6721343
|
A | T | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-3527A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721343 | ||||||
chr8:6721377
|
C | A | 4 | a0001c0003t0006g0009a0001c0003t0006g0305a0001c0003t0006g0306others(1): Show | 9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-3493C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721377 | ||||||
chr8:6721397
|
A | C | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-3473A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721397 | ||||||
chr8:6721405
|
G | C | 4 | a0001c0003t0006g0009a0001c0003t0006g0305a0001c0003t0006g0306others(1): Show | 9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-3465G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721405 | ||||||
chr8:6721421
|
G | A | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-3449G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721421 | ||||||
chr8:6721464
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(235): Show | 298 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.220-3406T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721464 | ||||||
chr8:6721506
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-3364A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721506 | ||||||
chr8:6721514
|
A | C | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3356A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721514 | ||||||
chr8:6721533
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3337C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721533 | ||||||
chr8:6721597
|
G | A | 1 | a0001c0003t0013g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.220-3273G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721597 | ||||||
chr8:6721657
|
T | C | 1 | a0001c0001t0033g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.220-3213T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721657 | ||||||
chr8:6721748
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.220-3122C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721748 | ||||||
chr8:6721753
|
G | T | 1 | a0001c0001t0005g0028 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.220-3117G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721753 | ||||||
chr8:6721780
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3090G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721780 | ||||||
chr8:6721800
|
T | A | 1 | a0001c0001t0002g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.220-3070T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721800 | ||||||
chr8:6721802
|
T | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(242): Show | 311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.220-3068T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721802 | ||||||
chr8:6721850
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.220-3020A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721850 | ||||||
chr8:6721914
|
A | G | 1 | a0001c0001t0045g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.220-2956A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721914 | ||||||
chr8:6721940
|
G | C | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-2930G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721940 | ||||||
chr8:6722042
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(244): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.220-2828A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722042 | ||||||
chr8:6722184
|
A | G | 1 | a0001c0001t0050g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-2686A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722184 | ||||||
chr8:6722196
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.220-2674A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722196 | ||||||
chr8:6722248
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220-2622G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722248 | ||||||
chr8:6722328
|
T | G | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-2542T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722328 | ||||||
chr8:6722355
|
T | C | 15 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(12): Show | 20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-2515T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722355 | ||||||
chr8:6722406
|
T | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-2464T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722406 | ||||||
chr8:6722407
|
A | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2463A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722407 | ||||||
chr8:6722447
|
G | T | 1 | a0001c0003t0014g0027 | 2 | HG01070.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.220-2423G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722447 | ||||||
chr8:6722566
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2304G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722566 | ||||||
chr8:6722606
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2264G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722606 | ||||||
chr8:6722658
|
C | T | 10 | a0001c0001t0001g0071a0001c0001t0004g0070a0001c0001t0010g0005others(7): Show | 13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.220-2212C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722658 | ||||||
chr8:6722674
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2196C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722674 | ||||||
chr8:6722687
|
G | C | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-2183G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722687 | ||||||
chr8:6722689
|
C | A | 7 | a0001c0001t0004g0066a0001c0001t0015g0065a0001c0001t0015g0067others(4): Show | 7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-2181C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722689 | ||||||
chr8:6722729
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(255): Show | 326 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.220-2141T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722729 | ||||||
chr8:6722745
|
A | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-2125A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722745 | ||||||
chr8:6722760
|
T | G | 8 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(5): Show | 13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.220-2110T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722760 | ||||||
chr8:6722793
|
T | G | 9 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(6): Show | 11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2077T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722793 | ||||||
chr8:6722826
|
A | C | 6 | a0001c0001t0004g0066a0001c0001t0015g0065a0001c0001t0015g0067others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-2044A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722826 | ||||||
chr8:6722830
|
A | AT | 11 | a0001c0001t0001g0071a0001c0001t0004g0070a0001c0001t0010g0005others(8): Show | 14 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2031dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6722830 | |||||
chr8:6722865
|
TA | T | 7 | a0001c0001t0004g0066a0001c0001t0015g0065a0001c0001t0015g0067others(4): Show | 7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-2000delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6722865 | |||||
chr8:6722905
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(226): Show | 293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.220-1965C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722905 | ||||||
chr8:6723061
|
A | T | 1 | a0001c0001t0015g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-1809A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723061 | ||||||
chr8:6723062
|
A | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(229): Show | 296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.220-1808A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723062 | ||||||
chr8:6723194
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1676A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723194 | ||||||
chr8:6723214
|
G | C | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-1656G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723214 | ||||||
chr8:6723255
|
T | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(32): Show | 49 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.220-1615T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723255 | ||||||
chr8:6723267
|
G | T | 1 | a0001c0001t0003g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-1603G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723267 | ||||||
chr8:6723320
|
T | C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1550T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723320 | ||||||
chr8:6723325
|
G | A | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1545G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723325 | ||||||
chr8:6723336
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1534C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723336 | ||||||
chr8:6723351
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-1519A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723351 | ||||||
chr8:6723528
|
A | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0275 | 5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-1342A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723528 | ||||||
chr8:6723566
|
A | G | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-1304A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723566 | ||||||
chr8:6723703
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(237): Show | 305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.220-1167G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723703 | ||||||
chr8:6723714
|
C | G | 2 | a0001c0001t0021g0131a0001c0001t0039g0044 | 2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.220-1156C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723714 | ||||||
chr8:6723892
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.220-978C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723892 | ||||||
chr8:6723999
|
A | G | 13 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(10): Show | 18 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.220-871A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723999 | ||||||
chr8:6724078
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.220-792C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724078 | ||||||
chr8:6724109
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG00741.hp2 HG01175.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-761A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724109 | ||||||
chr8:6724222
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220-648A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724222 | ||||||
chr8:6724251
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.220-619C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724251 | ||||||
chr8:6724282
|
T | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(236): Show | 303 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.220-588T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724282 | ||||||
chr8:6724409
|
A | T | 1 | a0001c0002t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.220-461A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724409 | ||||||
chr8:6724429
|
A | G | 4 | a0001c0001t0001g0071a0001c0005t0005g0130a0001c0005t0013g0072others(1): Show | 4 | HG02109.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-441A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724429 | ||||||
chr8:6724495
|
C | T | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-375C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724495 | ||||||
chr8:6724524
|
A | C | 12 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(9): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-346A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724524 | ||||||
chr8:6724661
|
A | G | 3 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0003t0014g0027 | 4 | HG01070.hp2 HG01099.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-209A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724661 | ||||||
chr8:6724667
|
TACCGTTA | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(247): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.220-199_220-193del others(7): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6724667 | |||||
chr8:6724708
|
C | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(235): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.220-162C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724708 | ||||||
chr8:6724839
|
C | G | 1 | a0001c0001t0002g0318 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220-31C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724839 | ||||||
chr8:6724964
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.289+25A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724964 | ||||||
chr8:6724974
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+35C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724974 | ||||||
chr8:6724975
|
T | C | 1 | a0001c0001t0011g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.289+36T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724975 | ||||||
chr8:6725071
|
C | A | 1 | a0004c0007t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.289+132C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725071 | ||||||
chr8:6725120
|
A | G | 1 | a0001c0001t0045g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.289+181A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725120 | ||||||
chr8:6725177
|
A | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+238A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725177 | ||||||
chr8:6725248
|
C | G | 13 | a0001c0001t0004g0070a0001c0001t0010g0005a0001c0001t0011g0048others(10): Show | 16 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.289+309C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725248 | ||||||
chr8:6725299
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(55): Show | 74 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.289+360T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725299 | ||||||
chr8:6725355
|
C | T | 1 | a0001c0001t0004g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.289+416C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725355 | ||||||
chr8:6725365
|
A | G | 8 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(5): Show | 13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+426A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725365 | ||||||
chr8:6725372
|
G | C | 7 | a0001c0001t0004g0070a0001c0001t0010g0005a0001c0001t0016g0069others(4): Show | 10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+433G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725372 | ||||||
chr8:6725460
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(238): Show | 306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.289+521C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725460 | ||||||
chr8:6725499
|
C | G | 3 | a0001c0001t0001g0071a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.289+560C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725499 | ||||||
chr8:6725527
|
C | A | 1 | a0001c0001t0008g0257 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.289+588C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725527 | ||||||
chr8:6725553
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.289+614T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725553 | ||||||
chr8:6725605
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0124a0001c0001t0005g0126others(5): Show | 9 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+666A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725605 | ||||||
chr8:6725638
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.289+699C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725638 | ||||||
chr8:6725639
|
T | G | 7 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+700T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725639 | ||||||
chr8:6725718
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.289+779G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725718 | ||||||
chr8:6725762
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+823C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725762 | ||||||
chr8:6725773
|
A | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+834A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725773 | ||||||
chr8:6725910
|
G | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(50): Show | 69 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.289+971G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725910 | ||||||
chr8:6725968
|
C | T | 1 | a0001c0001t0029g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289+1029C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725968 | ||||||
chr8:6725974
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.289+1035T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725974 | ||||||
chr8:6725979
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.289+1040A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725979 | ||||||
chr8:6726124
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1185C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726124 | ||||||
chr8:6726131
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(146): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.289+1192A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726131 | ||||||
chr8:6726189
|
C | T | 1 | a0001c0002t0001g0022 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.289+1250C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726189 | ||||||
chr8:6726225
|
T | C | 7 | a0001c0001t0004g0070a0001c0001t0010g0005a0001c0001t0016g0069others(4): Show | 10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+1286T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726225 | ||||||
chr8:6726299
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(131): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.289+1360A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726299 | ||||||
chr8:6726311
|
T | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+1372T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726311 | ||||||
chr8:6726445
|
G | A | 1 | a0001c0002t0001g0153 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.289+1506G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726445 | ||||||
chr8:6726626
|
C | T | 7 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1687C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726626 | ||||||
chr8:6726652
|
A | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1713A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726652 | ||||||
chr8:6726677
|
G | C | 1 | a0001c0001t0004g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.289+1738G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726677 | ||||||
chr8:6726740
|
T | A | 7 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1801T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726740 | ||||||
chr8:6726742
|
G | C | 1 | a0001c0003t0014g0027 | 2 | HG01070.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.289+1803G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726742 | ||||||
chr8:6726772
|
C | G | 23 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(20): Show | 29 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.289+1833C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726772 | ||||||
chr8:6726865
|
T | G | 7 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1926T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726865 | ||||||
chr8:6726944
|
C | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+2005C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726944 | ||||||
chr8:6726967
|
A | G | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289+2028A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726967 | ||||||
chr8:6727125
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(257): Show | 328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.289+2186T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727125 | ||||||
chr8:6727152
|
A | T | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+2213A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727152 | ||||||
chr8:6727189
|
A | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+2250A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727189 | ||||||
chr8:6727212
|
C | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.289+2273C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727212 | ||||||
chr8:6727316
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.289+2377G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727316 | ||||||
chr8:6727364
|
T | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(257): Show | 328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.289+2425T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727364 | ||||||
chr8:6727371
|
TTTTGACA others(4): Show |
T | 2 | a0001c0003t0013g0064a0001c0003t0041g0107 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.289+2437_289+2447d others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6727371 | |||||
chr8:6727414
|
C | T | 1 | a0001c0002t0001g0022 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.289+2475C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727414 | ||||||
chr8:6727423
|
C | G | 1 | a0001c0001t0020g0204 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.289+2484C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727423 | ||||||
chr8:6727448
|
C | T | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+2509C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727448 | ||||||
chr8:6727458
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.289+2519T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727458 | ||||||
chr8:6727474
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0202 | 3 | HG02622.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.289+2535C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727474 | ||||||
chr8:6727527
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.289+2588A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727527 | ||||||
chr8:6727538
|
C | T | 1 | a0001c0001t0004g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.289+2599C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727538 | ||||||
chr8:6727661
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+2722G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727661 | ||||||
chr8:6727704
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.289+2765T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727704 | ||||||
chr8:6727727
|
G | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+2788G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727727 | ||||||
chr8:6727811
|
G | C | 1 | a0001c0002t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.289+2872G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727811 | ||||||
chr8:6727883
|
C | G | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-2828C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727883 | ||||||
chr8:6727928
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2783C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727928 | ||||||
chr8:6727958
|
C | T | 2 | a0001c0001t0021g0131a0001c0001t0039g0044 | 2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.290-2753C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727958 | ||||||
chr8:6728023
|
A | C | 1 | a0001c0001t0003g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.290-2688A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728023 | ||||||
chr8:6728062
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0179a0001c0001t0038g0178 | 3 | HG01106.hp1 HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.290-2649A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728062 | ||||||
chr8:6728181
|
G | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2530G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728181 | ||||||
chr8:6728229
|
G | T | 1 | a0001c0001t0007g0031 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.290-2482G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728229 | ||||||
chr8:6728274
|
T | C | 1 | a0001c0001t0003g0106 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.290-2437T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728274 | ||||||
chr8:6728320
|
A | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2391A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728320 | ||||||
chr8:6728343
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(256): Show | 327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.290-2368A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728343 | ||||||
chr8:6728358
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(257): Show | 328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.290-2353G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728358 | ||||||
chr8:6728374
|
C | G | 1 | a0001c0001t0020g0204 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.290-2337C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728374 | ||||||
chr8:6728447
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2264C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728447 | ||||||
chr8:6728452
|
A | G | 1 | a0001c0001t0003g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.290-2259A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728452 | ||||||
chr8:6728461
|
C | G | 6 | a0001c0001t0001g0177a0001c0002t0001g0138a0001c0002t0001g0150others(3): Show | 6 | HG00280.hp2 HG01361.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2250C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728461 | ||||||
chr8:6728492
|
G | C | 1 | a0001c0001t0002g0040 | 2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.290-2219G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728492 | ||||||
chr8:6728513
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(120): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.290-2198A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728513 | ||||||
chr8:6728519
|
T | G | 1 | a0001c0001t0004g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.290-2192T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728519 | ||||||
chr8:6728649
|
G | GA | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-2056dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6728649 | |||||
chr8:6728713
|
C | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1998C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728713 | ||||||
chr8:6728714
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290-1997T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728714 | ||||||
chr8:6728721
|
C | G | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-1990C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728721 | ||||||
chr8:6728760
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.290-1951T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728760 | ||||||
chr8:6728833
|
A | G | 17 | a0001c0002t0001g0004a0001c0002t0001g0030a0001c0002t0001g0149others(14): Show | 23 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.290-1878A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728833 | ||||||
chr8:6728900
|
A | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1811A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728900 | ||||||
chr8:6728917
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00741.hp2 HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.290-1794A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728917 | ||||||
chr8:6728990
|
C | G | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1721C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728990 | ||||||
chr8:6729024
|
T | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1687T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729024 | ||||||
chr8:6729110
|
G | A | 1 | a0001c0001t0004g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.290-1601G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729110 | ||||||
chr8:6729173
|
T | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1538T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729173 | ||||||
chr8:6729197
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(238): Show | 306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.290-1514T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729197 | ||||||
chr8:6729219
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0086others(63): Show | 83 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.290-1492T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729219 | ||||||
chr8:6729345
|
C | CT | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0063others(63): Show | 86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.290-1352dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | |||||
chr8:6729345
|
C | CTT | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0032others(51): Show | 67 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.290-1353_290-1352d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | |||||
chr8:6729345
|
C | CTTT | 15 | a0001c0001t0001g0071a0001c0001t0003g0091a0001c0001t0004g0079others(12): Show | 16 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-1354_290-1352d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | |||||
chr8:6729345
|
C | CTTTT | 107 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0059others(104): Show | 138 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.290-1355_290-1352d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | |||||
chr8:6729345
|
C | CTTTTT | 15 | a0001c0001t0001g0060a0001c0001t0002g0242a0001c0001t0002g0318others(12): Show | 18 | HG01175.hp1 HG01934.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.290-1356_290-1352d others(7): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | |||||
chr8:6729431
|
T | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1280T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729431 | ||||||
chr8:6729470
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.290-1241C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729470 | ||||||
chr8:6729471
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1240G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729471 | ||||||
chr8:6729509
|
T | TA | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(239): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.290-1201dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729509 | |||||
chr8:6729546
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(239): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.290-1165T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729546 | ||||||
chr8:6729636
|
T | C | 1 | a0001c0003t0013g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.290-1075T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729636 | ||||||
chr8:6729663
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.290-1048C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729663 | ||||||
chr8:6729702
|
A | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0191a0001c0001t0001g0192others(6): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-1009A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729702 | ||||||
chr8:6729749
|
A | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.290-962A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729749 | ||||||
chr8:6729901
|
C | T | 4 | a0001c0003t0006g0009a0001c0003t0006g0305a0001c0003t0006g0306others(1): Show | 9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.290-810C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729901 | ||||||
chr8:6729952
|
A | T | 3 | a0001c0005t0005g0130a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.290-759A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729952 | ||||||
chr8:6730009
|
G | T | 2 | a0001c0003t0001g0152a0001c0003t0014g0027 | 3 | HG01070.hp2 HG01099.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.290-702G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730009 | ||||||
chr8:6730028
|
A | C | 1 | a0001c0001t0015g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-683A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730028 | ||||||
chr8:6730118
|
C | G | 1 | a0001c0001t0007g0031 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.290-593C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730118 | ||||||
chr8:6730306
|
CTAATCAT others(314): Show |
C | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-404_290-84del | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730306 | ||||||
chr8:6730308
|
AATCATAG others(314): Show |
A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(238): Show | 306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.290-395_290-75del | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6730308 | |||||
chr8:6730316
|
G | T | 83 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0001g0247others(80): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.290-395G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730316 | ||||||
chr8:6730318
|
C | CT | 25 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(22): Show | 29 | HG00621.hp2 HG00741.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.290-363dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6730318 | |||||
chr8:6730320
|
T | A | 1 | a0001c0006t0002g0290 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.290-391T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730320 | ||||||
chr8:6730349
|
G | T | 82 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0001g0247others(79): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.290-362G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730349 | ||||||
chr8:6730401
|
T | C | 83 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0001g0247others(80): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.290-310T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730401 | ||||||
chr8:6730441
|
C | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0294 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.290-270C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730441 | ||||||
chr8:6730629
|
C | A | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-82C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730629 | ||||||
chr8:6730871
|
A | AT | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(231): Show | 298 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.405+62dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6730871 | |||||
chr8:6730957
|
C | T | 1 | a0001c0001t0003g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.405+131C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6730957 | ||||||
chr8:6731463
|
A | G | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.405+637A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731463 | ||||||
chr8:6731464
|
C | T | 1 | a0001c0001t0002g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.405+638C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731464 | ||||||
chr8:6731564
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.405+738A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731564 | ||||||
chr8:6731615
|
A | G | 2 | a0001c0001t0002g0291a0001c0001t0002g0293 | 2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.405+789A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731615 | ||||||
chr8:6731631
|
A | C | 20 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(17): Show | 27 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.405+805A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731631 | ||||||
chr8:6731659
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.405+833C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731659 | ||||||
chr8:6731746
|
TA | T | 21 | a0001c0001t0002g0277a0001c0001t0002g0318a0001c0001t0004g0010others(18): Show | 28 | HG00673.hp1 HG01934.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.406-804delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6731746 | |||||
chr8:6731912
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.406-649C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731912 | ||||||
chr8:6731922
|
G | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(240): Show | 309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.406-639G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731922 | ||||||
chr8:6732116
|
G | A | 1 | a0001c0001t0002g0276 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.406-445G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732116 | ||||||
chr8:6732177
|
A | AGTATT | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(239): Show | 308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.406-383_406-382ins others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6732177 | |||||
chr8:6732183
|
G | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(240): Show | 309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.406-378G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732183 | ||||||
chr8:6732191
|
C | T | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.406-370C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732191 | ||||||
chr8:6732355
|
T | C | 1 | a0001c0003t0013g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.406-206T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732355 | ||||||
chr8:6732505
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.406-56C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732505 | ||||||
chr8:6733051
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.495+401T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733051 | ||||||
chr8:6733109
|
T | C | 1 | a0001c0001t0007g0031 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.495+459T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733109 | ||||||
chr8:6733212
|
C | T | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+562C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733212 | ||||||
chr8:6733232
|
C | G | 21 | a0001c0001t0002g0318a0001c0001t0004g0010a0001c0001t0004g0019others(18): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+582C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733232 | ||||||
chr8:6733261
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 8 | NA18950.hp2 NA18956.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+611G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733261 | ||||||
chr8:6733351
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(237): Show | 305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.495+701C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733351 | ||||||
chr8:6733367
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.495+717A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733367 | ||||||
chr8:6733416
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(116): Show | 152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.495+766C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733416 | ||||||
chr8:6733445
|
C | G | 1 | a0001c0001t0003g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.495+795C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733445 | ||||||
chr8:6733583
|
A | C | 1 | a0001c0002t0001g0030 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.495+933A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733583 | ||||||
chr8:6733681
|
A | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+1031A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733681 | ||||||
chr8:6733731
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.495+1081C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733731 | ||||||
chr8:6733844
|
T | C | 1 | a0001c0002t0044g0220 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.495+1194T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733844 | ||||||
chr8:6733859
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.495+1209G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733859 | ||||||
chr8:6733902
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(238): Show | 306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.495+1252C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733902 | ||||||
chr8:6734026
|
G | A | 2 | a0001c0001t0016g0074a0001c0001t0016g0076 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.495+1376G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734026 | ||||||
chr8:6734039
|
T | G | 2 | a0001c0001t0007g0231a0001c0001t0007g0232 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.495+1389T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734039 | ||||||
chr8:6734071
|
T | A | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+1421T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734071 | ||||||
chr8:6734095
|
G | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0002g0279others(3): Show | 7 | HG00621.hp2 HG02135.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1445G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734095 | ||||||
chr8:6734194
|
T | C | 1 | a0001c0006t0002g0290 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.495+1544T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734194 | ||||||
chr8:6734235
|
A | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+1585A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734235 | ||||||
chr8:6734242
|
A | G | 2 | a0001c0001t0021g0042a0001c0001t0053g0043 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.495+1592A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734242 | ||||||
chr8:6734257
|
GT | G | 25 | a0001c0001t0002g0132a0001c0001t0002g0318a0001c0001t0004g0010others(22): Show | 32 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.495+1617delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6734257 | |||||
chr8:6734266
|
T | A | 1 | a0001c0001t0050g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.495+1616T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734266 | ||||||
chr8:6734267
|
T | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(211): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.495+1617T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734267 | ||||||
chr8:6734270
|
T | A | 25 | a0001c0001t0002g0132a0001c0001t0002g0318a0001c0001t0004g0010others(22): Show | 32 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.495+1620T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734270 | ||||||
chr8:6734274
|
T | A | 11 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(8): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1624T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734274 | ||||||
chr8:6734307
|
G | C | 1 | a0001c0005t0013g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.495+1657G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734307 | ||||||
chr8:6734318
|
G | C | 3 | a0001c0005t0005g0130a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+1668G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734318 | ||||||
chr8:6734413
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0173 | 3 | HG00408.hp2 NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.495+1763C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734413 | ||||||
chr8:6734452
|
G | A | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1802G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734452 | ||||||
chr8:6734477
|
A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(59): Show | 78 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.495+1827A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734477 | ||||||
chr8:6734483
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.495+1833T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734483 | ||||||
chr8:6734509
|
G | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(60): Show | 80 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.495+1859G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734509 | ||||||
chr8:6734596
|
G | A | 3 | a0001c0001t0017g0020a0001c0001t0017g0047a0001c0001t0023g0020 | 3 | HG01109.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495+1946G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734596 | ||||||
chr8:6734691
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.495+2041T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734691 | ||||||
chr8:6734747
|
G | A | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+2097G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734747 | ||||||
chr8:6734762
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(122): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.495+2112C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734762 | ||||||
chr8:6734765
|
T | C | 1 | a0001c0003t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.495+2115T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734765 | ||||||
chr8:6734789
|
C | T | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.495+2139C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734789 | ||||||
chr8:6734879
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.495+2229T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734879 | ||||||
chr8:6735085
|
C | A | 7 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+2435C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735085 | ||||||
chr8:6735107
|
T | G | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+2457T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735107 | ||||||
chr8:6735178
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+2528G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735178 | ||||||
chr8:6735237
|
C | T | 1 | a0001c0002t0001g0033 | 2 | NA18961.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.495+2587C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735237 | ||||||
chr8:6735350
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.495+2700G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735350 | ||||||
chr8:6735354
|
G | A | 1 | a0001c0006t0002g0290 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.495+2704G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735354 | ||||||
chr8:6735367
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(123): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.495+2717C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735367 | ||||||
chr8:6735443
|
G | C | 11 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(8): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+2793G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735443 | ||||||
chr8:6735498
|
T | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(221): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.495+2848T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735498 | ||||||
chr8:6735587
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.495+2937T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735587 | ||||||
chr8:6735594
|
G | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(238): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.495+2944G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735594 | ||||||
chr8:6735684
|
GTGT | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(230): Show | 293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.495+3047_495+3049d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6735684 | |||||
chr8:6735712
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.495+3062A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735712 | ||||||
chr8:6735782
|
T | C | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3132T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735782 | ||||||
chr8:6735847
|
GC | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(123): Show | 159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.495+3199delC | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6735847 | |||||
chr8:6735848
|
C | CT | 61 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(58): Show | 77 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(3): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735848
|
C | CTT | 7 | a0001c0001t0003g0085a0001c0001t0003g0097a0001c0001t0003g0098others(4): Show | 7 | HG01346.hp2 HG02145.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735848
|
C | CTTT | 4 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232others(1): Show | 5 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735848
|
CCT | C | 6 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0002g0132others(3): Show | 6 | HG01081.hp1 HG01168.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3199_495+3200d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735848
|
CCTTTTT | C | 19 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(16): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.495+3199_495+3204d others(8): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735848
|
CCTTTTTT others(9): Show |
C | 6 | a0001c0003t0002g0303a0001c0003t0002g0304a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+3199_495+3214d others(18): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | ||||||
chr8:6735849
|
C | T | 167 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0063others(164): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.495+3199C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735849 | ||||||
chr8:6735905
|
A | C | 1 | a0001c0002t0001g0159 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+3255A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735905 | ||||||
chr8:6736016
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+3366G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736016 | ||||||
chr8:6736038
|
G | A | 3 | a0001c0001t0007g0034a0001c0001t0007g0231a0001c0001t0007g0232 | 4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3388G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736038 | ||||||
chr8:6736095
|
G | A | 3 | a0001c0005t0005g0130a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+3445G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736095 | ||||||
chr8:6736160
|
C | G | 8 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(5): Show | 13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.495+3510C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736160 | ||||||
chr8:6736196
|
A | G | 7 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0002g0304others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+3546A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736196 | ||||||
chr8:6736264
|
T | C | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736264 | ||||||
chr8:6736305
|
G | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(48): Show | 67 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.495+3655G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736305 | ||||||
chr8:6736359
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495+3709A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736359 | ||||||
chr8:6736371
|
C | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3721C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736371 | ||||||
chr8:6736373
|
T | C | 1 | a0001c0001t0017g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.495+3723T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736373 | ||||||
chr8:6736455
|
A | G | 1 | a0001c0002t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.495+3805A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736455 | ||||||
chr8:6736586
|
C | T | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3936C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736586 | ||||||
chr8:6736696
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00741.hp2 HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.495+4046C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736696 | ||||||
chr8:6736735
|
A | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+4085A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736735 | ||||||
chr8:6736756
|
A | T | 1 | a0001c0003t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.495+4106A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736756 | ||||||
chr8:6736834
|
G | T | 2 | a0001c0005t0013g0072a0001c0005t0013g0073 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.495+4184G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736834 | ||||||
chr8:6736842
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.495+4192G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736842 | ||||||
chr8:6736850
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+4200C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736850 | ||||||
chr8:6736864
|
C | G | 1 | a0001c0002t0001g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.495+4214C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736864 | ||||||
chr8:6736974
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.495+4324G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736974 | ||||||
chr8:6736976
|
C | G | 1 | a0001c0001t0003g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.495+4326C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736976 | ||||||
chr8:6736992
|
C | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+4342C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736992 | ||||||
chr8:6737085
|
A | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+4435A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737085 | ||||||
chr8:6737218
|
G | A | 1 | a0001c0001t0005g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496-4443G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737218 | ||||||
chr8:6737237
|
T | C | 1 | a0001c0001t0009g0234 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.496-4424T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737237 | ||||||
chr8:6737393
|
T | C | 4 | a0001c0001t0003g0110a0001c0001t0003g0113a0001c0001t0003g0114others(1): Show | 4 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-4268T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737393 | ||||||
chr8:6737419
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(123): Show | 159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.496-4242G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737419 | ||||||
chr8:6737503
|
A | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-4158A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737503 | ||||||
chr8:6737522
|
A | C | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-4139A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737522 | ||||||
chr8:6737635
|
A | C | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-4026A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737635 | ||||||
chr8:6737649
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.496-4012C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737649 | ||||||
chr8:6737812
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(137): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.496-3849A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737812 | ||||||
chr8:6738040
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496-3621C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738040 | ||||||
chr8:6738122
|
T | C | 1 | a0001c0001t0003g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.496-3539T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738122 | ||||||
chr8:6738128
|
C | T | 1 | a0001c0003t0006g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.496-3533C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738128 | ||||||
chr8:6738138
|
C | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0086others(83): Show | 108 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.496-3523C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738138 | ||||||
chr8:6738144
|
A | G | 11 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(8): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.496-3517A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738144 | ||||||
chr8:6738170
|
A | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(124): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.496-3491A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738170 | ||||||
chr8:6738204
|
A | AT | 10 | a0001c0001t0004g0066a0001c0001t0004g0070a0001c0001t0010g0005others(7): Show | 13 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3454dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6738204 | |||||
chr8:6738305
|
G | T | 1 | a0001c0001t0027g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.496-3356G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738305 | ||||||
chr8:6738431
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(126): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.496-3230G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738431 | ||||||
chr8:6738438
|
T | C | 1 | a0001c0003t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-3223T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738438 | ||||||
chr8:6738533
|
A | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3128A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738533 | ||||||
chr8:6738545
|
C | T | 2 | a0001c0005t0013g0072a0001c0005t0013g0073 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496-3116C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738545 | ||||||
chr8:6738587
|
C | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-3074C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738587 | ||||||
chr8:6738593
|
C | G | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.496-3068C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738593 | ||||||
chr8:6738640
|
C | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3021C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738640 | ||||||
chr8:6738643
|
G | A | 2 | a0001c0003t0013g0064a0001c0003t0041g0107 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496-3018G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738643 | ||||||
chr8:6738752
|
G | C | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-2909G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738752 | ||||||
chr8:6738758
|
T | G | 1 | a0001c0003t0013g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496-2903T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738758 | ||||||
chr8:6738818
|
C | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-2843C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738818 | ||||||
chr8:6738838
|
AT | A | 6 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2815delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6738838 | |||||
chr8:6738852
|
A | G | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.496-2809A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738852 | ||||||
chr8:6738853
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0294 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.496-2808T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738853 | ||||||
chr8:6738943
|
G | C | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.496-2718G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738943 | ||||||
chr8:6738985
|
A | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00741.hp2 HG01175.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2676A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738985 | ||||||
chr8:6739020
|
T | A | 1 | a0001c0001t0027g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.496-2641T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739020 | ||||||
chr8:6739146
|
C | CTA | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-2503_496-2502d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6739146 | |||||
chr8:6739233
|
A | G | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-2428A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739233 | ||||||
chr8:6739310
|
C | T | 6 | a0001c0001t0004g0070a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2351C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739310 | ||||||
chr8:6739567
|
G | A | 1 | a0001c0001t0002g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496-2094G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739567 | ||||||
chr8:6739681
|
A | G | 12 | a0001c0001t0003g0230a0001c0001t0004g0066a0001c0001t0004g0070others(9): Show | 15 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-1980A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739681 | ||||||
chr8:6739696
|
A | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(124): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.496-1965A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739696 | ||||||
chr8:6739789
|
C | G | 1 | a0001c0001t0002g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496-1872C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739789 | ||||||
chr8:6739834
|
C | A | 1 | a0001c0001t0051g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.496-1827C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739834 | ||||||
chr8:6739858
|
T | A | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1803T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739858 | ||||||
chr8:6740014
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-1647C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740014 | ||||||
chr8:6740020
|
A | C | 1 | a0001c0001t0002g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.496-1641A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740020 | ||||||
chr8:6740106
|
A | G | 5 | a0001c0003t0001g0152a0001c0003t0013g0064a0001c0003t0041g0107others(2): Show | 5 | HG02109.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-1555A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740106 | ||||||
chr8:6740279
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-1382A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740279 | ||||||
chr8:6740327
|
C | A | 6 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-1334C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740327 | ||||||
chr8:6740400
|
C | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1261C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740400 | ||||||
chr8:6740428
|
T | G | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-1233T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740428 | ||||||
chr8:6740456
|
A | G | 1 | a0001c0001t0033g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.496-1205A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740456 | ||||||
chr8:6740490
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0240 | 3 | NA18941.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.496-1171A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740490 | ||||||
chr8:6740543
|
ATAT | A | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1114_496-1112d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6740543 | |||||
chr8:6740584
|
A | G | 1 | a0001c0001t0051g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.496-1077A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740584 | ||||||
chr8:6740613
|
A | G | 3 | a0001c0003t0013g0064a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496-1048A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740613 | ||||||
chr8:6740627
|
G | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0122a0001c0001t0031g0118 | 3 | HG02145.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.496-1034G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740627 | ||||||
chr8:6740641
|
A | G | 8 | a0001c0001t0004g0070a0001c0001t0039g0044a0001c0003t0002g0303others(5): Show | 13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.496-1020A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740641 | ||||||
chr8:6740820
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.496-841C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740820 | ||||||
chr8:6740942
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.496-719G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740942 | ||||||
chr8:6741052
|
C | A | 1 | a0001c0001t0002g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.496-609C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741052 | ||||||
chr8:6741127
|
T | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-534T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741127 | ||||||
chr8:6741304
|
C | T | 2 | a0001c0001t0002g0291a0001c0001t0002g0293 | 2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.496-357C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741304 | ||||||
chr8:6741323
|
G | C | 1 | a0001c0001t0003g0111 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.496-338G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741323 | ||||||
chr8:6741357
|
C | T | 13 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0036others(10): Show | 16 | HG00408.hp1 HG01346.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-304C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741357 | ||||||
chr8:6741484
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(244): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.496-177T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741484 | ||||||
chr8:6741640
|
A | C | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.496-21A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741640 | ||||||
chr8:6741804
|
T | G | 1 | a0001c0001t0002g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.586+53T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741804 | ||||||
chr8:6741926
|
T | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0294 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.586+175T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741926 | ||||||
chr8:6741927
|
T | G | 27 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(24): Show | 38 | HG01884.hp1 HG01934.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.586+176T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741927 | ||||||
chr8:6742037
|
T | G | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG00741.hp2 HG01175.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+286T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742037 | ||||||
chr8:6742088
|
G | C | 5 | a0001c0003t0002g0303a0001c0003t0006g0009a0001c0003t0006g0305others(2): Show | 10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+337G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742088 | ||||||
chr8:6742153
|
G | C | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.586+402G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742153 | ||||||
chr8:6742237
|
T | A | 1 | a0001c0001t0003g0144 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.586+486T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742237 | ||||||
chr8:6742525
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+774C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742525 | ||||||
chr8:6742566
|
T | C | 1 | a0001c0003t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.586+815T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742566 | ||||||
chr8:6742664
|
T | G | 19 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(16): Show | 25 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.586+913T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742664 | ||||||
chr8:6742790
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+1039G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742790 | ||||||
chr8:6742793
|
T | G | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+1042T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742793 | ||||||
chr8:6742828
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(242): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.586+1077T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742828 | ||||||
chr8:6742873
|
C | G | 19 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(16): Show | 25 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.586+1122C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742873 | ||||||
chr8:6742901
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.586+1150A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742901 | ||||||
chr8:6743026
|
T | G | 1 | a0001c0001t0050g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+1275T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743026 | ||||||
chr8:6743161
|
G | C | 6 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+1410G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743161 | ||||||
chr8:6743169
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.586+1418C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743169 | ||||||
chr8:6743248
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.586+1497A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743248 | ||||||
chr8:6743283
|
T | C | 20 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(17): Show | 26 | HG01884.hp1 HG01934.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.586+1532T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743283 | ||||||
chr8:6743293
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0122a0001c0001t0031g0118 | 3 | HG02145.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.586+1542G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743293 | ||||||
chr8:6743308
|
G | A | 4 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(1): Show | 7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+1557G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743308 | ||||||
chr8:6743365
|
T | C | 6 | a0001c0001t0005g0124a0001c0001t0015g0065a0001c0001t0015g0067others(3): Show | 6 | HG02809.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743365 | ||||||
chr8:6743389
|
C | G | 1 | a0001c0001t0003g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.586+1638C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743389 | ||||||
chr8:6743458
|
A | T | 2 | a0001c0001t0007g0231a0001c0001t0007g0232 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.586+1707A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743458 | ||||||
chr8:6743581
|
A | G | 1 | a0001c0001t0050g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+1830A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743581 | ||||||
chr8:6743640
|
C | T | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.586+1889C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743640 | ||||||
chr8:6743701
|
G | A | 1 | a0001c0001t0027g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.586+1950G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743701 | ||||||
chr8:6743772
|
G | GT | 4 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0275others(1): Show | 6 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+2033dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6743772 | |||||
chr8:6743772
|
GT | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(115): Show | 151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.586+2033delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6743772 | |||||
chr8:6743828
|
C | T | 1 | a0001c0001t0019g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.586+2077C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743828 | ||||||
chr8:6743852
|
A | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(233): Show | 301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.586+2101A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743852 | ||||||
chr8:6743957
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.586+2206G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743957 | ||||||
chr8:6743971
|
G | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(233): Show | 301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.586+2220G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743971 | ||||||
chr8:6744048
|
A | T | 1 | a0001c0001t0019g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.586+2297A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744048 | ||||||
chr8:6744109
|
A | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+2358A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744109 | ||||||
chr8:6744323
|
C | G | 2 | a0001c0001t0007g0231a0001c0001t0007g0232 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.586+2572C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744323 | ||||||
chr8:6744447
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.586+2696A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744447 | ||||||
chr8:6744456
|
A | T | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.586+2705A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744456 | ||||||
chr8:6744574
|
G | T | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+2823G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744574 | ||||||
chr8:6744800
|
C | G | 1 | a0001c0001t0037g0269 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-2870C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744800 | ||||||
chr8:6744808
|
G | A | 4 | a0001c0001t0002g0132a0001c0001t0025g0021a0001c0001t0026g0021others(1): Show | 4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-2862G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744808 | ||||||
chr8:6744873
|
C | G | 1 | a0001c0001t0003g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.587-2797C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744873 | ||||||
chr8:6744913
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.587-2757G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744913 | ||||||
chr8:6745004
|
T | C | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-2666T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745004 | ||||||
chr8:6745043
|
T | G | 1 | a0001c0001t0028g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.587-2627T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745043 | ||||||
chr8:6745075
|
A | G | 2 | a0001c0001t0021g0042a0001c0001t0053g0043 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.587-2595A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745075 | ||||||
chr8:6745170
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0002g0243 | 2 | NA18965.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.587-2500G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745170 | ||||||
chr8:6745201
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-2469T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745201 | ||||||
chr8:6745273
|
C | A | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-2397C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745273 | ||||||
chr8:6745398
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.587-2272T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745398 | ||||||
chr8:6745402
|
G | A | 6 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-2268G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745402 | ||||||
chr8:6745410
|
C | G | 1 | a0001c0001t0037g0269 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-2260C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745410 | ||||||
chr8:6745670
|
T | C | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-2000T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745670 | ||||||
chr8:6745692
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.587-1978G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745692 | ||||||
chr8:6745752
|
T | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0275 | 5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-1918T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745752 | ||||||
chr8:6745808
|
G | A | 1 | a0001c0002t0001g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587-1862G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745808 | ||||||
chr8:6745819
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.587-1851C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745819 | ||||||
chr8:6745918
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.587-1752C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745918 | ||||||
chr8:6745945
|
C | G | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587-1725C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745945 | ||||||
chr8:6745970
|
G | A | 1 | a0001c0005t0013g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.587-1700G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745970 | ||||||
chr8:6746024
|
C | G | 1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.587-1646C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746024 | ||||||
chr8:6746032
|
C | T | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-1638C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746032 | ||||||
chr8:6746033
|
T | TCTTG | 10 | a0001c0001t0004g0070a0001c0001t0039g0044a0001c0003t0002g0303others(7): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.587-1625_587-1622d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6746033 | |||||
chr8:6746075
|
C | CTTTCTTT others(4): Show |
1 | a0001c0001t0042g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.587-1595_587-1594i others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746075 | ||||||
chr8:6746075
|
C | CTTTCTTT others(4): Show |
224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(221): Show | 286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.587-1595_587-1594i others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746075 | ||||||
chr8:6746183
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(215): Show | 278 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.587-1487G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746183 | ||||||
chr8:6746326
|
G | C | 3 | a0001c0003t0013g0064a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.587-1344G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746326 | ||||||
chr8:6746615
|
A | G | 6 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-1055A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746615 | ||||||
chr8:6746618
|
T | A | 1 | a0001c0001t0003g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.587-1052T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746618 | ||||||
chr8:6746635
|
G | C | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-1035G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746635 | ||||||
chr8:6746686
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0240 | 3 | NA18941.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.587-984C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746686 | ||||||
chr8:6746799
|
A | G | 29 | a0001c0001t0003g0105a0001c0001t0004g0019a0001c0001t0004g0066others(26): Show | 32 | HG00099.hp2 HG01884.hp1 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.587-871A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746799 | ||||||
chr8:6746830
|
T | C | 1 | a0001c0001t0003g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587-840T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746830 | ||||||
chr8:6746882
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(173): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.587-788T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746882 | ||||||
chr8:6747008
|
A | G | 4 | a0001c0001t0033g0125a0001c0003t0013g0064a0001c0005t0013g0072others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-662A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747008 | ||||||
chr8:6747019
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.587-651C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747019 | ||||||
chr8:6747023
|
T | C | 14 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0247others(11): Show | 16 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-647T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747023 | ||||||
chr8:6747097
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0147a0001c0001t0001g0177others(3): Show | 8 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-573A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747097 | ||||||
chr8:6747173
|
G | A | 7 | a0001c0001t0003g0207a0001c0001t0039g0044a0001c0003t0002g0303others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-497G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747173 | ||||||
chr8:6747192
|
G | T | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-478G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747192 | ||||||
chr8:6747259
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.587-411A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747259 | ||||||
chr8:6747286
|
G | A | 1 | a0001c0001t0039g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-384G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747286 | ||||||
chr8:6747307
|
G | A | 6 | a0001c0001t0003g0207a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-363G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747307 | ||||||
chr8:6747385
|
G | A | 47 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0023others(44): Show | 60 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.587-285G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747385 | ||||||
chr8:6747408
|
G | A | 2 | a0001c0001t0002g0212a0001c0001t0002g0288 | 2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.587-262G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747408 | ||||||
chr8:6747414
|
G | A | 7 | a0001c0001t0003g0207a0001c0001t0039g0044a0001c0003t0002g0303others(4): Show | 12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-256G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747414 | ||||||
chr8:6747568
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-102G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747568 | ||||||
chr8:6747583
|
G | A | 25 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(22): Show | 31 | HG01884.hp1 HG01934.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.587-87G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747583 | ||||||
chr8:6747621
|
G | A | 6 | a0001c0001t0002g0132a0001c0001t0002g0233a0001c0001t0002g0256others(3): Show | 6 | HG02602.hp2 HG03654.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-49G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747621 | ||||||
chr8:6747932
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(118): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.745+104T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6747932 | ||||||
chr8:6748013
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.745+185A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748013 | ||||||
chr8:6748141
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(122): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.745+313C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748141 | ||||||
chr8:6748166
|
G | A | 4 | a0001c0003t0002g0303a0001c0003t0006g0009a0001c0003t0006g0306others(1): Show | 9 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.745+338G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748166 | ||||||
chr8:6748186
|
G | C | 1 | a0001c0001t0042g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.745+358G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748186 | ||||||
chr8:6748264
|
T | C | 2 | a0001c0001t0003g0115a0001c0001t0003g0123 | 2 | HG01243.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.745+436T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748264 | ||||||
chr8:6748305
|
C | G | 1 | a0001c0001t0003g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.745+477C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748305 | ||||||
chr8:6748621
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(116): Show | 158 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.745+793C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748621 | ||||||
chr8:6748695
|
C | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(226): Show | 294 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.745+867C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748695 | ||||||
chr8:6748729
|
T | G | 1 | a0001c0001t0037g0269 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745+901T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748729 | ||||||
chr8:6748756
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.745+928C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748756 | ||||||
chr8:6748771
|
G | A | 6 | a0001c0001t0039g0044a0001c0003t0002g0303a0001c0003t0006g0009others(3): Show | 11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.745+943G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748771 | ||||||
chr8:6748792
|
A | G | 2 | a0001c0001t0003g0221a0001c0003t0014g0027 | 3 | HG01070.hp2 HG01099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.745+964A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748792 | ||||||
chr8:6749049
|
T | C | 5 | a0001c0001t0015g0065a0001c0001t0015g0067a0001c0001t0015g0068others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+1221T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749049 | ||||||
chr8:6749176
|
T | C | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.745+1348T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749176 | ||||||
chr8:6749265
|
G | A | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.745+1437G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749265 | ||||||
chr8:6749357
|
A | T | 3 | a0001c0001t0017g0020a0001c0001t0017g0047a0001c0001t0023g0020 | 3 | HG01109.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.745+1529A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749357 | ||||||
chr8:6749490
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0298 | 2 | NA18960.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.745+1662G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749490 | ||||||
chr8:6749496
|
C | T | 3 | a0001c0001t0001g0214a0001c0002t0001g0004a0001c0002t0001g0164 | 8 | HG00423.hp2 NA18950.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+1668C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749496 | ||||||
chr8:6749571
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.745+1743T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749571 | ||||||
chr8:6749576
|
G | A | 8 | a0001c0001t0001g0208a0001c0001t0002g0295a0001c0001t0002g0296others(5): Show | 10 | HG00558.hp2 HG00597.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.745+1748G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749576 | ||||||
chr8:6749591
|
T | A | 1 | a0001c0001t0033g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.745+1763T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749591 | ||||||
chr8:6749597
|
A | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+1769A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749597 | ||||||
chr8:6749607
|
A | C | 5 | a0001c0001t0039g0044a0001c0003t0006g0009a0001c0003t0006g0305others(2): Show | 10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.745+1779A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749607 | ||||||
chr8:6749668
|
A | G | 3 | a0001c0003t0013g0064a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.745+1840A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749668 | ||||||
chr8:6749700
|
G | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.745+1872G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749700 | ||||||
chr8:6749741
|
CAT | C | 3 | a0001c0001t0015g0065a0001c0001t0015g0067a0001c0001t0042g0222 | 3 | HG01884.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.745+1915_745+1916d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6749741 | |||||
chr8:6749785
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.745+1957A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749785 | ||||||
chr8:6749907
|
G | A | 4 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(1): Show | 7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+2079G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749907 | ||||||
chr8:6750094
|
C | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.745+2266C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750094 | ||||||
chr8:6750107
|
C | G | 1 | a0001c0002t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.745+2279C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750107 | ||||||
chr8:6750113
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.745+2285C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750113 | ||||||
chr8:6750124
|
G | A | 1 | a0001c0001t0004g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.745+2296G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750124 | ||||||
chr8:6750128
|
C | G | 2 | a0001c0001t0004g0066a0001c0001t0004g0070 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.745+2300C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750128 | ||||||
chr8:6750138
|
C | G | 1 | a0001c0002t0001g0030 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.745+2310C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750138 | ||||||
chr8:6750246
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.745+2418C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750246 | ||||||
chr8:6750295
|
A | T | 1 | a0001c0002t0001g0030 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.745+2467A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750295 | ||||||
chr8:6750300
|
C | T | 1 | a0001c0001t0003g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.745+2472C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750300 | ||||||
chr8:6750381
|
T | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.745+2553T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750381 | ||||||
chr8:6750389
|
T | G | 6 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0001g0261others(3): Show | 6 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+2561T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750389 | ||||||
chr8:6750483
|
A | G | 1 | a0001c0001t0022g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745+2655A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750483 | ||||||
chr8:6750508
|
C | G | 3 | a0001c0001t0025g0021a0001c0001t0026g0021a0001c0001t0027g0133 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.745+2680C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750508 | ||||||
chr8:6750551
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(235): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.745+2723A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750551 | ||||||
chr8:6750590
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.745+2762G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750590 | ||||||
chr8:6750596
|
T | C | 28 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(25): Show | 41 | HG01934.hp1 HG02055.hp1 HG02080.hp2 others(38): Show |
intron_variant | MODIFIER | c.745+2768T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750596 | ||||||
chr8:6750645
|
G | T | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.745+2817G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750645 | ||||||
chr8:6750724
|
C | CT | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(293): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.745+2908dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6750724 | |||||
chr8:6750724
|
C | CTT | 23 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(20): Show | 29 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.745+2907_745+2908d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6750724 | |||||
chr8:6750804
|
C | T | 5 | a0001c0003t0002g0303a0001c0003t0006g0009a0001c0003t0006g0305others(2): Show | 10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.745+2976C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750804 | ||||||
chr8:6750900
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.745+3072C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750900 | ||||||
chr8:6750955
|
G | A | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+3127G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750955 | ||||||
chr8:6751000
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143 | 3 | HG02280.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.745+3172C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751000 | ||||||
chr8:6751008
|
C | G | 1 | a0001c0001t0002g0287 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.745+3180C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751008 | ||||||
chr8:6751058
|
C | T | 1 | a0001c0001t0003g0091 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.745+3230C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751058 | ||||||
chr8:6751064
|
C | G | 1 | a0001c0002t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.745+3236C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751064 | ||||||
chr8:6751088
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.745+3260T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751088 | ||||||
chr8:6751308
|
T | G | 64 | a0001c0001t0001g0063a0001c0001t0001g0086a0001c0001t0001g0095others(61): Show | 77 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.745+3480T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751308 | ||||||
chr8:6751338
|
G | A | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.745+3510G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751338 | ||||||
chr8:6751464
|
G | T | 1 | a0001c0001t0003g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.746-3587G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751464 | ||||||
chr8:6751666
|
G | GA | 3 | a0001c0001t0025g0021a0001c0001t0026g0021a0001c0001t0027g0133 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-3384dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6751666 | |||||
chr8:6751691
|
A | G | 1 | a0001c0001t0024g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.746-3360A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751691 | ||||||
chr8:6751726
|
A | AT | 67 | a0001c0001t0001g0063a0001c0001t0001g0095a0001c0001t0001g0134others(64): Show | 80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.746-3320dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6751726 | |||||
chr8:6751887
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.746-3164A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751887 | ||||||
chr8:6751917
|
G | A | 1 | a0001c0003t0002g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.746-3134G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751917 | ||||||
chr8:6751950
|
G | A | 10 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(7): Show | 17 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.746-3101G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751950 | ||||||
chr8:6751994
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.746-3057C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751994 | ||||||
chr8:6752013
|
C | A | 4 | a0001c0001t0015g0065a0001c0001t0015g0067a0001c0001t0015g0068others(1): Show | 4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-3038C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752013 | ||||||
chr8:6752031
|
G | T | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.746-3020G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752031 | ||||||
chr8:6752049
|
C | T | 7 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(4): Show | 9 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-3002C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752049 | ||||||
chr8:6752086
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(233): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.746-2965G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752086 | ||||||
chr8:6752093
|
C | T | 2 | a0001c0001t0004g0066a0001c0001t0004g0070 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.746-2958C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752093 | ||||||
chr8:6752101
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.746-2950C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752101 | ||||||
chr8:6752132
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.746-2919G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752132 | ||||||
chr8:6752264
|
C | T | 7 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(4): Show | 9 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-2787C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752264 | ||||||
chr8:6752356
|
A | G | 1 | a0001c0001t0003g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.746-2695A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752356 | ||||||
chr8:6752392
|
A | G | 1 | a0001c0001t0015g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.746-2659A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752392 | ||||||
chr8:6752461
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.746-2590A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752461 | ||||||
chr8:6752500
|
T | A | 1 | a0001c0001t0002g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.746-2551T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752500 | ||||||
chr8:6752527
|
A | G | 1 | a0001c0001t0029g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.746-2524A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752527 | ||||||
chr8:6752582
|
T | TC | 76 | a0001c0001t0001g0063a0001c0001t0001g0095a0001c0001t0001g0134others(73): Show | 96 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.746-2469_746-2468i others(3): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752582 | ||||||
chr8:6752610
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.746-2441G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752610 | ||||||
chr8:6752642
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(241): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.746-2409T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752642 | ||||||
chr8:6752767
|
C | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(239): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.746-2284C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752767 | ||||||
chr8:6752878
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.746-2173G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752878 | ||||||
chr8:6752987
|
G | T | 1 | a0003c0009t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.746-2064G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752987 | ||||||
chr8:6753103
|
C | G | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1948C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753103 | ||||||
chr8:6753108
|
A | T | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.746-1943A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753108 | ||||||
chr8:6753163
|
C | G | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1888C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753163 | ||||||
chr8:6753178
|
T | A | 99 | a0001c0001t0001g0063a0001c0001t0001g0095a0001c0001t0001g0134others(96): Show | 125 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.746-1873T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753178 | ||||||
chr8:6753251
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.746-1800A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753251 | ||||||
chr8:6753348
|
A | C | 63 | a0001c0001t0001g0063a0001c0001t0001g0086a0001c0001t0001g0095others(60): Show | 76 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.746-1703A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753348 | ||||||
chr8:6753389
|
C | G | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1662C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753389 | ||||||
chr8:6753474
|
T | A | 1 | a0001c0001t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.746-1577T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753474 | ||||||
chr8:6753509
|
T | C | 1 | a0001c0001t0033g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.746-1542T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753509 | ||||||
chr8:6753540
|
G | C | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.746-1511G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753540 | ||||||
chr8:6753586
|
C | G | 16 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(13): Show | 23 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.746-1465C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753586 | ||||||
chr8:6753631
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.746-1420G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753631 | ||||||
chr8:6753785
|
A | G | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-1266A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753785 | ||||||
chr8:6753841
|
G | C | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-1210G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753841 | ||||||
chr8:6753929
|
A | C | 1 | a0001c0002t0001g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.746-1122A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753929 | ||||||
chr8:6754147
|
T | G | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746-904T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754147 | ||||||
chr8:6754149
|
C | G | 2 | a0001c0001t0001g0208a0001c0002t0001g0218 | 2 | NA19007.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.746-902C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754149 | ||||||
chr8:6754194
|
T | G | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-857T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754194 | ||||||
chr8:6754224
|
C | T | 1 | a0001c0001t0033g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.746-827C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754224 | ||||||
chr8:6754312
|
A | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0219 | 4 | HG00558.hp2 NA18954.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-739A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754312 | ||||||
chr8:6754537
|
G | A | 1 | a0001c0003t0041g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746-514G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754537 | ||||||
chr8:6754571
|
C | T | 5 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(2): Show | 8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.746-480C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754571 | ||||||
chr8:6754616
|
C | G | 3 | a0001c0001t0025g0021a0001c0001t0026g0021a0001c0001t0027g0133 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-435C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754616 | ||||||
chr8:6754620
|
T | A | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-431T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754620 | ||||||
chr8:6754698
|
C | T | 50 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0023others(47): Show | 63 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.746-353C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754698 | ||||||
chr8:6754800
|
A | G | 3 | a0001c0001t0025g0021a0001c0001t0026g0021a0001c0001t0027g0133 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-251A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754800 | ||||||
chr8:6754819
|
G | A | 1 | a0001c0001t0021g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.746-232G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754819 | ||||||
chr8:6754843
|
A | T | 1 | a0001c0001t0003g0091 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.746-208A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754843 | ||||||
chr8:6754895
|
C | CTT | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-148_746-147dup others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6754895 | |||||
chr8:6754913
|
T | C | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG00741.hp2 HG01106.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.746-138T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754913 | ||||||
chr8:6755190
|
T | A | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.869+16T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755190 | ||||||
chr8:6755191
|
C | G | 24 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0066others(21): Show | 30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.869+17C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755191 | ||||||
chr8:6755302
|
T | A | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+128T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755302 | ||||||
chr8:6755315
|
G | A | 7 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(4): Show | 9 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.869+141G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755315 | ||||||
chr8:6755318
|
C | T | 3 | a0001c0003t0013g0064a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.869+144C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755318 | ||||||
chr8:6755369
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.869+195G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755369 | ||||||
chr8:6755371
|
G | A | 1 | a0001c0001t0036g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.869+197G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755371 | ||||||
chr8:6755412
|
C | T | 11 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(8): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.869+238C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755412 | ||||||
chr8:6755482
|
C | T | 2 | a0001c0001t0002g0288a0001c0001t0003g0111 | 2 | HG01346.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.869+308C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755482 | ||||||
chr8:6755519
|
G | T | 22 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0079others(19): Show | 28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+345G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755519 | ||||||
chr8:6755771
|
G | C | 8 | a0001c0001t0010g0005a0001c0001t0016g0069a0001c0001t0016g0074others(5): Show | 11 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.869+597G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755771 | ||||||
chr8:6755840
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0046others(23): Show | 38 | HG01070.hp2 HG01099.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.869+666A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755840 | ||||||
chr8:6755882
|
C | T | 3 | a0001c0003t0013g0064a0001c0005t0013g0072a0001c0005t0013g0073 | 3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.869+708C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755882 | ||||||
chr8:6755901
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.869+727C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755901 | ||||||
chr8:6756035
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.869+861C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756035 | ||||||
chr8:6756097
|
G | A | 1 | a0001c0001t0030g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.869+923G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756097 | ||||||
chr8:6756109
|
T | C | 3 | a0001c0001t0025g0021a0001c0001t0026g0021a0001c0001t0027g0133 | 3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.869+935T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756109 | ||||||
chr8:6756133
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0003g0024a0001c0001t0003g0080others(1): Show | 5 | HG01943.hp1 HG01952.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+959C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756133 | ||||||
chr8:6756134
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.869+960G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756134 | ||||||
chr8:6756266
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(137): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.870-897C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756266 | ||||||
chr8:6756273
|
C | A | 3 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0121 | 3 | HG00438.hp1 HG02015.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.870-890C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756273 | ||||||
chr8:6756577
|
C | G | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-586C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756577 | ||||||
chr8:6756609
|
C | CA | 17 | a0001c0001t0001g0186a0001c0001t0004g0066a0001c0001t0004g0070others(14): Show | 18 | HG02572.hp2 HG02647.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.870-536dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | |||||
chr8:6756609
|
C | CAA | 10 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0307others(7): Show | 15 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-537_870-536dup others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | |||||
chr8:6756609
|
CA | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(248): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.870-536delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | |||||
chr8:6756609
|
CAA | C | 12 | a0001c0001t0001g0213a0001c0001t0011g0048a0001c0001t0011g0049others(9): Show | 17 | HG01257.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.870-537_870-536del others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | |||||
chr8:6756651
|
T | A | 1 | a0001c0001t0028g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.870-512T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756651 | ||||||
chr8:6756664
|
C | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0034a0001c0001t0007g0231others(1): Show | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-499C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756664 | ||||||
chr8:6756719
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.870-444C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756719 | ||||||
chr8:6756740
|
C | T | 55 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0023others(52): Show | 68 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.870-423C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756740 | ||||||
chr8:6756764
|
G | C | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-399G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756764 | ||||||
chr8:6756773
|
C | G | 1 | a0001c0001t0028g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.870-390C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756773 | ||||||
chr8:6756799
|
C | T | 1 | a0001c0001t0027g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.870-364C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756799 | ||||||
chr8:6756800
|
G | A | 5 | a0001c0001t0002g0016a0001c0001t0002g0041a0001c0001t0002g0089others(2): Show | 7 | HG02027.hp1 HG02040.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-363G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756800 | ||||||
chr8:6756962
|
A | G | 2 | a0001c0001t0004g0312a0001c0001t0055g0313 | 2 | HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.870-201A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756962 | ||||||
chr8:6757021
|
A | G | 65 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0023others(62): Show | 78 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.870-142A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757021 | ||||||
chr8:6757038
|
G | A | 58 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0023others(55): Show | 71 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.870-125G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757038 | ||||||
chr8:6757075
|
T | A | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-88T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757075 | ||||||
chr8:6757077
|
C | T | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-86C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757077 | ||||||
chr8:6757078
|
A | C | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-85A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757078 | ||||||
chr8:6757079
|
G | A | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-84G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757079 | ||||||
chr8:6757085
|
A | G | 64 | a0001c0001t0001g0063a0001c0001t0003g0003a0001c0001t0003g0006others(61): Show | 77 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.870-78A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757085 | ||||||
chr8:6757092
|
A | T | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-71A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757092 | ||||||
chr8:6757093
|
C | T | 1 | a0001c0001t0004g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-70C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757093 | ||||||
chr8:6757095
|
T | A | 3 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-68T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757095 |