geneid | 11057 |
---|---|
ensemblid | ENSG00000140526.18 |
hgncid | 18717 |
symbol | ABHD2 |
name | abhydrolase domain containing 2, acylglycerol lipase |
refseq_nuc | NM_152924.5 |
refseq_prot | NP_690888.1 |
ensembl_nuc | ENST00000352732.10 |
ensembl_prot | ENSP00000268129.5 |
mane_status | MANE Select |
chr | chr15 |
start | 89088456 |
end | 89202355 |
strand | + |
ver | v1.2 |
region | chr15:89088456-89202355 |
region5000 | chr15:89083456-89207355 |
regionname0 | ABHD2_chr15_89088456_89202355 |
regionname5000 | ABHD2_chr15_89083456_89207355 |
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 | 425 | 233 | 90 | 38 | 65 | 8 | 30 | 49 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0002 | 0/0 | 425 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
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 | 1278 | 217 | 77 | 36 | 64 | 8 | 30 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0002 | 0/0 | 1278 | 7 | 6 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0003 | 0/0 | 1278 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0004 | 0/0 | 1278 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0005 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0006 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0007 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0008 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
c0009 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
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 | 7146 | 88 | 22 | 15 | 36 | 2 | 13 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0002 | 0/0 | 7146 | 31 | 6 | 7 | 13 | 1 | 4 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0003 | 0/1 | 7146 | 20 | 0 | 3 | 8 | 2 | 6 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0004 | 0/0 | 7129 | 11 | 11 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0005 | 0/0 | 7144 | 6 | 0 | 1 | 5 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0006 | 0/0 | 7146 | 6 | 5 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0007 | 0/0 | 7147 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0008 | 0/0 | 7146 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0009 | 0/0 | 7145 | 5 | 3 | 2 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0010 | 0/0 | 7146 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0011 | 0/0 | 7146 | 4 | 1 | 1 | 0 | 0 | 2 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0012 | 0/0 | 7146 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0013 | 0/0 | 7146 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0014 | 0/0 | 7146 | 3 | 2 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0015 | 0/0 | 7146 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0016 | 0/0 | 7264 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0017 | 0/0 | 7147 | 2 | 1 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0018 | 0/0 | 7265 | 2 | 1 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0019 | 0/0 | 7146 | 2 | 0 | 0 | 0 | 0 | 2 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0020 | 0/0 | 7146 | 2 | 0 | 1 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0021 | 0/0 | 7146 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0022 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0023 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0024 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0025 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0026 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0027 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0028 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0029 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0030 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0031 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0032 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0033 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0034 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0035 | 0/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0036 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0037 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0038 | 0/0 | 7129 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0039 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0040 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0041 | 1/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0042 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0043 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0044 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
t0045 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
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 | 1278 | 217 | 77 | 36 | 64 | 8 | 30 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0002 | 0/0 | 1278 | 7 | 6 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0003 | 0/0 | 1278 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0004 | 0/0 | 1278 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0006 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0007 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0008 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0009 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0002c0005 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8423 | 86 | 22 | 14 | 35 | 2 | 13 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0002 | 0/0 | 8423 | 31 | 6 | 7 | 13 | 1 | 4 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0003 | 0/1 | 8423 | 20 | 0 | 3 | 8 | 2 | 6 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0004 | 0/0 | 8406 | 11 | 11 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0005 | 0/0 | 8421 | 5 | 0 | 1 | 4 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0006 | 0/0 | 8423 | 6 | 5 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0008 | 0/0 | 8423 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0009 | 0/0 | 8422 | 5 | 3 | 2 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0010 | 0/0 | 8423 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0011 | 0/0 | 8423 | 4 | 1 | 1 | 0 | 0 | 2 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0013 | 0/0 | 8423 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0014 | 0/0 | 8423 | 3 | 2 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0016 | 0/0 | 8541 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0018 | 0/0 | 8542 | 2 | 1 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0019 | 0/0 | 8423 | 2 | 0 | 0 | 0 | 0 | 2 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0020 | 0/0 | 8423 | 2 | 0 | 1 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0021 | 0/0 | 8423 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0022 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0024 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0025 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0026 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0027 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0028 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0029 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0030 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0031 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0032 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0033 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0034 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0035 | 0/0 | 8424 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0036 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0037 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0038 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0039 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0040 | 0/0 | 8542 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0041 | 1/0 | 8424 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0042 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0043 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0044 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0001t0045 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0002t0007 | 0/0 | 8424 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0002t0017 | 0/0 | 8424 | 2 | 1 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0002t0023 | 0/0 | 8424 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0003t0015 | 0/0 | 8423 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0004t0012 | 0/0 | 8423 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0006t0001 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0007t0007 | 0/0 | 8424 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0008t0001 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0001c0009t0012 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
a0002c0005t0005 | 0/0 | 8421 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | copy fasta | chr15 | 89083456 | 89207355 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0011g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0011g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0013g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0018g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0018g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0019g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0019g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0020g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0020g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0021g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0021g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0024g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0025g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0026g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0027g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0028g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0029g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0030g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0031g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0032g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0033g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0034g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0035g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0036g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0037g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0038g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0039g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0040g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0041g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0042g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0043g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0044g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0001t0045g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0017g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0002t0023g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0003t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0003t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0003t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0004t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0004t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0007t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0008t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0001c0009t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
a0002c0005t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0020 | g0058 | EUR | GBR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00140 | hp2 | a0001 | c0001 | t0034 | g0143 | EUR | GBR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00280 | hp1 | a0001 | c0001 | t0014 | g0059 | EUR | FIN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00438 | hp2 | a0001 | c0001 | t0027 | g0189 | EAS | CHS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00738 | hp1 | a0001 | c0001 | t0030 | g0128 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00741 | hp1 | a0001 | c0001 | t0029 | g0122 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG00741 | hp2 | a0001 | c0001 | t0009 | g0025 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01070 | hp2 | a0001 | c0001 | t0020 | g0104 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01106 | hp2 | a0001 | c0001 | t0024 | g0170 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01109 | hp1 | a0001 | c0008 | t0001 | g0228 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01243 | hp1 | a0001 | c0001 | t0018 | g0036 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01243 | hp2 | a0001 | c0002 | t0017 | g0008 | AMR | PUR | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0209 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01361 | hp1 | a0001 | c0001 | t0025 | g0199 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01361 | hp2 | a0001 | c0001 | t0009 | g0081 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | IBS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01884 | hp2 | a0001 | c0001 | t0022 | g0043 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01891 | hp2 | a0001 | c0004 | t0012 | g0226 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02004 | hp1 | a0001 | c0001 | t0011 | g0076 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0082 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | KHV | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02145 | hp2 | a0001 | c0002 | t0017 | g0005 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02165 | hp2 | a0001 | c0006 | t0001 | g0191 | EAS | CDX | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02273 | hp2 | a0001 | c0001 | t0026 | g0070 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02280 | hp1 | a0001 | c0002 | t0023 | g0112 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02280 | hp2 | a0001 | c0003 | t0015 | g0234 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0111 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0171 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02615 | hp1 | a0001 | c0001 | t0044 | g0090 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02630 | hp1 | a0001 | c0001 | t0038 | g0078 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02630 | hp2 | a0001 | c0001 | t0031 | g0229 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02717 | hp2 | a0001 | c0001 | t0018 | g0033 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02723 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02735 | hp1 | a0001 | c0001 | t0042 | g0057 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02895 | hp1 | a0001 | c0003 | t0015 | g0194 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0232 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02922 | hp1 | a0001 | c0009 | t0012 | g0027 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02970 | hp2 | a0001 | c0001 | t0040 | g0010 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0154 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02976 | hp2 | a0001 | c0001 | t0021 | g0105 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03041 | hp2 | a0001 | c0001 | t0032 | g0034 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0147 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0152 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03486 | hp2 | a0001 | c0001 | t0033 | g0164 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03490 | hp1 | a0001 | c0001 | t0019 | g0063 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03492 | hp2 | a0001 | c0001 | t0019 | g0064 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | ESN | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03540 | hp2 | a0001 | c0001 | t0045 | g0168 | AFR | GWD | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03579 | hp1 | a0001 | c0001 | t0039 | g0009 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03688 | hp2 | a0001 | c0001 | t0011 | g0208 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04115 | hp2 | a0001 | c0001 | t0043 | g0137 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04204 | hp1 | a0001 | c0001 | t0035 | g0136 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04228 | hp1 | a0001 | c0001 | t0011 | g0138 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18906 | hp1 | a0001 | c0002 | t0007 | g0040 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18962 | hp1 | a0001 | c0001 | t0037 | g0067 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18971 | hp2 | a0001 | c0001 | t0036 | g0178 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18990 | hp1 | a0001 | c0001 | t0028 | g0176 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19030 | hp1 | a0001 | c0002 | t0007 | g0020 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19089 | hp2 | a0002 | c0005 | t0005 | g0114 | EAS | JPT | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20129 | hp1 | a0001 | c0007 | t0007 | g0225 | AFR | ASW | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02109 | hp2 | a0001 | c0001 | t0013 | g0096 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0163 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02486 | hp2 | a0001 | c0003 | t0015 | g0101 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG02559 | hp2 | a0001 | c0001 | t0021 | g0167 | AFR | ACB | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0159 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG03471 | hp2 | a0001 | c0004 | t0012 | g0001 | AFR | MSL | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | USA | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
HG06807 | hp2 | a0001 | c0002 | t0007 | g0153 | AFR | USA | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | USA | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0056 | REF | REF | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0041 | g0211 | REF | REF | ABHD2_chr15_89083456_89207355 | ABHD2 | chr15 | 89083456 | 89207355 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:89175880
|
G | A | 1 | a0002 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.607G>A | p.Val203Ile | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/11 | 821/8424 | 607/1278 | 203/425 | chr15 | 89175880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:89155470
|
C | T | 3 | a0001c0007a0001c0008a0001c0009 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.474C>T | p.Ala158Ala | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/11 | 688/8424 | 474/1278 | 158/425 | chr15 | 89155470 | ||
chr15:89188244
|
G | A | 1 | a0001c0006 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.867G>A | p.Thr289Thr | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/11 | 1081/8424 | 867/1278 | 289/425 | chr15 | 89188244 | ||
chr15:89191089
|
C | T | 1 | a0001c0003 | 3 | HG02280.hp2 HG02486.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.936C>T | p.His312His | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/11 | 1150/8424 | 936/1278 | 312/425 | chr15 | 89191089 | ||
chr15:89193270
|
C | T | 2 | a0001c0004a0001c0009 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.1032C>T | p.Asp344Asp | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/11 | 1246/8424 | 1032/1278 | 344/425 | chr15 | 89193270 | ||
chr15:89195405
|
G | A | 2 | a0001c0002a0001c0007 | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.1260G>A | p.Val420Val | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1474/8424 | 1260/1278 | 420/425 | chr15 | 89195405 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:89113806
|
G | C | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/11 | 2522 | chr15 | 89113806 | |||||
chr15:89195523
|
G | C | 4 | a0001c0002t0007a0001c0002t0017a0001c0002t0023others(1): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*100G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 100 | chr15 | 89195523 | |||||
chr15:89195674
|
T | C | 1 | a0001c0001t0018 | 2 | HG01243.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*251T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 251 | chr15 | 89195674 | |||||
chr15:89195861
|
A | G | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*438A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 438 | chr15 | 89195861 | |||||
chr15:89195886
|
G | T | 1 | a0001c0001t0018 | 2 | HG01243.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*463G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 463 | chr15 | 89195886 | |||||
chr15:89196028
|
G | C | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(20): Show | 137 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*605G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 605 | chr15 | 89196028 | |||||
chr15:89196030
|
G | T | 1 | a0001c0001t0045 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 607 | chr15 | 89196030 | |||||
chr15:89196232
|
C | T | 1 | a0001c0001t0013 | 3 | HG02109.hp2 HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*809C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 809 | chr15 | 89196232 | |||||
chr15:89196782
|
G | A | 1 | a0001c0001t0033 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1359G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1359 | chr15 | 89196782 | |||||
chr15:89196794
|
A | G | 1 | a0001c0001t0021 | 2 | HG02559.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1371A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1371 | chr15 | 89196794 | |||||
chr15:89196811
|
G | A | 1 | a0001c0001t0019 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1388G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1388 | chr15 | 89196811 | |||||
chr15:89196841
|
G | A | 1 | a0001c0001t0024 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1418 | chr15 | 89196841 | |||||
chr15:89197142
|
G | C | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(12): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1719G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1719 | chr15 | 89197142 | |||||
chr15:89197153
|
T | G | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(13): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1730T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1730 | chr15 | 89197153 | |||||
chr15:89197238
|
T | C | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(12): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1815T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1815 | chr15 | 89197238 | |||||
chr15:89197350
|
G | A | 1 | a0001c0001t0008 | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1927G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1927 | chr15 | 89197350 | |||||
chr15:89197385
|
G | A | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1962G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 1962 | chr15 | 89197385 | |||||
chr15:89197589
|
C | T | 1 | a0001c0001t0040 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 2166 | chr15 | 89197589 | |||||
chr15:89197781
|
C | T | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2358C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 2358 | chr15 | 89197781 | |||||
chr15:89198291
|
C | G | 2 | a0001c0004t0012a0001c0009t0012 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2868C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 2868 | chr15 | 89198291 | |||||
chr15:89198449
|
CTG | C | 2 | a0001c0001t0005a0002c0005t0005 | 6 | HG01928.hp2 HG02129.hp2 NA18990.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3028_*3029delGT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3028 | INFO_REALIGN_3_PRIME | chr15 | 89198449 | ||||
chr15:89198757
|
C | T | 3 | a0001c0001t0018a0001c0001t0039a0001c0001t0044 | 4 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3334C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3334 | chr15 | 89198757 | |||||
chr15:89198855
|
G | A | 1 | a0001c0001t0025 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3432G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3432 | chr15 | 89198855 | |||||
chr15:89199019
|
G | A | 1 | a0001c0001t0031 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3596G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3596 | chr15 | 89199019 | |||||
chr15:89199031
|
G | A | 1 | a0001c0001t0026 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3608G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3608 | chr15 | 89199031 | |||||
chr15:89199226
|
A | G | 1 | a0001c0001t0038 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3803A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3803 | chr15 | 89199226 | |||||
chr15:89199296
|
TA | T | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*3877delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 3877 | INFO_REALIGN_3_PRIME | chr15 | 89199296 | ||||
chr15:89199702
|
T | C | 1 | a0001c0001t0034 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4279T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4279 | chr15 | 89199702 | |||||
chr15:89199712
|
G | A | 1 | a0001c0002t0017 | 2 | HG01243.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4289G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4289 | chr15 | 89199712 | |||||
chr15:89199801
|
G | C | 3 | a0001c0001t0013a0001c0001t0032a0001c0001t0044 | 5 | HG02109.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4378G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4378 | chr15 | 89199801 | |||||
chr15:89199812
|
C | T | 10 | a0001c0001t0001a0001c0001t0022a0001c0001t0024others(7): Show | 95 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*4389C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4389 | chr15 | 89199812 | |||||
chr15:89199831
|
C | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4408C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4408 | chr15 | 89199831 | |||||
chr15:89199849
|
C | A | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*4426C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4426 | chr15 | 89199849 | |||||
chr15:89199865
|
C | A | 1 | a0001c0001t0027 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4442C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4442 | chr15 | 89199865 | |||||
chr15:89199924
|
A | G | 4 | a0001c0001t0004a0001c0001t0013a0001c0001t0032others(1): Show | 16 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4501A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4501 | chr15 | 89199924 | |||||
chr15:89200105
|
G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4682G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4682 | chr15 | 89200105 | |||||
chr15:89200348
|
C | T | 1 | a0001c0001t0043 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4925C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4925 | chr15 | 89200348 | |||||
chr15:89200373
|
A | ACCTCACT others(111): Show |
3 | a0001c0001t0016a0001c0001t0018a0001c0001t0040 | 6 | HG01243.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4964_*4965insTGGT others(114): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 4965 | INFO_REALIGN_3_PRIME | chr15 | 89200373 | ||||
chr15:89200437
|
C | G | 10 | a0001c0001t0001a0001c0001t0014a0001c0001t0022others(7): Show | 97 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*5014C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5014 | chr15 | 89200437 | |||||
chr15:89200439
|
G | A | 2 | a0001c0004t0012a0001c0009t0012 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5016G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5016 | chr15 | 89200439 | |||||
chr15:89200540
|
AC | A | 1 | a0001c0001t0009 | 5 | HG00741.hp2 HG01361.hp2 HG01891.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5118delC | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5118 | chr15 | 89200540 | |||||
chr15:89200662
|
C | CA | 4 | a0001c0002t0007a0001c0002t0017a0001c0002t0023others(1): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5246dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5247 | INFO_REALIGN_3_PRIME | chr15 | 89200662 | ||||
chr15:89200729
|
G | GA | 5 | a0001c0001t0004a0001c0001t0018a0001c0001t0035others(2): Show | 16 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5316dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5317 | INFO_REALIGN_3_PRIME | chr15 | 89200729 | ||||
chr15:89200773
|
C | T | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*5350C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5350 | chr15 | 89200773 | |||||
chr15:89200784
|
A | G | 1 | a0001c0001t0008 | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5361A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5361 | chr15 | 89200784 | |||||
chr15:89200959
|
G | A | 2 | a0001c0001t0004a0001c0001t0038 | 12 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5536G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5536 | chr15 | 89200959 | |||||
chr15:89201245
|
G | T | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*5822G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 5822 | chr15 | 89201245 | |||||
chr15:89201450
|
A | C | 3 | a0001c0001t0016a0001c0001t0018a0001c0001t0040 | 6 | HG01243.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6027A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6027 | chr15 | 89201450 | |||||
chr15:89201593
|
T | G | 1 | a0001c0001t0030 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6170T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6170 | chr15 | 89201593 | |||||
chr15:89201684
|
C | T | 1 | a0001c0001t0006 | 6 | HG01258.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6261C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6261 | chr15 | 89201684 | |||||
chr15:89201715
|
T | C | 1 | a0001c0002t0023 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6292T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6292 | chr15 | 89201715 | |||||
chr15:89201720
|
G | A | 1 | a0001c0001t0028 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6297G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6297 | chr15 | 89201720 | |||||
chr15:89201751
|
C | T | 8 | a0001c0001t0004a0001c0001t0013a0001c0001t0032others(5): Show | 24 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6328C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6328 | chr15 | 89201751 | |||||
chr15:89201759
|
A | C | 2 | a0001c0001t0010a0001c0001t0044 | 5 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6336A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6336 | chr15 | 89201759 | |||||
chr15:89201822
|
AGGGGGCG others(11): Show |
A | 2 | a0001c0001t0004a0001c0001t0038 | 12 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6408_*6425delCTTG others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6408 | INFO_REALIGN_3_PRIME | chr15 | 89201822 | ||||
chr15:89201891
|
C | T | 1 | a0001c0001t0020 | 2 | HG00140.hp1 HG01070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6468C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6468 | chr15 | 89201891 | |||||
chr15:89201916
|
A | G | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6493A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6493 | chr15 | 89201916 | |||||
chr15:89202155
|
T | C | 1 | a0001c0001t0036 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6732T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6732 | chr15 | 89202155 | |||||
chr15:89202171
|
G | A | 1 | a0001c0001t0042 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6748G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6748 | chr15 | 89202171 | |||||
chr15:89202280
|
C | G | 2 | a0001c0001t0040a0001c0003t0015 | 4 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6857C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6857 | chr15 | 89202280 | |||||
chr15:89202294
|
A | G | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6871A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 11/11 | 6871 | chr15 | 89202294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:89088688
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-107+125T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89088688 | ||||||
chr15:89088689
|
G | C | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+126G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89088689 | ||||||
chr15:89088711
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014 | 3 | HG03540.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-107+148G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89088711 | ||||||
chr15:89088973
|
T | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00741.hp2 HG01106.hp1 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.-107+410T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89088973 | ||||||
chr15:89089386
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0004g0016 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-107+823T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089386 | ||||||
chr15:89089408
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02165.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-107+845T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089408 | ||||||
chr15:89089462
|
A | G | 3 | a0001c0001t0008g0232a0001c0001t0008g0233a0001c0003t0015g0234 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-107+899A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089462 | ||||||
chr15:89089687
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02165.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-107+1124G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089687 | ||||||
chr15:89089717
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-107+1154A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089717 | ||||||
chr15:89089786
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-107+1223G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89089786 | ||||||
chr15:89090060
|
T | G | 1 | a0001c0001t0010g0032 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-107+1497T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090060 | ||||||
chr15:89090104
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-107+1541A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090104 | ||||||
chr15:89090156
|
G | C | 2 | a0001c0001t0018g0033a0001c0001t0032g0034 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-107+1593G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090156 | ||||||
chr15:89090266
|
C | T | 4 | a0001c0001t0004g0227a0001c0001t0010g0032a0001c0001t0031g0229others(1): Show | 4 | HG01109.hp1 HG02630.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+1703C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090266 | ||||||
chr15:89090446
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02165.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-107+1883A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090446 | ||||||
chr15:89090505
|
TAAC | T | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-107+1944_-107+194 others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89090505 | |||||
chr15:89090516
|
A | G | 2 | a0001c0004t0012g0226a0001c0007t0007g0225 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-107+1953A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090516 | ||||||
chr15:89090668
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-107+2105C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090668 | ||||||
chr15:89090709
|
G | A | 56 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0042others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-107+2146G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090709 | ||||||
chr15:89090762
|
C | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0010g0012 | 3 | HG01106.hp1 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-107+2199C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090762 | ||||||
chr15:89090868
|
G | A | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+2305G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090868 | ||||||
chr15:89090876
|
A | C | 4 | a0001c0001t0004g0227a0001c0001t0010g0032a0001c0001t0031g0229others(1): Show | 4 | HG01109.hp1 HG02630.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+2313A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090876 | ||||||
chr15:89090878
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-107+2315G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89090878 | ||||||
chr15:89091061
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02165.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-107+2498G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091061 | ||||||
chr15:89091065
|
G | A | 56 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0042others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-107+2502G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091065 | ||||||
chr15:89091068
|
C | A | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-107+2505C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091068 | ||||||
chr15:89091102
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-107+2539G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091102 | ||||||
chr15:89091125
|
T | C | 1 | a0001c0004t0012g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-107+2562T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091125 | ||||||
chr15:89091183
|
G | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-107+2620G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091183 | ||||||
chr15:89091211
|
A | G | 46 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(43): Show | 46 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-107+2648A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091211 | ||||||
chr15:89091236
|
G | A | 14 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0097others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-107+2673G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091236 | ||||||
chr15:89091427
|
G | T | 14 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0097others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-107+2864G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091427 | ||||||
chr15:89091528
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00741.hp2 HG03453.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-107+2965C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091528 | ||||||
chr15:89091780
|
T | C | 3 | a0001c0001t0004g0227a0001c0001t0010g0032a0001c0008t0001g0228 | 3 | HG01109.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-107+3217T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091780 | ||||||
chr15:89091960
|
G | T | 1 | a0001c0001t0003g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-107+3397G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091960 | ||||||
chr15:89091975
|
C | A | 1 | a0001c0001t0020g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-107+3412C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89091975 | ||||||
chr15:89092037
|
A | G | 149 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-107+3474A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092037 | ||||||
chr15:89092122
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-107+3559T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092122 | ||||||
chr15:89092196
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-107+3633G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092196 | ||||||
chr15:89092548
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02165.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-107+3985G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092548 | ||||||
chr15:89092550
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-107+3987C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092550 | ||||||
chr15:89092740
|
G | C | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-107+4177G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092740 | ||||||
chr15:89092765
|
C | G | 2 | a0001c0001t0009g0144a0001c0001t0034g0143 | 2 | HG00140.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-107+4202C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092765 | ||||||
chr15:89092839
|
A | G | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-107+4276A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89092839 | ||||||
chr15:89093008
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0002g0219a0001c0001t0004g0220others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+4445T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093008 | ||||||
chr15:89093047
|
CCTT | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 17 | HG00741.hp2 HG01891.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.-107+4489_-107+449 others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89093047 | |||||
chr15:89093059
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0148others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-107+4496T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093059 | ||||||
chr15:89093173
|
C | CT | 8 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0217others(5): Show | 8 | HG02293.hp1 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-107+4634dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89093173 | |||||
chr15:89093173
|
CT | C | 150 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-107+4634delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89093173 | |||||
chr15:89093173
|
CTT | C | 7 | a0001c0001t0001g0028a0001c0001t0002g0156a0001c0001t0006g0157others(4): Show | 7 | HG02630.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-107+4633_-107+463 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89093173 | |||||
chr15:89093173
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0155 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-107+4621_-107+463 others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89093173 | |||||
chr15:89093183
|
T | A | 2 | a0001c0004t0012g0226a0001c0007t0007g0225 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-107+4620T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093183 | ||||||
chr15:89093236
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0002g0077a0001c0001t0011g0076others(1): Show | 4 | HG01099.hp2 HG02004.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+4673A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093236 | ||||||
chr15:89093245
|
A | C | 31 | a0001c0001t0001g0074a0001c0001t0001g0087a0001c0001t0001g0113others(28): Show | 31 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-107+4682A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093245 | ||||||
chr15:89093255
|
G | T | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-107+4692G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093255 | ||||||
chr15:89093283
|
C | T | 2 | a0001c0004t0012g0226a0001c0007t0007g0225 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-107+4720C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093283 | ||||||
chr15:89093750
|
G | C | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-107+5187G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093750 | ||||||
chr15:89093791
|
A | T | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+5228A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093791 | ||||||
chr15:89093964
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-107+5401C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093964 | ||||||
chr15:89093965
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-107+5402G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89093965 | ||||||
chr15:89094187
|
C | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-107+5624C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094187 | ||||||
chr15:89094208
|
T | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(25): Show | 28 | HG01106.hp1 HG01884.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.-107+5645T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094208 | ||||||
chr15:89094228
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-107+5665G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094228 | ||||||
chr15:89094256
|
T | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(25): Show | 28 | HG01106.hp1 HG01884.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.-107+5693T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094256 | ||||||
chr15:89094276
|
T | C | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-107+5713T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094276 | ||||||
chr15:89094474
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-107+5911G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094474 | ||||||
chr15:89094824
|
A | C | 1 | a0001c0001t0035g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-107+6261A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094824 | ||||||
chr15:89094860
|
C | T | 58 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-107+6297C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094860 | ||||||
chr15:89094921
|
G | A | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+6358G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094921 | ||||||
chr15:89094999
|
G | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(10): Show | 13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-107+6436G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89094999 | ||||||
chr15:89095063
|
C | CA | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(40): Show | 43 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.-107+6522dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89095063 | |||||
chr15:89095063
|
C | CAA | 6 | a0001c0001t0001g0028a0001c0001t0004g0227a0001c0001t0010g0032others(3): Show | 6 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+6521_-107+652 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89095063 | |||||
chr15:89095063
|
CA | C | 10 | a0001c0001t0001g0213a0001c0001t0002g0214a0001c0001t0003g0026others(7): Show | 10 | HG00544.hp1 HG01169.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-107+6522delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89095063 | |||||
chr15:89095193
|
A | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0005g0037 | 3 | NA18975.hp2 NA18978.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-107+6630A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095193 | ||||||
chr15:89095209
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-107+6646G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095209 | ||||||
chr15:89095275
|
G | C | 1 | a0001c0001t0006g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-107+6712G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095275 | ||||||
chr15:89095469
|
T | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(10): Show | 13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-107+6906T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095469 | ||||||
chr15:89095556
|
A | C | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+6993A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095556 | ||||||
chr15:89095629
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-107+7066A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095629 | ||||||
chr15:89095787
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-107+7224G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89095787 | ||||||
chr15:89096480
|
A | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-107+7917A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89096480 | ||||||
chr15:89096529
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-107+7966G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89096529 | ||||||
chr15:89096617
|
A | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-107+8054A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89096617 | ||||||
chr15:89096758
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-107+8195A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89096758 | ||||||
chr15:89097103
|
T | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0022g0043others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+8540T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097103 | ||||||
chr15:89097137
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-107+8574A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097137 | ||||||
chr15:89097193
|
A | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(25): Show | 28 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-107+8630A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097193 | ||||||
chr15:89097292
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-107+8729T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097292 | ||||||
chr15:89097494
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0002g0219 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-107+8931A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097494 | ||||||
chr15:89097507
|
A | T | 55 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.-107+8944A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097507 | ||||||
chr15:89097624
|
A | G | 69 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0041others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.-107+9061A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89097624 | ||||||
chr15:89098018
|
G | C | 13 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0103others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-107+9455G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098018 | ||||||
chr15:89098168
|
T | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-107+9605T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098168 | ||||||
chr15:89098200
|
A | G | 1 | a0001c0001t0009g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-107+9637A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098200 | ||||||
chr15:89098340
|
C | G | 39 | a0001c0001t0001g0087a0001c0001t0001g0113a0001c0001t0001g0115others(36): Show | 39 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-107+9777C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098340 | ||||||
chr15:89098405
|
C | T | 1 | a0001c0001t0006g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-107+9842C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098405 | ||||||
chr15:89098647
|
G | C | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+10084G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89098647 | ||||||
chr15:89099096
|
C | T | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-107+10533C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89099096 | ||||||
chr15:89099192
|
A | G | 1 | a0001c0001t0009g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-107+10629A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89099192 | ||||||
chr15:89099283
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(4): Show | 7 | HG01106.hp1 HG02451.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-107+10720G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89099283 | ||||||
chr15:89099868
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(4): Show | 7 | HG01106.hp1 HG02451.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-107+11305C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89099868 | ||||||
chr15:89099909
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG00741.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+11346A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89099909 | ||||||
chr15:89100043
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-107+11480C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100043 | ||||||
chr15:89100284
|
A | ATTT | 11 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-107+11736_-107+11 others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89100284 | |||||
chr15:89100284
|
AT | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01081.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-107+11738delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89100284 | |||||
chr15:89100309
|
A | G | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-107+11746A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100309 | ||||||
chr15:89100342
|
A | G | 29 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(26): Show | 29 | HG01106.hp1 HG01884.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.-107+11779A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100342 | ||||||
chr15:89100581
|
C | A | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-107+12018C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100581 | ||||||
chr15:89100713
|
C | A | 1 | a0001c0001t0021g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-107+12150C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100713 | ||||||
chr15:89100801
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG00741.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+12238G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100801 | ||||||
chr15:89100821
|
A | G | 2 | a0001c0002t0007g0111a0001c0002t0023g0112 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-107+12258A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89100821 | ||||||
chr15:89101050
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-107+12487T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101050 | ||||||
chr15:89101082
|
T | G | 21 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(18): Show | 21 | HG01106.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-107+12519T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101082 | ||||||
chr15:89101146
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-106-12579A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101146 | ||||||
chr15:89101322
|
A | G | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-106-12403A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101322 | ||||||
chr15:89101707
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-106-12018G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101707 | ||||||
chr15:89101756
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-106-11969C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101756 | ||||||
chr15:89101949
|
A | G | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-11776A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101949 | ||||||
chr15:89101972
|
T | C | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-11753T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101972 | ||||||
chr15:89101993
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106-11732C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101993 | ||||||
chr15:89101999
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-106-11726A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89101999 | ||||||
chr15:89102441
|
T | C | 2 | a0001c0004t0012g0226a0001c0007t0007g0225 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-106-11284T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102441 | ||||||
chr15:89102496
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0002g0151a0001c0001t0004g0150others(3): Show | 6 | HG01952.hp1 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-106-11229G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102496 | ||||||
chr15:89102711
|
C | T | 46 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.-106-11014C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102711 | ||||||
chr15:89102769
|
G | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0108a0001c0001t0001g0149others(9): Show | 12 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-106-10956G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102769 | ||||||
chr15:89102876
|
G | T | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-10849G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102876 | ||||||
chr15:89102974
|
G | C | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-106-10751G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89102974 | ||||||
chr15:89103002
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-106-10723G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103002 | ||||||
chr15:89103136
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-106-10589C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103136 | ||||||
chr15:89103200
|
A | C | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-10525A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103200 | ||||||
chr15:89103239
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-106-10486T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103239 | ||||||
chr15:89103268
|
C | G | 2 | a0001c0001t0009g0144a0001c0001t0034g0143 | 2 | HG00140.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-106-10457C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103268 | ||||||
chr15:89103279
|
T | C | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-106-10446T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103279 | ||||||
chr15:89103395
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-106-10330C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103395 | ||||||
chr15:89103637
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-106-10088G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103637 | ||||||
chr15:89103668
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-106-10057A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103668 | ||||||
chr15:89103695
|
C | G | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | NA18961.hp1 NA18965.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-106-10030C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103695 | ||||||
chr15:89103779
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-106-9946T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103779 | ||||||
chr15:89103831
|
A | C | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-9894A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89103831 | ||||||
chr15:89104097
|
A | G | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG00741.hp2 HG01243.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-106-9628A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104097 | ||||||
chr15:89104240
|
A | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-9485A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104240 | ||||||
chr15:89104457
|
A | G | 17 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-106-9268A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104457 | ||||||
chr15:89104551
|
C | T | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-9174C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104551 | ||||||
chr15:89104640
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0092others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-9085G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104640 | ||||||
chr15:89104758
|
A | C | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-106-8967A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89104758 | ||||||
chr15:89105043
|
A | T | 2 | a0001c0001t0019g0063a0001c0001t0019g0064 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-106-8682A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105043 | ||||||
chr15:89105135
|
G | A | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-106-8590G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105135 | ||||||
chr15:89105393
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-106-8332C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105393 | ||||||
chr15:89105402
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-106-8323T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105402 | ||||||
chr15:89105488
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-8237C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105488 | ||||||
chr15:89105530
|
T | C | 2 | a0001c0001t0002g0109a0001c0001t0002g0197 | 2 | HG02293.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-106-8195T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105530 | ||||||
chr15:89105551
|
A | G | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-106-8174A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105551 | ||||||
chr15:89105597
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-106-8128C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105597 | ||||||
chr15:89105602
|
A | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0002g0210others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-106-8123A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105602 | ||||||
chr15:89105712
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-106-8013C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105712 | ||||||
chr15:89105830
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-106-7895C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89105830 | ||||||
chr15:89106045
|
A | G | 112 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-106-7680A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106045 | ||||||
chr15:89106161
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0206others(1): Show | 4 | NA18965.hp2 NA18978.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-7564A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106161 | ||||||
chr15:89106277
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-106-7448G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106277 | ||||||
chr15:89106286
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-7439G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106286 | ||||||
chr15:89106425
|
A | G | 17 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-106-7300A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106425 | ||||||
chr15:89106434
|
ACTCAC | A | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-7286_-106-728 others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89106434 | |||||
chr15:89106438
|
A | G | 2 | a0001c0001t0003g0130a0001c0001t0003g0140 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-106-7287A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106438 | ||||||
chr15:89106455
|
C | G | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-106-7270C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106455 | ||||||
chr15:89106473
|
C | T | 42 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0046others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-106-7252C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106473 | ||||||
chr15:89106652
|
A | T | 35 | a0001c0001t0001g0075a0001c0001t0001g0087a0001c0001t0001g0113others(32): Show | 35 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-106-7073A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106652 | ||||||
chr15:89106789
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0039g0009 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-106-6936A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106789 | ||||||
chr15:89106804
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-106-6921A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89106804 | ||||||
chr15:89107015
|
A | G | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-106-6710A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89107015 | ||||||
chr15:89107080
|
G | A | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-6645G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89107080 | ||||||
chr15:89107099
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-6626G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89107099 | ||||||
chr15:89107238
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-106-6487T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89107238 | ||||||
chr15:89107564
|
C | T | 44 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0046others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.-106-6161C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89107564 | ||||||
chr15:89108017
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-106-5708T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108017 | ||||||
chr15:89108023
|
G | C | 112 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-106-5702G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108023 | ||||||
chr15:89108029
|
A | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-5696A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108029 | ||||||
chr15:89108066
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106-5659T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108066 | ||||||
chr15:89108147
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-106-5578G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108147 | ||||||
chr15:89108249
|
G | T | 2 | a0001c0001t0033g0164a0001c0002t0007g0020 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-106-5476G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108249 | ||||||
chr15:89108393
|
T | A | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.-106-5332T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108393 | ||||||
chr15:89108448
|
G | A | 1 | a0001c0001t0006g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-106-5277G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108448 | ||||||
chr15:89108699
|
A | G | 2 | a0001c0001t0004g0220a0001c0001t0010g0012 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-106-5026A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108699 | ||||||
chr15:89108783
|
G | A | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-4942G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108783 | ||||||
chr15:89108907
|
G | A | 67 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.-106-4818G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89108907 | ||||||
chr15:89109182
|
A | G | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.-106-4543A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109182 | ||||||
chr15:89109238
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-106-4487T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109238 | ||||||
chr15:89109321
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-106-4404G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109321 | ||||||
chr15:89109341
|
A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-106-4384A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109341 | ||||||
chr15:89109358
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG00438.hp2 HG01081.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-106-4367C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109358 | ||||||
chr15:89109431
|
G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106-4294G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109431 | ||||||
chr15:89109446
|
A | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-4279A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109446 | ||||||
chr15:89109485
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-106-4240G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109485 | ||||||
chr15:89109521
|
C | T | 1 | a0001c0001t0020g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-106-4204C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109521 | ||||||
chr15:89109891
|
C | G | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-106-3834C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89109891 | ||||||
chr15:89110031
|
A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-106-3694A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110031 | ||||||
chr15:89110034
|
G | C | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-3691G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110034 | ||||||
chr15:89110095
|
A | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-106-3630A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110095 | ||||||
chr15:89110152
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0091others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-106-3573C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110152 | ||||||
chr15:89110221
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0079 | 3 | NA18950.hp1 NA18983.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-106-3504G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110221 | ||||||
chr15:89110308
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-106-3417C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110308 | ||||||
chr15:89110345
|
GT | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00741.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-106-3379delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110345 | ||||||
chr15:89110404
|
C | G | 2 | a0001c0001t0016g0066a0001c0001t0031g0229 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-106-3321C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110404 | ||||||
chr15:89110460
|
A | G | 2 | a0001c0001t0008g0011a0001c0002t0017g0008 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-106-3265A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110460 | ||||||
chr15:89110533
|
A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-106-3192A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110533 | ||||||
chr15:89110595
|
C | T | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-3130C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110595 | ||||||
chr15:89110675
|
A | G | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-106-3050A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110675 | ||||||
chr15:89110837
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-106-2888T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110837 | ||||||
chr15:89110896
|
G | A | 1 | a0001c0001t0009g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-106-2829G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110896 | ||||||
chr15:89110915
|
C | T | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-106-2810C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110915 | ||||||
chr15:89110926
|
T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-106-2799T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110926 | ||||||
chr15:89110966
|
T | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-106-2759T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89110966 | ||||||
chr15:89111104
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-106-2621G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111104 | ||||||
chr15:89111151
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG00741.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-106-2574A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111151 | ||||||
chr15:89111413
|
A | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0148others(1): Show | 4 | HG01106.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-2312A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111413 | ||||||
chr15:89111501
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-106-2224G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111501 | ||||||
chr15:89111510
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-106-2215A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111510 | ||||||
chr15:89111533
|
A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-106-2192A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111533 | ||||||
chr15:89111723
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0092others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-2002C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111723 | ||||||
chr15:89111745
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-106-1980T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111745 | ||||||
chr15:89111747
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0091others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-106-1978C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111747 | ||||||
chr15:89111754
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0009g0163 | 2 | HG01433.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-106-1971A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111754 | ||||||
chr15:89111816
|
T | G | 4 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0092others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-1909T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111816 | ||||||
chr15:89111941
|
T | TTA | 16 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0091others(13): Show | 16 | HG01243.hp2 HG02040.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-106-1770_-106-176 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89111941 | |||||
chr15:89111981
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-106-1744A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89111981 | ||||||
chr15:89112174
|
C | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-106-1551C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89112174 | ||||||
chr15:89112175
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-106-1550G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89112175 | ||||||
chr15:89112388
|
C | A | 2 | a0001c0001t0001g0074a0001c0001t0003g0047 | 2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-106-1337C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89112388 | ||||||
chr15:89112443
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-106-1282G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89112443 | ||||||
chr15:89112635
|
T | C | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-106-1090T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89112635 | ||||||
chr15:89112857
|
G | GAC | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(8): Show | 11 | HG00741.hp2 HG01106.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-106-865_-106-864d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89112857 | |||||
chr15:89113136
|
T | G | 2 | a0001c0001t0008g0232a0001c0001t0008g0233 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-106-589T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113136 | ||||||
chr15:89113159
|
C | G | 1 | a0001c0001t0004g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-106-566C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113159 | ||||||
chr15:89113168
|
G | A | 1 | a0001c0001t0045g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-106-557G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113168 | ||||||
chr15:89113171
|
C | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106-554C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113171 | ||||||
chr15:89113236
|
T | C | 33 | a0001c0001t0001g0075a0001c0001t0001g0087a0001c0001t0001g0113others(30): Show | 33 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-106-489T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113236 | ||||||
chr15:89113240
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-106-485T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113240 | ||||||
chr15:89113382
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-106-343T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113382 | ||||||
chr15:89113454
|
CA | C | 4 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0092others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-270delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113454 | ||||||
chr15:89113505
|
T | C | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-106-220T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113505 | ||||||
chr15:89113596
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-106-129C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113596 | ||||||
chr15:89113664
|
T | TA | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0022g0043others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-60dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 89113664 | |||||
chr15:89113692
|
G | A | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-106-33G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113692 | ||||||
chr15:89113692
|
G | T | 2 | a0001c0001t0019g0063a0001c0001t0019g0064 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-106-33G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113692 | ||||||
chr15:89113704
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-106-21A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 1/10 | chr15 | 89113704 | ||||||
chr15:89114134
|
A | G | 4 | a0001c0001t0004g0220a0001c0001t0010g0012a0001c0001t0016g0066others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+310A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114134 | ||||||
chr15:89114198
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-7+374G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114198 | ||||||
chr15:89114349
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7+525G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114349 | ||||||
chr15:89114403
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-7+579G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114403 | ||||||
chr15:89114465
|
A | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(7): Show | 10 | HG00741.hp2 HG01106.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+641A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114465 | ||||||
chr15:89114487
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0206 | 2 | NA18965.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-7+663G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114487 | ||||||
chr15:89114508
|
C | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(9): Show | 12 | HG00741.hp2 HG01106.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+684C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114508 | ||||||
chr15:89114801
|
A | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(9): Show | 12 | HG00741.hp2 HG01106.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+977A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114801 | ||||||
chr15:89114920
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-7+1096A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114920 | ||||||
chr15:89114928
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1104A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89114928 | ||||||
chr15:89115190
|
G | A | 45 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0046others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.-6-1132G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115190 | ||||||
chr15:89115209
|
T | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(10): Show | 13 | HG00741.hp2 HG01106.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-1113T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115209 | ||||||
chr15:89115227
|
C | G | 1 | a0001c0001t0002g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-6-1095C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115227 | ||||||
chr15:89115365
|
G | T | 46 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0046others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.-6-957G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115365 | ||||||
chr15:89115367
|
GGTATGTG others(11): Show |
G | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-6-952_-6-935delAT others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(13): Show |
G | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-952_-6-933delAT others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(15): Show |
G | 12 | a0001c0001t0001g0028a0001c0001t0001g0074a0001c0001t0001g0091others(9): Show | 12 | HG02451.hp2 HG02965.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-952_-6-931delAT others(20): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(17): Show |
G | 41 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-6-952_-6-929delAT others(22): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(19): Show |
G | 6 | a0001c0001t0002g0107a0001c0001t0003g0162a0001c0001t0004g0065others(3): Show | 6 | HG00140.hp1 HG00280.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-952_-6-927delAT others(24): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(21): Show |
G | 4 | a0001c0001t0001g0060a0001c0001t0003g0061a0001c0001t0010g0012others(1): Show | 4 | HG01517.hp1 HG02602.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-952_-6-925delAT others(26): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(23): Show |
G | 2 | a0001c0001t0001g0148a0001c0001t0002g0219 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-6-952_-6-923delAT others(28): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115367
|
GGTATGTG others(27): Show |
G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0004t0012g0226 | 3 | HG01106.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-6-952_-6-919delAT others(32): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115367 | |||||
chr15:89115370
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0016g0147a0001c0001t0043g0137 | 3 | HG02602.hp1 HG03098.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-6-952A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115370 | ||||||
chr15:89115370
|
ATGTG | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0151others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-894_-6-891delGT others(2): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTG | A | 7 | a0001c0001t0001g0095a0001c0001t0003g0135a0001c0001t0004g0083others(4): Show | 7 | HG00544.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-896_-6-891delGT others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0001g0100a0001c0001t0001g0231a0001c0001t0006g0193others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-898_-6-891delGT others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(3): Show |
A | 25 | a0001c0001t0001g0029a0001c0001t0001g0075a0001c0001t0001g0097others(22): Show | 25 | HG00280.hp2 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-6-900_-6-891delGT others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(5): Show |
A | 37 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0087others(34): Show | 37 | HG00438.hp2 HG01099.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.-6-902_-6-891delGT others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(7): Show |
A | 31 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0084others(28): Show | 31 | HG00438.hp1 HG00741.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-6-904_-6-891delGT others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(9): Show |
A | 15 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0192others(12): Show | 15 | HG00738.hp1 HG01070.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-906_-6-891delGT others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(11): Show |
A | 6 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0195others(3): Show | 6 | HG01070.hp2 HG01928.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-908_-6-891delGT others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115370
|
ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-6-912_-6-891delGT others(20): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115370 | |||||
chr15:89115391
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6-931T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115391 | ||||||
chr15:89115393
|
T | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG00741.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-929T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115393 | ||||||
chr15:89115395
|
T | G | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-927T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115395 | ||||||
chr15:89115397
|
T | G | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-6-925T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115397 | ||||||
chr15:89115399
|
T | G | 2 | a0001c0001t0001g0148a0001c0001t0002g0219 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-6-923T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115399 | ||||||
chr15:89115403
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0004t0012g0226 | 3 | HG01106.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-6-919T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115403 | ||||||
chr15:89115406
|
GTGTGTGT others(18): Show |
G | 1 | a0001c0001t0043g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6-914_-6-890delGT others(23): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115406 | |||||
chr15:89115408
|
GTGTGTGT others(16): Show |
G | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-6-912_-6-890delGT others(21): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115408 | |||||
chr15:89115414
|
GTGTGTGT others(10): Show |
G | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-906_-6-890delGT others(15): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115414 | |||||
chr15:89115416
|
GTGTGTGT others(8): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-6-904_-6-890delGT others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115416 | |||||
chr15:89115420
|
GTGTGTGT others(4): Show |
G | 3 | a0001c0001t0001g0142a0001c0001t0003g0215a0001c0001t0006g0209 | 3 | HG01258.hp1 NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-6-900_-6-890delGT others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115420 | |||||
chr15:89115420
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-6-898_-6-886delGT others(11): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115420 | |||||
chr15:89115422
|
GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-6-896_-6-886delGT others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 89115422 | |||||
chr15:89115432
|
T | G | 14 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(11): Show | 14 | HG00741.hp2 HG01106.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-890T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115432 | ||||||
chr15:89115433
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6-889T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115433 | ||||||
chr15:89115499
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0091others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-823A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115499 | ||||||
chr15:89115732
|
G | C | 1 | a0001c0001t0035g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6-590G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89115732 | ||||||
chr15:89116194
|
C | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-6-128C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89116194 | ||||||
chr15:89116220
|
G | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-6-102G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89116220 | ||||||
chr15:89116236
|
C | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-6-86C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89116236 | ||||||
chr15:89116250
|
C | T | 2 | a0001c0001t0016g0066a0001c0001t0031g0229 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-6-72C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89116250 | ||||||
chr15:89116251
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-71G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 2/10 | chr15 | 89116251 | ||||||
chr15:89116983
|
G | C | 2 | a0001c0001t0010g0035a0001c0001t0018g0036 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.194+462G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89116983 | ||||||
chr15:89117047
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0091others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.194+526A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117047 | ||||||
chr15:89117061
|
A | C | 2 | a0001c0001t0016g0147a0001c0004t0012g0226 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+540A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117061 | ||||||
chr15:89117088
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.194+567T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117088 | ||||||
chr15:89117245
|
T | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.194+724T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117245 | ||||||
chr15:89117259
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.194+738C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117259 | ||||||
chr15:89117283
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194+762C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117283 | ||||||
chr15:89117621
|
CAG | C | 2 | a0001c0001t0001g0175a0001c0001t0028g0176 | 2 | HG00280.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.194+1106_194+1107d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89117621 | |||||
chr15:89117684
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.194+1163G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117684 | ||||||
chr15:89117742
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.194+1221G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117742 | ||||||
chr15:89117756
|
G | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.194+1235G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117756 | ||||||
chr15:89117808
|
C | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.194+1287C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117808 | ||||||
chr15:89117889
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+1368C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117889 | ||||||
chr15:89117958
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.194+1437C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89117958 | ||||||
chr15:89118191
|
C | CT | 5 | a0001c0001t0001g0088a0001c0001t0001g0129a0001c0001t0005g0125others(2): Show | 5 | HG01928.hp1 HG02129.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+1680dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89118191 | |||||
chr15:89118191
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0148others(1): Show | 4 | HG01106.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+1670C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118191 | ||||||
chr15:89118324
|
C | T | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.194+1803C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118324 | ||||||
chr15:89118325
|
G | A | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.194+1804G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118325 | ||||||
chr15:89118404
|
C | G | 2 | a0001c0001t0016g0147a0001c0004t0012g0226 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+1883C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118404 | ||||||
chr15:89118405
|
C | T | 2 | a0001c0001t0004g0220a0001c0001t0010g0012 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.194+1884C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118405 | ||||||
chr15:89118515
|
T | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.194+1994T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118515 | ||||||
chr15:89118608
|
A | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0022g0043others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+2087A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118608 | ||||||
chr15:89118626
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.194+2105C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118626 | ||||||
chr15:89118780
|
A | G | 1 | a0001c0001t0004g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.194+2259A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118780 | ||||||
chr15:89118881
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.194+2360C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118881 | ||||||
chr15:89118986
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.194+2465T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89118986 | ||||||
chr15:89119018
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0004g0013a0001c0001t0014g0014others(2): Show | 5 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+2497G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119018 | ||||||
chr15:89119103
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.194+2582G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119103 | ||||||
chr15:89119346
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+2825C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119346 | ||||||
chr15:89119360
|
C | A | 3 | a0001c0001t0001g0123a0001c0001t0029g0122a0001c0001t0030g0128 | 3 | HG00738.hp1 HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.194+2839C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119360 | ||||||
chr15:89119525
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.194+3004A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119525 | ||||||
chr15:89119568
|
T | C | 2 | a0001c0001t0004g0220a0001c0001t0010g0012 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.194+3047T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119568 | ||||||
chr15:89119605
|
C | T | 1 | a0001c0001t0014g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.194+3084C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119605 | ||||||
chr15:89119828
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.194+3307C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119828 | ||||||
chr15:89119862
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(11): Show | 14 | HG00741.hp2 HG01106.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+3341G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119862 | ||||||
chr15:89119879
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+3358G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89119879 | ||||||
chr15:89120015
|
G | A | 1 | a0001c0001t0009g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.194+3494G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120015 | ||||||
chr15:89120132
|
A | G | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(12): Show | 15 | HG00741.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+3611A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120132 | ||||||
chr15:89120413
|
G | A | 72 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.194+3892G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120413 | ||||||
chr15:89120534
|
C | T | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.194+4013C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120534 | ||||||
chr15:89120621
|
G | A | 2 | a0001c0001t0004g0220a0001c0001t0010g0012 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.194+4100G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120621 | ||||||
chr15:89120720
|
C | T | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.194+4199C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120720 | ||||||
chr15:89120732
|
G | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+4211G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89120732 | ||||||
chr15:89120846
|
GA | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.194+4335delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89120846 | |||||
chr15:89121126
|
G | A | 2 | a0001c0001t0008g0232a0001c0001t0008g0233 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194+4605G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121126 | ||||||
chr15:89121145
|
G | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0117 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.194+4624G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121145 | ||||||
chr15:89121146
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0117 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.194+4625A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121146 | ||||||
chr15:89121346
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0002g0219 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194+4825G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121346 | ||||||
chr15:89121458
|
CT | C | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(12): Show | 15 | HG00741.hp2 HG01106.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+4949delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89121458 | |||||
chr15:89121684
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.194+5163C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121684 | ||||||
chr15:89121895
|
C | T | 2 | a0001c0001t0004g0220a0001c0001t0010g0012 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.194+5374C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121895 | ||||||
chr15:89121906
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+5385G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89121906 | ||||||
chr15:89122083
|
G | A | 2 | a0001c0001t0018g0033a0001c0001t0032g0034 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.194+5562G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122083 | ||||||
chr15:89122121
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.194+5600T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122121 | ||||||
chr15:89122388
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.194+5867A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122388 | ||||||
chr15:89122447
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.194+5926C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122447 | ||||||
chr15:89122571
|
G | T | 47 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0046others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.194+6050G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122571 | ||||||
chr15:89122592
|
G | T | 56 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.194+6071G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122592 | ||||||
chr15:89122700
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0014g0014a0001c0001t0014g0159 | 3 | HG03471.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.194+6179C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122700 | ||||||
chr15:89122774
|
T | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0183a0001c0001t0001g0231others(5): Show | 8 | HG01109.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+6253T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122774 | ||||||
chr15:89122825
|
G | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.194+6304G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122825 | ||||||
chr15:89122865
|
T | C | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+6344T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122865 | ||||||
chr15:89122889
|
C | T | 1 | a0001c0001t0014g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.194+6368C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122889 | ||||||
chr15:89122927
|
G | A | 1 | a0001c0001t0006g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.194+6406G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89122927 | ||||||
chr15:89123276
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.194+6755C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123276 | ||||||
chr15:89123312
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+6791C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123312 | ||||||
chr15:89123503
|
G | A | 72 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.194+6982G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123503 | ||||||
chr15:89123593
|
C | CT | 11 | a0001c0001t0001g0116a0001c0001t0001g0142a0001c0001t0001g0182others(8): Show | 11 | HG00438.hp2 HG00544.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.194+7094dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89123593 | |||||
chr15:89123593
|
CT | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0173others(12): Show | 15 | HG00140.hp2 HG00544.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.194+7094delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89123593 | |||||
chr15:89123593
|
CTT | C | 22 | a0001c0001t0001g0108a0001c0001t0001g0146a0001c0001t0001g0149others(19): Show | 22 | HG01952.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.194+7093_194+7094d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89123593 | |||||
chr15:89123593
|
CTTT | C | 66 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.194+7092_194+7094d others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89123593 | |||||
chr15:89123593
|
CTTTT | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.194+7091_194+7094d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89123593 | |||||
chr15:89123596
|
T | TC | 5 | a0001c0001t0016g0147a0001c0001t0019g0063a0001c0001t0019g0064others(2): Show | 5 | HG01891.hp2 HG03098.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+7075_194+7076i others(3): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123596 | ||||||
chr15:89123599
|
T | C | 1 | a0001c0001t0008g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.194+7078T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123599 | ||||||
chr15:89123654
|
A | G | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.194+7133A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123654 | ||||||
chr15:89123727
|
G | A | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.194+7206G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123727 | ||||||
chr15:89123886
|
G | T | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.194+7365G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123886 | ||||||
chr15:89123910
|
T | G | 3 | a0001c0001t0001g0060a0001c0001t0002g0107a0001c0001t0020g0058 | 3 | HG00140.hp1 HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.194+7389T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123910 | ||||||
chr15:89123929
|
A | G | 2 | a0001c0001t0016g0147a0001c0004t0012g0226 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+7408A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89123929 | ||||||
chr15:89124079
|
T | G | 1 | a0001c0001t0010g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.194+7558T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89124079 | ||||||
chr15:89124429
|
TA | T | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.194+7916delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89124429 | |||||
chr15:89124580
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.194+8059A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89124580 | ||||||
chr15:89124580
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.194+8059A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89124580 | ||||||
chr15:89124942
|
G | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.194+8421G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89124942 | ||||||
chr15:89125044
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.194+8523G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125044 | ||||||
chr15:89125089
|
C | CA | 45 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(42): Show | 45 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.194+8581dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89125089 | |||||
chr15:89125127
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.194+8606A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125127 | ||||||
chr15:89125173
|
T | C | 2 | a0001c0001t0016g0147a0001c0004t0012g0226 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+8652T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125173 | ||||||
chr15:89125254
|
C | CA | 26 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(23): Show | 26 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.194+8746dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89125254 | |||||
chr15:89125387
|
C | G | 2 | a0001c0001t0004g0227a0001c0001t0010g0032 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.194+8866C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125387 | ||||||
chr15:89125625
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0016g0066a0001c0001t0016g0147others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.194+9104T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125625 | ||||||
chr15:89125634
|
G | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.194+9113G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125634 | ||||||
chr15:89125654
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.194+9133G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125654 | ||||||
chr15:89125823
|
A | C | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+9302A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125823 | ||||||
chr15:89125880
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0016g0066a0001c0001t0016g0147others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.194+9359T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125880 | ||||||
chr15:89125948
|
A | T | 2 | a0001c0001t0005g0127a0002c0005t0005g0114 | 2 | HG02129.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.194+9427A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89125948 | ||||||
chr15:89126014
|
A | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+9493A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126014 | ||||||
chr15:89126096
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+9575G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126096 | ||||||
chr15:89126167
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.194+9646A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126167 | ||||||
chr15:89126208
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(22): Show | 25 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.194+9687C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126208 | ||||||
chr15:89126357
|
A | G | 1 | a0001c0001t0005g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.194+9836A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126357 | ||||||
chr15:89126454
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(46): Show | 49 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.194+9933A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126454 | ||||||
chr15:89126475
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.194+9954G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126475 | ||||||
chr15:89126750
|
G | T | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.194+10229G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89126750 | ||||||
chr15:89126984
|
A | AG | 22 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.194+10464dupG | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89126984 | |||||
chr15:89127106
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.194+10585C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127106 | ||||||
chr15:89127273
|
C | T | 47 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.194+10752C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127273 | ||||||
chr15:89127450
|
A | AT | 22 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.194+10929_194+1093 others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127450 | ||||||
chr15:89127553
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.194+11032A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127553 | ||||||
chr15:89127596
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0116a0001c0001t0001g0198others(11): Show | 14 | HG00438.hp1 HG01099.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.194+11075C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127596 | ||||||
chr15:89127706
|
C | CATACATA others(9): Show |
1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194+11188_194+1118 others(20): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATACATA others(29): Show |
1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.194+11188_194+1118 others(40): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATAT | 4 | a0001c0001t0001g0146a0001c0001t0011g0138a0001c0001t0014g0059others(1): Show | 4 | HG00280.hp1 HG02602.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+11195_194+1119 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATAT | 2 | a0001c0001t0002g0094a0001c0001t0008g0102 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194+11193_194+1119 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(1): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0231a0001c0001t0004g0083others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+11191_194+1119 others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0091a0001c0001t0001g0148a0001c0001t0002g0219others(2): Show | 5 | HG02451.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+11189_194+1119 others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(5): Show |
6 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0013g0096others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+11187_194+1119 others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(7): Show |
2 | a0001c0001t0001g0042a0001c0001t0022g0043 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(9): Show |
2 | a0001c0001t0002g0151a0001c0001t0008g0011 | 2 | HG01952.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(20): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(11): Show |
1 | a0001c0001t0004g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+11198_194+1119 others(22): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(13): Show |
1 | a0001c0001t0001g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.194+11198_194+1119 others(24): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.194+11198_194+1119 others(28): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(19): Show |
1 | a0001c0001t0008g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.194+11198_194+1119 others(30): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(15): Show |
2 | a0001c0001t0013g0154a0001c0002t0007g0153 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(26): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(21): Show |
2 | a0001c0001t0040g0010a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(32): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127706
|
C | CATATATA others(21): Show |
1 | a0001c0001t0010g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.194+11198_194+1119 others(32): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127706 | |||||
chr15:89127708
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.194+11199_194+1121 others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127708 | |||||
chr15:89127710
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0009g0025 | 2 | HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.194+11199_194+1121 others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127710 | |||||
chr15:89127712
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.194+11199_194+1120 others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127712 | |||||
chr15:89127716
|
TATACAC | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.194+11199_194+1120 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127716 | |||||
chr15:89127718
|
T | TATAC | 3 | a0001c0001t0002g0039a0001c0001t0004g0045a0001c0001t0038g0078 | 3 | HG02630.hp1 HG03139.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127718 | |||||
chr15:89127718
|
T | TATACAC | 2 | a0001c0001t0004g0227a0001c0001t0010g0032 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.194+11198_194+1119 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127718 | |||||
chr15:89127720
|
C | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(92): Show | 95 | HG00140.hp1 HG00738.hp2 HG01081.hp2 others(92): Show |
intron_variant | MODIFIER | c.194+11199C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127720 | ||||||
chr15:89127722
|
C | CACACACA others(7): Show |
1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+11202_194+1120 others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CACACATA others(1): Show |
10 | a0001c0001t0001g0068a0001c0001t0001g0108a0001c0001t0001g0183others(7): Show | 10 | HG02280.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.194+11202_194+1120 others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CACACATA others(3): Show |
1 | a0001c0001t0021g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.194+11202_194+1120 others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CACATAT | 32 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0044others(29): Show | 32 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.194+11202_194+1120 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CACATATA others(1): Show |
9 | a0001c0001t0001g0046a0001c0001t0001g0060a0001c0001t0002g0107others(6): Show | 9 | HG00140.hp1 HG01169.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+11202_194+1120 others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CACATATA others(5): Show |
1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.194+11202_194+1120 others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CATAT | 3 | a0001c0001t0001g0146a0001c0001t0004g0016a0001c0001t0014g0059 | 3 | HG00280.hp1 HG02602.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.194+11216_194+1121 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | CATATAT | 2 | a0001c0001t0011g0138a0001c0001t0042g0057 | 2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.194+11214_194+1121 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127722
|
C | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0041others(45): Show | 48 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.194+11201C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127722 | ||||||
chr15:89127722
|
CAT | C | 38 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0087others(35): Show | 38 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.194+11218_194+1121 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127722 | |||||
chr15:89127724
|
T | C | 1 | a0001c0001t0010g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.194+11203T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127724 | ||||||
chr15:89127724
|
T | TATATATA others(15): Show |
1 | a0001c0004t0012g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.194+11219_194+1122 others(26): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127724 | |||||
chr15:89127724
|
T | TATATATA others(19): Show |
1 | a0001c0001t0002g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.194+11219_194+1122 others(30): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127724 | |||||
chr15:89127724
|
T | TATATATA others(21): Show |
2 | a0001c0001t0001g0006a0001c0002t0017g0005 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.194+11219_194+1122 others(32): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127724 | |||||
chr15:89127724
|
T | TATATATA others(29): Show |
1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.194+11219_194+1122 others(40): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127724 | |||||
chr15:89127724
|
T | TATATATA others(31): Show |
1 | a0001c0001t0001g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.194+11219_194+1122 others(42): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89127724 | |||||
chr15:89127726
|
T | C | 2 | a0001c0001t0040g0010a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.194+11205T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127726 | ||||||
chr15:89127741
|
G | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+11220G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127741 | ||||||
chr15:89127803
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194+11282G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127803 | ||||||
chr15:89127836
|
C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(5): Show | 8 | HG01106.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+11315C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89127836 | ||||||
chr15:89128002
|
C | T | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+11481C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128002 | ||||||
chr15:89128058
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0002others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+11537C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128058 | ||||||
chr15:89128581
|
C | A | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.194+12060C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128581 | ||||||
chr15:89128690
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+12169C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128690 | ||||||
chr15:89128790
|
G | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG00741.hp2 HG02922.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.194+12269G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128790 | ||||||
chr15:89128814
|
C | A | 2 | a0001c0001t0011g0138a0001c0001t0042g0057 | 2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.194+12293C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89128814 | ||||||
chr15:89129038
|
G | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.194+12517G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129038 | ||||||
chr15:89129048
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0002g0214 | 3 | HG01167.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.194+12527A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129048 | ||||||
chr15:89129077
|
A | C | 1 | a0001c0001t0002g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.194+12556A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129077 | ||||||
chr15:89129134
|
G | A | 2 | a0001c0001t0018g0033a0001c0001t0032g0034 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.194+12613G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129134 | ||||||
chr15:89129209
|
G | T | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+12688G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129209 | ||||||
chr15:89129408
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+12887C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129408 | ||||||
chr15:89129637
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+13116C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129637 | ||||||
chr15:89129716
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0002g0107a0001c0001t0020g0058 | 3 | HG00140.hp1 HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.194+13195C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129716 | ||||||
chr15:89129937
|
A | G | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.194+13416A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89129937 | ||||||
chr15:89130005
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.194+13484T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130005 | ||||||
chr15:89130073
|
CAATG | C | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+13555_194+1355 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89130073 | |||||
chr15:89130398
|
C | A | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.194+13877C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130398 | ||||||
chr15:89130459
|
C | G | 1 | a0001c0001t0001g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.194+13938C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130459 | ||||||
chr15:89130594
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.194+14073A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130594 | ||||||
chr15:89130595
|
C | T | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+14074C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130595 | ||||||
chr15:89130650
|
T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.194+14129T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130650 | ||||||
chr15:89130797
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.194+14276G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130797 | ||||||
chr15:89130823
|
A | G | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+14302A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130823 | ||||||
chr15:89130872
|
TA | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(5): Show | 8 | HG01106.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+14354delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89130872 | |||||
chr15:89130927
|
G | A | 3 | a0001c0001t0016g0066a0001c0001t0016g0147a0001c0001t0031g0229 | 3 | HG02258.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194+14406G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89130927 | ||||||
chr15:89131018
|
C | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.194+14497C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131018 | ||||||
chr15:89131152
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+14631C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131152 | ||||||
chr15:89131213
|
T | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+14692T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131213 | ||||||
chr15:89131362
|
G | T | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194+14841G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131362 | ||||||
chr15:89131443
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0095others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.194+14922G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131443 | ||||||
chr15:89131487
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0196 | 2 | NA19005.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.194+14966G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131487 | ||||||
chr15:89131525
|
C | A | 1 | a0001c0004t0012g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.194+15004C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131525 | ||||||
chr15:89131583
|
C | A | 2 | a0001c0001t0020g0104a0001c0001t0024g0170 | 2 | HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.194+15062C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131583 | ||||||
chr15:89131691
|
A | G | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.194+15170A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131691 | ||||||
chr15:89131953
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0017others(57): Show | 60 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.194+15432G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89131953 | ||||||
chr15:89132025
|
T | C | 3 | a0001c0001t0008g0232a0001c0001t0008g0233a0001c0003t0015g0234 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194+15504T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89132025 | ||||||
chr15:89132311
|
T | C | 2 | a0001c0001t0005g0127a0002c0005t0005g0114 | 2 | HG02129.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.194+15790T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89132311 | ||||||
chr15:89132389
|
A | T | 12 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0103others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.194+15868A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89132389 | ||||||
chr15:89132521
|
A | C | 5 | a0001c0001t0004g0013a0001c0001t0010g0032a0001c0001t0014g0014others(2): Show | 5 | HG02895.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+16000A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89132521 | ||||||
chr15:89132630
|
T | G | 1 | a0001c0001t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194+16109T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89132630 | ||||||
chr15:89133182
|
T | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.194+16661T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133182 | ||||||
chr15:89133182
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0021g0105a0001c0001t0021g0167 | 3 | HG02559.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.194+16661T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133182 | ||||||
chr15:89133192
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.194+16671A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133192 | ||||||
chr15:89133267
|
T | TA | 41 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.194+16753dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133267 | |||||
chr15:89133326
|
T | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.194+16805T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133326 | ||||||
chr15:89133353
|
T | G | 1 | a0001c0001t0003g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.194+16832T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133353 | ||||||
chr15:89133374
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.194+16853C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133374 | ||||||
chr15:89133534
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0021g0105a0001c0001t0021g0167 | 3 | HG02559.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.194+17013A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133534 | ||||||
chr15:89133555
|
G | A | 1 | a0001c0001t0032g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.194+17034G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133555 | ||||||
chr15:89133834
|
A | AT | 9 | a0001c0001t0001g0041a0001c0001t0001g0085a0001c0001t0001g0086others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+17333dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
A | ATT | 16 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0098others(13): Show | 16 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+17332_194+1733 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
A | ATTT | 34 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 34 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.194+17331_194+1733 others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
A | ATTTT | 6 | a0001c0001t0001g0088a0001c0001t0001g0179a0001c0001t0001g0196others(3): Show | 6 | HG01891.hp2 HG03579.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+17330_194+1733 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
AT | A | 23 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0060others(20): Show | 23 | HG00741.hp1 HG01109.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.194+17333delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
ATT | A | 20 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0172others(17): Show | 20 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.194+17332_194+1733 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133834
|
ATTTTTTT | A | 8 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0148others(5): Show | 8 | HG02622.hp2 HG02965.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.194+17327_194+1733 others(11): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133834 | |||||
chr15:89133850
|
T | TTG | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0149others(6): Show | 9 | HG01952.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+17330_194+1733 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89133850 | |||||
chr15:89133867
|
C | T | 1 | a0001c0003t0015g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194+17346C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133867 | ||||||
chr15:89133985
|
T | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.194+17464T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89133985 | ||||||
chr15:89134040
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0021g0105a0001c0001t0021g0167 | 3 | HG02559.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.194+17519A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134040 | ||||||
chr15:89134059
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.194+17538C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134059 | ||||||
chr15:89134073
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0028g0176 | 2 | HG00280.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.194+17552C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134073 | ||||||
chr15:89134129
|
C | T | 1 | a0001c0001t0011g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.195-17548C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134129 | ||||||
chr15:89134161
|
A | G | 1 | a0001c0001t0020g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.195-17516A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134161 | ||||||
chr15:89134222
|
GTCT | G | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0149others(6): Show | 9 | HG01952.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-17449_195-1744 others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89134222 | |||||
chr15:89134735
|
A | C | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195-16942A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134735 | ||||||
chr15:89134775
|
C | T | 2 | a0001c0001t0040g0010a0001c0007t0007g0225 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.195-16902C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134775 | ||||||
chr15:89134887
|
C | G | 8 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0148others(5): Show | 8 | HG02622.hp2 HG02965.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-16790C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134887 | ||||||
chr15:89134964
|
A | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0004g0083others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-16713A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89134964 | ||||||
chr15:89135009
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.195-16668C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135009 | ||||||
chr15:89135045
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.195-16632A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135045 | ||||||
chr15:89135072
|
A | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-16605A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135072 | ||||||
chr15:89135138
|
T | TTTTTC | 144 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 144 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.195-16534_195-1653 others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135138 | |||||
chr15:89135140
|
T | TTTCTTTT others(1): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG01081.hp1 HG02004.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-16530_195-1652 others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135140 | |||||
chr15:89135143
|
C | CTTTTCT | 19 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0097others(16): Show | 19 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-16530_195-1652 others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135143 | |||||
chr15:89135143
|
C | CTTTTCTT others(1): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 32 | HG00438.hp1 HG01070.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.195-16530_195-1652 others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135143 | |||||
chr15:89135143
|
C | CTTTTCTT others(2): Show |
5 | a0001c0001t0001g0072a0001c0001t0003g0145a0001c0001t0008g0232others(2): Show | 5 | HG01243.hp1 HG02071.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-16530_195-1652 others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135143 | |||||
chr15:89135144
|
T | TTTTC | 25 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0158others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.195-16530_195-1652 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135144 | |||||
chr15:89135406
|
C | CA | 12 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0001g0099others(9): Show | 12 | HG01952.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.195-16260dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89135406 | |||||
chr15:89135440
|
A | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-16237A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135440 | ||||||
chr15:89135725
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.195-15952G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135725 | ||||||
chr15:89135993
|
C | A | 1 | a0001c0001t0002g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.195-15684C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89135993 | ||||||
chr15:89136076
|
G | A | 1 | a0001c0001t0026g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.195-15601G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136076 | ||||||
chr15:89136078
|
C | A | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195-15599C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136078 | ||||||
chr15:89136081
|
C | A | 2 | a0001c0001t0040g0010a0001c0007t0007g0225 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.195-15596C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136081 | ||||||
chr15:89136092
|
A | ATT | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-15571_195-1557 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89136092 | |||||
chr15:89136092
|
AT | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0004g0083others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-15570delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89136092 | |||||
chr15:89136144
|
G | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-15533G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136144 | ||||||
chr15:89136193
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0011g0171a0001c0009t0012g0027 | 3 | HG02572.hp2 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.195-15484T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136193 | ||||||
chr15:89136208
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0150a0001c0002t0007g0153 | 3 | HG01952.hp1 HG02809.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.195-15469C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136208 | ||||||
chr15:89136284
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.195-15393G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136284 | ||||||
chr15:89136290
|
G | C | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195-15387G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136290 | ||||||
chr15:89136556
|
G | GC | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-15117dupC | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89136556 | |||||
chr15:89136638
|
G | A | 12 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0149others(9): Show | 12 | HG01952.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.195-15039G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136638 | ||||||
chr15:89136659
|
G | A | 1 | a0001c0001t0011g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.195-15018G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136659 | ||||||
chr15:89136684
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0018g0036a0001c0001t0039g0009 | 3 | HG01243.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195-14993C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136684 | ||||||
chr15:89136759
|
G | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0075a0001c0001t0001g0087others(12): Show | 15 | HG00741.hp1 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.195-14918G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136759 | ||||||
chr15:89136810
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-14867A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136810 | ||||||
chr15:89136813
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.195-14864G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136813 | ||||||
chr15:89136813
|
G | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.195-14864G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136813 | ||||||
chr15:89136895
|
T | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-14782T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136895 | ||||||
chr15:89136900
|
G | A | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195-14777G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89136900 | ||||||
chr15:89137153
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.195-14524T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137153 | ||||||
chr15:89137219
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.195-14458C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137219 | ||||||
chr15:89137275
|
G | C | 2 | a0001c0001t0001g0028a0001c0009t0012g0027 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.195-14402G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137275 | ||||||
chr15:89137386
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.195-14291T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137386 | ||||||
chr15:89137478
|
T | C | 2 | a0001c0001t0040g0010a0001c0007t0007g0225 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.195-14199T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137478 | ||||||
chr15:89137545
|
C | T | 55 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.195-14132C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137545 | ||||||
chr15:89137566
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0032g0034 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.195-14111C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137566 | ||||||
chr15:89137579
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0004g0083others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-14098A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137579 | ||||||
chr15:89137785
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-13892T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89137785 | ||||||
chr15:89138854
|
CT | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0097others(14): Show | 17 | HG01109.hp1 HG01952.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.195-12812delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89138854 | |||||
chr15:89138857
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0018g0036a0001c0001t0039g0009 | 3 | HG01243.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195-12820T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89138857 | ||||||
chr15:89138864
|
TTC | T | 41 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.195-12811_195-1281 others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89138864 | |||||
chr15:89138867
|
T | C | 41 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.195-12810T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89138867 | ||||||
chr15:89138875
|
T | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.195-12802T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89138875 | ||||||
chr15:89138916
|
G | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(37): Show | 40 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.195-12761G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89138916 | ||||||
chr15:89139018
|
C | CA | 19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-12659_195-1265 others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139018 | ||||||
chr15:89139019
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-12658C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139019 | ||||||
chr15:89139022
|
C | CAAGACAT others(5): Show |
19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-12655_195-1265 others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139022 | ||||||
chr15:89139023
|
C | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-12654C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139023 | ||||||
chr15:89139287
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.195-12390C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139287 | ||||||
chr15:89139304
|
T | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(127): Show | 130 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.195-12373T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139304 | ||||||
chr15:89139791
|
A | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.195-11886A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139791 | ||||||
chr15:89139936
|
T | C | 1 | a0001c0006t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.195-11741T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89139936 | ||||||
chr15:89140144
|
G | C | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.195-11533G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140144 | ||||||
chr15:89140146
|
C | G | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.195-11531C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140146 | ||||||
chr15:89140353
|
G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00738.hp1 HG00741.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-11324G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140353 | ||||||
chr15:89140411
|
A | T | 3 | a0001c0001t0002g0219a0001c0001t0033g0164a0001c0002t0023g0112 | 3 | HG02280.hp1 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.195-11266A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140411 | ||||||
chr15:89140415
|
G | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0185a0001c0001t0001g0187 | 3 | HG01081.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.195-11262G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140415 | ||||||
chr15:89140585
|
A | C | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.195-11092A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140585 | ||||||
chr15:89140672
|
C | G | 1 | a0001c0001t0003g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.195-11005C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140672 | ||||||
chr15:89140698
|
G | A | 47 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.195-10979G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140698 | ||||||
chr15:89140958
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.195-10719A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89140958 | ||||||
chr15:89140972
|
CT | C | 48 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0052others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.195-10693delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89140972 | |||||
chr15:89141032
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.195-10645G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141032 | ||||||
chr15:89141132
|
C | CTAAT | 4 | a0001c0001t0011g0138a0001c0001t0021g0105a0001c0001t0021g0167others(1): Show | 4 | HG02559.hp2 HG02735.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-10523_195-1052 others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89141132 | |||||
chr15:89141132
|
C | CTAATTAA others(5): Show |
1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195-10531_195-1052 others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89141132 | |||||
chr15:89141318
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.195-10359G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141318 | ||||||
chr15:89141540
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0231others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-10137C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141540 | ||||||
chr15:89141605
|
C | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.195-10072C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141605 | ||||||
chr15:89141622
|
C | CA | 12 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0097others(9): Show | 12 | HG01952.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.195-10045dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89141622 | |||||
chr15:89141643
|
G | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0108others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-10034G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141643 | ||||||
chr15:89141738
|
C | T | 1 | a0001c0001t0002g0200 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.195-9939C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141738 | ||||||
chr15:89141761
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.195-9916C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141761 | ||||||
chr15:89141894
|
T | C | 5 | a0001c0001t0004g0013a0001c0001t0010g0032a0001c0001t0014g0014others(2): Show | 5 | HG02895.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-9783T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141894 | ||||||
chr15:89141966
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0016others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-9711T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89141966 | ||||||
chr15:89142037
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.195-9640G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142037 | ||||||
chr15:89142056
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0001g0091others(23): Show | 26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.195-9621A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142056 | ||||||
chr15:89142089
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG00738.hp1 HG01099.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.195-9588G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142089 | ||||||
chr15:89142122
|
C | T | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195-9555C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142122 | ||||||
chr15:89142193
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0097others(7): Show | 10 | HG01952.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.195-9484G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142193 | ||||||
chr15:89142197
|
T | C | 1 | a0001c0003t0015g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.195-9480T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142197 | ||||||
chr15:89142337
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(40): Show | 43 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.195-9340G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142337 | ||||||
chr15:89142435
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.195-9242T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142435 | ||||||
chr15:89142555
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0060others(34): Show | 37 | HG01256.hp1 HG01258.hp1 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.195-9122C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89142555 | ||||||
chr15:89143061
|
A | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.195-8616A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143061 | ||||||
chr15:89143099
|
T | C | 4 | a0001c0001t0001g0099a0001c0001t0014g0014a0001c0001t0014g0159others(1): Show | 4 | HG02895.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-8578T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143099 | ||||||
chr15:89143253
|
A | G | 22 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(19): Show | 22 | HG02004.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-8424A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143253 | ||||||
chr15:89143310
|
T | C | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.195-8367T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143310 | ||||||
chr15:89143374
|
T | C | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.195-8303T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143374 | ||||||
chr15:89143393
|
T | C | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-8284T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143393 | ||||||
chr15:89143396
|
G | A | 1 | a0001c0001t0045g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.195-8281G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143396 | ||||||
chr15:89143588
|
A | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-8089A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143588 | ||||||
chr15:89143616
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.195-8061G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143616 | ||||||
chr15:89143627
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.195-8050G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143627 | ||||||
chr15:89143680
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.195-7997T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143680 | ||||||
chr15:89143688
|
CA | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(124): Show | 127 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.195-7976delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89143688 | |||||
chr15:89143721
|
A | AGAGATGA others(46): Show |
1 | a0001c0001t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.195-7954_195-7902d others(55): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89143721 | |||||
chr15:89143782
|
A | C | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.195-7895A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143782 | ||||||
chr15:89143835
|
C | T | 2 | a0001c0001t0018g0036a0001c0001t0031g0229 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.195-7842C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143835 | ||||||
chr15:89143852
|
A | G | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.195-7825A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143852 | ||||||
chr15:89143853
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-7824T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143853 | ||||||
chr15:89143916
|
T | C | 2 | a0001c0003t0015g0101a0001c0003t0015g0234 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.195-7761T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89143916 | ||||||
chr15:89144209
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-7468C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144209 | ||||||
chr15:89144424
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(112): Show | 115 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.195-7253C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144424 | ||||||
chr15:89144459
|
A | C | 2 | a0001c0002t0017g0005a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.195-7218A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144459 | ||||||
chr15:89144477
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-7200G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144477 | ||||||
chr15:89144700
|
G | T | 5 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0016others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-6977G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144700 | ||||||
chr15:89144751
|
C | G | 9 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(6): Show | 9 | HG01258.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.195-6926C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144751 | ||||||
chr15:89144803
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-6874T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144803 | ||||||
chr15:89144884
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(168): Show | 171 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.195-6793T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144884 | ||||||
chr15:89144985
|
A | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.195-6692A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89144985 | ||||||
chr15:89145117
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-6560G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145117 | ||||||
chr15:89145164
|
C | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-6513C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145164 | ||||||
chr15:89145291
|
G | T | 2 | a0001c0002t0017g0005a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.195-6386G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145291 | ||||||
chr15:89145421
|
A | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-6256A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145421 | ||||||
chr15:89145477
|
G | A | 1 | a0001c0003t0015g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.195-6200G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145477 | ||||||
chr15:89145521
|
G | A | 5 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-6156G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145521 | ||||||
chr15:89145619
|
A | G | 1 | a0001c0001t0025g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195-6058A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145619 | ||||||
chr15:89145711
|
C | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-5966C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145711 | ||||||
chr15:89145798
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-5879A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145798 | ||||||
chr15:89145837
|
T | C | 2 | a0001c0001t0018g0036a0001c0001t0031g0229 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.195-5840T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145837 | ||||||
chr15:89145882
|
T | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195-5795T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89145882 | ||||||
chr15:89146079
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-5598G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146079 | ||||||
chr15:89146352
|
G | T | 19 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(16): Show | 19 | HG02004.hp1 HG02602.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-5325G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146352 | ||||||
chr15:89146355
|
C | CGT | 15 | a0001c0001t0001g0139a0001c0001t0001g0198a0001c0001t0001g0213others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-5279_195-5278d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGT | 7 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0182others(4): Show | 7 | HG02647.hp2 HG02895.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-5281_195-5278d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGT | 5 | a0001c0001t0001g0118a0001c0001t0002g0024a0001c0001t0004g0013others(2): Show | 5 | HG01433.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-5283_195-5278d others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGTG others(1): Show |
6 | a0001c0001t0004g0150a0001c0001t0006g0157a0001c0001t0006g0166others(3): Show | 6 | HG02723.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-5285_195-5278d others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0021g0167a0001c0001t0042g0057a0001c0007t0007g0225 | 3 | HG02559.hp2 HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.195-5287_195-5278d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGTG others(5): Show |
5 | a0001c0001t0001g0087a0001c0001t0001g0117a0001c0001t0002g0002others(2): Show | 5 | HG02004.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-5289_195-5278d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGTG others(7): Show |
6 | a0001c0001t0001g0075a0001c0001t0006g0209a0001c0001t0011g0138others(3): Show | 6 | HG01258.hp1 HG01891.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-5291_195-5278d others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0060 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.195-5293_195-5278d others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGT | C | 17 | a0001c0001t0001g0044a0001c0001t0001g0120a0001c0001t0001g0160others(14): Show | 17 | HG00140.hp1 HG01109.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.195-5279_195-5278d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGTGT | C | 13 | a0001c0001t0001g0202a0001c0001t0001g0218a0001c0001t0003g0048others(10): Show | 13 | HG00544.hp1 HG01109.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-5281_195-5278d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGTGTGT | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0084others(28): Show | 31 | HG00438.hp2 HG01243.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.195-5283_195-5278d others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGTGTGTG others(1): Show |
C | 80 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.195-5285_195-5278d others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.195-5287_195-5278d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146355
|
CGTGTGTG others(11): Show |
C | 9 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0008g0011others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.195-5295_195-5278d others(20): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89146355 | |||||
chr15:89146524
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(10): Show | 13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-5153A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146524 | ||||||
chr15:89146642
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.195-5035A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146642 | ||||||
chr15:89146731
|
C | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-4946C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146731 | ||||||
chr15:89146733
|
T | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(111): Show | 114 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.195-4944T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146733 | ||||||
chr15:89146835
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0004g0065a0001c0001t0004g0092 | 3 | HG01109.hp2 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.195-4842A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146835 | ||||||
chr15:89146850
|
A | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-4827A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146850 | ||||||
chr15:89146966
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.195-4711A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89146966 | ||||||
chr15:89147000
|
G | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195-4677G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147000 | ||||||
chr15:89147016
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-4661G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147016 | ||||||
chr15:89147029
|
C | G | 2 | a0001c0001t0019g0063a0001c0001t0019g0064 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.195-4648C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147029 | ||||||
chr15:89147170
|
C | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-4507C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147170 | ||||||
chr15:89147179
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.195-4498A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147179 | ||||||
chr15:89147182
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-4495C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147182 | ||||||
chr15:89147350
|
C | CTTTTT | 14 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(11): Show | 14 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.195-4310_195-4306d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89147350 | |||||
chr15:89147350
|
CT | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(138): Show | 141 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.195-4306delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89147350 | |||||
chr15:89147374
|
G | C | 1 | a0001c0002t0007g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195-4303G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147374 | ||||||
chr15:89147384
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-4293C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147384 | ||||||
chr15:89147415
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0184 | 3 | HG01167.hp2 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.195-4262G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147415 | ||||||
chr15:89147447
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-4230A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147447 | ||||||
chr15:89147452
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(162): Show | 165 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.195-4225T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147452 | ||||||
chr15:89147455
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.195-4222G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147455 | ||||||
chr15:89147632
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.195-4045C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147632 | ||||||
chr15:89147642
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-4035T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147642 | ||||||
chr15:89147652
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-4025T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147652 | ||||||
chr15:89147663
|
T | C | 2 | a0001c0003t0015g0101a0001c0003t0015g0234 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.195-4014T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147663 | ||||||
chr15:89147903
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.195-3774G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147903 | ||||||
chr15:89147973
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-3704C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89147973 | ||||||
chr15:89148068
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.195-3609G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148068 | ||||||
chr15:89148114
|
G | A | 19 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(16): Show | 19 | HG02004.hp1 HG02602.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.195-3563G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148114 | ||||||
chr15:89148118
|
C | CA | 15 | a0001c0001t0002g0039a0001c0001t0002g0055a0001c0001t0002g0094others(12): Show | 15 | HG01070.hp1 HG01070.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-3536dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89148118 | |||||
chr15:89148118
|
CA | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(135): Show | 138 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.195-3536delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89148118 | |||||
chr15:89148118
|
CAA | C | 7 | a0001c0001t0001g0072a0001c0001t0003g0177a0001c0001t0006g0166others(4): Show | 7 | HG01109.hp1 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-3537_195-3536d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89148118 | |||||
chr15:89148118
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0010g0032a0001c0001t0010g0035 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.195-3546_195-3536d others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89148118 | |||||
chr15:89148198
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-3479G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148198 | ||||||
chr15:89148254
|
A | G | 1 | a0001c0001t0011g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.195-3423A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148254 | ||||||
chr15:89148308
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-3369T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148308 | ||||||
chr15:89148322
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.195-3355C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148322 | ||||||
chr15:89148456
|
T | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195-3221T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148456 | ||||||
chr15:89148511
|
A | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(162): Show | 165 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.195-3166A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148511 | ||||||
chr15:89148512
|
A | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-3165A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148512 | ||||||
chr15:89148561
|
G | A | 1 | a0001c0006t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.195-3116G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148561 | ||||||
chr15:89148741
|
A | G | 1 | a0001c0001t0014g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.195-2936A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148741 | ||||||
chr15:89148815
|
A | G | 2 | a0001c0001t0040g0010a0001c0002t0023g0112 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.195-2862A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148815 | ||||||
chr15:89148929
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-2748A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148929 | ||||||
chr15:89148995
|
T | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.195-2682T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89148995 | ||||||
chr15:89149000
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-2677A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149000 | ||||||
chr15:89149028
|
T | G | 2 | a0001c0001t0003g0130a0001c0001t0003g0140 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.195-2649T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149028 | ||||||
chr15:89149187
|
C | G | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-2490C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149187 | ||||||
chr15:89149214
|
A | AAC | 4 | a0001c0001t0018g0036a0001c0001t0040g0010a0001c0002t0023g0112others(1): Show | 4 | HG01243.hp1 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-2436_195-2435d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
A | AACAC | 21 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(18): Show | 21 | HG01109.hp1 HG01258.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.195-2438_195-2435d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
A | AACACAC | 13 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(10): Show | 13 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-2440_195-2435d others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
A | AACACACA others(1): Show |
3 | a0001c0001t0004g0150a0001c0001t0014g0014a0001c0001t0043g0137 | 3 | HG02809.hp1 HG03540.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.195-2442_195-2435d others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
A | AACACACA others(5): Show |
2 | a0001c0003t0015g0101a0001c0003t0015g0234 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.195-2446_195-2435d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
AAC | A | 102 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(99): Show | 102 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.195-2436_195-2435d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
AACAC | A | 2 | a0001c0001t0018g0033a0001c0001t0039g0009 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195-2438_195-2435d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149214
|
AACACAC | A | 2 | a0001c0001t0002g0214a0001c0001t0026g0070 | 2 | HG01256.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.195-2440_195-2435d others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 89149214 | |||||
chr15:89149383
|
A | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-2294A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149383 | ||||||
chr15:89149442
|
T | C | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195-2235T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149442 | ||||||
chr15:89149484
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.195-2193C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149484 | ||||||
chr15:89149489
|
GA | G | 2 | a0001c0001t0019g0063a0001c0001t0019g0064 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.195-2187delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149489 | ||||||
chr15:89149615
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-2062C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149615 | ||||||
chr15:89149646
|
G | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(157): Show | 160 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.195-2031G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149646 | ||||||
chr15:89149713
|
C | T | 1 | a0001c0001t0004g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-1964C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149713 | ||||||
chr15:89149798
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195-1879G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89149798 | ||||||
chr15:89150244
|
A | G | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-1433A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150244 | ||||||
chr15:89150474
|
G | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0202others(1): Show | 4 | NA18965.hp2 NA18989.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1203G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150474 | ||||||
chr15:89150483
|
T | C | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195-1194T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150483 | ||||||
chr15:89150662
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.195-1015G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150662 | ||||||
chr15:89150682
|
A | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0051a0001c0001t0003g0061others(1): Show | 4 | HG01517.hp1 HG01517.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-995A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150682 | ||||||
chr15:89150932
|
T | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-745T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150932 | ||||||
chr15:89150948
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.195-729G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89150948 | ||||||
chr15:89151157
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.195-520C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89151157 | ||||||
chr15:89151449
|
T | C | 1 | a0001c0001t0027g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.195-228T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 3/10 | chr15 | 89151449 | ||||||
chr15:89152043
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.370+191C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152043 | ||||||
chr15:89152067
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+215T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152067 | ||||||
chr15:89152077
|
GT | G | 125 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(122): Show | 125 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.370+241delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 89152077 | |||||
chr15:89152110
|
G | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.370+258G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152110 | ||||||
chr15:89152145
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.370+293G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152145 | ||||||
chr15:89152184
|
G | A | 4 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0079others(1): Show | 4 | HG00544.hp1 NA18950.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+332G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152184 | ||||||
chr15:89152224
|
A | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.370+372A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152224 | ||||||
chr15:89152245
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.370+393T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152245 | ||||||
chr15:89152330
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.370+478C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152330 | ||||||
chr15:89152362
|
A | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.370+510A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152362 | ||||||
chr15:89152378
|
C | T | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.370+526C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152378 | ||||||
chr15:89152489
|
A | G | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.370+637A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152489 | ||||||
chr15:89152696
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.370+844C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152696 | ||||||
chr15:89152700
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.370+848T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152700 | ||||||
chr15:89152750
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.370+898T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152750 | ||||||
chr15:89152796
|
G | T | 5 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+944G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152796 | ||||||
chr15:89152939
|
T | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.370+1087T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89152939 | ||||||
chr15:89153062
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.370+1210C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153062 | ||||||
chr15:89153346
|
A | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.370+1494A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153346 | ||||||
chr15:89153406
|
A | G | 2 | a0001c0001t0021g0105a0001c0001t0021g0167 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.370+1554A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153406 | ||||||
chr15:89153523
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+1671A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153523 | ||||||
chr15:89153641
|
C | G | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.371-1726C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153641 | ||||||
chr15:89153700
|
A | C | 5 | a0001c0001t0001g0091a0001c0001t0004g0003a0001c0001t0004g0016others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-1667A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153700 | ||||||
chr15:89153846
|
C | A | 1 | a0001c0001t0043g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.371-1521C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89153846 | ||||||
chr15:89154369
|
A | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.371-998A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154369 | ||||||
chr15:89154487
|
A | G | 3 | a0001c0001t0014g0014a0001c0001t0014g0159a0001c0003t0015g0194 | 3 | HG02895.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.371-880A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154487 | ||||||
chr15:89154514
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.371-853C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154514 | ||||||
chr15:89154813
|
A | G | 19 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(16): Show | 19 | HG00738.hp2 HG02004.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.371-554A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154813 | ||||||
chr15:89154872
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.371-495A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154872 | ||||||
chr15:89154923
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.371-444T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89154923 | ||||||
chr15:89155102
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(186): Show | 189 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.371-265C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89155102 | ||||||
chr15:89155122
|
C | CT | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.371-241dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 89155122 | |||||
chr15:89155167
|
A | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.371-200A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89155167 | ||||||
chr15:89155170
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.371-197C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89155170 | ||||||
chr15:89155307
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.371-60A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89155307 | ||||||
chr15:89155360
|
G | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.371-7G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 4/10 | chr15 | 89155360 | ||||||
chr15:89155555
|
T | C | 1 | a0001c0001t0008g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538+21T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155555 | ||||||
chr15:89155569
|
G | T | 1 | a0001c0001t0004g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.538+35G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155569 | ||||||
chr15:89155608
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+74T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155608 | ||||||
chr15:89155659
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.538+125G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155659 | ||||||
chr15:89155802
|
A | G | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.538+268A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155802 | ||||||
chr15:89155814
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+280A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155814 | ||||||
chr15:89155835
|
C | T | 1 | a0001c0001t0026g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.538+301C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155835 | ||||||
chr15:89155878
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+344G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155878 | ||||||
chr15:89155882
|
G | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+348G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89155882 | ||||||
chr15:89156008
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.538+474C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156008 | ||||||
chr15:89156016
|
G | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0075others(30): Show | 33 | HG01243.hp2 HG02004.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.538+482G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156016 | ||||||
chr15:89156115
|
C | CT | 11 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0002g0055others(8): Show | 11 | HG00280.hp1 HG01361.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+604dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156115 | |||||
chr15:89156115
|
CT | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(100): Show | 103 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.538+604delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156115 | |||||
chr15:89156115
|
CTT | C | 22 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0075others(19): Show | 22 | HG01099.hp1 HG02004.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.538+603_538+604del others(2): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156115 | |||||
chr15:89156184
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.538+650G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156184 | ||||||
chr15:89156417
|
C | A | 161 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(158): Show | 161 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.538+883C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156417 | ||||||
chr15:89156510
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.538+976G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156510 | ||||||
chr15:89156559
|
A | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.538+1025A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156559 | ||||||
chr15:89156566
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.538+1032G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156566 | ||||||
chr15:89156617
|
A | C | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+1083A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156617 | ||||||
chr15:89156721
|
G | GA | 111 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.538+1201dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156721 | |||||
chr15:89156721
|
G | GAA | 7 | a0001c0001t0001g0046a0001c0001t0001g0095a0001c0001t0001g0217others(4): Show | 7 | HG01109.hp1 HG01361.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.538+1200_538+1201d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156721 | |||||
chr15:89156771
|
T | TTG | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+1239_538+1240d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89156771 | |||||
chr15:89156825
|
A | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+1291A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156825 | ||||||
chr15:89156895
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+1361T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156895 | ||||||
chr15:89156914
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.538+1380T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156914 | ||||||
chr15:89156928
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+1394A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156928 | ||||||
chr15:89156940
|
T | C | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538+1406T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89156940 | ||||||
chr15:89157120
|
G | C | 2 | a0001c0001t0040g0010a0001c0002t0023g0112 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.538+1586G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157120 | ||||||
chr15:89157336
|
G | A | 1 | a0001c0001t0011g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.538+1802G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157336 | ||||||
chr15:89157441
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+1907G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157441 | ||||||
chr15:89157444
|
T | C | 161 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(158): Show | 161 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.538+1910T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157444 | ||||||
chr15:89157447
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+1913G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157447 | ||||||
chr15:89157673
|
C | G | 2 | a0001c0001t0019g0063a0001c0001t0019g0064 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.538+2139C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157673 | ||||||
chr15:89157821
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+2287T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157821 | ||||||
chr15:89157850
|
T | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+2316T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157850 | ||||||
chr15:89157895
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+2361A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157895 | ||||||
chr15:89157936
|
G | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.538+2402G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89157936 | ||||||
chr15:89157982
|
TGG | T | 5 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+2451_538+2452d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89157982 | |||||
chr15:89158053
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+2519G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158053 | ||||||
chr15:89158180
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.538+2646C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158180 | ||||||
chr15:89158208
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.538+2674C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158208 | ||||||
chr15:89158237
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+2703T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158237 | ||||||
chr15:89158248
|
A | C | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.538+2714A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158248 | ||||||
chr15:89158557
|
T | C | 1 | a0001c0002t0007g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+3023T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158557 | ||||||
chr15:89158651
|
G | C | 4 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0232others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+3117G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158651 | ||||||
chr15:89158680
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.538+3146T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158680 | ||||||
chr15:89158684
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.538+3150T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89158684 | ||||||
chr15:89159058
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.538+3524A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159058 | ||||||
chr15:89159067
|
T | C | 168 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(165): Show | 168 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.538+3533T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159067 | ||||||
chr15:89159075
|
G | A | 2 | a0001c0002t0017g0005a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.538+3541G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159075 | ||||||
chr15:89159147
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+3613T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159147 | ||||||
chr15:89159164
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+3630G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159164 | ||||||
chr15:89159210
|
C | A | 6 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(3): Show | 6 | HG01258.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+3676C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159210 | ||||||
chr15:89159234
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.538+3700A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159234 | ||||||
chr15:89159236
|
G | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0022g0043 | 3 | HG01884.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.538+3702G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159236 | ||||||
chr15:89159308
|
C | T | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+3774C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159308 | ||||||
chr15:89159372
|
A | G | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.538+3838A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159372 | ||||||
chr15:89159390
|
T | G | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.538+3856T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159390 | ||||||
chr15:89159400
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.538+3866G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159400 | ||||||
chr15:89159418
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(156): Show | 159 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.538+3884C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159418 | ||||||
chr15:89159423
|
C | T | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+3889C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159423 | ||||||
chr15:89159583
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.538+4049T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159583 | ||||||
chr15:89159589
|
G | T | 1 | a0001c0001t0004g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.538+4055G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159589 | ||||||
chr15:89159597
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+4063C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159597 | ||||||
chr15:89159705
|
G | A | 1 | a0001c0001t0013g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+4171G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159705 | ||||||
chr15:89159766
|
A | ATCC | 20 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(17): Show | 20 | HG02004.hp1 HG02602.hp2 HG02717.hp2 others(17): Show |
intron_variant | MODIFIER | c.538+4232_538+4233i others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159766 | ||||||
chr15:89159826
|
GT | G | 20 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(17): Show | 20 | HG02004.hp1 HG02602.hp2 HG02717.hp2 others(17): Show |
intron_variant | MODIFIER | c.538+4295delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89159826 | |||||
chr15:89159902
|
A | G | 2 | a0001c0008t0001g0228a0001c0009t0012g0027 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.538+4368A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89159902 | ||||||
chr15:89160053
|
G | A | 3 | a0001c0001t0002g0094a0001c0001t0002g0151a0001c0001t0016g0147 | 3 | HG01952.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.538+4519G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160053 | ||||||
chr15:89160201
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+4667A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160201 | ||||||
chr15:89160204
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+4670G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160204 | ||||||
chr15:89160235
|
T | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+4701T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160235 | ||||||
chr15:89160251
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+4717A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160251 | ||||||
chr15:89160462
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+4928A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160462 | ||||||
chr15:89160487
|
TACCTG | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+4954_538+4958d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160487 | ||||||
chr15:89160492
|
G | GT | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0084others(15): Show | 18 | HG02602.hp2 HG02735.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.538+4970dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89160492 | |||||
chr15:89160492
|
GT | G | 5 | a0001c0001t0001g0187a0001c0001t0008g0011a0001c0001t0008g0082others(2): Show | 5 | HG02004.hp2 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+4970delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89160492 | |||||
chr15:89160493
|
T | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+4959T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160493 | ||||||
chr15:89160521
|
C | G | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.538+4987C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160521 | ||||||
chr15:89160598
|
A | C | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5064A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160598 | ||||||
chr15:89160666
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5132G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160666 | ||||||
chr15:89160756
|
G | A | 112 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(109): Show | 112 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.538+5222G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160756 | ||||||
chr15:89160789
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.538+5255A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160789 | ||||||
chr15:89160834
|
A | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5300A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160834 | ||||||
chr15:89160836
|
G | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5302G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160836 | ||||||
chr15:89160914
|
G | A | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.538+5380G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89160914 | ||||||
chr15:89161141
|
C | G | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5607C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161141 | ||||||
chr15:89161193
|
C | T | 1 | a0001c0001t0014g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538+5659C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161193 | ||||||
chr15:89161287
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.538+5753C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161287 | ||||||
chr15:89161317
|
T | C | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+5783T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161317 | ||||||
chr15:89161331
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+5797G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161331 | ||||||
chr15:89161334
|
C | A | 3 | a0001c0007t0007g0225a0001c0008t0001g0228a0001c0009t0012g0027 | 3 | HG01109.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+5800C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161334 | ||||||
chr15:89161425
|
C | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.538+5891C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161425 | ||||||
chr15:89161426
|
T | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(167): Show | 170 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.538+5892T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161426 | ||||||
chr15:89161457
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.538+5923A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161457 | ||||||
chr15:89161633
|
T | C | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6099T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161633 | ||||||
chr15:89161634
|
T | C | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6100T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161634 | ||||||
chr15:89161642
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.538+6108C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161642 | ||||||
chr15:89161652
|
C | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6118C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161652 | ||||||
chr15:89161876
|
C | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6342C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161876 | ||||||
chr15:89161903
|
A | G | 1 | a0001c0001t0024g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.538+6369A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161903 | ||||||
chr15:89161943
|
C | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6409C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89161943 | ||||||
chr15:89162147
|
C | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.538+6613C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162147 | ||||||
chr15:89162179
|
T | C | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6645T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162179 | ||||||
chr15:89162302
|
T | G | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+6768T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162302 | ||||||
chr15:89162497
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.538+6963C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162497 | ||||||
chr15:89162503
|
A | G | 1 | a0001c0001t0011g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.538+6969A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162503 | ||||||
chr15:89162626
|
A | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+7092A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162626 | ||||||
chr15:89162690
|
C | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7156C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162690 | ||||||
chr15:89162697
|
C | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7163C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162697 | ||||||
chr15:89162802
|
G | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7268G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162802 | ||||||
chr15:89162808
|
A | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7274A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162808 | ||||||
chr15:89162826
|
G | A | 136 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(133): Show | 136 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.538+7292G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162826 | ||||||
chr15:89162856
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.538+7322C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162856 | ||||||
chr15:89162873
|
T | C | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7339T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162873 | ||||||
chr15:89162991
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.538+7457C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89162991 | ||||||
chr15:89163021
|
T | C | 2 | a0001c0001t0003g0056a0001c0001t0003g0230 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+7487T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163021 | ||||||
chr15:89163050
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.538+7516T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163050 | ||||||
chr15:89163067
|
A | G | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.538+7533A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163067 | ||||||
chr15:89163092
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+7558C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163092 | ||||||
chr15:89163172
|
G | C | 112 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(109): Show | 112 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.538+7638G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163172 | ||||||
chr15:89163266
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.538+7732G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163266 | ||||||
chr15:89163332
|
A | T | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7798A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163332 | ||||||
chr15:89163354
|
C | T | 1 | a0001c0001t0025g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.538+7820C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163354 | ||||||
chr15:89163453
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.538+7919C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163453 | ||||||
chr15:89163457
|
A | G | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7923A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163457 | ||||||
chr15:89163539
|
A | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0075others(47): Show | 50 | HG00738.hp2 HG01109.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.538+8005A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163539 | ||||||
chr15:89163543
|
G | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+8009G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163543 | ||||||
chr15:89163568
|
A | G | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+8034A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163568 | ||||||
chr15:89163675
|
G | A | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+8141G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163675 | ||||||
chr15:89163873
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.538+8339A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89163873 | ||||||
chr15:89164011
|
G | C | 1 | a0001c0002t0007g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+8477G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164011 | ||||||
chr15:89164112
|
C | G | 1 | a0001c0001t0036g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.538+8578C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164112 | ||||||
chr15:89164341
|
T | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+8807T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164341 | ||||||
chr15:89164433
|
T | G | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+8899T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164433 | ||||||
chr15:89164474
|
TGAGA | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.538+8941_538+8944d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164474 | ||||||
chr15:89164517
|
T | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.538+8983T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164517 | ||||||
chr15:89164549
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+9015C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164549 | ||||||
chr15:89164777
|
T | TA | 12 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(9): Show | 12 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.538+9256dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89164777 | |||||
chr15:89164847
|
C | T | 2 | a0001c0001t0018g0033a0001c0001t0039g0009 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.538+9313C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164847 | ||||||
chr15:89164935
|
G | A | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.538+9401G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164935 | ||||||
chr15:89164970
|
G | A | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.538+9436G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89164970 | ||||||
chr15:89165007
|
G | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9473G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165007 | ||||||
chr15:89165134
|
G | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9600G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165134 | ||||||
chr15:89165143
|
C | A | 1 | a0001c0001t0011g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.538+9609C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165143 | ||||||
chr15:89165300
|
T | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9766T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165300 | ||||||
chr15:89165301
|
T | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9767T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165301 | ||||||
chr15:89165302
|
T | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9768T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165302 | ||||||
chr15:89165303
|
T | A | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+9769T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165303 | ||||||
chr15:89165304
|
T | A | 6 | a0001c0001t0001g0074a0001c0001t0002g0002a0001c0002t0007g0020others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+9770T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165304 | ||||||
chr15:89165305
|
T | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(126): Show | 129 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.538+9771T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165305 | ||||||
chr15:89165322
|
C | T | 1 | a0001c0008t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.538+9788C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165322 | ||||||
chr15:89165468
|
T | C | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.538+9934T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165468 | ||||||
chr15:89165599
|
T | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(121): Show | 124 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.538+10065T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165599 | ||||||
chr15:89165907
|
C | T | 17 | a0001c0001t0001g0029a0001c0001t0001g0113a0001c0001t0001g0120others(14): Show | 17 | HG00438.hp2 HG00544.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-9905C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165907 | ||||||
chr15:89165908
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.539-9904G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89165908 | ||||||
chr15:89166146
|
A | G | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.539-9666A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89166146 | ||||||
chr15:89166148
|
C | A | 1 | a0001c0001t0026g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.539-9664C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89166148 | ||||||
chr15:89166156
|
T | G | 1 | a0001c0001t0009g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.539-9656T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89166156 | ||||||
chr15:89166555
|
G | T | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-9257G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89166555 | ||||||
chr15:89166911
|
C | T | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.539-8901C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89166911 | ||||||
chr15:89167030
|
A | C | 1 | a0001c0001t0016g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.539-8782A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89167030 | ||||||
chr15:89167210
|
T | C | 2 | a0001c0007t0007g0225a0001c0009t0012g0027 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-8602T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89167210 | ||||||
chr15:89167443
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.539-8369G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89167443 | ||||||
chr15:89167817
|
C | T | 2 | a0001c0002t0017g0005a0001c0002t0017g0008 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.539-7995C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89167817 | ||||||
chr15:89167878
|
G | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.539-7934G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89167878 | ||||||
chr15:89168044
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.539-7768T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168044 | ||||||
chr15:89168106
|
AT | A | 7 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-7705delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168106 | ||||||
chr15:89168127
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0118a0001c0001t0001g0198others(1): Show | 4 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-7685G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168127 | ||||||
chr15:89168248
|
T | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(111): Show | 114 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.539-7564T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168248 | ||||||
chr15:89168342
|
C | T | 2 | a0001c0001t0021g0105a0001c0001t0021g0167 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.539-7470C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168342 | ||||||
chr15:89168662
|
A | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-7150A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168662 | ||||||
chr15:89168816
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.539-6996A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89168816 | ||||||
chr15:89169086
|
CG | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0022g0043 | 3 | HG01884.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.539-6725delG | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169086 | ||||||
chr15:89169087
|
G | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.539-6725G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169087 | ||||||
chr15:89169196
|
T | C | 1 | a0001c0001t0002g0200 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.539-6616T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169196 | ||||||
chr15:89169220
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-6592G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169220 | ||||||
chr15:89169534
|
C | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(186): Show | 189 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.539-6278C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169534 | ||||||
chr15:89169647
|
C | A | 1 | a0001c0001t0009g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.539-6165C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169647 | ||||||
chr15:89169662
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.539-6150A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169662 | ||||||
chr15:89169682
|
T | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-6130T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169682 | ||||||
chr15:89169711
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-6101T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169711 | ||||||
chr15:89169724
|
C | T | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.539-6088C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89169724 | ||||||
chr15:89170007
|
G | A | 1 | a0001c0001t0035g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.539-5805G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170007 | ||||||
chr15:89170028
|
C | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0115a0001c0001t0001g0129others(2): Show | 5 | HG01081.hp1 HG01928.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-5784C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170028 | ||||||
chr15:89170031
|
G | GT | 8 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.539-5776dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170031 | |||||
chr15:89170080
|
C | CTTT | 22 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0072others(19): Show | 22 | HG00280.hp2 HG01099.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-5701_539-5699d others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
C | CTTTT | 32 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(29): Show | 32 | HG00438.hp1 HG00544.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.539-5702_539-5699d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
C | CTTTTT | 36 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(33): Show | 36 | HG00438.hp2 HG00544.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.539-5703_539-5699d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
C | CTTTTTT | 19 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0074others(16): Show | 19 | HG00741.hp1 HG01109.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-5704_539-5699d others(8): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
C | CTTTTTTT | 6 | a0001c0001t0001g0204a0001c0001t0006g0165a0001c0001t0011g0171others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.539-5705_539-5699d others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CT | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0181others(15): Show | 18 | HG00280.hp1 HG01361.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-5699delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTT | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0087others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.539-5700_539-5699d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTT | C | 15 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0002g0024others(12): Show | 15 | HG01109.hp2 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.539-5701_539-5699d others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.539-5709_539-5699d others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0004g0003a0001c0001t0004g0093a0001c0001t0008g0011others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-5710_539-5699d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0018g0036a0001c0001t0031g0229 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.539-5711_539-5699d others(15): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTTTTTT others(7): Show |
C | 15 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0158others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-5712_539-5699d others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170080
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0098a0001c0007t0007g0225 | 2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.539-5713_539-5699d others(17): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170080 | |||||
chr15:89170119
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0022g0043 | 3 | HG01884.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.539-5693C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170119 | ||||||
chr15:89170135
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.539-5677C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170135 | ||||||
chr15:89170197
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-5615G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170197 | ||||||
chr15:89170233
|
C | T | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539-5579C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170233 | ||||||
chr15:89170242
|
C | T | 2 | a0001c0001t0018g0036a0001c0001t0031g0229 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.539-5570C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170242 | ||||||
chr15:89170253
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.539-5559T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170253 | ||||||
chr15:89170278
|
G | T | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539-5534G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170278 | ||||||
chr15:89170339
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.539-5473C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170339 | ||||||
chr15:89170343
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-5469C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170343 | ||||||
chr15:89170379
|
C | G | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-5433C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170379 | ||||||
chr15:89170494
|
C | CA | 112 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(109): Show | 112 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-5314dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89170494 | |||||
chr15:89170562
|
G | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-5250G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170562 | ||||||
chr15:89170563
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-5249C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170563 | ||||||
chr15:89170652
|
C | T | 149 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(146): Show | 149 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.539-5160C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170652 | ||||||
chr15:89170679
|
G | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-5133G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170679 | ||||||
chr15:89170691
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-5121T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170691 | ||||||
chr15:89170908
|
G | T | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.539-4904G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170908 | ||||||
chr15:89170914
|
A | G | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.539-4898A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170914 | ||||||
chr15:89170931
|
C | A | 2 | a0001c0003t0015g0101a0001c0003t0015g0234 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.539-4881C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170931 | ||||||
chr15:89170977
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-4835G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89170977 | ||||||
chr15:89171010
|
C | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(167): Show | 170 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.539-4802C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171010 | ||||||
chr15:89171066
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0022g0043 | 3 | HG01884.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.539-4746A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171066 | ||||||
chr15:89171115
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-4693_539-4692i others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89171115 | |||||
chr15:89171219
|
G | C | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-4593G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171219 | ||||||
chr15:89171313
|
A | G | 3 | a0001c0001t0002g0002a0001c0004t0012g0226a0001c0007t0007g0225 | 3 | HG01891.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-4499A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171313 | ||||||
chr15:89171369
|
A | G | 1 | a0001c0002t0023g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.539-4443A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171369 | ||||||
chr15:89171449
|
C | T | 1 | a0001c0004t0012g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.539-4363C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171449 | ||||||
chr15:89171498
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.539-4314G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171498 | ||||||
chr15:89171562
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.539-4250G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171562 | ||||||
chr15:89171604
|
T | A | 3 | a0001c0001t0014g0014a0001c0001t0014g0159a0001c0003t0015g0194 | 3 | HG02895.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.539-4208T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171604 | ||||||
chr15:89171629
|
T | C | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-4183T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171629 | ||||||
chr15:89171667
|
C | A | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.539-4145C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171667 | ||||||
chr15:89171846
|
A | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0075others(33): Show | 36 | HG01243.hp2 HG01891.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.539-3966A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89171846 | ||||||
chr15:89172003
|
C | T | 108 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(105): Show | 108 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.539-3809C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172003 | ||||||
chr15:89172024
|
C | CT | 15 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(12): Show | 15 | HG02602.hp2 HG02735.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-3779dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89172024 | |||||
chr15:89172024
|
CT | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.539-3779delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89172024 | |||||
chr15:89172032
|
T | TA | 115 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(112): Show | 115 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.539-3780_539-3779i others(3): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172032 | ||||||
chr15:89172033
|
T | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(117): Show | 120 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.539-3779T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172033 | ||||||
chr15:89172033
|
T | TA | 17 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0093others(14): Show | 17 | HG01258.hp1 HG02004.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.539-3771dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89172033 | |||||
chr15:89172034
|
A | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(15): Show | 18 | HG00738.hp2 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.539-3778A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172034 | ||||||
chr15:89172161
|
AC | A | 2 | a0001c0001t0018g0033a0001c0001t0039g0009 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.539-3650delC | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172161 | ||||||
chr15:89172250
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0115a0001c0001t0001g0129others(2): Show | 5 | HG01081.hp1 HG01928.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-3562A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172250 | ||||||
chr15:89172271
|
A | T | 1 | a0001c0001t0027g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.539-3541A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172271 | ||||||
chr15:89172284
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(119): Show | 122 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.539-3528C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172284 | ||||||
chr15:89172308
|
C | T | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-3504C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172308 | ||||||
chr15:89172412
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.539-3400T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172412 | ||||||
chr15:89172452
|
G | A | 3 | a0001c0001t0002g0002a0001c0004t0012g0226a0001c0007t0007g0225 | 3 | HG01891.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-3360G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172452 | ||||||
chr15:89172506
|
T | C | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.539-3306T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172506 | ||||||
chr15:89172709
|
T | C | 21 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(18): Show | 21 | HG01891.hp2 HG02004.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.539-3103T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172709 | ||||||
chr15:89172721
|
C | G | 8 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.539-3091C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172721 | ||||||
chr15:89172731
|
A | G | 2 | a0001c0001t0009g0163a0001c0001t0009g0180 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.539-3081A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89172731 | ||||||
chr15:89173333
|
G | A | 1 | a0001c0001t0029g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.539-2479G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173333 | ||||||
chr15:89173421
|
A | G | 3 | a0001c0001t0002g0002a0001c0004t0012g0226a0001c0007t0007g0225 | 3 | HG01891.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-2391A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173421 | ||||||
chr15:89173583
|
G | A | 29 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(26): Show | 29 | HG01243.hp1 HG01884.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.539-2229G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173583 | ||||||
chr15:89173615
|
G | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(105): Show | 108 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.539-2197G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173615 | ||||||
chr15:89173739
|
C | G | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-2073C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173739 | ||||||
chr15:89173741
|
A | G | 3 | a0001c0001t0002g0002a0001c0004t0012g0226a0001c0007t0007g0225 | 3 | HG01891.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-2071A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173741 | ||||||
chr15:89173756
|
A | T | 3 | a0001c0001t0002g0002a0001c0004t0012g0226a0001c0007t0007g0225 | 3 | HG01891.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-2056A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89173756 | ||||||
chr15:89174086
|
G | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0093others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-1726G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174086 | ||||||
chr15:89174137
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-1675T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174137 | ||||||
chr15:89174166
|
C | A | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.539-1646C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174166 | ||||||
chr15:89174377
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.539-1435C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174377 | ||||||
chr15:89174621
|
A | C | 1 | a0001c0001t0002g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.539-1191A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174621 | ||||||
chr15:89174674
|
G | A | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-1138G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174674 | ||||||
chr15:89174767
|
G | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(105): Show | 108 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.539-1045G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174767 | ||||||
chr15:89174871
|
T | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(13): Show | 16 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-941T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174871 | ||||||
chr15:89174933
|
C | G | 50 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0075others(47): Show | 50 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.539-879C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89174933 | ||||||
chr15:89175015
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0022g0043 | 3 | HG01884.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.539-797C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175015 | ||||||
chr15:89175153
|
G | T | 1 | a0001c0001t0018g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.539-659G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175153 | ||||||
chr15:89175288
|
G | A | 1 | a0001c0001t0040g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.539-524G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175288 | ||||||
chr15:89175367
|
A | G | 49 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0075others(46): Show | 49 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.539-445A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175367 | ||||||
chr15:89175442
|
G | T | 18 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(15): Show | 18 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.539-370G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175442 | ||||||
chr15:89175682
|
C | T | 19 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(16): Show | 19 | HG02004.hp1 HG02602.hp2 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-130C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175682 | ||||||
chr15:89175703
|
TTCTC | T | 3 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0093 | 3 | HG02965.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.539-103_539-100del others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 89175703 | |||||
chr15:89175728
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.539-84C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 5/10 | chr15 | 89175728 | ||||||
chr15:89176009
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.722+14G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176009 | ||||||
chr15:89176086
|
G | A | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+91G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176086 | ||||||
chr15:89176144
|
C | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(158): Show | 161 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.722+149C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176144 | ||||||
chr15:89176395
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0034g0143 | 2 | HG00140.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.722+400C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176395 | ||||||
chr15:89176435
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.722+440A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176435 | ||||||
chr15:89176547
|
C | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(27): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.722+552C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176547 | ||||||
chr15:89176594
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(27): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.722+599C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176594 | ||||||
chr15:89176636
|
C | T | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+641C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176636 | ||||||
chr15:89176820
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(27): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.722+825C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89176820 | ||||||
chr15:89177105
|
A | G | 1 | a0001c0001t0004g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.722+1110A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177105 | ||||||
chr15:89177186
|
G | A | 2 | a0001c0001t0002g0002a0001c0004t0012g0226 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.722+1191G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177186 | ||||||
chr15:89177234
|
A | G | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.722+1239A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177234 | ||||||
chr15:89177245
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.722+1250C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177245 | ||||||
chr15:89177275
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.722+1280C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177275 | ||||||
chr15:89177318
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.722+1323G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177318 | ||||||
chr15:89177370
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(25): Show | 28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.722+1375C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177370 | ||||||
chr15:89177578
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.722+1583C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177578 | ||||||
chr15:89177668
|
T | C | 8 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(5): Show | 8 | HG01258.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.722+1673T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177668 | ||||||
chr15:89177690
|
T | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(143): Show | 146 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.722+1695T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177690 | ||||||
chr15:89177715
|
T | A | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(143): Show | 146 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.722+1720T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177715 | ||||||
chr15:89177846
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.722+1851T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177846 | ||||||
chr15:89177888
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.722+1893C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89177888 | ||||||
chr15:89178058
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(27): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.722+2063T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178058 | ||||||
chr15:89178180
|
A | G | 1 | a0001c0009t0012g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.722+2185A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178180 | ||||||
chr15:89178192
|
T | C | 2 | a0001c0003t0015g0101a0001c0003t0015g0234 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.722+2197T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178192 | ||||||
chr15:89178230
|
T | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.722+2235T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178230 | ||||||
chr15:89178290
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.722+2295T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178290 | ||||||
chr15:89178308
|
G | C | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+2313G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178308 | ||||||
chr15:89178316
|
C | G | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+2321C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178316 | ||||||
chr15:89178428
|
C | T | 1 | a0001c0007t0007g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.722+2433C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178428 | ||||||
chr15:89178462
|
G | A | 1 | a0001c0001t0020g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.722+2467G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178462 | ||||||
chr15:89178510
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.722+2515G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178510 | ||||||
chr15:89178543
|
C | G | 2 | a0001c0001t0018g0033a0001c0001t0039g0009 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.722+2548C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178543 | ||||||
chr15:89178547
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.722+2552C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178547 | ||||||
chr15:89178576
|
G | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(127): Show | 130 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.722+2581G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178576 | ||||||
chr15:89178696
|
C | T | 14 | a0001c0001t0001g0108a0001c0001t0002g0024a0001c0001t0004g0013others(11): Show | 14 | HG02004.hp1 HG02735.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.722+2701C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178696 | ||||||
chr15:89178699
|
T | A | 1 | a0002c0005t0005g0114 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.722+2704T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178699 | ||||||
chr15:89178833
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(27): Show | 30 | HG00280.hp1 HG01243.hp2 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.722+2838C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178833 | ||||||
chr15:89178854
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(116): Show | 119 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.722+2859A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178854 | ||||||
chr15:89178929
|
C | T | 1 | a0001c0001t0018g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+2934C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89178929 | ||||||
chr15:89179077
|
T | C | 6 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(3): Show | 6 | HG01258.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+3082T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179077 | ||||||
chr15:89179333
|
A | G | 7 | a0001c0001t0004g0227a0001c0001t0008g0102a0001c0001t0010g0032others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.722+3338A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179333 | ||||||
chr15:89179361
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.722+3366T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179361 | ||||||
chr15:89179563
|
T | C | 14 | a0001c0001t0002g0156a0001c0001t0004g0013a0001c0001t0004g0045others(11): Show | 14 | HG01884.hp1 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.722+3568T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179563 | ||||||
chr15:89179847
|
C | T | 3 | a0001c0004t0012g0001a0001c0004t0012g0226a0001c0009t0012g0027 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.722+3852C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179847 | ||||||
chr15:89179936
|
A | G | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.722+3941A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89179936 | ||||||
chr15:89180011
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.722+4016T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180011 | ||||||
chr15:89180139
|
A | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.722+4144A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180139 | ||||||
chr15:89180146
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.722+4151C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180146 | ||||||
chr15:89180147
|
G | A | 151 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(148): Show | 151 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.722+4152G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180147 | ||||||
chr15:89180592
|
A | G | 3 | a0001c0002t0007g0020a0001c0002t0007g0040a0001c0007t0007g0225 | 3 | NA18906.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.722+4597A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180592 | ||||||
chr15:89180627
|
T | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(128): Show | 131 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.722+4632T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180627 | ||||||
chr15:89180715
|
A | G | 23 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.723-4709A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180715 | ||||||
chr15:89180768
|
C | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(129): Show | 132 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.723-4656C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89180768 | ||||||
chr15:89181094
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.723-4330C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181094 | ||||||
chr15:89181095
|
G | A | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.723-4329G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181095 | ||||||
chr15:89181097
|
G | A | 9 | a0001c0001t0010g0007a0001c0001t0010g0012a0001c0001t0010g0032others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.723-4327G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181097 | ||||||
chr15:89181133
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(156): Show | 159 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.723-4291G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181133 | ||||||
chr15:89181214
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0118a0001c0001t0001g0198others(1): Show | 4 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-4210G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181214 | ||||||
chr15:89181223
|
T | C | 1 | a0001c0002t0023g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.723-4201T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181223 | ||||||
chr15:89181228
|
C | CA | 31 | a0001c0001t0002g0038a0001c0001t0002g0132a0001c0001t0002g0133others(28): Show | 31 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.723-4174dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89181228 | |||||
chr15:89181228
|
C | CAA | 18 | a0001c0001t0003g0051a0001c0001t0003g0140a0001c0001t0008g0011others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.723-4175_723-4174d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89181228 | |||||
chr15:89181228
|
C | CAAA | 8 | a0001c0001t0001g0052a0001c0001t0016g0066a0001c0001t0033g0164others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.723-4176_723-4174d others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89181228 | |||||
chr15:89181228
|
C | CAAAA | 82 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(79): Show | 82 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.723-4177_723-4174d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89181228 | |||||
chr15:89181228
|
C | CAAAAA | 45 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 45 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.723-4178_723-4174d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89181228 | |||||
chr15:89181280
|
T | C | 3 | a0001c0002t0007g0020a0001c0002t0007g0040a0001c0007t0007g0225 | 3 | NA18906.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.723-4144T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181280 | ||||||
chr15:89181295
|
A | T | 2 | a0001c0004t0012g0226a0001c0009t0012g0027 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.723-4129A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181295 | ||||||
chr15:89181368
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.723-4056C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181368 | ||||||
chr15:89181369
|
G | A | 1 | a0001c0001t0009g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.723-4055G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181369 | ||||||
chr15:89181415
|
G | A | 25 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.723-4009G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181415 | ||||||
chr15:89181489
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 184 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.723-3935A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181489 | ||||||
chr15:89181563
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 184 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.723-3861C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181563 | ||||||
chr15:89181604
|
A | G | 3 | a0001c0001t0018g0033a0001c0001t0018g0036a0001c0001t0032g0034 | 3 | HG01243.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.723-3820A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181604 | ||||||
chr15:89181610
|
G | T | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.723-3814G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181610 | ||||||
chr15:89181738
|
G | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 184 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.723-3686G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181738 | ||||||
chr15:89181802
|
A | G | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.723-3622A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181802 | ||||||
chr15:89181890
|
G | A | 1 | a0001c0001t0029g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.723-3534G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181890 | ||||||
chr15:89181910
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723-3514A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181910 | ||||||
chr15:89181914
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723-3510T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181914 | ||||||
chr15:89181915
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723-3509C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181915 | ||||||
chr15:89181927
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 184 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.723-3497G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181927 | ||||||
chr15:89181971
|
T | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(150): Show | 153 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.723-3453T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89181971 | ||||||
chr15:89182708
|
G | A | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.723-2716G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89182708 | ||||||
chr15:89182866
|
C | T | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.723-2558C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89182866 | ||||||
chr15:89182905
|
G | A | 16 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(13): Show | 16 | HG01258.hp1 HG02004.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.723-2519G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89182905 | ||||||
chr15:89182972
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723-2452C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89182972 | ||||||
chr15:89182974
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723-2450T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89182974 | ||||||
chr15:89183056
|
G | A | 25 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.723-2368G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183056 | ||||||
chr15:89183152
|
G | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.723-2272G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183152 | ||||||
chr15:89183161
|
G | A | 6 | a0001c0001t0039g0009a0001c0001t0040g0010a0001c0001t0044g0090others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.723-2263G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183161 | ||||||
chr15:89183195
|
C | CTGTTTGT others(1): Show |
5 | a0001c0002t0007g0111a0001c0002t0007g0153a0001c0002t0017g0005others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-2215_723-2208d others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183195 | |||||
chr15:89183222
|
G | C | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.723-2202G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183222 | ||||||
chr15:89183274
|
T | C | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.723-2150T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183274 | ||||||
chr15:89183322
|
T | C | 13 | a0001c0001t0002g0039a0001c0001t0002g0050a0001c0001t0002g0062others(10): Show | 13 | HG01167.hp1 HG02040.hp2 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.723-2102T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183322 | ||||||
chr15:89183368
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0010g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.723-2048_723-2039d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183368 | |||||
chr15:89183368
|
CAAAA | C | 5 | a0001c0001t0001g0084a0001c0001t0006g0157a0001c0001t0006g0166others(2): Show | 5 | HG01258.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-2042_723-2039d others(6): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183368 | |||||
chr15:89183374
|
AAAAAAAA others(19): Show |
A | 4 | a0001c0001t0008g0102a0001c0002t0007g0020a0001c0002t0007g0040others(1): Show | 4 | HG01884.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-2048_723-2023d others(28): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183374 | |||||
chr15:89183376
|
AAAAAAAA others(19): Show |
A | 19 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(16): Show | 19 | HG02055.hp2 HG02451.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.723-2046_723-2021d others(28): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183376 | |||||
chr15:89183378
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.723-2046A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183378 | ||||||
chr15:89183380
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | HG02004.hp1 HG02165.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.723-2044A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183380 | ||||||
chr15:89183380
|
AAAAAATA others(5): Show |
A | 1 | a0001c0001t0003g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.723-2042_723-2031d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183380 | |||||
chr15:89183380
|
AAAAAATA others(7): Show |
A | 2 | a0001c0001t0001g0106a0001c0001t0044g0090 | 2 | HG02615.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.723-2042_723-2029d others(16): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183380 | |||||
chr15:89183380
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0040g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.723-2042_723-2027d others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183380 | |||||
chr15:89183380
|
AAAAAATA others(19): Show |
A | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.723-2042_723-2017d others(28): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183380 | |||||
chr15:89183381
|
AAAAATAT others(8): Show |
A | 2 | a0001c0002t0007g0111a0001c0002t0007g0153 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.723-2041_723-2027d others(17): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183381 | |||||
chr15:89183382
|
A | AAT | 10 | a0001c0001t0001g0019a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG00741.hp1 HG02735.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.723-2041_723-2040i others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183382
|
A | AATATATA others(3): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0160a0001c0001t0001g0174others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-2041_723-2040i others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183382
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0175 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.723-2041_723-2040i others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183382
|
A | ATAT | 2 | a0001c0001t0001g0028a0001c0001t0001g0183 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.723-2042_723-2041i others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183382 | ||||||
chr15:89183382
|
A | ATATATAT others(2): Show |
2 | a0001c0001t0001g0134a0001c0001t0002g0002 | 2 | HG02027.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.723-2042_723-2041i others(11): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183382 | ||||||
chr15:89183382
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.723-2042_723-2041i others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183382 | ||||||
chr15:89183382
|
A | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG00438.hp1 HG00544.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.723-2042A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183382 | ||||||
chr15:89183382
|
AAAATATA others(3): Show |
A | 3 | a0001c0001t0013g0096a0001c0001t0013g0152a0001c0001t0013g0154 | 3 | HG02109.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.723-2040_723-2031d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183382
|
AAAATATA others(5): Show |
A | 7 | a0001c0001t0003g0026a0001c0001t0003g0121a0001c0001t0003g0124others(4): Show | 7 | HG01099.hp1 HG01169.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.723-2040_723-2029d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183382
|
AAAATATA others(9): Show |
A | 3 | a0001c0001t0011g0138a0001c0002t0017g0008a0001c0003t0015g0194 | 3 | HG01243.hp2 HG02895.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.723-2040_723-2025d others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183382 | |||||
chr15:89183383
|
AAATAT | A | 5 | a0001c0001t0016g0066a0001c0001t0016g0080a0001c0001t0016g0147others(2): Show | 5 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-2039_723-2035d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183383 | |||||
chr15:89183383
|
AAATATAT others(4): Show |
A | 1 | a0001c0001t0003g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.723-2039_723-2029d others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183383 | |||||
chr15:89183383
|
AAATATAT others(6): Show |
A | 2 | a0001c0001t0003g0047a0001c0001t0003g0155 | 2 | HG01070.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.723-2039_723-2027d others(15): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183383 | |||||
chr15:89183383
|
AAATATAT others(8): Show |
A | 4 | a0001c0002t0017g0005a0001c0002t0023g0112a0001c0003t0015g0101others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.723-2039_723-2025d others(17): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183383 | |||||
chr15:89183384
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0131a0001c0001t0005g0125 | 2 | NA18961.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.723-2039_723-2038i others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0005g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.723-2039_723-2038i others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0010g0032 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.723-2039_723-2038i others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAATA others(1): Show |
6 | a0001c0001t0001g0017a0001c0001t0002g0050a0001c0001t0009g0025others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-2039_723-2038i others(10): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAATA others(3): Show |
6 | a0001c0001t0002g0054a0001c0001t0002g0071a0001c0001t0002g0107others(3): Show | 6 | HG00738.hp2 HG01256.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.723-2039_723-2038i others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0002g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.723-2039_723-2038i others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0002g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.723-2039_723-2038i others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAATAT others(4): Show |
2 | a0001c0001t0002g0053a0001c0001t0002g0210 | 2 | HG01081.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.723-2039_723-2038i others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAAATAT others(6): Show |
2 | a0001c0001t0010g0007a0001c0001t0010g0012 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.723-2039_723-2038i others(15): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.723-2039_723-2038i others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAATATAT others(4): Show |
1 | a0001c0001t0036g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.723-2039_723-2038i others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AAT | 8 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(5): Show | 8 | HG01361.hp1 HG02293.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.723-2009_723-2008d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0100 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.723-2017_723-2008d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
A | ATAT | 4 | a0001c0001t0001g0110a0001c0001t0001g0172a0001c0001t0001g0185others(1): Show | 4 | HG02273.hp1 HG02273.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-2040_723-2039i others(5): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183384 | ||||||
chr15:89183384
|
A | ATATATAT | 2 | a0001c0001t0001g0097a0001c0001t0001g0113 | 2 | HG02622.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.723-2040_723-2039i others(9): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183384 | ||||||
chr15:89183384
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723-2040A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183384 | ||||||
chr15:89183384
|
A | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(54): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.723-2040A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183384 | ||||||
chr15:89183384
|
AAT | A | 5 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0002g0077others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-2009_723-2008d others(4): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0032g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.723-2017_723-2008d others(12): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
AATATATA others(5): Show |
A | 7 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0056others(4): Show | 7 | HG00438.hp2 HG02738.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.723-2019_723-2008d others(14): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183384
|
AATATATA others(9): Show |
A | 2 | a0001c0001t0031g0229a0001c0001t0033g0164 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.723-2023_723-2008d others(18): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183384 | |||||
chr15:89183385
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0132a0001c0001t0003g0061 | 2 | HG01517.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.723-2038_723-2028d others(13): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183385 | ||||||
chr15:89183385
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0003g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.723-2038_723-2026d others(15): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183385 | ||||||
chr15:89183386
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0002g0038a0001c0001t0011g0208 | 3 | HG03688.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.723-2038T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183386 | ||||||
chr15:89183388
|
T | A | 2 | a0001c0001t0002g0077a0001c0001t0024g0170 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.723-2036T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183388 | ||||||
chr15:89183390
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.723-2034T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183390 | ||||||
chr15:89183398
|
T | A | 1 | a0001c0001t0002g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.723-2026T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183398 | ||||||
chr15:89183400
|
T | A | 1 | a0001c0001t0002g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.723-2024T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183400 | ||||||
chr15:89183535
|
A | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(128): Show | 131 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.723-1889A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183535 | ||||||
chr15:89183630
|
G | A | 5 | a0001c0002t0007g0111a0001c0002t0007g0153a0001c0002t0017g0005others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-1794G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183630 | ||||||
chr15:89183658
|
G | C | 1 | a0001c0001t0002g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.723-1766G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183658 | ||||||
chr15:89183677
|
T | TA | 53 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.723-1738dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 89183677 | |||||
chr15:89183873
|
C | G | 1 | a0001c0001t0001g0072 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.723-1551C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89183873 | ||||||
chr15:89184026
|
T | C | 1 | a0001c0004t0012g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.723-1398T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184026 | ||||||
chr15:89184207
|
A | G | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.723-1217A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184207 | ||||||
chr15:89184226
|
A | G | 2 | a0001c0001t0002g0024a0001c0001t0002g0071 | 2 | HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.723-1198A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184226 | ||||||
chr15:89184228
|
T | G | 3 | a0001c0001t0016g0066a0001c0001t0016g0080a0001c0001t0016g0147 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.723-1196T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184228 | ||||||
chr15:89184409
|
C | T | 1 | a0001c0003t0015g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.723-1015C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184409 | ||||||
chr15:89184410
|
G | A | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.723-1014G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184410 | ||||||
chr15:89184520
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.723-904G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184520 | ||||||
chr15:89184521
|
C | G | 2 | a0001c0001t0010g0032a0001c0001t0010g0035 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.723-903C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184521 | ||||||
chr15:89184605
|
T | G | 5 | a0001c0002t0007g0111a0001c0002t0007g0153a0001c0002t0017g0005others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-819T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184605 | ||||||
chr15:89184861
|
T | C | 1 | a0001c0001t0003g0224 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.723-563T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184861 | ||||||
chr15:89184888
|
C | T | 20 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(17): Show | 20 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.723-536C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184888 | ||||||
chr15:89184991
|
G | A | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.723-433G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89184991 | ||||||
chr15:89185017
|
G | C | 20 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(17): Show | 20 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.723-407G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89185017 | ||||||
chr15:89185226
|
C | T | 9 | a0001c0001t0039g0009a0001c0001t0040g0010a0001c0001t0044g0090others(6): Show | 9 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.723-198C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 6/10 | chr15 | 89185226 | ||||||
chr15:89185697
|
G | A | 27 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(24): Show | 27 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.815+181G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89185697 | ||||||
chr15:89185830
|
A | G | 71 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.815+314A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89185830 | ||||||
chr15:89185904
|
C | T | 103 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.815+388C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89185904 | ||||||
chr15:89185934
|
C | A | 1 | a0001c0001t0028g0176 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.815+418C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89185934 | ||||||
chr15:89186292
|
C | G | 22 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.815+776C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186292 | ||||||
chr15:89186418
|
T | C | 72 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.815+902T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186418 | ||||||
chr15:89186467
|
G | T | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.815+951G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186467 | ||||||
chr15:89186489
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.815+973C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186489 | ||||||
chr15:89186518
|
C | A | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.815+1002C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186518 | ||||||
chr15:89186521
|
G | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.815+1005G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186521 | ||||||
chr15:89186568
|
A | G | 28 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(25): Show | 28 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.815+1052A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186568 | ||||||
chr15:89186584
|
G | A | 5 | a0001c0002t0007g0111a0001c0002t0007g0153a0001c0002t0017g0005others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+1068G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186584 | ||||||
chr15:89186599
|
A | G | 2 | a0001c0001t0010g0032a0001c0001t0010g0035 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.815+1083A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186599 | ||||||
chr15:89186713
|
C | A | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.815+1197C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186713 | ||||||
chr15:89186716
|
G | A | 1 | a0001c0001t0003g0124 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.815+1200G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186716 | ||||||
chr15:89186827
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.815+1311C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186827 | ||||||
chr15:89186854
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.815+1338G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186854 | ||||||
chr15:89186917
|
A | G | 3 | a0001c0004t0012g0001a0001c0004t0012g0226a0001c0009t0012g0027 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.816-1276A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89186917 | ||||||
chr15:89187044
|
G | A | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.816-1149G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187044 | ||||||
chr15:89187318
|
G | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.816-875G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187318 | ||||||
chr15:89187480
|
C | G | 3 | a0001c0004t0012g0001a0001c0004t0012g0226a0001c0009t0012g0027 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.816-713C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187480 | ||||||
chr15:89187481
|
C | T | 2 | a0001c0001t0003g0049a0001c0002t0007g0040 | 2 | NA18906.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.816-712C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187481 | ||||||
chr15:89187729
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.816-464T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187729 | ||||||
chr15:89187737
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.816-456C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187737 | ||||||
chr15:89187944
|
A | G | 73 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.816-249A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89187944 | ||||||
chr15:89188116
|
G | C | 73 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.816-77G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 7/10 | chr15 | 89188116 | ||||||
chr15:89188314
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.926+11G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89188314 | ||||||
chr15:89188333
|
T | G | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.926+30T>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89188333 | ||||||
chr15:89188545
|
T | C | 32 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(29): Show | 32 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.926+242T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89188545 | ||||||
chr15:89188794
|
G | A | 2 | a0001c0001t0014g0014a0001c0001t0014g0159 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.926+491G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89188794 | ||||||
chr15:89188883
|
T | TA | 52 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.926+595dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 89188883 | |||||
chr15:89188883
|
TA | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0212a0001c0001t0003g0155others(2): Show | 5 | HG01070.hp1 HG02809.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.926+595delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 89188883 | |||||
chr15:89188884
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.926+581A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89188884 | ||||||
chr15:89189020
|
A | G | 3 | a0001c0001t0016g0066a0001c0001t0016g0080a0001c0001t0016g0147 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.926+717A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189020 | ||||||
chr15:89189240
|
T | C | 108 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.926+937T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189240 | ||||||
chr15:89189242
|
G | T | 2 | a0001c0001t0031g0229a0001c0001t0044g0090 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.926+939G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189242 | ||||||
chr15:89189331
|
T | C | 22 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.926+1028T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189331 | ||||||
chr15:89189776
|
C | T | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.927-1304C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189776 | ||||||
chr15:89189783
|
TG | T | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.927-1295delG | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 89189783 | |||||
chr15:89189796
|
CAAATT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-1278_927-1274d others(7): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 89189796 | |||||
chr15:89189825
|
T | A | 3 | a0001c0001t0016g0066a0001c0001t0016g0080a0001c0001t0016g0147 | 3 | HG02258.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.927-1255T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189825 | ||||||
chr15:89189899
|
A | T | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927-1181A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189899 | ||||||
chr15:89189983
|
C | A | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927-1097C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89189983 | ||||||
chr15:89190000
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.927-1080C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190000 | ||||||
chr15:89190016
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(91): Show | 94 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.927-1064G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190016 | ||||||
chr15:89190091
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.927-989T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190091 | ||||||
chr15:89190164
|
C | A | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.927-916C>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190164 | ||||||
chr15:89190315
|
C | T | 3 | a0001c0004t0012g0001a0001c0004t0012g0226a0001c0009t0012g0027 | 3 | HG01891.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.927-765C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190315 | ||||||
chr15:89190429
|
T | C | 22 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.927-651T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190429 | ||||||
chr15:89190481
|
C | G | 9 | a0001c0001t0006g0157a0001c0001t0006g0165a0001c0001t0006g0166others(6): Show | 9 | HG01258.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.927-599C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190481 | ||||||
chr15:89190597
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.927-483A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190597 | ||||||
chr15:89190701
|
C | G | 1 | a0001c0001t0034g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.927-379C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190701 | ||||||
chr15:89190811
|
C | T | 1 | a0001c0001t0003g0124 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.927-269C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190811 | ||||||
chr15:89190860
|
A | T | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927-220A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 8/10 | chr15 | 89190860 | ||||||
chr15:89191164
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0103others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+15C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191164 | ||||||
chr15:89191165
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0034g0143 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.996+16G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191165 | ||||||
chr15:89191235
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(91): Show | 94 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.996+86G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191235 | ||||||
chr15:89191299
|
G | T | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.996+150G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191299 | ||||||
chr15:89191346
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.996+197T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191346 | ||||||
chr15:89191428
|
G | A | 1 | a0001c0001t0033g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.996+279G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191428 | ||||||
chr15:89191509
|
G | T | 8 | a0001c0002t0007g0020a0001c0002t0007g0040a0001c0002t0007g0111others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+360G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191509 | ||||||
chr15:89191627
|
CT | C | 102 | a0001c0001t0001g0113a0001c0001t0001g0213a0001c0001t0002g0002others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.996+496delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 89191627 | |||||
chr15:89191631
|
T | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(107): Show | 110 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.996+482T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191631 | ||||||
chr15:89191632
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0213 | 2 | HG01256.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.996+483T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191632 | ||||||
chr15:89191633
|
T | C | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.996+484T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191633 | ||||||
chr15:89191644
|
T | A | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.996+495T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191644 | ||||||
chr15:89191716
|
CT | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.996+569delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 89191716 | |||||
chr15:89191906
|
C | T | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.996+757C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191906 | ||||||
chr15:89191907
|
G | A | 1 | a0001c0001t0008g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.996+758G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191907 | ||||||
chr15:89191929
|
G | GC | 106 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.996+780_996+781ins others(1): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89191929 | ||||||
chr15:89192017
|
A | G | 104 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.996+868A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192017 | ||||||
chr15:89192025
|
CAT | C | 11 | a0001c0001t0016g0066a0001c0001t0016g0080a0001c0001t0016g0147others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+879_996+880del others(2): Show |
ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 89192025 | |||||
chr15:89192206
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.997-1029C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192206 | ||||||
chr15:89192254
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.997-981G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192254 | ||||||
chr15:89192351
|
G | A | 104 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.997-884G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192351 | ||||||
chr15:89192509
|
C | CT | 5 | a0001c0001t0008g0011a0001c0001t0008g0082a0001c0001t0008g0102others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-711dupT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 89192509 | |||||
chr15:89192509
|
CT | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0001t0001g0113others(11): Show | 14 | HG01517.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.997-711delT | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 89192509 | |||||
chr15:89192571
|
A | G | 104 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.997-664A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192571 | ||||||
chr15:89192632
|
C | T | 1 | a0001c0001t0031g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.997-603C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192632 | ||||||
chr15:89192666
|
G | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.997-569G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192666 | ||||||
chr15:89192853
|
C | T | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.997-382C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192853 | ||||||
chr15:89192905
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.997-330C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192905 | ||||||
chr15:89192987
|
C | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.997-248C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89192987 | ||||||
chr15:89193014
|
C | T | 1 | a0001c0003t0015g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.997-221C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89193014 | ||||||
chr15:89193070
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.997-165T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89193070 | ||||||
chr15:89193145
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.997-90A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 9/10 | chr15 | 89193145 | ||||||
chr15:89193327
|
T | C | 73 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1081+8T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193327 | ||||||
chr15:89193608
|
G | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1081+289G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193608 | ||||||
chr15:89193617
|
C | T | 8 | a0001c0002t0007g0020a0001c0002t0007g0040a0001c0002t0007g0111others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081+298C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193617 | ||||||
chr15:89193641
|
A | C | 22 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1081+322A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193641 | ||||||
chr15:89193659
|
A | C | 8 | a0001c0002t0007g0020a0001c0002t0007g0040a0001c0002t0007g0111others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081+340A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193659 | ||||||
chr15:89193690
|
C | G | 1 | a0001c0001t0002g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1081+371C>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193690 | ||||||
chr15:89193719
|
A | G | 3 | a0001c0003t0015g0101a0001c0003t0015g0194a0001c0003t0015g0234 | 3 | HG02280.hp2 HG02486.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1081+400A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193719 | ||||||
chr15:89193730
|
G | A | 1 | a0001c0001t0039g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1081+411G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193730 | ||||||
chr15:89193759
|
G | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0093others(1): Show | 4 | HG02717.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+440G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89193759 | ||||||
chr15:89193920
|
C | CA | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG01106.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1081+619dupA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 89193920 | |||||
chr15:89193920
|
CA | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(188): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1081+619delA | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 89193920 | |||||
chr15:89194155
|
G | A | 1 | a0001c0001t0011g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1081+836G>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194155 | ||||||
chr15:89194230
|
G | T | 1 | a0001c0001t0002g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1081+911G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194230 | ||||||
chr15:89194247
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1081+928C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194247 | ||||||
chr15:89194273
|
C | T | 21 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1081+954C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194273 | ||||||
chr15:89194390
|
G | T | 2 | a0001c0001t0018g0033a0001c0001t0018g0036 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1082-837G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194390 | ||||||
chr15:89194412
|
A | G | 216 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1082-815A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194412 | ||||||
chr15:89194701
|
A | T | 15 | a0001c0001t0002g0156a0001c0001t0004g0003a0001c0001t0004g0013others(12): Show | 15 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1082-526A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194701 | ||||||
chr15:89194712
|
A | C | 21 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1082-515A>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194712 | ||||||
chr15:89194718
|
G | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(133): Show | 136 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1082-509G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194718 | ||||||
chr15:89194749
|
C | T | 21 | a0001c0001t0003g0026a0001c0001t0003g0047a0001c0001t0003g0048others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1082-478C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194749 | ||||||
chr15:89194758
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1082-469A>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194758 | ||||||
chr15:89194800
|
A | G | 72 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0038others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.1082-427A>G | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194800 | ||||||
chr15:89194817
|
G | T | 1 | a0001c0004t0012g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1082-410G>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194817 | ||||||
chr15:89194825
|
G | C | 4 | a0001c0001t0013g0096a0001c0001t0013g0152a0001c0001t0013g0154others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-402G>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194825 | ||||||
chr15:89194854
|
C | T | 1 | a0001c0001t0026g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1082-373C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194854 | ||||||
chr15:89194892
|
T | C | 1 | a0001c0001t0020g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1082-335T>C | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89194892 | ||||||
chr15:89195034
|
C | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1082-193C>T | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89195034 | ||||||
chr15:89195127
|
T | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0087others(1): Show | 4 | HG02602.hp2 HG03831.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-100T>A | ABHD2 | ENSG00000140526.18 | transcript | ENST00000352732.10 | protein_coding | 10/10 | chr15 | 89195127 |