geneid | 2515 |
---|---|
ensemblid | ENSG00000104755.16 |
hgncid | 198 |
symbol | ADAM2 |
name | ADAM metallopeptidase domain 2 |
refseq_nuc | NM_001464.5 |
refseq_prot | NP_001455.3 |
ensembl_nuc | ENST00000265708.9 |
ensembl_prot | ENSP00000265708.4 |
mane_status | MANE Select |
chr | chr8 |
start | 39743735 |
end | 39838227 |
strand | - |
ver | v1.2 |
region | chr8:39743735-39838227 |
region5000 | chr8:39738735-39843227 |
regionname0 | ADAM2_chr8_39743735_39838227 |
regionname5000 | ADAM2_chr8_39738735_39843227 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 735 | 303 | 82 | 59 | 121 | 12 | 28 | 93 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0002 | 0/0 | 735 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0003 | 0/0 | 735 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0004 | 0/0 | 735 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0005 | 0/0 | 735 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0006 | 0/0 | 735 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0007 | 0/0 | 735 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0008 | 0/0 | 735 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0009 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0010 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0011 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0012 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0013 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2208 | 295 | 79 | 59 | 118 | 12 | 26 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0002 | 0/0 | 2208 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0003 | 0/0 | 2208 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0004 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0005 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0006 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0007 | 0/0 | 2208 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0008 | 0/0 | 2208 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0009 | 0/0 | 2208 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0010 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0011 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0012 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0013 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0014 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0015 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0016 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0017 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0018 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0019 | 0/0 | 2071 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
c0020 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 403 | 327 | 94 | 59 | 132 | 14 | 27 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
t0002 | 0/0 | 403 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
t0003 | 0/0 | 403 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2208 | 295 | 79 | 59 | 118 | 12 | 26 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0006 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0007 | 0/0 | 2208 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0014 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0015 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0018 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0020 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0002c0002 | 0/0 | 2208 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0003c0003 | 0/0 | 2208 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0004c0008 | 0/0 | 2208 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0005c0009 | 0/0 | 2208 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0006c0005 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0007c0004 | 0/0 | 2208 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0008c0010 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0008c0011 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0009c0013 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0010c0016 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0011c0017 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0012c0019 | 0/0 | 2071 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0013c0012 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2610 | 293 | 79 | 58 | 118 | 12 | 25 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0001t0002 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0001t0003 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0006t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0007t0001 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0014t0001 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0015t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0018t0001 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0001c0020t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0002c0002t0001 | 0/0 | 2610 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0003c0003t0001 | 0/0 | 2610 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0004c0008t0001 | 0/0 | 2610 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0005c0009t0001 | 0/0 | 2610 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0006c0005t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0007c0004t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0008c0010t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0008c0011t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0009c0013t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0010c0016t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0011c0017t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0012c0019t0001 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
a0013c0012t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | copy fasta | chr8 | 39738735 | 39843227 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0006t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0014t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0015t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0018t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0001c0020t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0004c0008t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0005c0009t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0006c0005t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0007c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0007c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0008c0010t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0008c0011t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0009c0013t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0010c0016t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0011c0017t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0012c0019t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
a0013c0012t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01070 | hp2 | a0004 | c0008 | t0001 | g0008 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01515 | hp2 | a0005 | c0009 | t0001 | g0007 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01517 | hp1 | a0005 | c0009 | t0001 | g0007 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01884 | hp1 | a0010 | c0016 | t0001 | g0294 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01891 | hp1 | a0006 | c0005 | t0001 | g0006 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01891 | hp2 | a0001 | c0006 | t0001 | g0182 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02040 | hp2 | a0004 | c0008 | t0001 | g0008 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02080 | hp1 | a0012 | c0019 | t0001 | g0123 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02602 | hp1 | a0001 | c0014 | t0001 | g0046 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02615 | hp2 | a0006 | c0005 | t0001 | g0006 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0167 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02738 | hp1 | a0001 | c0018 | t0001 | g0232 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02886 | hp1 | a0007 | c0004 | t0001 | g0165 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0307 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03486 | hp1 | a0007 | c0004 | t0001 | g0166 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03486 | hp2 | a0001 | c0015 | t0001 | g0224 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18961 | hp2 | a0013 | c0012 | t0001 | g0021 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18992 | hp1 | a0008 | c0010 | t0001 | g0020 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA18999 | hp2 | a0009 | c0013 | t0001 | g0034 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19004 | hp2 | a0011 | c0017 | t0001 | g0125 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19012 | hp1 | a0001 | c0020 | t0001 | g0136 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0309 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19066 | hp1 | a0008 | c0011 | t0001 | g0019 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19068 | hp2 | a0001 | c0007 | t0001 | g0244 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19072 | hp1 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19079 | hp1 | a0001 | c0007 | t0001 | g0066 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | GIH | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0306 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0178 | REF | REF | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:39746584
|
G | C | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2062C>G | p.Pro688Ala | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/21 | 2104/2610 | 2062/2208 | 688/735 | chr8 | 39746584 | ||
chr8:39749416
|
G | A | 1 | a0004 | 2 | HG01070.hp2 HG02040.hp2 |
missense_variant | MODERATE | c.1910C>T | p.Ala637Val | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/21 | 1952/2610 | 1910/2208 | 637/735 | chr8 | 39749416 | ||
chr8:39755764
|
C | A | 1 | a0006 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1761G>T | p.Met587Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1803/2610 | 1761/2208 | 587/735 | chr8 | 39755764 | ||
chr8:39755887
|
T | C | 1 | a0011 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.1638A>G | p.Ile546Met | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1680/2610 | 1638/2208 | 546/735 | chr8 | 39755887 | ||
chr8:39767202
|
A | G | 1 | a0005 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.1262T>C | p.Phe421Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 13/21 | 1304/2610 | 1262/2208 | 421/735 | chr8 | 39767202 | ||
chr8:39769403
|
C | T | 1 | a0006 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1201G>A | p.Gly401Arg | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/21 | 1243/2610 | 1201/2208 | 401/735 | chr8 | 39769403 | ||
chr8:39769462
|
A | G | 1 | a0003 | 4 | NA18954.hp1 NA18998.hp2 NA19007.hp2 others(1): Show |
missense_variant | MODERATE | c.1142T>C | p.Phe381Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/21 | 1184/2610 | 1142/2208 | 381/735 | chr8 | 39769462 | ||
chr8:39774918
|
TACTCTAA others(11035): Show |
T | 1 | a0012 | 1 | HG02080.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.891+1014_1028+2106 others(3): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/21 | chr8 | 39774918 | ||||||
chr8:39788707
|
C | T | 1 | a0007 | 2 | HG02886.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.604G>A | p.Ala202Thr | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/21 | 646/2610 | 604/2208 | 202/735 | chr8 | 39788707 | ||
chr8:39837167
|
C | T | 1 | a0009 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.101G>A | p.Arg34Gln | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/21 | 143/2610 | 101/2208 | 34/735 | chr8 | 39837167 | ||
chr8:39838152
|
C | T | 1 | a0013 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.34G>A | p.Gly12Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 76/2610 | 34/2208 | 12/735 | chr8 | 39838152 | ||
chr8:39838158
|
C | A | 1 | a0002 | 7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
missense_variant | MODERATE | c.28G>T | p.Gly10Trp | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 70/2610 | 28/2208 | 10/735 | chr8 | 39838158 | ||
chr8:39838168
|
A | C | 1 | a0008 | 2 | NA18992.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.18T>G | p.Phe6Leu | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 60/2610 | 18/2208 | 6/735 | chr8 | 39838168 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:39746552
|
A | G | 2 | a0001c0007a0008c0010 | 3 | NA18992.hp1 NA19068.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.2094T>C | p.Ile698Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/21 | 2136/2610 | 2094/2208 | 698/735 | chr8 | 39746552 | ||
chr8:39755743
|
A | G | 1 | a0001c0006 | 2 | HG01891.hp2 HG02622.hp2 |
synonymous_variant | LOW | c.1782T>C | p.Ser594Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1824/2610 | 1782/2208 | 594/735 | chr8 | 39755743 | ||
chr8:39766873
|
T | C | 1 | a0001c0018 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1482A>G | p.Lys494Lys | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/21 | 1524/2610 | 1482/2208 | 494/735 | chr8 | 39766873 | ||
chr8:39788702
|
T | C | 1 | a0005c0009 | 2 | HG01515.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.609A>G | p.Gln203Gln | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/21 | 651/2610 | 609/2208 | 203/735 | chr8 | 39788702 | ||
chr8:39821636
|
A | G | 1 | a0001c0015 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.294T>C | p.Ile98Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/21 | 336/2610 | 294/2208 | 98/735 | chr8 | 39821636 | ||
chr8:39833967
|
T | C | 1 | a0001c0020 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.165A>G | p.Pro55Pro | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/21 | 207/2610 | 165/2208 | 55/735 | chr8 | 39833967 | ||
chr8:39837139
|
C | T | 1 | a0001c0014 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.129G>A | p.Ser43Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/21 | 171/2610 | 129/2208 | 43/735 | chr8 | 39837139 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:39743941
|
A | G | 1 | a0001c0001t0003 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 21/21 | 919 | chr8 | 39743941 | |||||
chr8:39743968
|
A | C | 1 | a0001c0001t0002 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 21/21 | 892 | chr8 | 39743968 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:39744075
|
GA | G | 127 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(124): Show | 129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.*31-12delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744075 | ||||||
chr8:39744245
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(125): Show | 130 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.*31-181T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744245 | ||||||
chr8:39744287
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.*31-223A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744287 | ||||||
chr8:39744469
|
C | G | 2 | a0001c0001t0001g0296a0002c0002t0001g0304 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*30+361G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744469 | ||||||
chr8:39744528
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.*30+302T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744528 | ||||||
chr8:39744685
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*30+145C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744685 | ||||||
chr8:39744708
|
G | A | 9 | a0001c0001t0001g0108a0001c0001t0001g0178a0001c0001t0001g0208others(6): Show | 9 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.*30+122C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744708 | ||||||
chr8:39744747
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*30+83G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744747 | ||||||
chr8:39744809
|
A | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0228 | 2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*30+21T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744809 | ||||||
chr8:39744897
|
C | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.2175-4G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39744897 | ||||||
chr8:39745009
|
C | A | 1 | a0001c0001t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2175-116G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745009 | ||||||
chr8:39745126
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00673.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2175-233C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745126 | ||||||
chr8:39745263
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2175-370G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745263 | ||||||
chr8:39745298
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2175-405G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745298 | ||||||
chr8:39745402
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175-509A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745402 | ||||||
chr8:39745459
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2175-566T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745459 | ||||||
chr8:39745532
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2175-639C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745532 | ||||||
chr8:39745545
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 243 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2175-652A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745545 | ||||||
chr8:39745984
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2174+488A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745984 | ||||||
chr8:39746017
|
G | GTA | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.2174+453_2174+454d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746017 | ||||||
chr8:39746037
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 212 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2174+435G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746037 | ||||||
chr8:39746094
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2174+378G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746094 | ||||||
chr8:39746157
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2174+315G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746157 | ||||||
chr8:39746171
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2174+301C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746171 | ||||||
chr8:39746226
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2174+246G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746226 | ||||||
chr8:39746257
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174+215G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746257 | ||||||
chr8:39746289
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2174+183T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746289 | ||||||
chr8:39746306
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174+166G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746306 | ||||||
chr8:39746335
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2174+137A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746335 | ||||||
chr8:39746376
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2174+96A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746376 | ||||||
chr8:39746650
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0196 | 2 | HG01175.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2015-19T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746650 | ||||||
chr8:39746706
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-75C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746706 | ||||||
chr8:39746714
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2015-83T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746714 | ||||||
chr8:39746855
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2015-224G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746855 | ||||||
chr8:39746972
|
G | A | 19 | a0001c0001t0001g0052a0001c0001t0001g0149a0001c0001t0001g0151others(16): Show | 20 | HG00733.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2015-341C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746972 | ||||||
chr8:39746980
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2015-349G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746980 | ||||||
chr8:39747073
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2015-442C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747073 | ||||||
chr8:39747101
|
A | T | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-470T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747101 | ||||||
chr8:39747167
|
C | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2015-536G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747167 | ||||||
chr8:39747187
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2015-556G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747187 | ||||||
chr8:39747384
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2015-753A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747384 | ||||||
chr8:39747541
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2015-910C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747541 | ||||||
chr8:39747561
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2015-930A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747561 | ||||||
chr8:39747594
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2015-963G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747594 | ||||||
chr8:39747673
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2015-1042G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747673 | ||||||
chr8:39747685
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2015-1054A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747685 | ||||||
chr8:39747905
|
C | T | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-1274G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747905 | ||||||
chr8:39747996
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2014+1316A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747996 | ||||||
chr8:39748235
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 6 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2014+1077G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748235 | ||||||
chr8:39748309
|
G | C | 1 | a0007c0004t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2014+1003C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748309 | ||||||
chr8:39748437
|
T | C | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2014+875A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748437 | ||||||
chr8:39748669
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0233 | 3 | HG02818.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2014+643C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748669 | ||||||
chr8:39748701
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2014+611C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748701 | ||||||
chr8:39749038
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 243 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2014+274C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749038 | ||||||
chr8:39749176
|
C | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.2014+136G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749176 | ||||||
chr8:39749311
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0144 | 2 | HG02922.hp1 NA19030.hp2 |
splice_donor_variant&intron_variant | HIGH | c.2014+1G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749311 | ||||||
chr8:39749584
|
T | C | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1875+83A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749584 | ||||||
chr8:39749585
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1875+82C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749585 | ||||||
chr8:39749586
|
C | CATGT | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1875+80_1875+81ins others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749586 | ||||||
chr8:39749586
|
C | T | 2 | a0001c0001t0001g0163a0010c0016t0001g0294 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1875+81G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749586 | ||||||
chr8:39749608
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1875+59G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749608 | ||||||
chr8:39749778
|
A | C | 3 | a0001c0007t0001g0066a0001c0007t0001g0244a0008c0010t0001g0020 | 3 | NA18992.hp1 NA19068.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1798-34T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39749778 | ||||||
chr8:39749825
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1798-81T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39749825 | ||||||
chr8:39750341
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1798-597A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750341 | ||||||
chr8:39750424
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1798-680A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750424 | ||||||
chr8:39750550
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-806A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750550 | ||||||
chr8:39750577
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1798-833G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750577 | ||||||
chr8:39750755
|
T | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0285 | 2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1798-1011A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750755 | ||||||
chr8:39750843
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1798-1099C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750843 | ||||||
chr8:39750995
|
A | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1798-1251T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750995 | ||||||
chr8:39751112
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1798-1368G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751112 | ||||||
chr8:39751203
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1798-1459A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751203 | ||||||
chr8:39751291
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1798-1547A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751291 | ||||||
chr8:39751423
|
G | A | 14 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0051others(11): Show | 14 | HG00621.hp1 HG02040.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1798-1679C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751423 | ||||||
chr8:39751466
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-1722C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751466 | ||||||
chr8:39751497
|
TTTTG | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1798-1757_1798-175 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751497 | ||||||
chr8:39751513
|
GT | G | 11 | a0001c0001t0001g0071a0001c0001t0001g0108a0001c0001t0001g0140others(8): Show | 11 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1798-1770delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751513 | ||||||
chr8:39751620
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1798-1876A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751620 | ||||||
chr8:39751662
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1798-1918T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751662 | ||||||
chr8:39751839
|
CT | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-2096delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751839 | ||||||
chr8:39751955
|
C | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-2211G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751955 | ||||||
chr8:39752041
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1798-2297G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752041 | ||||||
chr8:39752107
|
A | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1798-2363T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752107 | ||||||
chr8:39752109
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1798-2365A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752109 | ||||||
chr8:39752202
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1798-2458G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752202 | ||||||
chr8:39752222
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1798-2478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752222 | ||||||
chr8:39752408
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1798-2664C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752408 | ||||||
chr8:39752517
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0284 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1798-2773C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752517 | ||||||
chr8:39752532
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1798-2788A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752532 | ||||||
chr8:39752537
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1798-2793T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752537 | ||||||
chr8:39752588
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1798-2844C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752588 | ||||||
chr8:39752651
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1798-2907C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752651 | ||||||
chr8:39752827
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+2901A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752827 | ||||||
chr8:39753100
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0178 | 2 | HG02083.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1797+2628G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753100 | ||||||
chr8:39753163
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1797+2565C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753163 | ||||||
chr8:39753196
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1797+2532C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753196 | ||||||
chr8:39753286
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18961.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1797+2442G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753286 | ||||||
chr8:39753426
|
G | GA | 6 | a0001c0001t0001g0104a0001c0001t0001g0128a0001c0001t0001g0146others(3): Show | 6 | HG01433.hp1 NA18906.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+2301dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753426 | ||||||
chr8:39753426
|
GA | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(28): Show | 33 | HG01255.hp1 HG01928.hp1 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.1797+2301delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753426 | ||||||
chr8:39753439
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1797+2289G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753439 | ||||||
chr8:39753662
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0158others(8): Show | 12 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1797+2066A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753662 | ||||||
chr8:39753752
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1797+1976C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753752 | ||||||
chr8:39753812
|
A | AAC | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(142): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1797+1914_1797+191 others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753812 | ||||||
chr8:39753872
|
A | T | 6 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0183others(3): Show | 6 | HG00733.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+1856T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753872 | ||||||
chr8:39753886
|
G | A | 1 | a0006c0005t0001g0006 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1797+1842C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753886 | ||||||
chr8:39753994
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1797+1734A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753994 | ||||||
chr8:39754034
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+1694T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754034 | ||||||
chr8:39754464
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(5): Show | 8 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1797+1264C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754464 | ||||||
chr8:39754473
|
C | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1797+1255G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754473 | ||||||
chr8:39754484
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1797+1244T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754484 | ||||||
chr8:39754664
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797+1064T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754664 | ||||||
chr8:39754804
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1797+924G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754804 | ||||||
chr8:39754813
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1797+915T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754813 | ||||||
chr8:39754897
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1797+831T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754897 | ||||||
chr8:39754954
|
A | C | 5 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | NA18949.hp2 NA19005.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+774T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754954 | ||||||
chr8:39754978
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0075others(3): Show | 6 | HG00423.hp1 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+750C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754978 | ||||||
chr8:39755013
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1797+715G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755013 | ||||||
chr8:39755138
|
T | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797+590A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755138 | ||||||
chr8:39755249
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1797+479C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755249 | ||||||
chr8:39755337
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1797+391A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755337 | ||||||
chr8:39755448
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1797+280C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755448 | ||||||
chr8:39755458
|
C | T | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1797+270G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755458 | ||||||
chr8:39755524
|
A | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1797+204T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755524 | ||||||
chr8:39756032
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-121G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756032 | ||||||
chr8:39756069
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1614-158C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756069 | ||||||
chr8:39756134
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(15): Show | 19 | HG02040.hp1 HG02080.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.1614-223A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756134 | ||||||
chr8:39756142
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1614-231T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756142 | ||||||
chr8:39756364
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-453A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756364 | ||||||
chr8:39756366
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-455G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756366 | ||||||
chr8:39756420
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614-509C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756420 | ||||||
chr8:39756501
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1614-590G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756501 | ||||||
chr8:39756659
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1614-748T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756659 | ||||||
chr8:39756800
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 274 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1614-889T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756800 | ||||||
chr8:39756902
|
A | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 267 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1614-991T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756902 | ||||||
chr8:39756924
|
C | G | 1 | a0001c0001t0001g0098 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1614-1013G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756924 | ||||||
chr8:39757075
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1614-1164A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757075 | ||||||
chr8:39757295
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614-1384T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757295 | ||||||
chr8:39757352
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1614-1441A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757352 | ||||||
chr8:39757646
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1614-1735T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757646 | ||||||
chr8:39757777
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1614-1866C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757777 | ||||||
chr8:39758316
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1614-2405T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758316 | ||||||
chr8:39758370
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1614-2459A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758370 | ||||||
chr8:39758573
|
T | A | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1613+2603A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758573 | ||||||
chr8:39758575
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(74): Show | 87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1613+2601A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758575 | ||||||
chr8:39758694
|
A | C | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1613+2482T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758694 | ||||||
chr8:39758784
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1613+2392C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758784 | ||||||
chr8:39759274
|
A | C | 1 | a0001c0001t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1613+1902T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39759274 | ||||||
chr8:39759933
|
C | T | 1 | a0002c0002t0001g0303 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1613+1243G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39759933 | ||||||
chr8:39760055
|
C | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1613+1121G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760055 | ||||||
chr8:39760162
|
C | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1613+1014G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760162 | ||||||
chr8:39760361
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0233 | 3 | HG02818.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1613+815G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760361 | ||||||
chr8:39760363
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1613+813T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760363 | ||||||
chr8:39760450
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1613+726C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760450 | ||||||
chr8:39760549
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1613+627C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760549 | ||||||
chr8:39760582
|
G | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1613+594C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760582 | ||||||
chr8:39760698
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1613+478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760698 | ||||||
chr8:39760739
|
T | TA | 93 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(90): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1613+436dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760739 | ||||||
chr8:39760838
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1613+338C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760838 | ||||||
chr8:39760846
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1613+330C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760846 | ||||||
chr8:39760882
|
C | CA | 35 | a0001c0001t0001g0009a0001c0001t0001g0151a0001c0001t0001g0152others(32): Show | 37 | HG00544.hp2 HG01175.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1613+293dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
C | CAA | 10 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG00733.hp2 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1613+292_1613+293d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1613+284_1613+293d others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0015t0001g0224 | 3 | HG02145.hp2 HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1613+283_1613+293d others(13): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1613+279_1613+293d others(17): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CA | C | 14 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0178others(11): Show | 15 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1613+293delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CAA | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0111others(3): Show | 7 | HG01175.hp1 HG01952.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+292_1613+293d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CAAA | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0023others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1613+291_1613+293d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CAAAA | C | 63 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0049others(60): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1613+290_1613+293d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CAAAAA | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0041others(5): Show | 9 | HG00323.hp1 HG02080.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613+289_1613+293d others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39760882
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+282_1613+293d others(14): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | ||||||
chr8:39761031
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(5): Show | 8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1613+145C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39761031 | ||||||
chr8:39761118
|
G | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1613+58C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39761118 | ||||||
chr8:39761346
|
C | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-65G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761346 | ||||||
chr8:39761365
|
G | T | 1 | a0002c0002t0001g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1508-84C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761365 | ||||||
chr8:39761402
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1508-121A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761402 | ||||||
chr8:39761429
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1508-148T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761429 | ||||||
chr8:39761641
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-360A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761641 | ||||||
chr8:39761927
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1508-646T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761927 | ||||||
chr8:39762058
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1508-777A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762058 | ||||||
chr8:39762104
|
C | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-823G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762104 | ||||||
chr8:39762496
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1508-1215T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762496 | ||||||
chr8:39762568
|
T | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1508-1287A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762568 | ||||||
chr8:39762759
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1508-1478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762759 | ||||||
chr8:39762910
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1508-1629A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762910 | ||||||
chr8:39762990
|
G | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1508-1709C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762990 | ||||||
chr8:39763099
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-1818C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763099 | ||||||
chr8:39763142
|
A | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(90): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1508-1861T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763142 | ||||||
chr8:39763274
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(4): Show | 7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1508-1993A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763274 | ||||||
chr8:39763457
|
C | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-2176G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763457 | ||||||
chr8:39763568
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1508-2287C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763568 | ||||||
chr8:39763571
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1508-2290T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763571 | ||||||
chr8:39763610
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0164 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1508-2329G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763610 | ||||||
chr8:39763791
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1508-2510C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763791 | ||||||
chr8:39763881
|
CAA | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1508-2602_1508-260 others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763881 | ||||||
chr8:39763892
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1508-2611A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763892 | ||||||
chr8:39763955
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1508-2674T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763955 | ||||||
chr8:39763998
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(5): Show | 8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1508-2717G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763998 | ||||||
chr8:39764042
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1508-2761A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764042 | ||||||
chr8:39764045
|
G | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(26): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1508-2764C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764045 | ||||||
chr8:39764130
|
A | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18959.hp2 NA19005.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507+2718T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764130 | ||||||
chr8:39764148
|
T | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507+2700A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764148 | ||||||
chr8:39764400
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+2448A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764400 | ||||||
chr8:39764416
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0213 | 3 | HG01361.hp1 HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1507+2432T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764416 | ||||||
chr8:39764456
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+2392G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764456 | ||||||
chr8:39764655
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1507+2193C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764655 | ||||||
chr8:39764754
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1507+2094C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764754 | ||||||
chr8:39764921
|
G | A | 1 | a0007c0004t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1507+1927C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764921 | ||||||
chr8:39764921
|
G | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0147 | 2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1507+1927C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764921 | ||||||
chr8:39764992
|
C | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+1856G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764992 | ||||||
chr8:39764998
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1507+1850C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764998 | ||||||
chr8:39765026
|
A | AAAAT | 18 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0246others(15): Show | 18 | HG00544.hp2 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1507+1818_1507+182 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | ||||||
chr8:39765026
|
AAAAT | A | 38 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(35): Show | 38 | HG00621.hp1 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1507+1818_1507+182 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | ||||||
chr8:39765026
|
AAAATAAA others(1): Show |
A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1507+1814_1507+182 others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | ||||||
chr8:39765026
|
AAAATAAA others(5): Show |
A | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(71): Show | 83 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1507+1810_1507+182 others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | ||||||
chr8:39765026
|
AAAATAAA others(9): Show |
A | 4 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0127others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507+1806_1507+182 others(20): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | ||||||
chr8:39765033
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+1815T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765033 | ||||||
chr8:39765079
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1507+1769T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765079 | ||||||
chr8:39765148
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+1700C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765148 | ||||||
chr8:39765207
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1507+1641G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765207 | ||||||
chr8:39765214
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 273 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1507+1634A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765214 | ||||||
chr8:39765231
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(83): Show | 96 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1507+1617A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765231 | ||||||
chr8:39765385
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1507+1463C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765385 | ||||||
chr8:39765400
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+1448C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765400 | ||||||
chr8:39765475
|
T | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507+1373A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765475 | ||||||
chr8:39765504
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1507+1344C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765504 | ||||||
chr8:39765541
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+1307T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765541 | ||||||
chr8:39765551
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(16): Show | 20 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1507+1297G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765551 | ||||||
chr8:39765564
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1507+1284G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765564 | ||||||
chr8:39765826
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1507+1022T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765826 | ||||||
chr8:39765920
|
GT | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+927delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765920 | ||||||
chr8:39766052
|
C | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(7): Show | 10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507+796G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766052 | ||||||
chr8:39766107
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0284 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1507+741A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766107 | ||||||
chr8:39766268
|
G | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+580C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766268 | ||||||
chr8:39766438
|
CT | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507+409delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766438 | ||||||
chr8:39766490
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+358T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766490 | ||||||
chr8:39766494
|
C | A | 1 | a0002c0002t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1507+354G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766494 | ||||||
chr8:39766551
|
G | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1507+297C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766551 | ||||||
chr8:39766805
|
C | A | 1 | a0001c0001t0001g0146 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+43G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766805 | ||||||
chr8:39766806
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+42T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766806 | ||||||
chr8:39766807
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+41C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766807 | ||||||
chr8:39767133
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1311+20T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 13/20 | chr8 | 39767133 | ||||||
chr8:39767328
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1213-77T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767328 | ||||||
chr8:39767341
|
T | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1213-90A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767341 | ||||||
chr8:39767458
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1213-207C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767458 | ||||||
chr8:39767891
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1213-640A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767891 | ||||||
chr8:39767896
|
T | TCA | 13 | a0001c0001t0001g0018a0001c0001t0001g0142a0001c0001t0001g0254others(10): Show | 14 | HG00423.hp1 HG01433.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1213-647_1213-646d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
T | TCACA | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(102): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1213-649_1213-646d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
T | TCACACA | 33 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0026others(30): Show | 35 | HG00140.hp2 HG00673.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1213-651_1213-646d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0058a0001c0001t0001g0067a0001c0001t0001g0158others(10): Show | 13 | HG00621.hp1 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1213-653_1213-646d others(10): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
T | TCACACAC others(3): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0225others(1): Show | 4 | HG00323.hp2 HG03453.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213-655_1213-646d others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
T | TCACACAC others(7): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0179a0001c0001t0001g0235others(1): Show | 4 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-659_1213-646d others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767896
|
TCA | T | 37 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(34): Show | 37 | HG00733.hp2 HG01192.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1213-647_1213-646d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | ||||||
chr8:39767914
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0089 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1213-664_1213-663i others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767914 | ||||||
chr8:39768020
|
T | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-769A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768020 | ||||||
chr8:39768161
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1213-910A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768161 | ||||||
chr8:39768260
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-1009G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768260 | ||||||
chr8:39768320
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1213-1069C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768320 | ||||||
chr8:39768560
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1212+832C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768560 | ||||||
chr8:39768787
|
A | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+605T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768787 | ||||||
chr8:39768900
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1212+492T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768900 | ||||||
chr8:39769072
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0299 | 2 | HG03540.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1212+320C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769072 | ||||||
chr8:39769135
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1212+257T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769135 | ||||||
chr8:39769300
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1212+92A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769300 | ||||||
chr8:39769624
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1029-49A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769624 | ||||||
chr8:39769722
|
T | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(7): Show | 10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029-147A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769722 | ||||||
chr8:39769848
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1029-273C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769848 | ||||||
chr8:39769943
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0168others(3): Show | 8 | HG00738.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-368G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769943 | ||||||
chr8:39769950
|
C | CT | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 234 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1029-376dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769950 | ||||||
chr8:39770040
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(26): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1029-465C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770040 | ||||||
chr8:39770094
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-519G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770094 | ||||||
chr8:39770190
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1029-615C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770190 | ||||||
chr8:39770356
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029-781G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770356 | ||||||
chr8:39770361
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1029-786A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770361 | ||||||
chr8:39770372
|
C | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1029-797G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770372 | ||||||
chr8:39770638
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(5): Show | 8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1063C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770638 | ||||||
chr8:39770670
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1029-1095G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770670 | ||||||
chr8:39770687
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1029-1112T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770687 | ||||||
chr8:39770855
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(5): Show | 8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1280G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770855 | ||||||
chr8:39771062
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1029-1487C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771062 | ||||||
chr8:39771171
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 244 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1029-1596C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771171 | ||||||
chr8:39771182
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-1607G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771182 | ||||||
chr8:39771219
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029-1644C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771219 | ||||||
chr8:39771344
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-1769C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771344 | ||||||
chr8:39771467
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1029-1892A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771467 | ||||||
chr8:39771537
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1029-1962A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771537 | ||||||
chr8:39771549
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1029-1974A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771549 | ||||||
chr8:39771648
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1029-2073C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771648 | ||||||
chr8:39772039
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1029-2464C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772039 | ||||||
chr8:39772109
|
T | TA | 93 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(90): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1029-2535dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772109 | ||||||
chr8:39772220
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0208 | 2 | HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1029-2645G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772220 | ||||||
chr8:39772231
|
C | CT | 15 | a0001c0001t0001g0022a0001c0001t0001g0152a0001c0001t0001g0153others(12): Show | 15 | HG01167.hp1 HG02040.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-2657dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772231 | ||||||
chr8:39772239
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1029-2664A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772239 | ||||||
chr8:39772291
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-2716A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772291 | ||||||
chr8:39772324
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1029-2749G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772324 | ||||||
chr8:39772530
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029-2955C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772530 | ||||||
chr8:39772732
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1029-3157C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772732 | ||||||
chr8:39772741
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1029-3166A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772741 | ||||||
chr8:39772754
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1029-3179A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772754 | ||||||
chr8:39772777
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1029-3202C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772777 | ||||||
chr8:39772980
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1029-3405C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772980 | ||||||
chr8:39773031
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-3456G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773031 | ||||||
chr8:39773043
|
C | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-3468G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773043 | ||||||
chr8:39773091
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1029-3516C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773091 | ||||||
chr8:39773263
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1029-3688G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773263 | ||||||
chr8:39773484
|
A | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+3541T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773484 | ||||||
chr8:39773859
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1028+3166G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773859 | ||||||
chr8:39773884
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1028+3141A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773884 | ||||||
chr8:39774047
|
C | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1028+2978G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774047 | ||||||
chr8:39774430
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1028+2595C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774430 | ||||||
chr8:39774446
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG01243.hp2 HG03491.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1028+2579A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774446 | ||||||
chr8:39774493
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1028+2532T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774493 | ||||||
chr8:39774496
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0126 | 2 | NA18953.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1028+2529A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774496 | ||||||
chr8:39774529
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1028+2496T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774529 | ||||||
chr8:39774693
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1028+2332T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774693 | ||||||
chr8:39774789
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1028+2236T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774789 | ||||||
chr8:39774831
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+2194T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774831 | ||||||
chr8:39774923
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+2102A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774923 | ||||||
chr8:39775007
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00738.hp1 HG01361.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028+2018C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775007 | ||||||
chr8:39775021
|
C | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0105others(5): Show | 8 | HG02135.hp1 NA18969.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+2004G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775021 | ||||||
chr8:39775138
|
C | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(26): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1028+1887G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775138 | ||||||
chr8:39775249
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0168others(3): Show | 8 | HG00738.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+1776G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775249 | ||||||
chr8:39775576
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1028+1449T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775576 | ||||||
chr8:39775803
|
T | C | 1 | a0007c0004t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1028+1222A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775803 | ||||||
chr8:39775990
|
A | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1028+1035T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775990 | ||||||
chr8:39776346
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0116a0005c0009t0001g0007 | 4 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028+679T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776346 | ||||||
chr8:39776438
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1028+587T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776438 | ||||||
chr8:39776446
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028+579G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776446 | ||||||
chr8:39776448
|
G | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1028+577C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776448 | ||||||
chr8:39776449
|
G | T | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0002c0002t0001g0303others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028+576C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776449 | ||||||
chr8:39776495
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1028+530C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776495 | ||||||
chr8:39776511
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1028+514A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776511 | ||||||
chr8:39776727
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1028+298C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776727 | ||||||
chr8:39776744
|
G | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1028+281C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776744 | ||||||
chr8:39777240
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.892-79G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777240 | ||||||
chr8:39777362
|
A | T | 1 | a0002c0002t0001g0307 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-201T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777362 | ||||||
chr8:39777398
|
T | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-237A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777398 | ||||||
chr8:39777490
|
A | G | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-329T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777490 | ||||||
chr8:39777643
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-482T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777643 | ||||||
chr8:39777659
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.892-498T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777659 | ||||||
chr8:39777771
|
G | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.892-610C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777771 | ||||||
chr8:39777988
|
G | T | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.892-827C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777988 | ||||||
chr8:39778030
|
A | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-869T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778030 | ||||||
chr8:39778189
|
T | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-1028A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778189 | ||||||
chr8:39778403
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.892-1242T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778403 | ||||||
chr8:39778655
|
G | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1494C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778655 | ||||||
chr8:39778686
|
A | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.892-1525T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778686 | ||||||
chr8:39778766
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.892-1605T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778766 | ||||||
chr8:39778802
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.892-1641T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778802 | ||||||
chr8:39778822
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.892-1661A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778822 | ||||||
chr8:39778949
|
A | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-1788T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778949 | ||||||
chr8:39778989
|
G | A | 1 | a0002c0002t0001g0307 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-1828C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778989 | ||||||
chr8:39779068
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.892-1907A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779068 | ||||||
chr8:39779204
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.892-2043G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779204 | ||||||
chr8:39779297
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-2136G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779297 | ||||||
chr8:39779344
|
C | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.892-2183G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779344 | ||||||
chr8:39779578
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.892-2417C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779578 | ||||||
chr8:39779895
|
C | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0200 | 3 | HG01261.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.892-2734G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779895 | ||||||
chr8:39780160
|
C | T | 2 | a0001c0001t0001g0081a0010c0016t0001g0294 | 2 | HG01884.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.892-2999G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780160 | ||||||
chr8:39780194
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.892-3033C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780194 | ||||||
chr8:39780276
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.892-3115G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780276 | ||||||
chr8:39780547
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0147 | 2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.892-3386G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780547 | ||||||
chr8:39780783
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.892-3622G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780783 | ||||||
chr8:39780898
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.892-3737G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780898 | ||||||
chr8:39780927
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.892-3766C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780927 | ||||||
chr8:39780988
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-3827A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780988 | ||||||
chr8:39780996
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.892-3835G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780996 | ||||||
chr8:39781012
|
CT | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0170others(5): Show | 8 | HG02451.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-3852delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781012 | ||||||
chr8:39781069
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-3908G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781069 | ||||||
chr8:39781190
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-4029A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781190 | ||||||
chr8:39781225
|
T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(121): Show | 129 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.892-4064A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781225 | ||||||
chr8:39781269
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.892-4108C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781269 | ||||||
chr8:39781278
|
TGTG | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-4120_892-4118d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781278 | ||||||
chr8:39781288
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.892-4127A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781288 | ||||||
chr8:39781290
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892-4129G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781290 | ||||||
chr8:39781291
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-4130C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781291 | ||||||
chr8:39781506
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.892-4345C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781506 | ||||||
chr8:39781637
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.892-4476A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781637 | ||||||
chr8:39781892
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.892-4731T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781892 | ||||||
chr8:39781923
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.892-4762C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781923 | ||||||
chr8:39782186
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00735.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.891+4788C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782186 | ||||||
chr8:39782305
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.891+4669A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782305 | ||||||
chr8:39782369
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.891+4605T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782369 | ||||||
chr8:39782705
|
G | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+4269C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782705 | ||||||
chr8:39782805
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.891+4169A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782805 | ||||||
chr8:39782958
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+4016T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782958 | ||||||
chr8:39783332
|
A | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0023others(63): Show | 68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.891+3642T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783332 | ||||||
chr8:39783349
|
T | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0031others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+3625A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783349 | ||||||
chr8:39783389
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+3585A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783389 | ||||||
chr8:39783670
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.891+3304C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783670 | ||||||
chr8:39783701
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+3273G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783701 | ||||||
chr8:39783820
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+3154G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783820 | ||||||
chr8:39783899
|
C | T | 2 | a0001c0001t0001g0068a0005c0009t0001g0007 | 3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.891+3075G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783899 | ||||||
chr8:39783931
|
C | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+3043G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783931 | ||||||
chr8:39783950
|
G | GA | 77 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(74): Show | 87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.891+3023dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783950 | ||||||
chr8:39784101
|
C | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.891+2873G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784101 | ||||||
chr8:39784401
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.891+2573C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784401 | ||||||
chr8:39784600
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.891+2374C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784600 | ||||||
chr8:39784848
|
T | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(118): Show | 126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.891+2126A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784848 | ||||||
chr8:39784925
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.891+2049A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784925 | ||||||
chr8:39785003
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.891+1971C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785003 | ||||||
chr8:39785159
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.891+1815G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785159 | ||||||
chr8:39785165
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.891+1809C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785165 | ||||||
chr8:39785206
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0205a0001c0001t0001g0218others(1): Show | 5 | HG00544.hp1 NA19003.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1768G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785206 | ||||||
chr8:39785289
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.891+1685C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785289 | ||||||
chr8:39785380
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+1594C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785380 | ||||||
chr8:39785405
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+1569A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785405 | ||||||
chr8:39785426
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.891+1548T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785426 | ||||||
chr8:39785443
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.891+1531C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785443 | ||||||
chr8:39785449
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.891+1525G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785449 | ||||||
chr8:39785745
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.891+1229G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785745 | ||||||
chr8:39785754
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.891+1220C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785754 | ||||||
chr8:39785796
|
T | TAAA | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+1175_891+1177d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | ||||||
chr8:39785796
|
TA | T | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(145): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.891+1177delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | ||||||
chr8:39785796
|
TAAA | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0158others(7): Show | 11 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1175_891+1177d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | ||||||
chr8:39785920
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.891+1054G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785920 | ||||||
chr8:39785935
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.891+1039C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785935 | ||||||
chr8:39785983
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.891+991A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785983 | ||||||
chr8:39786133
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+841T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786133 | ||||||
chr8:39786230
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(122): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.891+744G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786230 | ||||||
chr8:39786287
|
A | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0173a0001c0001t0001g0188others(1): Show | 4 | HG00423.hp2 HG00673.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+687T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786287 | ||||||
chr8:39786301
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+673C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786301 | ||||||
chr8:39786341
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.891+633A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786341 | ||||||
chr8:39786348
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+626A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786348 | ||||||
chr8:39786526
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.891+448G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786526 | ||||||
chr8:39786564
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0127others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+410G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786564 | ||||||
chr8:39786583
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00738.hp1 HG01361.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+391G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786583 | ||||||
chr8:39786595
|
T | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+379A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786595 | ||||||
chr8:39786673
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0302 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.891+301G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786673 | ||||||
chr8:39786712
|
A | G | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+262T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786712 | ||||||
chr8:39786716
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.891+258G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786716 | ||||||
chr8:39786753
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.891+221G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786753 | ||||||
chr8:39787172
|
C | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.810-117G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787172 | ||||||
chr8:39787264
|
A | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-209T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787264 | ||||||
chr8:39787295
|
A | T | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.810-240T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787295 | ||||||
chr8:39787387
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.810-332C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787387 | ||||||
chr8:39787414
|
T | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.810-359A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787414 | ||||||
chr8:39787436
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.810-381T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787436 | ||||||
chr8:39787453
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.810-398C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787453 | ||||||
chr8:39787531
|
A | ACT | 3 | a0001c0001t0001g0065a0001c0001t0001g0296a0001c0015t0001g0224 | 3 | HG01978.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.810-478_810-477dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787531 | ||||||
chr8:39787542
|
C | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0179others(8): Show | 12 | HG00408.hp2 HG01070.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.810-487G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | ||||||
chr8:39787542
|
C | CTA | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-489_810-488dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | ||||||
chr8:39787542
|
CTA | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.810-489_810-488del others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | ||||||
chr8:39787544
|
A | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.810-489T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787544 | ||||||
chr8:39787546
|
A | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0122a0001c0001t0001g0228others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.810-491T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787546 | ||||||
chr8:39787557
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810-502G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787557 | ||||||
chr8:39787581
|
ATG | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 262 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.809+502_809+503del others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787581 | ||||||
chr8:39787583
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.809+502C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787583 | ||||||
chr8:39787732
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.809+353T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787732 | ||||||
chr8:39787870
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809+215C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787870 | ||||||
chr8:39787925
|
A | G | 1 | a0002c0002t0001g0303 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809+160T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787925 | ||||||
chr8:39787944
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.809+141G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787944 | ||||||
chr8:39787975
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.809+110C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787975 | ||||||
chr8:39787977
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.809+108C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787977 | ||||||
chr8:39788036
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+49C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39788036 | ||||||
chr8:39788053
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.809+32T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39788053 | ||||||
chr8:39788567
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.642+102G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/20 | chr8 | 39788567 | ||||||
chr8:39788742
|
T | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0203a0001c0001t0001g0208 | 3 | HG03239.hp2 NA19030.hp1 NA21309.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.571-2A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39788742 | ||||||
chr8:39789049
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-309C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789049 | ||||||
chr8:39789410
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0179a0001c0001t0001g0235others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-670G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789410 | ||||||
chr8:39789462
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0203a0001c0001t0001g0208 | 3 | HG03239.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.571-722C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789462 | ||||||
chr8:39789808
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.571-1068C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789808 | ||||||
chr8:39789889
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-1149T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789889 | ||||||
chr8:39789926
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.571-1186G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789926 | ||||||
chr8:39789927
|
A | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-1187T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789927 | ||||||
chr8:39790133
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-1393G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790133 | ||||||
chr8:39790317
|
T | G | 1 | a0001c0001t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.571-1577A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790317 | ||||||
chr8:39790320
|
G | A | 1 | a0009c0013t0001g0034 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571-1580C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790320 | ||||||
chr8:39790369
|
C | T | 1 | a0006c0005t0001g0006 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.571-1629G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790369 | ||||||
chr8:39790399
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571-1659G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790399 | ||||||
chr8:39790400
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18961.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.571-1660C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790400 | ||||||
chr8:39790483
|
T | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(122): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.571-1743A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790483 | ||||||
chr8:39790544
|
G | A | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.571-1804C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790544 | ||||||
chr8:39790549
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.571-1809A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790549 | ||||||
chr8:39790549
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.571-1809A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790549 | ||||||
chr8:39790586
|
T | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0207 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.571-1846A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790586 | ||||||
chr8:39790698
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-1958G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790698 | ||||||
chr8:39790789
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18949.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.571-2049A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790789 | ||||||
chr8:39790923
|
C | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-2183G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790923 | ||||||
chr8:39791085
|
C | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.571-2345G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791085 | ||||||
chr8:39791352
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.571-2612A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791352 | ||||||
chr8:39791518
|
A | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-2778T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791518 | ||||||
chr8:39791665
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.571-2925C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791665 | ||||||
chr8:39791866
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.571-3126C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791866 | ||||||
chr8:39791928
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(4): Show | 7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3188G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791928 | ||||||
chr8:39792112
|
C | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3372G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792112 | ||||||
chr8:39792143
|
C | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-3403G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792143 | ||||||
chr8:39792286
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.571-3546C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792286 | ||||||
chr8:39792288
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-3548C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792288 | ||||||
chr8:39792520
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.571-3780C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792520 | ||||||
chr8:39792528
|
C | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3788G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792528 | ||||||
chr8:39792709
|
C | CA | 6 | a0001c0001t0001g0249a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG02129.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-3970dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792709 | ||||||
chr8:39792750
|
T | C | 2 | a0003c0003t0001g0010a0003c0003t0001g0174 | 3 | NA18998.hp2 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.571-4010A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792750 | ||||||
chr8:39792768
|
G | A | 3 | a0001c0001t0001g0067a0001c0007t0001g0066a0001c0007t0001g0244 | 3 | NA18992.hp2 NA19068.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.571-4028C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792768 | ||||||
chr8:39792837
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.571-4097A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792837 | ||||||
chr8:39793046
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-4306G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793046 | ||||||
chr8:39793144
|
T | G | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.571-4404A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793144 | ||||||
chr8:39793212
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.571-4472C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793212 | ||||||
chr8:39793229
|
T | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-4489A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793229 | ||||||
chr8:39793250
|
C | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-4510G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793250 | ||||||
chr8:39793313
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.571-4573C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793313 | ||||||
chr8:39793322
|
T | TAAGAAAT others(358): Show |
1 | a0001c0001t0001g0129 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.571-4583_571-4582i others(367): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793322 | ||||||
chr8:39793421
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-4681T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793421 | ||||||
chr8:39793682
|
C | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.571-4942G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793682 | ||||||
chr8:39793829
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18959.hp2 NA19005.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5089T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793829 | ||||||
chr8:39793861
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-5121G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793861 | ||||||
chr8:39793968
|
C | T | 26 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0073others(23): Show | 26 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-5228G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793968 | ||||||
chr8:39794031
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.571-5291T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794031 | ||||||
chr8:39794283
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-5543A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794283 | ||||||
chr8:39794422
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-5682C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794422 | ||||||
chr8:39794452
|
C | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0040others(59): Show | 64 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.571-5712G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794452 | ||||||
chr8:39794701
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-5961G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794701 | ||||||
chr8:39794740
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.571-6000G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794740 | ||||||
chr8:39794883
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-6143A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794883 | ||||||
chr8:39795411
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.571-6671A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795411 | ||||||
chr8:39795441
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.571-6701T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795441 | ||||||
chr8:39795543
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-6803G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795543 | ||||||
chr8:39795717
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6977A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795717 | ||||||
chr8:39795718
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6978C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795718 | ||||||
chr8:39795719
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6979A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795719 | ||||||
chr8:39795721
|
C | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0222 | 2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.571-6981G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795721 | ||||||
chr8:39795723
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6983A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795723 | ||||||
chr8:39795726
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6986G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795726 | ||||||
chr8:39795727
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6987G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795727 | ||||||
chr8:39795729
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6989A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795729 | ||||||
chr8:39795836
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571-7096T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795836 | ||||||
chr8:39795887
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.571-7147A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795887 | ||||||
chr8:39796064
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.571-7324A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796064 | ||||||
chr8:39796081
|
TA | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-7342delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796081 | ||||||
chr8:39796099
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.571-7359G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796099 | ||||||
chr8:39796254
|
A | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(4): Show | 7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-7514T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796254 | ||||||
chr8:39796492
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-7752G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796492 | ||||||
chr8:39796671
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.571-7931C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796671 | ||||||
chr8:39796679
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 265 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.571-7939G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796679 | ||||||
chr8:39796787
|
T | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.571-8047A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796787 | ||||||
chr8:39796811
|
T | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-8071A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796811 | ||||||
chr8:39796992
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-8252C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796992 | ||||||
chr8:39797008
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571-8268G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797008 | ||||||
chr8:39797029
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-8289G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797029 | ||||||
chr8:39797071
|
T | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG01109.hp2 HG01255.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-8331A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797071 | ||||||
chr8:39797087
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-8347T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797087 | ||||||
chr8:39797153
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.571-8413C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797153 | ||||||
chr8:39797330
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.571-8590C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797330 | ||||||
chr8:39797422
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.571-8682G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797422 | ||||||
chr8:39797523
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(78): Show | 91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.571-8783G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797523 | ||||||
chr8:39797638
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-8898G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797638 | ||||||
chr8:39797749
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(78): Show | 91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.571-9009A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797749 | ||||||
chr8:39797884
|
T | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-9144A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797884 | ||||||
chr8:39797950
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-9210C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797950 | ||||||
chr8:39798015
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-9275A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798015 | ||||||
chr8:39798434
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.571-9694C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798434 | ||||||
chr8:39798604
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-9864T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798604 | ||||||
chr8:39798688
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0146 | 3 | NA18987.hp1 NA19007.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.571-9948T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798688 | ||||||
chr8:39798853
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-10113C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798853 | ||||||
chr8:39798889
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-10149G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798889 | ||||||
chr8:39799005
|
AT | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.571-10266delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799005 | ||||||
chr8:39799020
|
T | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-10280A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799020 | ||||||
chr8:39799176
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.570+10234C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799176 | ||||||
chr8:39799630
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+9780C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799630 | ||||||
chr8:39799707
|
C | G | 1 | a0002c0002t0001g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+9703G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799707 | ||||||
chr8:39799719
|
T | C | 5 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0155others(2): Show | 5 | HG02148.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+9691A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799719 | ||||||
chr8:39799780
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0289others(4): Show | 7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+9630G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799780 | ||||||
chr8:39799936
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+9474C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799936 | ||||||
chr8:39800040
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.570+9370A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800040 | ||||||
chr8:39800078
|
TG | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+9331delC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800078 | ||||||
chr8:39800265
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0042 | 2 | HG02148.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.570+9145T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800265 | ||||||
chr8:39800384
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.570+9026A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800384 | ||||||
chr8:39800497
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+8913A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800497 | ||||||
chr8:39800641
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+8769G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800641 | ||||||
chr8:39800810
|
C | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(89): Show | 102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.570+8600G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800810 | ||||||
chr8:39800823
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+8587C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800823 | ||||||
chr8:39800824
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+8586T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800824 | ||||||
chr8:39801024
|
A | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.570+8386T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801024 | ||||||
chr8:39801118
|
T | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.570+8292A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801118 | ||||||
chr8:39801585
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+7825C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801585 | ||||||
chr8:39801653
|
G | A | 26 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0073others(23): Show | 26 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+7757C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801653 | ||||||
chr8:39801773
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+7637C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801773 | ||||||
chr8:39802022
|
G | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.570+7388C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802022 | ||||||
chr8:39802112
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+7298G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802112 | ||||||
chr8:39802175
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.570+7235A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802175 | ||||||
chr8:39802182
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.570+7228G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802182 | ||||||
chr8:39802240
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0284 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.570+7170G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802240 | ||||||
chr8:39802263
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+7147G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802263 | ||||||
chr8:39802311
|
G | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+7099C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802311 | ||||||
chr8:39802359
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.570+7051A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802359 | ||||||
chr8:39802428
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+6982C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802428 | ||||||
chr8:39802435
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+6975G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802435 | ||||||
chr8:39802438
|
C | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0282 | 2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.570+6972G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802438 | ||||||
chr8:39802511
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.570+6899C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802511 | ||||||
chr8:39802529
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 267 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.570+6881A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802529 | ||||||
chr8:39802749
|
T | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(65): Show | 78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.570+6661A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802749 | ||||||
chr8:39802964
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.570+6446C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802964 | ||||||
chr8:39803063
|
A | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0170a0001c0001t0001g0248others(7): Show | 10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+6347T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803063 | ||||||
chr8:39803076
|
T | C | 1 | a0009c0013t0001g0034 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.570+6334A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803076 | ||||||
chr8:39803109
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | HG01081.hp1 HG02486.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.570+6301C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803109 | ||||||
chr8:39803160
|
T | C | 3 | a0001c0001t0001g0259a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01496.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.570+6250A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803160 | ||||||
chr8:39803227
|
G | A | 1 | a0005c0009t0001g0007 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.570+6183C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803227 | ||||||
chr8:39803409
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+6001C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803409 | ||||||
chr8:39803454
|
C | G | 1 | a0001c0001t0001g0217 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+5956G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803454 | ||||||
chr8:39803455
|
G | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+5955C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803455 | ||||||
chr8:39803505
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.570+5905G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803505 | ||||||
chr8:39803554
|
A | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.570+5856T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803554 | ||||||
chr8:39803670
|
G | A | 20 | a0001c0001t0001g0071a0001c0001t0001g0172a0001c0001t0001g0203others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+5740C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803670 | ||||||
chr8:39803743
|
T | C | 1 | a0001c0020t0001g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.570+5667A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803743 | ||||||
chr8:39803987
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0161 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.570+5423C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803987 | ||||||
chr8:39804002
|
A | G | 4 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0015t0001g0224others(1): Show | 4 | HG01884.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+5408T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804002 | ||||||
chr8:39804169
|
C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0261a0008c0010t0001g0020others(1): Show | 4 | HG00621.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+5241G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804169 | ||||||
chr8:39804249
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.570+5161A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804249 | ||||||
chr8:39804338
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+5072G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804338 | ||||||
chr8:39804382
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+5028G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804382 | ||||||
chr8:39804423
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.570+4987T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804423 | ||||||
chr8:39804920
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.570+4490A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804920 | ||||||
chr8:39804921
|
G | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+4489C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804921 | ||||||
chr8:39805009
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0015t0001g0224others(1): Show | 4 | HG01884.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+4401A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805009 | ||||||
chr8:39805420
|
C | A | 1 | a0003c0003t0001g0174 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.570+3990G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805420 | ||||||
chr8:39805439
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570+3971C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805439 | ||||||
chr8:39805551
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0156 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.570+3859T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805551 | ||||||
chr8:39805642
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+3768T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805642 | ||||||
chr8:39806045
|
G | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570+3365C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806045 | ||||||
chr8:39806139
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+3271A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806139 | ||||||
chr8:39806585
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.570+2825C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806585 | ||||||
chr8:39806678
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | NA18949.hp2 NA19010.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2732G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806678 | ||||||
chr8:39806683
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570+2727G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806683 | ||||||
chr8:39807077
|
C | T | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+2333G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807077 | ||||||
chr8:39807177
|
G | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+2233C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807177 | ||||||
chr8:39807260
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.570+2150T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807260 | ||||||
chr8:39807428
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.570+1982C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807428 | ||||||
chr8:39807874
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0222 | 2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.570+1536T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807874 | ||||||
chr8:39807947
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.570+1463A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807947 | ||||||
chr8:39808108
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.570+1302T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808108 | ||||||
chr8:39808122
|
T | A | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+1288A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808122 | ||||||
chr8:39808189
|
T | TAC | 46 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0063others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.570+1219_570+1220d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
T | TACAC | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.570+1217_570+1220d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
T | TACACAC | 11 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0023others(8): Show | 13 | HG01496.hp1 HG02148.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+1215_570+1220d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
TAC | T | 5 | a0001c0001t0001g0184a0001c0001t0001g0295a0001c0001t0001g0299others(2): Show | 5 | HG02809.hp1 HG02886.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1219_570+1220d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
TACAC | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+1217_570+1220d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
TACACAC | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0002c0002t0001g0305 | 3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.570+1215_570+1220d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808189
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.570+1199_570+1220d others(24): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | ||||||
chr8:39808467
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.570+943C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808467 | ||||||
chr8:39808634
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+776A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808634 | ||||||
chr8:39808683
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.570+727G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808683 | ||||||
chr8:39808731
|
T | C | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+679A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808731 | ||||||
chr8:39808847
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.570+563G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808847 | ||||||
chr8:39808848
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.570+562C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808848 | ||||||
chr8:39808903
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.570+507C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808903 | ||||||
chr8:39808982
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.570+428G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808982 | ||||||
chr8:39809080
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.570+330T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809080 | ||||||
chr8:39809110
|
A | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+300T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809110 | ||||||
chr8:39809111
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+299C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809111 | ||||||
chr8:39809133
|
T | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570+277A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809133 | ||||||
chr8:39809879
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514-413C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39809879 | ||||||
chr8:39809913
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0265a0001c0001t0001g0301 | 4 | NA18991.hp1 NA19058.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-447T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39809913 | ||||||
chr8:39810040
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.514-574A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810040 | ||||||
chr8:39810261
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-795T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810261 | ||||||
chr8:39810500
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0082a0001c0001t0001g0173others(7): Show | 11 | HG00423.hp2 HG00673.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-1034G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810500 | ||||||
chr8:39810522
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.514-1056T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810522 | ||||||
chr8:39810900
|
C | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0179a0001c0001t0001g0254others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1434G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810900 | ||||||
chr8:39811101
|
G | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.514-1635C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811101 | ||||||
chr8:39811151
|
T | C | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(132): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.514-1685A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811151 | ||||||
chr8:39811641
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.514-2175C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811641 | ||||||
chr8:39811693
|
C | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084others(8): Show | 11 | HG00621.hp2 NA18949.hp2 NA18992.hp1 others(8): Show |
intron_variant | MODIFIER | c.514-2227G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811693 | ||||||
chr8:39811729
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0045others(33): Show | 38 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.514-2263C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811729 | ||||||
chr8:39811862
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.514-2396A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811862 | ||||||
chr8:39811884
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.514-2418G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811884 | ||||||
chr8:39811940
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.514-2474T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811940 | ||||||
chr8:39811966
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-2500A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811966 | ||||||
chr8:39811988
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.514-2522C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811988 | ||||||
chr8:39812074
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-2608C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812074 | ||||||
chr8:39812238
|
AAGG | A | 6 | a0001c0001t0001g0248a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-2775_514-2773d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812238 | ||||||
chr8:39812316
|
GGAAGAAT others(7): Show |
G | 1 | a0001c0001t0001g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.514-2864_514-2851d others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812316 | ||||||
chr8:39812345
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2879T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812345 | ||||||
chr8:39812392
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.514-2926A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812392 | ||||||
chr8:39812439
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0116a0005c0009t0001g0007 | 4 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2973A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812439 | ||||||
chr8:39812457
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | NA19002.hp2 NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.514-2991G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812457 | ||||||
chr8:39812463
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.514-2997C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812463 | ||||||
chr8:39812620
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.514-3154G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812620 | ||||||
chr8:39812648
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.514-3182G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812648 | ||||||
chr8:39812809
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(103): Show | 117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.514-3343C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812809 | ||||||
chr8:39812825
|
AAC | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG00558.hp2 HG00597.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-3361_514-3360d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812825 | ||||||
chr8:39812924
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-3458G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812924 | ||||||
chr8:39812981
|
C | T | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(132): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.514-3515G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812981 | ||||||
chr8:39812988
|
T | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0274others(2): Show | 5 | NA18954.hp2 NA18962.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-3522A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812988 | ||||||
chr8:39813081
|
C | G | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.514-3615G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813081 | ||||||
chr8:39813100
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.514-3634C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813100 | ||||||
chr8:39813164
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.514-3698T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813164 | ||||||
chr8:39813174
|
C | T | 1 | a0002c0002t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.514-3708G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813174 | ||||||
chr8:39813315
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.514-3849C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813315 | ||||||
chr8:39813700
|
C | G | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.514-4234G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813700 | ||||||
chr8:39813732
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.514-4266C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813732 | ||||||
chr8:39813782
|
C | T | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.514-4316G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813782 | ||||||
chr8:39813832
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-4366C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813832 | ||||||
chr8:39813903
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.514-4437T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813903 | ||||||
chr8:39814084
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514-4618C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814084 | ||||||
chr8:39814093
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0170a0001c0001t0001g0179others(8): Show | 11 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-4627G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814093 | ||||||
chr8:39814119
|
A | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.514-4653T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814119 | ||||||
chr8:39814146
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(122): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.514-4680G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814146 | ||||||
chr8:39814407
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0071others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-4941T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814407 | ||||||
chr8:39814467
|
T | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0053others(2): Show | 7 | NA18983.hp2 NA18987.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-5001A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814467 | ||||||
chr8:39814927
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514-5461T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814927 | ||||||
chr8:39815178
|
G | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.514-5712C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815178 | ||||||
chr8:39815358
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.513+5644A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815358 | ||||||
chr8:39815483
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(85): Show | 98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.513+5519C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815483 | ||||||
chr8:39815610
|
C | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513+5392G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815610 | ||||||
chr8:39815743
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513+5259T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815743 | ||||||
chr8:39815769
|
A | G | 3 | a0003c0003t0001g0010a0003c0003t0001g0174a0003c0003t0001g0187 | 4 | NA18954.hp1 NA18998.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+5233T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815769 | ||||||
chr8:39815953
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.513+5049T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815953 | ||||||
chr8:39815977
|
T | A | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+5025A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815977 | ||||||
chr8:39816153
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+4849G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816153 | ||||||
chr8:39816154
|
G | A | 1 | a0010c0016t0001g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.513+4848C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816154 | ||||||
chr8:39816222
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 83 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.513+4780C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816222 | ||||||
chr8:39816261
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513+4741G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816261 | ||||||
chr8:39816304
|
T | TA | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+4697dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816304 | ||||||
chr8:39816367
|
T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(123): Show | 131 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.513+4635A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816367 | ||||||
chr8:39816541
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+4461C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816541 | ||||||
chr8:39816599
|
C | A | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+4403G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816599 | ||||||
chr8:39816736
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.513+4266T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816736 | ||||||
chr8:39817001
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+4001C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817001 | ||||||
chr8:39817169
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.513+3833C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817169 | ||||||
chr8:39817181
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3821T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817181 | ||||||
chr8:39817350
|
G | A | 1 | a0003c0003t0001g0174 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.513+3652C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817350 | ||||||
chr8:39817393
|
TAGA | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0170a0001c0001t0001g0179others(8): Show | 11 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.513+3606_513+3608d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817393 | ||||||
chr8:39817466
|
C | A | 2 | a0001c0015t0001g0224a0010c0016t0001g0294 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+3536G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817466 | ||||||
chr8:39817479
|
G | A | 1 | a0002c0002t0001g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.513+3523C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817479 | ||||||
chr8:39817584
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513+3418T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817584 | ||||||
chr8:39817658
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+3344C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817658 | ||||||
chr8:39817728
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(124): Show | 132 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.513+3274G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817728 | ||||||
chr8:39817792
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.513+3210C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817792 | ||||||
chr8:39817953
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+3049G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817953 | ||||||
chr8:39818071
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.513+2931T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818071 | ||||||
chr8:39818529
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.513+2473G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818529 | ||||||
chr8:39818532
|
T | G | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+2470A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818532 | ||||||
chr8:39818619
|
G | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513+2383C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818619 | ||||||
chr8:39818771
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+2231A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818771 | ||||||
chr8:39818772
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.513+2230C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818772 | ||||||
chr8:39818909
|
C | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(125): Show | 139 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+2093G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818909 | ||||||
chr8:39818981
|
G | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.513+2021C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818981 | ||||||
chr8:39819106
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.513+1896C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819106 | ||||||
chr8:39819376
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0180 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.513+1626T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819376 | ||||||
chr8:39819865
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0003g0080 | 2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.513+1137A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819865 | ||||||
chr8:39819871
|
A | AT | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.513+1130dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819871 | ||||||
chr8:39819911
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.513+1091A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819911 | ||||||
chr8:39819917
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.513+1085C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819917 | ||||||
chr8:39820219
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(125): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+783G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820219 | ||||||
chr8:39820220
|
A | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(125): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+782T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820220 | ||||||
chr8:39820238
|
T | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+764A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820238 | ||||||
chr8:39820424
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.513+578T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820424 | ||||||
chr8:39820428
|
G | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0175a0001c0001t0001g0205others(5): Show | 9 | HG00408.hp2 HG00544.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.513+574C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820428 | ||||||
chr8:39820627
|
A | G | 1 | a0001c0020t0001g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.513+375T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820627 | ||||||
chr8:39820649
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.513+353G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820649 | ||||||
chr8:39820810
|
T | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+192A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820810 | ||||||
chr8:39820848
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG02055.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+154T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820848 | ||||||
chr8:39820993
|
A | G | 3 | a0001c0001t0001g0024a0007c0004t0001g0165a0007c0004t0001g0166 | 3 | HG02572.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+9T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820993 | ||||||
chr8:39821204
|
C | T | 40 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-34G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/20 | chr8 | 39821204 | ||||||
chr8:39821286
|
G | A | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-116C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/20 | chr8 | 39821286 | ||||||
chr8:39821765
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268-103T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821765 | ||||||
chr8:39821805
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-143C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821805 | ||||||
chr8:39821971
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.268-309A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821971 | ||||||
chr8:39821974
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0222 | 2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.268-312T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821974 | ||||||
chr8:39822086
|
C | G | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-424G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822086 | ||||||
chr8:39822281
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.268-619C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822281 | ||||||
chr8:39822324
|
T | C | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-662A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822324 | ||||||
chr8:39822506
|
T | TTGCATTG others(313): Show |
1 | a0001c0001t0001g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.268-845_268-844ins others(320): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(314): Show |
1 | a0001c0001t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268-845_268-844ins others(321): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(321): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(328): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(322): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0162 | 3 | HG02723.hp1 HG03471.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(329): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(323): Show |
1 | a0001c0001t0001g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(330): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(323): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG02148.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(330): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(324): Show |
1 | a0001c0001t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(331): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTG others(329): Show |
1 | a0001c0001t0001g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(336): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTT others(320): Show |
1 | a0001c0001t0001g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(327): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822506
|
T | TTGCATTT others(321): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02109.hp1 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(328): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | ||||||
chr8:39822569
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.268-907A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822569 | ||||||
chr8:39822658
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.268-996C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822658 | ||||||
chr8:39822712
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.268-1050T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822712 | ||||||
chr8:39822715
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.268-1053T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822715 | ||||||
chr8:39822752
|
T | G | 1 | a0002c0002t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.268-1090A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822752 | ||||||
chr8:39822752
|
T | TG | 19 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.268-1091_268-1090i others(3): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822752 | ||||||
chr8:39822754
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-1092A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822754 | ||||||
chr8:39822830
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.268-1168C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822830 | ||||||
chr8:39823013
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.268-1351G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823013 | ||||||
chr8:39823013
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268-1351G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823013 | ||||||
chr8:39823044
|
G | A | 1 | a0002c0002t0001g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.268-1382C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823044 | ||||||
chr8:39823139
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0285 | 2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.268-1477T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823139 | ||||||
chr8:39823212
|
G | T | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.268-1550C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823212 | ||||||
chr8:39823237
|
G | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.268-1575C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823237 | ||||||
chr8:39823482
|
C | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.267+1337G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823482 | ||||||
chr8:39823530
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0127 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.267+1289A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823530 | ||||||
chr8:39823547
|
T | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(69): Show | 77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.267+1272A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823547 | ||||||
chr8:39823652
|
G | A | 2 | a0008c0010t0001g0020a0008c0011t0001g0019 | 2 | NA18992.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.267+1167C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823652 | ||||||
chr8:39824105
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.267+714C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824105 | ||||||
chr8:39824203
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.267+616T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824203 | ||||||
chr8:39824219
|
G | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.267+600C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824219 | ||||||
chr8:39824249
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.267+570G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824249 | ||||||
chr8:39824274
|
C | CA | 57 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(54): Show | 61 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.267+544dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | ||||||
chr8:39824274
|
C | CAA | 17 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 18 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.267+543_267+544dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | ||||||
chr8:39824274
|
CA | C | 28 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0081others(25): Show | 28 | HG00733.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.267+544delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | ||||||
chr8:39824318
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.267+501G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824318 | ||||||
chr8:39824345
|
TA | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG01109.hp2 HG01255.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+473delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824345 | ||||||
chr8:39824352
|
T | TA | 10 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(7): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.267+466dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824352 | ||||||
chr8:39824487
|
C | A | 1 | a0001c0001t0001g0015 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.267+332G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824487 | ||||||
chr8:39824676
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.267+143C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824676 | ||||||
chr8:39824751
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.267+68C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824751 | ||||||
chr8:39824932
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0145 | 2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.189-35G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39824932 | ||||||
chr8:39824994
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(69): Show | 77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.189-97C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39824994 | ||||||
chr8:39825325
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189-428T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39825325 | ||||||
chr8:39825763
|
G | T | 20 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.189-866C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39825763 | ||||||
chr8:39826217
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1320C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826217 | ||||||
chr8:39826328
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189-1431T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826328 | ||||||
chr8:39826383
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189-1486G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826383 | ||||||
chr8:39826444
|
C | T | 1 | a0001c0015t0001g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.189-1547G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826444 | ||||||
chr8:39826478
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.189-1581G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826478 | ||||||
chr8:39826506
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.189-1609C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826506 | ||||||
chr8:39826636
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 50 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.189-1739A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826636 | ||||||
chr8:39826976
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.189-2079T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826976 | ||||||
chr8:39826999
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-2102A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826999 | ||||||
chr8:39827037
|
AAAC | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 9 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-2143_189-2141d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827037 | ||||||
chr8:39827047
|
GA | G | 6 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-2151delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827047 | ||||||
chr8:39827107
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.189-2210T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827107 | ||||||
chr8:39827161
|
A | T | 38 | a0001c0001t0001g0023a0001c0001t0001g0149a0001c0001t0001g0150others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.189-2264T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827161 | ||||||
chr8:39827468
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.189-2571G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827468 | ||||||
chr8:39827849
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(47): Show | 54 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.189-2952G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827849 | ||||||
chr8:39827912
|
T | A | 1 | a0002c0002t0001g0307 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.189-3015A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827912 | ||||||
chr8:39827940
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189-3043A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827940 | ||||||
chr8:39827963
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.189-3066G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827963 | ||||||
chr8:39828075
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.189-3178G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828075 | ||||||
chr8:39828317
|
A | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.189-3420T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828317 | ||||||
chr8:39828426
|
A | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.189-3529T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828426 | ||||||
chr8:39828519
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.189-3622A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828519 | ||||||
chr8:39828664
|
G | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 50 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.189-3767C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828664 | ||||||
chr8:39828674
|
C | G | 1 | a0001c0015t0001g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.189-3777G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828674 | ||||||
chr8:39828792
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.189-3895T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828792 | ||||||
chr8:39828814
|
A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(2): Show | 5 | HG00323.hp2 HG01243.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-3917T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828814 | ||||||
chr8:39829218
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.189-4321T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829218 | ||||||
chr8:39829280
|
A | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.189-4383T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829280 | ||||||
chr8:39829326
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0284 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189-4429A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829326 | ||||||
chr8:39829376
|
C | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.189-4479G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829376 | ||||||
chr8:39829414
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.189-4517A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829414 | ||||||
chr8:39829466
|
C | T | 21 | a0001c0001t0001g0023a0001c0001t0001g0225a0001c0001t0001g0226others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.188+4478G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829466 | ||||||
chr8:39829505
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+4439T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829505 | ||||||
chr8:39829594
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.188+4350G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829594 | ||||||
chr8:39829736
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.188+4208A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829736 | ||||||
chr8:39829807
|
C | T | 1 | a0001c0001t0001g0009 | 2 | NA18984.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.188+4137G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829807 | ||||||
chr8:39829821
|
C | T | 4 | a0001c0001t0001g0288a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01884.hp1 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+4123G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829821 | ||||||
chr8:39829941
|
T | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0008c0010t0001g0020others(1): Show | 4 | HG00673.hp2 NA18968.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+4003A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829941 | ||||||
chr8:39829973
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+3971G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829973 | ||||||
chr8:39830190
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.188+3754T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830190 | ||||||
chr8:39830236
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.188+3708G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830236 | ||||||
chr8:39830238
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.188+3706G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830238 | ||||||
chr8:39830444
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.188+3500A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830444 | ||||||
chr8:39830523
|
T | C | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3421A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830523 | ||||||
chr8:39830782
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188+3162T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830782 | ||||||
chr8:39830805
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.188+3139A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830805 | ||||||
chr8:39830831
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188+3113A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830831 | ||||||
chr8:39831193
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.188+2751T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831193 | ||||||
chr8:39831204
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188+2740G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831204 | ||||||
chr8:39831251
|
TCTAAA | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.188+2688_188+2692d others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831251 | ||||||
chr8:39831499
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG00735.hp2 HG01074.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+2445G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831499 | ||||||
chr8:39831529
|
A | G | 7 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0305others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+2415T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831529 | ||||||
chr8:39831639
|
T | C | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188+2305A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831639 | ||||||
chr8:39831747
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.188+2197C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831747 | ||||||
chr8:39831806
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.188+2138C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831806 | ||||||
chr8:39831971
|
T | C | 7 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0305others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+1973A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831971 | ||||||
chr8:39832399
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.188+1545T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832399 | ||||||
chr8:39832606
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1338A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832606 | ||||||
chr8:39832610
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1334T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832610 | ||||||
chr8:39832611
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1333G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832611 | ||||||
chr8:39832612
|
A | ATATTTGA others(13): Show |
1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1331_188+1332i others(22): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832612 | ||||||
chr8:39832726
|
C | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+1218G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832726 | ||||||
chr8:39832758
|
G | T | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188+1186C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832758 | ||||||
chr8:39832834
|
ATATG | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.188+1106_188+1109d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832834 | ||||||
chr8:39832866
|
T | C | 1 | a0007c0004t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188+1078A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832866 | ||||||
chr8:39833237
|
G | T | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.188+707C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833237 | ||||||
chr8:39833246
|
A | T | 1 | a0002c0002t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.188+698T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833246 | ||||||
chr8:39833420
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG00544.hp2 NA18942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.188+524T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833420 | ||||||
chr8:39833657
|
A | T | 1 | a0001c0015t0001g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.188+287T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833657 | ||||||
chr8:39833694
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.188+250G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833694 | ||||||
chr8:39833825
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.188+119C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833825 | ||||||
chr8:39833842
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.188+102G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833842 | ||||||
chr8:39834045
|
G | T | 1 | a0001c0015t0001g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133-46C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834045 | ||||||
chr8:39834240
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.133-241A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834240 | ||||||
chr8:39834424
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.133-425A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834424 | ||||||
chr8:39834445
|
TG | T | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.133-447delC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834445 | ||||||
chr8:39834471
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.133-472T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834471 | ||||||
chr8:39834508
|
G | C | 1 | a0001c0015t0001g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133-509C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834508 | ||||||
chr8:39834516
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.133-517A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834516 | ||||||
chr8:39834591
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.133-592G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834591 | ||||||
chr8:39834592
|
G | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.133-593C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834592 | ||||||
chr8:39834602
|
C | T | 19 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.133-603G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834602 | ||||||
chr8:39834635
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0221 | 3 | NA18990.hp1 NA18994.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.133-636C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834635 | ||||||
chr8:39834666
|
C | T | 2 | a0001c0001t0001g0071a0006c0005t0001g0006 | 3 | HG01891.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133-667G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834666 | ||||||
chr8:39834713
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133-714G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834713 | ||||||
chr8:39834732
|
C | CA | 67 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(64): Show | 71 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.133-734dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
C | CAA | 36 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0026others(33): Show | 37 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.133-735_133-734dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
C | CAAAA | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG00423.hp2 HG01074.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-737_133-734dup others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
C | CAAAAA | 53 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(50): Show | 61 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.133-738_133-734dup others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
C | CAAAAAA | 13 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0211others(10): Show | 15 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-739_133-734dup others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
CA | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0049others(7): Show | 10 | HG00735.hp1 HG01978.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.133-734delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834732
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133-743_133-734del others(10): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | ||||||
chr8:39834742
|
A | G | 8 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 8 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-743T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834742 | ||||||
chr8:39834972
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 6 | NA18983.hp2 NA18987.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-973T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834972 | ||||||
chr8:39835254
|
C | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0288others(9): Show | 12 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-1255G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835254 | ||||||
chr8:39835412
|
C | CG | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(69): Show | 77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.133-1414dupC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835412 | ||||||
chr8:39835498
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133-1499G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835498 | ||||||
chr8:39835509
|
C | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.133-1510G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835509 | ||||||
chr8:39835542
|
G | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.133-1543C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835542 | ||||||
chr8:39835544
|
T | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.133-1545A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835544 | ||||||
chr8:39835681
|
C | CA | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(98): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.132+1454dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835681 | ||||||
chr8:39835681
|
C | CAA | 20 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0225others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.132+1453_132+1454d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835681 | ||||||
chr8:39835764
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.132+1372T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835764 | ||||||
chr8:39835765
|
T | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.132+1371A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835765 | ||||||
chr8:39836067
|
A | G | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+1069T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836067 | ||||||
chr8:39836204
|
CATTTTTT | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0301 | 5 | NA19007.hp1 NA19058.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+925_132+931del others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836204 | ||||||
chr8:39836205
|
A | AT | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+930dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836205 | ||||||
chr8:39836218
|
T | A | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+918A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836218 | ||||||
chr8:39836228
|
A | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.132+908T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836228 | ||||||
chr8:39836247
|
A | G | 20 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.132+889T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836247 | ||||||
chr8:39836257
|
GT | G | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+878delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836257 | ||||||
chr8:39836301
|
C | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.132+835G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836301 | ||||||
chr8:39836491
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.132+645G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836491 | ||||||
chr8:39836538
|
CA | C | 21 | a0001c0001t0001g0047a0001c0001t0001g0225a0001c0001t0001g0226others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+597delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836538 | ||||||
chr8:39836696
|
TAATCATT others(11): Show |
T | 1 | a0001c0006t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.132+422_132+439del others(18): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836696 | ||||||
chr8:39836707
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.132+429T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836707 | ||||||
chr8:39836855
|
T | A | 2 | a0007c0004t0001g0165a0007c0004t0001g0166 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.132+281A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836855 | ||||||
chr8:39837091
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.132+45G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39837091 | ||||||
chr8:39837248
|
C | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-36G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837248 | ||||||
chr8:39837280
|
T | C | 7 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0305others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-68A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837280 | ||||||
chr8:39837334
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56-122G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837334 | ||||||
chr8:39837341
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(72): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.56-129G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837341 | ||||||
chr8:39837352
|
T | C | 20 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-140A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837352 | ||||||
chr8:39837381
|
G | GT | 17 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 18 | HG00639.hp2 HG01515.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.56-170dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837381 | ||||||
chr8:39837382
|
T | G | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-170A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837382 | ||||||
chr8:39837537
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.56-325G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837537 | ||||||
chr8:39837547
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-335G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837547 | ||||||
chr8:39837666
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.56-454A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837666 | ||||||
chr8:39837687
|
A | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.55+444T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837687 | ||||||
chr8:39837841
|
C | A | 1 | a0001c0007t0001g0244 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.55+290G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837841 | ||||||
chr8:39838016
|
T | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.55+115A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838016 | ||||||
chr8:39838020
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.55+111A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838020 | ||||||
chr8:39838097
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.55+34G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838097 |