geneid | 8756 |
---|---|
ensemblid | ENSG00000069206.15 |
hgncid | 214 |
symbol | ADAM7 |
name | ADAM metallopeptidase domain 7 |
refseq_nuc | NM_003817.4 |
refseq_prot | NP_003808.2 |
ensembl_nuc | ENST00000175238.10 |
ensembl_prot | ENSP00000175238.5 |
mane_status | MANE Select |
chr | chr8 |
start | 24441026 |
end | 24509565 |
strand | + |
ver | v1.2 |
region | chr8:24441026-24509565 |
region5000 | chr8:24436026-24514565 |
regionname0 | ADAM7_chr8_24441026_24509565 |
regionname5000 | ADAM7_chr8_24436026_24514565 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 755 | 234 | 60 | 49 | 93 | 10 | 21 | 69 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002 | 0/1 | 755 | 77 | 5 | 16 | 39 | 3 | 13 | 31 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003 | 0/0 | 755 | 16 | 12 | 2 | 1 | 0 | 1 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0004 | 0/0 | 755 | 10 | 0 | 5 | 5 | 0 | 0 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0005 | 0/0 | 755 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0006 | 0/0 | 755 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0007 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0008 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0009 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0010 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0011 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0012 | 0/0 | 755 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0013 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0014 | 0/0 | 755 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0015 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0016 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0017 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3275 | 129 | 18 | 22 | 72 | 6 | 10 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0002 | 0/0 | 3272 | 69 | 29 | 17 | 13 | 3 | 7 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0003 | 0/1 | 3272 | 64 | 5 | 14 | 30 | 3 | 11 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0004 | 0/0 | 3272 | 15 | 1 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0005 | 0/0 | 3272 | 10 | 0 | 5 | 5 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0006 | 0/0 | 3272 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0007 | 0/0 | 3273 | 9 | 0 | 0 | 9 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0008 | 0/0 | 3273 | 9 | 2 | 0 | 7 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0009 | 0/0 | 3269 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0010 | 0/0 | 3272 | 6 | 5 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0011 | 0/0 | 3272 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0012 | 0/0 | 3272 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0013 | 0/0 | 3273 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0014 | 0/0 | 3269 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0015 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0016 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0017 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0018 | 0/0 | 3275 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0019 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0020 | 0/0 | 3272 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0021 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0022 | 0/0 | 3272 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0023 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0024 | 0/0 | 3272 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0025 | 0/0 | 3272 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0026 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0027 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0028 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0029 | 0/0 | 3274 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0030 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0031 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0032 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0033 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0034 | 0/0 | 3275 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0035 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
c0036 | 0/0 | 3275 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
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 | 1103 | 183 | 51 | 36 | 68 | 7 | 20 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0002 | 0/0 | 1103 | 125 | 16 | 22 | 71 | 6 | 10 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0003 | 0/0 | 1103 | 16 | 2 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0004 | 0/0 | 1101 | 10 | 9 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0005 | 0/0 | 1103 | 9 | 7 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0006 | 1/0 | 1103 | 4 | 3 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0007 | 0/0 | 1103 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0008 | 0/0 | 1103 | 3 | 2 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0009 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0010 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0011 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0012 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0013 | 0/0 | 1103 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0014 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
t0015 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
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 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3275 | 129 | 18 | 22 | 72 | 6 | 10 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0002 | 0/0 | 3272 | 69 | 29 | 17 | 13 | 3 | 7 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0004 | 0/0 | 3272 | 15 | 1 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0008 | 0/0 | 3273 | 9 | 2 | 0 | 7 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0010 | 0/0 | 3272 | 6 | 5 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0013 | 0/0 | 3273 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0017 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0027 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0028 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0029 | 0/0 | 3274 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0003 | 0/1 | 3272 | 64 | 5 | 14 | 30 | 3 | 11 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0007 | 0/0 | 3273 | 9 | 0 | 0 | 9 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0012 | 0/0 | 3272 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0020 | 0/0 | 3272 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0022 | 0/0 | 3272 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0009 | 0/0 | 3269 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0011 | 0/0 | 3272 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0030 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0031 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0032 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0033 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0034 | 0/0 | 3275 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0004c0005 | 0/0 | 3272 | 10 | 0 | 5 | 5 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0005c0006 | 0/0 | 3272 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0006c0014 | 0/0 | 3269 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0007c0036 | 0/0 | 3275 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0008c0018 | 0/0 | 3275 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0009c0019 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0010c0021 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0011c0023 | 0/0 | 3272 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0012c0025 | 0/0 | 3272 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0013c0026 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0014c0024 | 0/0 | 3272 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0015c0035 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0016c0015 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0017c0016 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4377 | 122 | 15 | 22 | 69 | 6 | 10 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0001t0006 | 1/0 | 4377 | 4 | 3 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0001t0009 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0001t0010 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0001t0011 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0002t0001 | 0/0 | 4374 | 60 | 22 | 16 | 13 | 3 | 6 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0002t0004 | 0/0 | 4372 | 8 | 7 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0002t0013 | 0/0 | 4374 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0004t0003 | 0/0 | 4374 | 15 | 1 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0008t0001 | 0/0 | 4375 | 7 | 0 | 0 | 7 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0008t0007 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0010t0001 | 0/0 | 4374 | 6 | 5 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0013t0001 | 0/0 | 4375 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0017t0003 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0027t0001 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0028t0001 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0001c0029t0002 | 0/0 | 4376 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0003t0001 | 0/1 | 4374 | 62 | 5 | 12 | 30 | 3 | 11 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0003t0012 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0003t0015 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0007t0001 | 0/0 | 4375 | 9 | 0 | 0 | 9 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0012t0001 | 0/0 | 4374 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0020t0001 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0002c0022t0001 | 0/0 | 4374 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0009t0005 | 0/0 | 4371 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0011t0001 | 0/0 | 4374 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0030t0001 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0031t0014 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0032t0001 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0033t0004 | 0/0 | 4373 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0003c0034t0008 | 0/0 | 4377 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0004c0005t0001 | 0/0 | 4374 | 10 | 0 | 5 | 5 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0005c0006t0001 | 0/0 | 4374 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0006c0014t0005 | 0/0 | 4371 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0007c0036t0002 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0008c0018t0002 | 0/0 | 4377 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0009c0019t0001 | 0/0 | 4374 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0010c0021t0001 | 0/0 | 4374 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0011c0023t0001 | 0/0 | 4374 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0012c0025t0001 | 0/0 | 4374 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0013c0026t0007 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0014c0024t0001 | 0/0 | 4374 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0015c0035t0008 | 0/0 | 4374 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0016c0015t0004 | 0/0 | 4373 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
a0017c0016t0008 | 0/0 | 4375 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | copy fasta | chr8 | 24436026 | 24514565 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0006g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0002t0013g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0008t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0010t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0010t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0010t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0010t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0010t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0013t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0013t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0017t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0027t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0028t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0001c0029t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0012g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0003t0015g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0012t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0012t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0020t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0002c0022t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0009t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0009t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0009t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0009t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0009t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0011t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0011t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0011t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0030t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0031t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0032t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0033t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0003c0034t0008g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0004c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0005c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0006c0014t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0007c0036t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0008c0018t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0009c0019t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0010c0021t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0011c0023t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0012c0025t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0013c0026t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0014c0024t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0015c0035t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0016c0015t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
a0017c0016t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0255 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0113 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00140 | hp1 | a0001 | c0004 | t0003 | g0150 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0299 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0089 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0102 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0196 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00438 | hp1 | a0007 | c0036 | t0002 | g0250 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00438 | hp2 | a0002 | c0007 | t0001 | g0112 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0097 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00733 | hp1 | a0003 | c0009 | t0005 | g0317 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00733 | hp2 | a0001 | c0004 | t0003 | g0059 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00735 | hp1 | a0002 | c0022 | t0001 | g0134 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00735 | hp2 | a0001 | c0004 | t0003 | g0057 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00738 | hp1 | a0002 | c0003 | t0001 | g0078 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00738 | hp2 | a0003 | c0009 | t0005 | g0318 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01069 | hp1 | a0002 | c0003 | t0012 | g0093 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01081 | hp1 | a0004 | c0005 | t0001 | g0111 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01106 | hp2 | a0001 | c0004 | t0003 | g0058 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0130 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01167 | hp2 | a0001 | c0004 | t0003 | g0062 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01168 | hp2 | a0001 | c0004 | t0003 | g0065 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01192 | hp1 | a0004 | c0005 | t0001 | g0002 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0161 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01256 | hp1 | a0002 | c0003 | t0015 | g0138 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01257 | hp1 | a0001 | c0004 | t0003 | g0010 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0096 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01258 | hp1 | a0001 | c0004 | t0003 | g0010 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01261 | hp2 | a0002 | c0020 | t0001 | g0137 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0094 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01358 | hp1 | a0004 | c0005 | t0001 | g0002 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01358 | hp2 | a0001 | c0004 | t0003 | g0060 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0302 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01433 | hp2 | a0001 | c0010 | t0001 | g0305 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0290 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0303 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01891 | hp2 | a0013 | c0026 | t0007 | g0147 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01978 | hp1 | a0001 | c0004 | t0003 | g0061 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0136 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0012 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0209 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02055 | hp1 | a0001 | c0028 | t0001 | g0204 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0156 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02056 | hp2 | a0001 | c0001 | t0010 | g0257 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02080 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02080 | hp2 | a0004 | c0005 | t0001 | g0086 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02145 | hp1 | a0003 | c0009 | t0005 | g0034 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02257 | hp2 | a0001 | c0010 | t0001 | g0050 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02258 | hp1 | a0017 | c0016 | t0008 | g0056 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02258 | hp2 | a0005 | c0006 | t0001 | g0043 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0087 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02293 | hp1 | a0004 | c0005 | t0001 | g0129 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02300 | hp2 | a0004 | c0005 | t0001 | g0002 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02451 | hp2 | a0005 | c0006 | t0001 | g0042 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02572 | hp1 | a0003 | c0011 | t0001 | g0011 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02602 | hp2 | a0001 | c0004 | t0003 | g0151 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02615 | hp2 | a0001 | c0027 | t0001 | g0167 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02622 | hp1 | a0008 | c0018 | t0002 | g0222 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02622 | hp2 | a0003 | c0033 | t0004 | g0205 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02630 | hp2 | a0005 | c0006 | t0001 | g0044 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02647 | hp2 | a0006 | c0014 | t0005 | g0026 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0073 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0079 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0162 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02738 | hp1 | a0001 | c0004 | t0003 | g0152 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02738 | hp2 | a0003 | c0034 | t0008 | g0125 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02809 | hp1 | a0005 | c0006 | t0001 | g0038 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02886 | hp1 | a0003 | c0011 | t0001 | g0143 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02895 | hp1 | a0001 | c0010 | t0001 | g0009 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0008 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02897 | hp1 | a0005 | c0006 | t0001 | g0008 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02922 | hp1 | a0005 | c0006 | t0001 | g0039 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02965 | hp1 | a0001 | c0004 | t0003 | g0064 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02970 | hp1 | a0003 | c0011 | t0001 | g0074 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02976 | hp1 | a0005 | c0006 | t0001 | g0041 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03098 | hp2 | a0003 | c0031 | t0014 | g0171 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03139 | hp1 | a0001 | c0010 | t0001 | g0009 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03139 | hp2 | a0003 | c0011 | t0001 | g0011 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03195 | hp1 | a0001 | c0013 | t0001 | g0052 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03209 | hp1 | a0001 | c0017 | t0003 | g0066 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0133 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0090 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03225 | hp2 | a0016 | c0015 | t0004 | g0055 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0101 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03239 | hp2 | a0001 | c0004 | t0003 | g0063 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03453 | hp1 | a0003 | c0009 | t0005 | g0165 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03486 | hp1 | a0005 | c0006 | t0001 | g0037 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03486 | hp2 | a0001 | c0008 | t0007 | g0022 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03490 | hp2 | a0002 | c0012 | t0001 | g0109 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0141 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0131 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0140 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0155 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0132 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0157 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03579 | hp1 | a0003 | c0032 | t0001 | g0216 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0126 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0071 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03710 | hp2 | a0001 | c0004 | t0003 | g0149 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03942 | hp2 | a0012 | c0025 | t0001 | g0164 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04184 | hp1 | a0002 | c0012 | t0001 | g0082 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0124 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0070 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG04228 | hp2 | a0002 | c0003 | t0001 | g0072 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18522 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18906 | hp2 | a0003 | c0009 | t0005 | g0034 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18940 | hp2 | a0004 | c0005 | t0001 | g0115 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18942 | hp1 | a0001 | c0029 | t0002 | g0311 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18942 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18947 | hp2 | a0002 | c0007 | t0001 | g0120 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18948 | hp1 | a0001 | c0008 | t0001 | g0295 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18950 | hp2 | a0001 | c0008 | t0001 | g0298 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18952 | hp1 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18952 | hp2 | a0009 | c0019 | t0001 | g0122 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0105 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18954 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18959 | hp1 | a0001 | c0008 | t0001 | g0286 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18962 | hp2 | a0002 | c0007 | t0001 | g0036 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0272 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18966 | hp1 | a0002 | c0007 | t0001 | g0119 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18979 | hp1 | a0004 | c0005 | t0001 | g0116 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18980 | hp2 | a0004 | c0005 | t0001 | g0017 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18989 | hp1 | a0001 | c0008 | t0001 | g0297 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18989 | hp2 | a0002 | c0007 | t0001 | g0127 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18993 | hp1 | a0010 | c0021 | t0001 | g0123 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19003 | hp1 | a0002 | c0007 | t0001 | g0108 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19043 | hp1 | a0003 | c0009 | t0005 | g0020 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19055 | hp1 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19055 | hp2 | a0004 | c0005 | t0001 | g0092 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19062 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19065 | hp1 | a0002 | c0007 | t0001 | g0035 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19068 | hp1 | a0011 | c0023 | t0001 | g0017 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19080 | hp2 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19081 | hp2 | a0002 | c0007 | t0001 | g0121 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19083 | hp1 | a0003 | c0030 | t0001 | g0291 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19087 | hp2 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19090 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19240 | hp1 | a0006 | c0014 | t0005 | g0026 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20129 | hp1 | a0015 | c0035 | t0008 | g0045 | AFR | ASW | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ASW | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0199 | EUR | TSI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20805 | hp2 | a0014 | c0024 | t0001 | g0170 | EUR | TSI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20905 | hp1 | a0001 | c0002 | t0013 | g0163 | SAS | GIH | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | GIH | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02109 | hp1 | a0001 | c0008 | t0007 | g0022 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02109 | hp2 | a0001 | c0010 | t0001 | g0054 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02486 | hp1 | a0001 | c0010 | t0001 | g0051 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0158 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0159 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG06807 | hp1 | a0005 | c0006 | t0001 | g0040 | AFR | USA | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | USA | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18955 | hp1 | a0002 | c0007 | t0001 | g0100 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA21309 | hp1 | a0001 | c0013 | t0001 | g0053 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
NA21309 | hp2 | a0003 | c0009 | t0005 | g0020 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0103 | REF | REF | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0210 | REF | REF | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24442493
|
G | C | 2 | a0016a0017 | 2 | HG02258.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.73G>C | p.Glu25Gln | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 156/3367 | 73/2265 | 25/754 | chr8 | 24442493 | ||
chr8:24447190
|
C | T | 1 | a0007 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.161C>T | p.Thr54Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/22 | 244/3367 | 161/2265 | 54/754 | chr8 | 24447190 | ||
chr8:24447241
|
T | C | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.212T>C | p.Val71Ala | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/22 | 295/3367 | 212/2265 | 71/754 | chr8 | 24447241 | ||
chr8:24468800
|
A | G | 2 | a0015a0017 | 2 | HG02258.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.613A>G | p.Ile205Val | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/22 | 696/3367 | 613/2265 | 205/754 | chr8 | 24468800 | ||
chr8:24482166
|
G | A | 5 | a0002a0004a0009others(2): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
missense_variant | MODERATE | c.730G>A | p.Val244Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/22 | 813/3367 | 730/2265 | 244/754 | chr8 | 24482166 | ||
chr8:24482227
|
T | C | 1 | a0014 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.791T>C | p.Ile264Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/22 | 874/3367 | 791/2265 | 264/754 | chr8 | 24482227 | ||
chr8:24487298
|
G | A | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1072G>A | p.Val358Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/22 | 1155/3367 | 1072/2265 | 358/754 | chr8 | 24487298 | ||
chr8:24487317
|
G | A | 1 | a0009 | 1 | NA18952.hp2 | missense_variant&splice_region_variant | MODERATE | c.1091G>A | p.Ser364Asn | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/22 | 1174/3367 | 1091/2265 | 364/754 | chr8 | 24487317 | ||
chr8:24490841
|
A | G | 1 | a0011 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1309A>G | p.Lys437Glu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1392/3367 | 1309/2265 | 437/754 | chr8 | 24490841 | ||
chr8:24490842
|
A | T | 1 | a0011 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1310A>T | p.Lys437Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1393/3367 | 1310/2265 | 437/754 | chr8 | 24490842 | ||
chr8:24491904
|
T | C | 2 | a0004a0011 | 11 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(8): Show |
missense_variant&splice_region_variant | MODERATE | c.1358T>C | p.Ile453Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/22 | 1441/3367 | 1358/2265 | 453/754 | chr8 | 24491904 | ||
chr8:24492049
|
G | A | 1 | a0013 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1503G>A | p.Met501Ile | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/22 | 1586/3367 | 1503/2265 | 501/754 | chr8 | 24492049 | ||
chr8:24499305
|
A | C | 11 | a0002a0003a0004others(8): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
missense_variant | MODERATE | c.1912A>C | p.Asn638His | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/22 | 1995/3367 | 1912/2265 | 638/754 | chr8 | 24499305 | ||
chr8:24500837
|
G | A | 1 | a0010 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.2050G>A | p.Gly684Arg | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/22 | 2133/3367 | 2050/2265 | 684/754 | chr8 | 24500837 | ||
chr8:24501572
|
T | C | 1 | a0005 | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.2204T>C | p.Leu735Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/22 | 2287/3367 | 2204/2265 | 735/754 | chr8 | 24501572 | ||
chr8:24507484
|
C | T | 1 | a0006 | 2 | HG02647.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.2213C>T | p.Pro738Leu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/22 | 2296/3367 | 2213/2265 | 738/754 | chr8 | 24507484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24442528
|
T | C | 1 | a0002c0012 | 2 | HG03490.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.108T>C | p.Pro36Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 191/3367 | 108/2265 | 36/754 | chr8 | 24442528 | ||
chr8:24442558
|
C | A | 1 | a0001c0017 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.138C>A | p.Thr46Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 221/3367 | 138/2265 | 46/754 | chr8 | 24442558 | ||
chr8:24465731
|
C | T | 1 | a0008c0018 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.345C>T | p.His115His | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/22 | 428/3367 | 345/2265 | 115/754 | chr8 | 24465731 | ||
chr8:24489327
|
T | C | 1 | a0002c0020 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1260T>C | p.Pro420Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/22 | 1343/3367 | 1260/2265 | 420/754 | chr8 | 24489327 | ||
chr8:24490849
|
A | T | 1 | a0011c0023 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1317A>T | p.Gly439Gly | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1400/3367 | 1317/2265 | 439/754 | chr8 | 24490849 | ||
chr8:24492592
|
G | A | 1 | a0005c0006 | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.1650G>A | p.Glu550Glu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/22 | 1733/3367 | 1650/2265 | 550/754 | chr8 | 24492592 | ||
chr8:24493202
|
G | A | 2 | a0001c0004a0001c0017 | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
synonymous_variant | LOW | c.1815G>A | p.Ala605Ala | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/22 | 1898/3367 | 1815/2265 | 605/754 | chr8 | 24493202 | ||
chr8:24501555
|
G | A | 10 | a0002c0003a0002c0007a0002c0012others(7): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
synonymous_variant | LOW | c.2187G>A | p.Leu729Leu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/22 | 2270/3367 | 2187/2265 | 729/754 | chr8 | 24501555 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24441058
|
T | C | 1 | a0001c0001t0009 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 51 | chr8 | 24441058 | |||||
chr8:24441070
|
C | T | 1 | a0002c0003t0015 | 1 | HG01256.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 39 | chr8 | 24441070 | |||||
chr8:24441079
|
T | G | 2 | a0001c0008t0007a0013c0026t0007 | 3 | HG01891.hp2 HG02109.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-30T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 30 | chr8 | 24441079 | |||||
chr8:24508703
|
A | C | 3 | a0003c0009t0005a0003c0031t0014a0006c0014t0005 | 10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*157A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 157 | chr8 | 24508703 | |||||
chr8:24508824
|
T | C | 2 | a0003c0009t0005a0006c0014t0005 | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 278 | chr8 | 24508824 | |||||
chr8:24509016
|
G | A | 2 | a0003c0009t0005a0006c0014t0005 | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 470 | chr8 | 24509016 | |||||
chr8:24509042
|
C | T | 2 | a0003c0009t0005a0006c0014t0005 | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 496 | chr8 | 24509042 | |||||
chr8:24509107
|
T | C | 1 | a0001c0001t0010 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 561 | chr8 | 24509107 | |||||
chr8:24509147
|
T | C | 2 | a0001c0004t0003a0001c0017t0003 | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 601 | chr8 | 24509147 | |||||
chr8:24509199
|
CAG | C | 3 | a0001c0002t0004a0003c0033t0004a0016c0015t0004 | 10 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*658delGA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 657 | INFO_REALIGN_3_PRIME | chr8 | 24509199 | ||||
chr8:24509367
|
A | G | 44 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(41): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*821A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 821 | chr8 | 24509367 | |||||
chr8:24509381
|
G | T | 32 | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(29): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*835G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 835 | chr8 | 24509381 | |||||
chr8:24509498
|
T | C | 1 | a0002c0003t0012 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 952 | chr8 | 24509498 | |||||
chr8:24509520
|
A | G | 37 | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(34): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*974A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 974 | chr8 | 24509520 | |||||
chr8:24509529
|
C | T | 1 | a0001c0002t0013 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 983 | chr8 | 24509529 | |||||
chr8:24509530
|
G | A | 1 | a0001c0001t0011 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*984G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 984 | chr8 | 24509530 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24441385
|
A | G | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+225A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441385 | ||||||
chr8:24441494
|
G | C | 2 | a0002c0007t0001g0035a0002c0007t0001g0036 | 2 | NA18962.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.52+334G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441494 | ||||||
chr8:24441756
|
G | A | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.52+596G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441756 | ||||||
chr8:24441781
|
A | G | 3 | a0003c0009t0005g0034a0003c0009t0005g0317a0003c0009t0005g0318 | 4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+621A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441781 | ||||||
chr8:24441911
|
T | C | 202 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0046others(199): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.53-562T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441911 | ||||||
chr8:24441917
|
T | C | 2 | a0016c0015t0004g0055a0017c0016t0008g0056 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.53-556T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441917 | ||||||
chr8:24442003
|
G | A | 14 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(11): Show | 15 | HG00733.hp2 HG00735.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-470G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442003 | ||||||
chr8:24442132
|
C | CCACT | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0003t0001g0072 | 3 | HG03710.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53-340_53-337dupCA others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 24442132 | |||||
chr8:24442137
|
A | G | 316 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(313): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.53-336A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442137 | ||||||
chr8:24442195
|
A | G | 1 | a0002c0003t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.53-278A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442195 | ||||||
chr8:24442261
|
T | C | 1 | a0002c0003t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.53-212T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442261 | ||||||
chr8:24442357
|
C | T | 9 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(6): Show | 10 | HG01106.hp1 HG01361.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-116C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442357 | ||||||
chr8:24442470
|
T | C | 2 | a0003c0011t0001g0011a0003c0011t0001g0074 | 3 | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.53-3T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442470 | ||||||
chr8:24442639
|
T | A | 1 | a0001c0001t0002g0075 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.156+63T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442639 | ||||||
chr8:24442821
|
C | CT | 238 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0024others(235): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.156+248dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24442821 | |||||
chr8:24442836
|
A | G | 3 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285 | 3 | NA18995.hp1 NA19002.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.156+260A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442836 | ||||||
chr8:24442912
|
T | C | 87 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(84): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.156+336T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442912 | ||||||
chr8:24442926
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.156+350T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442926 | ||||||
chr8:24443057
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.156+481C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443057 | ||||||
chr8:24443209
|
T | C | 1 | a0002c0003t0001g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.156+633T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443209 | ||||||
chr8:24443303
|
C | G | 4 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+727C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443303 | ||||||
chr8:24443393
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.156+817T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443393 | ||||||
chr8:24443443
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(24): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+867G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443443 | ||||||
chr8:24443542
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.156+966C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443542 | ||||||
chr8:24443608
|
A | G | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(24): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+1032A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443608 | ||||||
chr8:24443719
|
C | T | 1 | a0003c0033t0004g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.156+1143C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443719 | ||||||
chr8:24443720
|
G | A | 1 | a0002c0003t0001g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.156+1144G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443720 | ||||||
chr8:24443726
|
C | T | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+1150C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443726 | ||||||
chr8:24443852
|
T | C | 1 | a0013c0026t0007g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.156+1276T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443852 | ||||||
chr8:24443861
|
G | C | 3 | a0002c0003t0001g0012a0002c0003t0001g0078a0002c0003t0001g0079 | 4 | HG00738.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1285G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443861 | ||||||
chr8:24443886
|
A | T | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.156+1310A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443886 | ||||||
chr8:24443939
|
A | AAAAAT | 13 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0048others(10): Show | 15 | HG00642.hp1 HG00741.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+1398_156+1402d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | |||||
chr8:24443939
|
AAAAAT | A | 189 | a0001c0001t0002g0095a0001c0001t0002g0174a0001c0001t0002g0215others(186): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.156+1398_156+1402d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | |||||
chr8:24443939
|
AAAAATAA others(3): Show |
A | 2 | a0001c0001t0002g0047a0002c0003t0001g0080 | 2 | HG01106.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.156+1393_156+1402d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | |||||
chr8:24443939
|
AAAAATAA others(13): Show |
A | 1 | a0001c0002t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.156+1383_156+1402d others(22): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | |||||
chr8:24443954
|
T | A | 1 | a0001c0008t0001g0286 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.156+1378T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443954 | ||||||
chr8:24444309
|
G | T | 2 | a0002c0007t0001g0035a0002c0007t0001g0036 | 2 | NA18962.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.156+1733G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444309 | ||||||
chr8:24444365
|
G | A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+1789G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444365 | ||||||
chr8:24444548
|
G | A | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+1972G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444548 | ||||||
chr8:24444679
|
C | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG00673.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.156+2103C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444679 | ||||||
chr8:24444680
|
G | A | 4 | a0001c0002t0001g0019a0001c0002t0001g0148a0001c0002t0001g0153others(1): Show | 5 | HG01192.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+2104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444680 | ||||||
chr8:24444691
|
A | C | 42 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(39): Show | 49 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+2115A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444691 | ||||||
chr8:24444695
|
C | CA | 4 | a0001c0001t0002g0048a0001c0001t0002g0217a0002c0003t0001g0076others(1): Show | 4 | HG01934.hp2 HG02027.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+2126dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24444695 | |||||
chr8:24444731
|
C | G | 319 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.156+2155C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444731 | ||||||
chr8:24444760
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.156+2184C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444760 | ||||||
chr8:24444856
|
A | C | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.156+2280A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444856 | ||||||
chr8:24444861
|
G | C | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.156+2285G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444861 | ||||||
chr8:24444913
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157-2273A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444913 | ||||||
chr8:24445148
|
C | T | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-2038C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445148 | ||||||
chr8:24445229
|
A | G | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-1957A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445229 | ||||||
chr8:24445262
|
C | G | 1 | a0001c0002t0001g0306 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.157-1924C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445262 | ||||||
chr8:24445281
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.157-1905C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445281 | ||||||
chr8:24445282
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.157-1904G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445282 | ||||||
chr8:24445310
|
C | T | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(24): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.157-1876C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445310 | ||||||
chr8:24445367
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.157-1819A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445367 | ||||||
chr8:24445433
|
A | G | 1 | a0002c0003t0001g0142 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.157-1753A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445433 | ||||||
chr8:24445479
|
T | C | 1 | a0001c0002t0004g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.157-1707T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445479 | ||||||
chr8:24445479
|
T | G | 1 | a0001c0001t0002g0309 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.157-1707T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445479 | ||||||
chr8:24445563
|
G | C | 203 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(200): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.157-1623G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445563 | ||||||
chr8:24445574
|
T | A | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1612T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445574 | ||||||
chr8:24445657
|
G | T | 121 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(118): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.157-1529G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445657 | ||||||
chr8:24445760
|
T | A | 1 | a0002c0012t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.157-1426T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445760 | ||||||
chr8:24445856
|
T | C | 1 | a0001c0002t0013g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.157-1330T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445856 | ||||||
chr8:24446020
|
G | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-1166G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446020 | ||||||
chr8:24446049
|
G | A | 1 | a0012c0025t0001g0164 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.157-1137G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446049 | ||||||
chr8:24446070
|
A | G | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.157-1116A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446070 | ||||||
chr8:24446101
|
T | C | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-1085T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446101 | ||||||
chr8:24446187
|
A | T | 79 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(76): Show | 90 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.157-999A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446187 | ||||||
chr8:24446652
|
T | C | 1 | a0002c0003t0001g0083 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.157-534T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446652 | ||||||
chr8:24446672
|
C | G | 238 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0024others(235): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.157-514C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446672 | ||||||
chr8:24446727
|
GA | G | 2 | a0003c0011t0001g0011a0003c0011t0001g0074 | 3 | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.157-458delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446727 | ||||||
chr8:24446756
|
C | T | 6 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(3): Show | 6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-430C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446756 | ||||||
chr8:24447405
|
A | C | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+143A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447405 | ||||||
chr8:24447438
|
G | T | 1 | a0001c0002t0001g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.233+176G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447438 | ||||||
chr8:24447444
|
C | T | 34 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(31): Show | 38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+182C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447444 | ||||||
chr8:24447450
|
T | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0309a0001c0001t0002g0310others(2): Show | 7 | HG02015.hp1 NA18612.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+188T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447450 | ||||||
chr8:24447457
|
G | C | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+195G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447457 | ||||||
chr8:24447464
|
C | T | 183 | a0001c0001t0002g0095a0001c0001t0002g0174a0001c0002t0001g0005others(180): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.233+202C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447464 | ||||||
chr8:24447679
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.233+417G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447679 | ||||||
chr8:24447794
|
C | T | 183 | a0001c0001t0002g0095a0001c0001t0002g0174a0001c0002t0001g0005others(180): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.233+532C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447794 | ||||||
chr8:24447840
|
T | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0168a0001c0027t0001g0167 | 3 | HG02280.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.233+578T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447840 | ||||||
chr8:24447840
|
T | C | 1 | a0001c0002t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.233+578T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447840 | ||||||
chr8:24447886
|
A | G | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+624A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447886 | ||||||
chr8:24447936
|
A | C | 1 | a0002c0003t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.233+674A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447936 | ||||||
chr8:24447937
|
A | AAC | 47 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(44): Show | 54 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.233+721_233+722dup others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
A | AACAC | 15 | a0001c0001t0002g0032a0001c0001t0002g0198a0001c0001t0002g0199others(12): Show | 16 | HG01516.hp1 HG01517.hp1 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+719_233+722dup others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
A | AACACAC | 6 | a0001c0001t0002g0024a0001c0001t0002g0201a0001c0001t0002g0276others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+717_233+722dup others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AAC | A | 52 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0174others(49): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.233+721_233+722del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACAC | A | 57 | a0001c0001t0002g0095a0001c0001t0002g0223a0001c0001t0002g0224others(54): Show | 67 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.233+719_233+722del others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACAC | A | 17 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0002t0001g0025others(14): Show | 18 | HG01070.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+717_233+722del others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(1): Show |
A | 10 | a0001c0002t0001g0085a0001c0002t0001g0166a0001c0002t0001g0169others(7): Show | 10 | HG01243.hp1 HG02129.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+715_233+722del others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(3): Show |
A | 28 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0184others(25): Show | 35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.233+713_233+722del others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(5): Show |
A | 11 | a0002c0003t0001g0084a0005c0006t0001g0008a0005c0006t0001g0037others(8): Show | 12 | HG02071.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.233+711_233+722del others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(7): Show |
A | 3 | a0001c0002t0001g0033a0003c0033t0004g0205a0016c0015t0004g0055 | 4 | HG01123.hp2 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+709_233+722del others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.233+707_233+722del others(16): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24447937
|
AACACACA others(11): Show |
A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+705_233+722del others(18): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | |||||
chr8:24448352
|
T | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1090T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448352 | ||||||
chr8:24448364
|
C | T | 1 | a0001c0002t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.233+1102C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448364 | ||||||
chr8:24448397
|
T | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+1135T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448397 | ||||||
chr8:24448440
|
A | G | 2 | a0003c0009t0005g0020a0003c0009t0005g0165 | 3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.233+1178A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448440 | ||||||
chr8:24448646
|
C | T | 5 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0001g0106others(2): Show | 5 | NA18943.hp1 NA18944.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+1384C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448646 | ||||||
chr8:24448657
|
T | TTTA | 28 | a0001c0001t0002g0007a0001c0001t0002g0200a0001c0001t0002g0309others(25): Show | 37 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.233+1421_233+1423d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | |||||
chr8:24448657
|
T | TTTATTA | 4 | a0001c0001t0002g0313a0001c0001t0002g0315a0001c0001t0002g0316others(1): Show | 4 | HG01517.hp2 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1418_233+1423d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | |||||
chr8:24448657
|
TTTA | T | 174 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(171): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.233+1421_233+1423d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | |||||
chr8:24448735
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.233+1473G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448735 | ||||||
chr8:24448815
|
A | C | 1 | a0002c0003t0015g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+1553A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448815 | ||||||
chr8:24448829
|
T | C | 1 | a0005c0006t0001g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+1567T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448829 | ||||||
chr8:24448861
|
T | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1599T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448861 | ||||||
chr8:24448899
|
G | A | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0010t0001g0050 | 3 | HG02257.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.233+1637G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448899 | ||||||
chr8:24449183
|
C | G | 2 | a0001c0001t0002g0285a0003c0032t0001g0216 | 2 | HG03579.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.233+1921C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449183 | ||||||
chr8:24449256
|
T | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1994T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449256 | ||||||
chr8:24449275
|
TAA | T | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+2016_233+2017d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24449275 | |||||
chr8:24449276
|
A | G | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+2014A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449276 | ||||||
chr8:24449407
|
C | T | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(26): Show | 37 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.233+2145C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449407 | ||||||
chr8:24449471
|
A | G | 1 | a0001c0001t0002g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.233+2209A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449471 | ||||||
chr8:24449474
|
G | T | 203 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(200): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.233+2212G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449474 | ||||||
chr8:24449480
|
G | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2218G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449480 | ||||||
chr8:24449534
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.233+2272A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449534 | ||||||
chr8:24449573
|
C | T | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+2311C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449573 | ||||||
chr8:24449574
|
G | A | 1 | a0003c0031t0014g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.233+2312G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449574 | ||||||
chr8:24449616
|
A | G | 1 | a0001c0002t0001g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+2354A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449616 | ||||||
chr8:24449660
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.233+2398C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449660 | ||||||
chr8:24449677
|
G | T | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+2415G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449677 | ||||||
chr8:24449787
|
A | G | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+2525A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449787 | ||||||
chr8:24449789
|
A | C | 1 | a0001c0002t0001g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.233+2527A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449789 | ||||||
chr8:24449830
|
G | A | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+2568G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449830 | ||||||
chr8:24449833
|
G | A | 6 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+2571G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449833 | ||||||
chr8:24449926
|
T | C | 5 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(2): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+2664T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449926 | ||||||
chr8:24449937
|
T | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2675T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449937 | ||||||
chr8:24449951
|
G | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+2689G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449951 | ||||||
chr8:24450024
|
T | C | 44 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0024others(41): Show | 48 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.233+2762T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450024 | ||||||
chr8:24450025
|
G | C | 44 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0024others(41): Show | 48 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.233+2763G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450025 | ||||||
chr8:24450082
|
A | C | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2820A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450082 | ||||||
chr8:24450125
|
C | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2863C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450125 | ||||||
chr8:24450131
|
G | A | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2869G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450131 | ||||||
chr8:24450153
|
C | G | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2891C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450153 | ||||||
chr8:24450257
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.233+2995C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450257 | ||||||
chr8:24450307
|
G | T | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+3045G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450307 | ||||||
chr8:24450365
|
C | T | 57 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(54): Show | 65 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.233+3103C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450365 | ||||||
chr8:24450366
|
G | A | 22 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(19): Show | 25 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.233+3104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450366 | ||||||
chr8:24450450
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.233+3188T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450450 | ||||||
chr8:24450549
|
G | A | 1 | a0017c0016t0008g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.233+3287G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450549 | ||||||
chr8:24450583
|
G | A | 22 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(19): Show | 25 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.233+3321G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450583 | ||||||
chr8:24450601
|
G | A | 2 | a0002c0003t0001g0013a0002c0003t0001g0089 | 3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.233+3339G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450601 | ||||||
chr8:24450603
|
C | T | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+3341C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450603 | ||||||
chr8:24450715
|
C | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3453C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450715 | ||||||
chr8:24450777
|
G | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+3515G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450777 | ||||||
chr8:24450793
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3531G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450793 | ||||||
chr8:24450802
|
T | C | 1 | a0001c0001t0002g0283 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.233+3540T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450802 | ||||||
chr8:24450825
|
T | C | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+3563T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450825 | ||||||
chr8:24450837
|
G | A | 83 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(80): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.233+3575G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450837 | ||||||
chr8:24450853
|
G | A | 5 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0271others(2): Show | 5 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+3591G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450853 | ||||||
chr8:24450861
|
G | C | 177 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(174): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.233+3599G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450861 | ||||||
chr8:24450862
|
G | A | 1 | a0005c0006t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.233+3600G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450862 | ||||||
chr8:24450883
|
C | A | 1 | a0001c0010t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.233+3621C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450883 | ||||||
chr8:24450948
|
A | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+3686A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450948 | ||||||
chr8:24450964
|
G | A | 10 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0223others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3702G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450964 | ||||||
chr8:24450964
|
G | T | 2 | a0001c0004t0003g0057a0001c0004t0003g0062 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.233+3702G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450964 | ||||||
chr8:24451032
|
T | C | 87 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(84): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.233+3770T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451032 | ||||||
chr8:24451044
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233+3782C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451044 | ||||||
chr8:24451055
|
C | T | 1 | a0001c0002t0001g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233+3793C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451055 | ||||||
chr8:24451080
|
A | T | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+3818A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451080 | ||||||
chr8:24451174
|
T | G | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233+3912T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451174 | ||||||
chr8:24451281
|
C | G | 13 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(10): Show | 15 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.233+4019C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451281 | ||||||
chr8:24451282
|
G | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+4020G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451282 | ||||||
chr8:24451304
|
A | G | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+4042A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451304 | ||||||
chr8:24451329
|
C | T | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.233+4067C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451329 | ||||||
chr8:24451335
|
A | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+4073A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451335 | ||||||
chr8:24451366
|
G | A | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.233+4104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451366 | ||||||
chr8:24451382
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.233+4120G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451382 | ||||||
chr8:24451435
|
G | A | 84 | a0001c0001t0002g0095a0001c0002t0001g0027a0001c0002t0001g0085others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.233+4173G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451435 | ||||||
chr8:24451486
|
G | A | 1 | a0001c0001t0006g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+4224G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451486 | ||||||
chr8:24451490
|
G | A | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG00673.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.233+4228G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451490 | ||||||
chr8:24451518
|
C | T | 26 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(23): Show | 28 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.233+4256C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451518 | ||||||
chr8:24451538
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(19): Show | 29 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.233+4276C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451538 | ||||||
chr8:24451567
|
T | C | 1 | a0017c0016t0008g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.233+4305T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451567 | ||||||
chr8:24451569
|
T | C | 1 | a0002c0003t0015g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+4307T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451569 | ||||||
chr8:24451699
|
C | A | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0004t0003g0057others(1): Show | 4 | HG00735.hp2 HG01167.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+4437C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451699 | ||||||
chr8:24451761
|
T | A | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+4499T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451761 | ||||||
chr8:24451780
|
G | A | 1 | a0002c0003t0001g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.233+4518G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451780 | ||||||
chr8:24451955
|
C | T | 1 | a0002c0020t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.233+4693C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451955 | ||||||
chr8:24451983
|
G | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.233+4721G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451983 | ||||||
chr8:24452013
|
G | T | 1 | a0003c0011t0001g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+4751G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452013 | ||||||
chr8:24452055
|
G | A | 1 | a0001c0004t0003g0058 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.233+4793G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452055 | ||||||
chr8:24452198
|
G | A | 182 | a0001c0001t0002g0095a0001c0001t0002g0174a0001c0002t0001g0005others(179): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.233+4936G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452198 | ||||||
chr8:24452209
|
A | G | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+4947A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452209 | ||||||
chr8:24452222
|
G | A | 1 | a0016c0015t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.233+4960G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452222 | ||||||
chr8:24452296
|
C | T | 125 | a0001c0001t0002g0095a0001c0002t0001g0005a0001c0002t0001g0006others(122): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.233+5034C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452296 | ||||||
chr8:24452319
|
C | T | 1 | a0002c0003t0001g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233+5057C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452319 | ||||||
chr8:24452338
|
A | G | 2 | a0005c0006t0001g0043a0005c0006t0001g0044 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.233+5076A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452338 | ||||||
chr8:24452441
|
C | A | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.233+5179C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452441 | ||||||
chr8:24452455
|
A | C | 83 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(80): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.233+5193A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452455 | ||||||
chr8:24452493
|
C | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+5231C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452493 | ||||||
chr8:24452575
|
G | C | 1 | a0005c0006t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.233+5313G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452575 | ||||||
chr8:24452641
|
T | C | 2 | a0005c0006t0001g0008a0005c0006t0001g0038 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.233+5379T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452641 | ||||||
chr8:24452717
|
G | C | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+5455G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452717 | ||||||
chr8:24452759
|
A | G | 1 | a0001c0002t0013g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+5497A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452759 | ||||||
chr8:24452810
|
C | A | 21 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(18): Show | 24 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.233+5548C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452810 | ||||||
chr8:24452885
|
G | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+5623G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452885 | ||||||
chr8:24452921
|
G | T | 2 | a0005c0006t0001g0008a0005c0006t0001g0038 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.233+5659G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452921 | ||||||
chr8:24452981
|
C | T | 2 | a0003c0009t0005g0020a0003c0009t0005g0165 | 3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.233+5719C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452981 | ||||||
chr8:24453010
|
C | T | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+5748C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453010 | ||||||
chr8:24453011
|
G | A | 1 | a0001c0001t0002g0278 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.233+5749G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453011 | ||||||
chr8:24453033
|
T | C | 1 | a0003c0009t0005g0165 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+5771T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453033 | ||||||
chr8:24453055
|
C | T | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+5793C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453055 | ||||||
chr8:24453128
|
G | C | 4 | a0001c0002t0001g0144a0001c0002t0001g0145a0003c0033t0004g0205others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+5866G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453128 | ||||||
chr8:24453164
|
A | G | 1 | a0001c0028t0001g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233+5902A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453164 | ||||||
chr8:24453259
|
TC | T | 4 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+5999delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24453259 | |||||
chr8:24453292
|
C | G | 88 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(85): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.233+6030C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453292 | ||||||
chr8:24453296
|
C | T | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(24): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.233+6034C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453296 | ||||||
chr8:24453320
|
T | C | 2 | a0001c0001t0002g0224a0001c0001t0002g0231 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.233+6058T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453320 | ||||||
chr8:24453384
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.233+6122G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453384 | ||||||
chr8:24453479
|
C | T | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+6217C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453479 | ||||||
chr8:24453651
|
C | T | 1 | a0001c0002t0001g0025 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.233+6389C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453651 | ||||||
chr8:24453683
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+6421G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453683 | ||||||
chr8:24453724
|
G | A | 15 | a0001c0001t0002g0174a0001c0002t0001g0166a0001c0002t0001g0168others(12): Show | 15 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.233+6462G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453724 | ||||||
chr8:24453734
|
A | T | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+6472A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453734 | ||||||
chr8:24453815
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.233+6553A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453815 | ||||||
chr8:24453942
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233+6680G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453942 | ||||||
chr8:24453979
|
G | A | 5 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+6717G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453979 | ||||||
chr8:24453999
|
A | G | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.233+6737A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453999 | ||||||
chr8:24454032
|
C | T | 1 | a0008c0018t0002g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.233+6770C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454032 | ||||||
chr8:24454230
|
T | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+6968T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454230 | ||||||
chr8:24454358
|
C | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7096C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454358 | ||||||
chr8:24454362
|
C | A | 1 | a0001c0001t0002g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.233+7100C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454362 | ||||||
chr8:24454386
|
G | A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7124G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454386 | ||||||
chr8:24454453
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.233+7191G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454453 | ||||||
chr8:24454459
|
G | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7197G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454459 | ||||||
chr8:24454464
|
G | A | 34 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(31): Show | 38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+7202G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454464 | ||||||
chr8:24454470
|
T | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+7208T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454470 | ||||||
chr8:24454533
|
C | T | 1 | a0001c0001t0002g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+7271C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454533 | ||||||
chr8:24454570
|
A | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7308A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454570 | ||||||
chr8:24454573
|
A | C | 1 | a0001c0004t0003g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.233+7311A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454573 | ||||||
chr8:24454624
|
C | T | 1 | a0002c0003t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+7362C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454624 | ||||||
chr8:24454651
|
G | A | 1 | a0002c0003t0001g0084 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.233+7389G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454651 | ||||||
chr8:24454677
|
G | C | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+7415G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454677 | ||||||
chr8:24454705
|
G | A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7443G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454705 | ||||||
chr8:24454713
|
A | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.233+7451A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454713 | ||||||
chr8:24454754
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(24): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.233+7492G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454754 | ||||||
chr8:24454770
|
C | T | 1 | a0005c0006t0001g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+7508C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454770 | ||||||
chr8:24454828
|
T | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7566T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454828 | ||||||
chr8:24454838
|
T | C | 9 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0148others(6): Show | 11 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+7576T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454838 | ||||||
chr8:24454949
|
C | T | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+7687C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454949 | ||||||
chr8:24455042
|
G | A | 1 | a0001c0001t0010g0257 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233+7780G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455042 | ||||||
chr8:24455111
|
T | C | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+7849T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455111 | ||||||
chr8:24455193
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.233+7931C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455193 | ||||||
chr8:24455392
|
A | G | 1 | a0001c0002t0013g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+8130A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455392 | ||||||
chr8:24455504
|
G | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+8242G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455504 | ||||||
chr8:24455597
|
T | C | 4 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-8285T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455597 | ||||||
chr8:24455643
|
C | A | 1 | a0002c0007t0001g0108 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.234-8239C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455643 | ||||||
chr8:24455664
|
C | T | 1 | a0001c0002t0001g0181 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.234-8218C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455664 | ||||||
chr8:24455668
|
A | T | 1 | a0001c0001t0002g0218 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.234-8214A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455668 | ||||||
chr8:24456011
|
C | T | 2 | a0001c0001t0002g0255a0001c0001t0002g0256 | 2 | HG00099.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.234-7871C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456011 | ||||||
chr8:24456058
|
G | A | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.234-7824G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456058 | ||||||
chr8:24456212
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.234-7670G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456212 | ||||||
chr8:24456299
|
A | C | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | NA18978.hp1 NA18999.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-7583A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456299 | ||||||
chr8:24456383
|
C | T | 1 | a0002c0003t0015g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.234-7499C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456383 | ||||||
chr8:24456480
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.234-7402C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456480 | ||||||
chr8:24456503
|
G | T | 1 | a0002c0003t0001g0016 | 2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.234-7379G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456503 | ||||||
chr8:24456630
|
G | T | 1 | a0001c0001t0002g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.234-7252G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456630 | ||||||
chr8:24456632
|
AT | A | 296 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(293): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.234-7232delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24456632 | |||||
chr8:24456721
|
A | G | 4 | a0002c0007t0001g0108a0002c0007t0001g0119a0002c0007t0001g0120others(1): Show | 4 | NA18947.hp2 NA18966.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-7161A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456721 | ||||||
chr8:24456740
|
A | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(19): Show | 29 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.234-7142A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456740 | ||||||
chr8:24456759
|
T | C | 1 | a0002c0003t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.234-7123T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456759 | ||||||
chr8:24456884
|
T | C | 3 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289 | 3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.234-6998T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456884 | ||||||
chr8:24456961
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.234-6921A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456961 | ||||||
chr8:24457123
|
A | G | 1 | a0001c0004t0003g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.234-6759A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457123 | ||||||
chr8:24457213
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-6669C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457213 | ||||||
chr8:24457293
|
A | AT | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-6580dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457293 | |||||
chr8:24457310
|
C | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-6572C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457310 | ||||||
chr8:24457389
|
C | T | 2 | a0001c0002t0001g0181a0001c0002t0001g0182 | 2 | NA18999.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.234-6493C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457389 | ||||||
chr8:24457475
|
C | T | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-6407C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457475 | ||||||
chr8:24457550
|
ACAGGC | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-6331_234-6327d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457550 | ||||||
chr8:24457556
|
A | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-6326A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457556 | ||||||
chr8:24457606
|
G | A | 1 | a0008c0018t0002g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234-6276G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457606 | ||||||
chr8:24457780
|
G | C | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.234-6102G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457780 | ||||||
chr8:24457854
|
A | ATG | 5 | a0002c0003t0001g0015a0002c0003t0001g0073a0002c0003t0001g0102others(2): Show | 6 | HG00323.hp1 HG02683.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-6021_234-6020d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457854 | |||||
chr8:24457854
|
A | ATGTG | 3 | a0001c0001t0002g0313a0001c0001t0002g0315a0001c0001t0002g0316 | 3 | NA18962.hp1 NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.234-6023_234-6020d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457854 | |||||
chr8:24457855
|
T | TGTGTGTG others(1): Show |
16 | a0001c0002t0001g0021a0001c0004t0003g0010a0001c0004t0003g0057others(13): Show | 18 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-6019_234-6012d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457855 | |||||
chr8:24457861
|
TGA | T | 2 | a0002c0003t0001g0012a0002c0003t0015g0138 | 3 | HG01256.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.234-6019_234-6018d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457861 | |||||
chr8:24457863
|
A | AGT | 77 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0046others(74): Show | 84 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.234-5992_234-5991d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | |||||
chr8:24457863
|
A | AGTGT | 66 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0029others(63): Show | 74 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.234-5994_234-5991d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | |||||
chr8:24457863
|
A | AGTGTGT | 11 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(8): Show | 12 | HG01074.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-5996_234-5991d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | |||||
chr8:24457863
|
A | AGTGTGTG others(5): Show |
1 | a0001c0010t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234-6002_234-5991d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | |||||
chr8:24457863
|
A | T | 41 | a0001c0001t0002g0095a0001c0001t0002g0313a0001c0001t0002g0315others(38): Show | 48 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.234-6019A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457863 | ||||||
chr8:24457863
|
AGT | A | 17 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(14): Show | 18 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-5992_234-5991d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | |||||
chr8:24458441
|
T | C | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-5441T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458441 | ||||||
chr8:24458517
|
A | G | 11 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5365A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458517 | ||||||
chr8:24458552
|
G | A | 1 | a0001c0004t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.234-5330G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458552 | ||||||
chr8:24458602
|
C | T | 84 | a0001c0001t0002g0095a0001c0002t0001g0085a0001c0002t0001g0117others(81): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.234-5280C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458602 | ||||||
chr8:24458633
|
T | A | 7 | a0001c0001t0002g0023a0001c0001t0002g0185a0001c0001t0002g0188others(4): Show | 8 | NA18612.hp1 NA18747.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-5249T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458633 | ||||||
chr8:24458817
|
T | C | 3 | a0001c0004t0003g0059a0001c0004t0003g0063a0001c0004t0003g0150 | 3 | HG00140.hp1 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.234-5065T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458817 | ||||||
chr8:24458848
|
T | A | 1 | a0002c0003t0001g0104 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.234-5034T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458848 | ||||||
chr8:24458873
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-5009G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458873 | ||||||
chr8:24458877
|
A | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0269 | 3 | HG03834.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.234-5005A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458877 | ||||||
chr8:24459045
|
C | T | 2 | a0001c0008t0007g0022a0013c0026t0007g0147 | 3 | HG01891.hp2 HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234-4837C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459045 | ||||||
chr8:24459199
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234-4683G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459199 | ||||||
chr8:24459415
|
G | C | 1 | a0002c0003t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.234-4467G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459415 | ||||||
chr8:24459429
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.234-4453C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459429 | ||||||
chr8:24459434
|
T | TTTTA | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-4432_234-4429d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24459434 | |||||
chr8:24459622
|
G | A | 2 | a0002c0003t0001g0013a0002c0003t0001g0089 | 3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.234-4260G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459622 | ||||||
chr8:24459814
|
G | T | 1 | a0008c0018t0002g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234-4068G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459814 | ||||||
chr8:24459952
|
T | A | 3 | a0002c0003t0001g0073a0002c0003t0001g0102a0002c0003t0001g0103 | 3 | HG00323.hp1 HG02683.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.234-3930T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459952 | ||||||
chr8:24459970
|
A | AT | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3904dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24459970 | |||||
chr8:24460009
|
T | G | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-3873T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460009 | ||||||
chr8:24460083
|
AT | A | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-3792delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460083 | |||||
chr8:24460090
|
T | A | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-3792T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460090 | ||||||
chr8:24460167
|
T | A | 1 | a0002c0003t0001g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.234-3715T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460167 | ||||||
chr8:24460263
|
T | A | 1 | a0002c0020t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234-3619T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460263 | ||||||
chr8:24460385
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.234-3497C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460385 | ||||||
chr8:24460386
|
G | A | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-3496G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460386 | ||||||
chr8:24460583
|
T | C | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3299T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460583 | ||||||
chr8:24460648
|
TAA | T | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3230_234-3229d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460648 | |||||
chr8:24460650
|
A | G | 3 | a0003c0009t0005g0034a0003c0009t0005g0317a0003c0009t0005g0318 | 4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-3232A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460650 | ||||||
chr8:24460703
|
A | G | 1 | a0001c0002t0001g0033 | 2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.234-3179A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460703 | ||||||
chr8:24460751
|
ATG | A | 113 | a0001c0001t0002g0095a0001c0002t0001g0005a0001c0002t0001g0006others(110): Show | 131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.234-3115_234-3114d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460751 | |||||
chr8:24460753
|
G | A | 10 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(7): Show | 11 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-3129G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460753 | ||||||
chr8:24460765
|
GTGTA | G | 80 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(77): Show | 90 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.234-3115_234-3112d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460765 | |||||
chr8:24460767
|
G | A | 1 | a0002c0003t0012g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.234-3115G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460767 | ||||||
chr8:24460767
|
G | GTA | 5 | a0001c0001t0002g0244a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG02559.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-3097_234-3096d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460767 | |||||
chr8:24460767
|
GTATA | G | 2 | a0001c0002t0001g0021a0001c0002t0001g0177 | 3 | HG02135.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.234-3099_234-3096d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460767 | |||||
chr8:24460846
|
T | C | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-3036T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460846 | ||||||
chr8:24460869
|
CTTCTT | C | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3012_234-3008d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460869 | ||||||
chr8:24460881
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3001C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460881 | ||||||
chr8:24461246
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.234-2636C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461246 | ||||||
chr8:24461337
|
C | CCT | 239 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0024others(236): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.234-2542_234-2541d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24461337 | |||||
chr8:24461346
|
G | A | 1 | a0001c0001t0002g0245 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.234-2536G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461346 | ||||||
chr8:24461580
|
C | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0233a0001c0001t0002g0234 | 4 | HG00609.hp2 HG02132.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-2302C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461580 | ||||||
chr8:24461788
|
C | CTT | 316 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(313): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.234-2093_234-2092d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24461788 | |||||
chr8:24462032
|
T | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1850T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462032 | ||||||
chr8:24462161
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.234-1721C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462161 | ||||||
chr8:24462293
|
A | C | 1 | a0002c0003t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.234-1589A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462293 | ||||||
chr8:24462434
|
C | T | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234-1448C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462434 | ||||||
chr8:24462526
|
C | A | 3 | a0003c0009t0005g0034a0003c0009t0005g0317a0003c0009t0005g0318 | 4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-1356C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462526 | ||||||
chr8:24462597
|
C | T | 2 | a0001c0001t0002g0265a0001c0001t0002g0274 | 2 | NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.234-1285C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462597 | ||||||
chr8:24462598
|
G | A | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234-1284G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462598 | ||||||
chr8:24462613
|
G | T | 201 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(198): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.234-1269G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462613 | ||||||
chr8:24462692
|
A | C | 1 | a0001c0002t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-1190A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462692 | ||||||
chr8:24462812
|
A | G | 21 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(18): Show | 23 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-1070A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462812 | ||||||
chr8:24462907
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234-975T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462907 | ||||||
chr8:24462922
|
A | T | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(21): Show | 31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.234-960A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462922 | ||||||
chr8:24463050
|
G | C | 180 | a0001c0001t0002g0095a0001c0001t0002g0174a0001c0002t0001g0005others(177): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.234-832G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463050 | ||||||
chr8:24463151
|
C | A | 1 | a0001c0001t0002g0267 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.234-731C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463151 | ||||||
chr8:24463481
|
G | A | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.234-401G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463481 | ||||||
chr8:24463518
|
A | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.234-364A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463518 | ||||||
chr8:24463592
|
A | G | 21 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(18): Show | 23 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-290A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463592 | ||||||
chr8:24463711
|
G | C | 3 | a0002c0003t0001g0073a0002c0003t0001g0102a0002c0003t0001g0103 | 3 | HG00323.hp1 HG02683.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.234-171G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463711 | ||||||
chr8:24463983
|
G | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+23G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24463983 | ||||||
chr8:24464010
|
G | A | 1 | a0002c0003t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.312+50G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464010 | ||||||
chr8:24464053
|
G | T | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+93G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464053 | ||||||
chr8:24464262
|
A | C | 1 | a0001c0001t0002g0252 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.312+302A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464262 | ||||||
chr8:24464263
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.312+303G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464263 | ||||||
chr8:24464316
|
AC | A | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(21): Show | 31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.312+357delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464316 | ||||||
chr8:24464370
|
G | T | 6 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(3): Show | 6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+410G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464370 | ||||||
chr8:24464418
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+458G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464418 | ||||||
chr8:24464494
|
A | T | 4 | a0001c0001t0002g0030a0001c0001t0002g0032a0001c0001t0002g0255others(1): Show | 6 | HG00099.hp1 HG00140.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+534A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464494 | ||||||
chr8:24464653
|
C | T | 1 | a0001c0002t0004g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.312+693C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464653 | ||||||
chr8:24464699
|
C | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.312+739C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464699 | ||||||
chr8:24464749
|
TGCCACCG others(179): Show |
T | 95 | a0001c0001t0002g0095a0002c0003t0001g0001a0002c0003t0001g0012others(92): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.312+868_313-686del | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 24464749 | |||||
chr8:24464844
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-855C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464844 | ||||||
chr8:24464872
|
C | T | 1 | a0001c0002t0001g0301 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.313-827C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464872 | ||||||
chr8:24465085
|
G | A | 1 | a0002c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.313-614G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465085 | ||||||
chr8:24465085
|
G | T | 1 | a0001c0001t0002g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.313-614G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465085 | ||||||
chr8:24465161
|
C | A | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.313-538C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465161 | ||||||
chr8:24465291
|
G | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-408G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465291 | ||||||
chr8:24465612
|
A | G | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-87A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465612 | ||||||
chr8:24465856
|
A | T | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389+81A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24465856 | ||||||
chr8:24465884
|
G | A | 2 | a0001c0002t0001g0181a0001c0002t0001g0182 | 2 | NA18999.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.389+109G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24465884 | ||||||
chr8:24466127
|
T | C | 1 | a0001c0001t0002g0031 | 2 | HG01433.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.389+352T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466127 | ||||||
chr8:24466189
|
T | A | 319 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.389+414T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466189 | ||||||
chr8:24466243
|
C | T | 1 | a0001c0004t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.389+468C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466243 | ||||||
chr8:24466375
|
T | A | 2 | a0003c0033t0004g0205a0016c0015t0004g0055 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-424T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466375 | ||||||
chr8:24466441
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.390-358A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466441 | ||||||
chr8:24466668
|
C | T | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.390-131C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466668 | ||||||
chr8:24466678
|
T | C | 11 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(8): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.390-121T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466678 | ||||||
chr8:24466989
|
GTGAGTAC others(23): Show |
G | 1 | a0001c0001t0002g0267 | 1 | NA19090.hp2 | splice_region_variant&intron_variant | LOW | c.579+5_579+34delGTA others(27): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24466989 | |||||
chr8:24467128
|
G | A | 3 | a0001c0004t0003g0059a0001c0004t0003g0063a0001c0004t0003g0150 | 3 | HG00140.hp1 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.579+140G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467128 | ||||||
chr8:24467145
|
T | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+157T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467145 | ||||||
chr8:24467289
|
A | C | 1 | a0001c0002t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+301A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467289 | ||||||
chr8:24467318
|
A | AT | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(21): Show | 31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.579+339dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24467318 | |||||
chr8:24467513
|
T | C | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.579+525T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467513 | ||||||
chr8:24467588
|
A | C | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.579+600A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467588 | ||||||
chr8:24467640
|
T | C | 41 | a0001c0001t0002g0095a0002c0003t0001g0001a0002c0003t0001g0012others(38): Show | 49 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.579+652T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467640 | ||||||
chr8:24467656
|
C | A | 3 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143 | 4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+668C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467656 | ||||||
chr8:24467674
|
A | G | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+686A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467674 | ||||||
chr8:24467698
|
A | G | 82 | a0001c0001t0002g0095a0002c0003t0001g0001a0002c0003t0001g0012others(79): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.579+710A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467698 | ||||||
chr8:24468026
|
A | C | 1 | a0002c0012t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580-741A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468026 | ||||||
chr8:24468093
|
A | T | 1 | a0002c0003t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580-674A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468093 | ||||||
chr8:24468264
|
A | G | 1 | a0001c0002t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.580-503A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468264 | ||||||
chr8:24468290
|
GA | G | 13 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(10): Show | 14 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-465delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24468290 | |||||
chr8:24468404
|
A | T | 11 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(8): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-363A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468404 | ||||||
chr8:24468413
|
T | G | 1 | a0001c0002t0001g0290 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.580-354T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468413 | ||||||
chr8:24468592
|
C | A | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.580-175C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468592 | ||||||
chr8:24468644
|
T | C | 2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.580-123T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468644 | ||||||
chr8:24469028
|
T | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0309a0001c0001t0002g0310others(2): Show | 7 | HG02015.hp1 NA18612.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+208T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469028 | ||||||
chr8:24469055
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.633+235C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469055 | ||||||
chr8:24469117
|
T | G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.633+297T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469117 | ||||||
chr8:24469235
|
A | C | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 8 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+415A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469235 | ||||||
chr8:24469380
|
A | G | 2 | a0002c0003t0001g0013a0002c0003t0001g0089 | 3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.633+560A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469380 | ||||||
chr8:24469383
|
G | C | 1 | a0001c0001t0002g0275 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.633+563G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469383 | ||||||
chr8:24469569
|
T | C | 1 | a0002c0003t0001g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.633+749T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469569 | ||||||
chr8:24469583
|
A | G | 10 | a0001c0002t0001g0166a0001c0002t0001g0168a0001c0002t0001g0173others(7): Show | 10 | HG02135.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+763A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469583 | ||||||
chr8:24469643
|
T | C | 11 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(8): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.633+823T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469643 | ||||||
chr8:24469686
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+866C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469686 | ||||||
chr8:24469688
|
C | T | 110 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(107): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.633+868C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469688 | ||||||
chr8:24470006
|
A | T | 1 | a0001c0001t0002g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.633+1186A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470006 | ||||||
chr8:24470156
|
T | C | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.633+1336T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470156 | ||||||
chr8:24470181
|
G | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+1361G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470181 | ||||||
chr8:24470449
|
G | A | 7 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(4): Show | 8 | HG02451.hp2 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+1629G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470449 | ||||||
chr8:24470711
|
A | C | 1 | a0010c0021t0001g0123 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.633+1891A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470711 | ||||||
chr8:24470875
|
A | T | 1 | a0002c0003t0001g0016 | 2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.633+2055A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470875 | ||||||
chr8:24470989
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.633+2169G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470989 | ||||||
chr8:24471228
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.633+2408A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471228 | ||||||
chr8:24471257
|
C | T | 10 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0148others(7): Show | 12 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.633+2437C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471257 | ||||||
chr8:24471465
|
G | GT | 140 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0025others(137): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.633+2657dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | |||||
chr8:24471465
|
G | GTT | 54 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(51): Show | 62 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.633+2656_633+2657d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | |||||
chr8:24471465
|
G | GTTT | 10 | a0001c0002t0001g0182a0005c0006t0001g0008a0005c0006t0001g0037others(7): Show | 11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+2655_633+2657d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | |||||
chr8:24471503
|
C | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(26): Show | 36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.633+2683C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471503 | ||||||
chr8:24471575
|
C | G | 1 | a0002c0003t0001g0080 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.633+2755C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471575 | ||||||
chr8:24471656
|
C | T | 5 | a0004c0005t0001g0017a0004c0005t0001g0092a0004c0005t0001g0115others(2): Show | 5 | NA18940.hp2 NA18979.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+2836C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471656 | ||||||
chr8:24471793
|
A | G | 6 | a0002c0003t0001g0001a0002c0003t0001g0077a0002c0003t0001g0080others(3): Show | 8 | HG01978.hp2 HG02080.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+2973A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471793 | ||||||
chr8:24471933
|
T | C | 4 | a0002c0007t0001g0108a0002c0007t0001g0119a0002c0007t0001g0120others(1): Show | 4 | NA18947.hp2 NA18966.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+3113T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471933 | ||||||
chr8:24471968
|
C | T | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.633+3148C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471968 | ||||||
chr8:24472014
|
T | A | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.633+3194T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472014 | ||||||
chr8:24472019
|
G | C | 34 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(31): Show | 38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.633+3199G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472019 | ||||||
chr8:24472122
|
C | CA | 46 | a0001c0001t0002g0067a0001c0001t0002g0095a0001c0001t0002g0193others(43): Show | 51 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.633+3318dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | |||||
chr8:24472122
|
CA | C | 28 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(25): Show | 29 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.633+3318delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | |||||
chr8:24472122
|
CAAA | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+3316_633+3318d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | |||||
chr8:24472124
|
A | AC | 3 | a0001c0001t0002g0174a0001c0002t0001g0183a0014c0024t0001g0170 | 3 | HG00639.hp1 HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.633+3304_633+3305i others(3): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472124 | ||||||
chr8:24472125
|
A | C | 1 | a0001c0001t0002g0256 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+3305A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472125 | ||||||
chr8:24472255
|
A | G | 1 | a0017c0016t0008g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+3435A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472255 | ||||||
chr8:24472286
|
A | T | 10 | a0002c0003t0001g0073a0005c0006t0001g0008a0005c0006t0001g0037others(7): Show | 11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+3466A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472286 | ||||||
chr8:24472493
|
C | T | 3 | a0001c0001t0002g0174a0001c0002t0001g0183a0014c0024t0001g0170 | 3 | HG00639.hp1 HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.633+3673C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472493 | ||||||
chr8:24472793
|
C | G | 1 | a0002c0007t0001g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.634-3640C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472793 | ||||||
chr8:24472882
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.634-3551A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472882 | ||||||
chr8:24473093
|
G | A | 4 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-3340G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473093 | ||||||
chr8:24473112
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.634-3321T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473112 | ||||||
chr8:24473219
|
C | A | 65 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(62): Show | 74 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.634-3214C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473219 | ||||||
chr8:24473235
|
T | G | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.634-3198T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473235 | ||||||
chr8:24473292
|
G | A | 2 | a0001c0001t0002g0258a0001c0002t0001g0153 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.634-3141G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473292 | ||||||
chr8:24473304
|
A | G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.634-3129A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473304 | ||||||
chr8:24473326
|
T | C | 2 | a0001c0001t0002g0227a0001c0001t0002g0243 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634-3107T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473326 | ||||||
chr8:24473370
|
T | C | 1 | a0001c0001t0002g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.634-3063T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473370 | ||||||
chr8:24473593
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.634-2840G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473593 | ||||||
chr8:24473691
|
A | G | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(21): Show | 31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.634-2742A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473691 | ||||||
chr8:24473808
|
G | A | 3 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143 | 4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-2625G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473808 | ||||||
chr8:24474082
|
C | T | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.634-2351C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474082 | ||||||
chr8:24474186
|
A | G | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.634-2247A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474186 | ||||||
chr8:24474245
|
C | T | 5 | a0002c0003t0001g0084a0002c0003t0001g0087a0002c0003t0001g0107others(2): Show | 5 | HG02071.hp2 HG02273.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-2188C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474245 | ||||||
chr8:24474352
|
G | A | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.634-2081G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474352 | ||||||
chr8:24474517
|
A | G | 42 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(39): Show | 50 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.634-1916A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474517 | ||||||
chr8:24474530
|
A | T | 3 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0268 | 3 | HG01993.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.634-1903A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474530 | ||||||
chr8:24474577
|
A | C | 11 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.634-1856A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474577 | ||||||
chr8:24474670
|
T | C | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1763T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474670 | ||||||
chr8:24475118
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.634-1315C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475118 | ||||||
chr8:24475162
|
A | G | 1 | a0002c0003t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.634-1271A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475162 | ||||||
chr8:24475268
|
T | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1165T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475268 | ||||||
chr8:24475372
|
T | C | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1061T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475372 | ||||||
chr8:24475637
|
G | A | 2 | a0001c0001t0002g0265a0001c0001t0002g0274 | 2 | NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.634-796G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475637 | ||||||
chr8:24475699
|
T | C | 1 | a0002c0003t0001g0104 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.634-734T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475699 | ||||||
chr8:24475719
|
T | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-714T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475719 | ||||||
chr8:24476088
|
G | A | 189 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(186): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.634-345G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24476088 | ||||||
chr8:24476335
|
A | AT | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(26): Show | 36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.634-91dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24476335 | |||||
chr8:24476387
|
C | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-46C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24476387 | ||||||
chr8:24476587
|
T | C | 1 | a0002c0003t0001g0084 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.705+83T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476587 | ||||||
chr8:24476615
|
G | A | 1 | a0002c0003t0001g0096 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.705+111G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476615 | ||||||
chr8:24476756
|
C | T | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.705+252C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476756 | ||||||
chr8:24476758
|
A | G | 1 | a0002c0020t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.705+254A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476758 | ||||||
chr8:24476827
|
C | A | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.705+323C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476827 | ||||||
chr8:24477024
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.705+520T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477024 | ||||||
chr8:24477104
|
G | A | 1 | a0001c0004t0003g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.705+600G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477104 | ||||||
chr8:24477107
|
A | G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+603A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477107 | ||||||
chr8:24477289
|
C | T | 1 | a0001c0004t0003g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.705+785C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477289 | ||||||
chr8:24477297
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+793G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477297 | ||||||
chr8:24477481
|
T | C | 2 | a0003c0033t0004g0205a0016c0015t0004g0055 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.705+977T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477481 | ||||||
chr8:24477560
|
AC | A | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.705+1059delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477560 | |||||
chr8:24477569
|
A | AGTGTGTG others(3): Show |
1 | a0003c0033t0004g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.705+1072_705+1073i others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(5): Show |
11 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(7): Show |
15 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 17 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(16): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(9): Show |
112 | a0001c0002t0001g0166a0001c0002t0001g0288a0001c0002t0001g0307others(109): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(18): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(11): Show |
50 | a0001c0001t0002g0174a0001c0002t0001g0005a0001c0002t0001g0006others(47): Show | 61 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(20): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(13): Show |
6 | a0001c0002t0001g0027a0001c0002t0001g0117a0001c0002t0001g0172others(3): Show | 7 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(22): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(15): Show |
7 | a0001c0002t0001g0021a0001c0002t0001g0169a0001c0002t0001g0175others(4): Show | 8 | HG00280.hp1 HG02129.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(24): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477569
|
A | AGTGTGTG others(17): Show |
1 | a0001c0002t0001g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.705+1072_705+1073i others(26): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | |||||
chr8:24477584
|
G | A | 4 | a0001c0001t0002g0246a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | NA18995.hp1 NA19002.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+1080G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477584 | ||||||
chr8:24477610
|
G | T | 1 | a0002c0003t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.705+1106G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477610 | ||||||
chr8:24477772
|
C | T | 1 | a0002c0007t0001g0127 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.705+1268C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477772 | ||||||
chr8:24477881
|
C | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1377C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477881 | ||||||
chr8:24477914
|
A | G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+1410A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477914 | ||||||
chr8:24477929
|
G | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(26): Show | 36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.705+1425G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477929 | ||||||
chr8:24478004
|
G | C | 3 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0001g0106 | 3 | NA18943.hp1 NA18953.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.705+1500G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478004 | ||||||
chr8:24478009
|
T | TC | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1506dupC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24478009 | |||||
chr8:24478032
|
C | T | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(21): Show | 31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.705+1528C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478032 | ||||||
chr8:24478157
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1653G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478157 | ||||||
chr8:24478204
|
T | G | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.705+1700T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478204 | ||||||
chr8:24478310
|
G | A | 1 | a0013c0026t0007g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.705+1806G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478310 | ||||||
chr8:24478377
|
C | G | 7 | a0001c0002t0004g0155a0001c0002t0004g0157a0001c0002t0004g0158others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.705+1873C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478377 | ||||||
chr8:24478507
|
T | A | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+2003T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478507 | ||||||
chr8:24478616
|
G | A | 1 | a0002c0003t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.705+2112G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478616 | ||||||
chr8:24478844
|
T | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+2340T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478844 | ||||||
chr8:24478889
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.705+2385C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478889 | ||||||
chr8:24478906
|
G | A | 1 | a0002c0003t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.705+2402G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478906 | ||||||
chr8:24478919
|
T | A | 1 | a0001c0002t0001g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+2415T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478919 | ||||||
chr8:24479052
|
C | T | 1 | a0002c0003t0001g0104 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.705+2548C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479052 | ||||||
chr8:24479172
|
C | T | 1 | a0002c0003t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.705+2668C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479172 | ||||||
chr8:24479174
|
T | A | 3 | a0002c0003t0001g0094a0002c0003t0001g0096a0002c0003t0001g0098 | 3 | HG00642.hp2 HG01257.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.705+2670T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479174 | ||||||
chr8:24479193
|
C | T | 33 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(30): Show | 37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.705+2689C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479193 | ||||||
chr8:24479247
|
A | G | 7 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(4): Show | 10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.705+2743A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479247 | ||||||
chr8:24479307
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+2803G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479307 | ||||||
chr8:24479361
|
T | TTTTTG | 5 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2756_706-2752d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24479361 | |||||
chr8:24479469
|
T | A | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-2673T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479469 | ||||||
chr8:24479493
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.706-2649C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479493 | ||||||
chr8:24479626
|
C | G | 194 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(191): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.706-2516C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479626 | ||||||
chr8:24479668
|
T | C | 7 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(4): Show | 10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.706-2474T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479668 | ||||||
chr8:24479737
|
C | T | 1 | a0001c0002t0001g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.706-2405C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479737 | ||||||
chr8:24479889
|
A | T | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-2253A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479889 | ||||||
chr8:24479978
|
G | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-2164G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479978 | ||||||
chr8:24480019
|
G | A | 1 | a0002c0012t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.706-2123G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480019 | ||||||
chr8:24480103
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.706-2039C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480103 | ||||||
chr8:24480125
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-2017G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480125 | ||||||
chr8:24480334
|
G | A | 1 | a0001c0001t0009g0272 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.706-1808G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480334 | ||||||
chr8:24480393
|
C | G | 3 | a0001c0004t0003g0010a0001c0004t0003g0058a0001c0004t0003g0060 | 4 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1749C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480393 | ||||||
chr8:24480513
|
C | T | 1 | a0001c0002t0004g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.706-1629C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480513 | ||||||
chr8:24480590
|
A | T | 2 | a0002c0003t0001g0131a0002c0003t0001g0140 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.706-1552A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480590 | ||||||
chr8:24480622
|
G | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1520G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480622 | ||||||
chr8:24480626
|
G | A | 2 | a0005c0006t0001g0043a0005c0006t0001g0044 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.706-1516G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480626 | ||||||
chr8:24480650
|
G | A | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-1492G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480650 | ||||||
chr8:24480691
|
G | A | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-1451G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480691 | ||||||
chr8:24480698
|
T | C | 1 | a0002c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-1444T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480698 | ||||||
chr8:24480718
|
T | C | 1 | a0002c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-1424T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480718 | ||||||
chr8:24480736
|
C | T | 190 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(187): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.706-1406C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480736 | ||||||
chr8:24480776
|
C | T | 5 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(2): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-1366C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480776 | ||||||
chr8:24480870
|
T | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.706-1272T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480870 | ||||||
chr8:24480897
|
G | T | 1 | a0002c0003t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.706-1245G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480897 | ||||||
chr8:24481063
|
A | AAAAC | 24 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(21): Show | 26 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-1048_706-1045d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | |||||
chr8:24481063
|
A | AAAACAAA others(1): Show |
2 | a0001c0002t0001g0025a0003c0011t0001g0074 | 3 | HG01167.hp1 HG01169.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.706-1052_706-1045d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | |||||
chr8:24481063
|
AAAAC | A | 80 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0029others(77): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.706-1048_706-1045d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | |||||
chr8:24481063
|
AAAACAAA others(1): Show |
A | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289others(2): Show | 5 | HG01257.hp2 HG01261.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1052_706-1045d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | |||||
chr8:24481092
|
AAAC | A | 10 | a0001c0002t0001g0166a0001c0002t0001g0168a0001c0002t0001g0173others(7): Show | 10 | HG02135.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-1047_706-1045d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481092 | |||||
chr8:24481199
|
C | A | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.706-943C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481199 | ||||||
chr8:24481275
|
T | A | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-867T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481275 | ||||||
chr8:24481313
|
A | G | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.706-829A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481313 | ||||||
chr8:24481346
|
T | C | 1 | a0002c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-796T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481346 | ||||||
chr8:24481559
|
G | A | 1 | a0003c0011t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.706-583G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481559 | ||||||
chr8:24481585
|
G | T | 2 | a0003c0033t0004g0205a0016c0015t0004g0055 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.706-557G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481585 | ||||||
chr8:24481823
|
T | C | 1 | a0005c0006t0001g0042 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.706-319T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481823 | ||||||
chr8:24481897
|
T | C | 193 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(190): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.706-245T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481897 | ||||||
chr8:24482383
|
GA | G | 199 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(196): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.875+80delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24482383 | |||||
chr8:24482473
|
A | C | 2 | a0002c0003t0001g0131a0002c0003t0001g0140 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.875+162A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482473 | ||||||
chr8:24482510
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0289 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.875+199G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482510 | ||||||
chr8:24482543
|
T | A | 1 | a0013c0026t0007g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.875+232T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482543 | ||||||
chr8:24482952
|
A | C | 1 | a0001c0001t0002g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.875+641A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482952 | ||||||
chr8:24482955
|
G | A | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.875+644G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482955 | ||||||
chr8:24483493
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.875+1182T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483493 | ||||||
chr8:24483505
|
C | T | 4 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+1194C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483505 | ||||||
chr8:24483600
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+1289C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483600 | ||||||
chr8:24483650
|
A | C | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.875+1339A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483650 | ||||||
chr8:24483667
|
G | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1356G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483667 | ||||||
chr8:24483724
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1413G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483724 | ||||||
chr8:24483779
|
T | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1468T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483779 | ||||||
chr8:24483823
|
A | G | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180 | 3 | NA18978.hp1 NA19004.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.876-1454A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483823 | ||||||
chr8:24483835
|
G | T | 2 | a0005c0006t0001g0043a0005c0006t0001g0044 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.876-1442G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483835 | ||||||
chr8:24483872
|
G | T | 203 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(200): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.876-1405G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483872 | ||||||
chr8:24484000
|
C | T | 7 | a0001c0002t0004g0155a0001c0002t0004g0157a0001c0002t0004g0158others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1277C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484000 | ||||||
chr8:24484001
|
C | T | 49 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0029others(46): Show | 56 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.876-1276C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484001 | ||||||
chr8:24484038
|
G | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-1239G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484038 | ||||||
chr8:24484081
|
T | A | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-1196T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484081 | ||||||
chr8:24484089
|
C | G | 1 | a0001c0013t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.876-1188C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484089 | ||||||
chr8:24484114
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.876-1163G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484114 | ||||||
chr8:24484177
|
C | A | 7 | a0001c0002t0004g0155a0001c0002t0004g0157a0001c0002t0004g0158others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1100C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484177 | ||||||
chr8:24484195
|
C | A | 10 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0148others(7): Show | 12 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-1082C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484195 | ||||||
chr8:24484333
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.876-944C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484333 | ||||||
chr8:24484427
|
A | G | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.876-850A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484427 | ||||||
chr8:24484530
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-747C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484530 | ||||||
chr8:24484802
|
C | CT | 18 | a0001c0001t0002g0031a0001c0001t0002g0220a0001c0001t0002g0238others(15): Show | 23 | HG00733.hp1 HG00738.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.876-453dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | |||||
chr8:24484802
|
CT | C | 46 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0068others(43): Show | 49 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.876-453delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | |||||
chr8:24484802
|
CTT | C | 119 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0019others(116): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.876-454_876-453del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | |||||
chr8:24484802
|
CTTT | C | 6 | a0002c0003t0001g0072a0002c0003t0001g0097a0002c0003t0001g0118others(3): Show | 6 | HG00639.hp2 HG01081.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-455_876-453del others(3): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | |||||
chr8:24484892
|
G | T | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-385G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484892 | ||||||
chr8:24484985
|
C | T | 14 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(11): Show | 16 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.876-292C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484985 | ||||||
chr8:24484986
|
A | G | 1 | a0002c0003t0001g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.876-291A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484986 | ||||||
chr8:24485055
|
C | T | 2 | a0002c0003t0001g0133a0002c0022t0001g0134 | 2 | HG00735.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.876-222C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24485055 | ||||||
chr8:24485409
|
G | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0168a0001c0027t0001g0167 | 3 | HG02280.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.960+48G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485409 | ||||||
chr8:24485461
|
T | A | 2 | a0001c0001t0002g0227a0001c0001t0002g0243 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.960+100T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485461 | ||||||
chr8:24485588
|
A | G | 1 | a0001c0001t0002g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.960+227A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485588 | ||||||
chr8:24485636
|
T | TG | 12 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0223others(9): Show | 12 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.960+276dupG | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 24485636 | |||||
chr8:24485672
|
T | A | 66 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(63): Show | 75 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.960+311T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485672 | ||||||
chr8:24485856
|
A | T | 194 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(191): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.960+495A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485856 | ||||||
chr8:24485858
|
A | T | 1 | a0002c0003t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+497A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485858 | ||||||
chr8:24485879
|
C | T | 1 | a0013c0026t0007g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.960+518C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485879 | ||||||
chr8:24485952
|
T | G | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.960+591T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485952 | ||||||
chr8:24486009
|
T | G | 6 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(3): Show | 6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+648T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486009 | ||||||
chr8:24486100
|
T | C | 1 | a0002c0003t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+739T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486100 | ||||||
chr8:24486239
|
T | C | 1 | a0006c0014t0005g0026 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.960+878T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486239 | ||||||
chr8:24486282
|
A | G | 1 | a0002c0003t0001g0118 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.961-905A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486282 | ||||||
chr8:24486291
|
T | C | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.961-896T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486291 | ||||||
chr8:24486303
|
A | C | 2 | a0005c0006t0001g0008a0005c0006t0001g0038 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.961-884A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486303 | ||||||
chr8:24486362
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.961-825G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486362 | ||||||
chr8:24486402
|
G | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-785G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486402 | ||||||
chr8:24486442
|
A | G | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.961-745A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486442 | ||||||
chr8:24486572
|
G | T | 116 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(113): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.961-615G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486572 | ||||||
chr8:24486576
|
A | G | 1 | a0001c0002t0001g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.961-611A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486576 | ||||||
chr8:24486639
|
C | T | 84 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.961-548C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486639 | ||||||
chr8:24486762
|
G | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-425G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486762 | ||||||
chr8:24486773
|
A | G | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.961-414A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486773 | ||||||
chr8:24486859
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0069 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.961-328A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486859 | ||||||
chr8:24486870
|
A | C | 1 | a0001c0028t0001g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.961-317A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486870 | ||||||
chr8:24486888
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.961-299A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486888 | ||||||
chr8:24487126
|
G | T | 1 | a0001c0004t0003g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.961-61G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24487126 | ||||||
chr8:24487369
|
G | GGTGCA | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+53_1091+54ins others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 24487369 | |||||
chr8:24487412
|
C | T | 1 | a0001c0002t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1091+95C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487412 | ||||||
chr8:24487520
|
G | A | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1091+203G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487520 | ||||||
chr8:24487584
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1091+267G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487584 | ||||||
chr8:24487635
|
C | CA | 7 | a0001c0001t0002g0198a0001c0002t0001g0025a0001c0002t0001g0144others(4): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+329dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 24487635 | |||||
chr8:24487668
|
A | T | 1 | a0001c0001t0002g0226 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1091+351A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487668 | ||||||
chr8:24487762
|
G | T | 1 | a0002c0003t0001g0104 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1091+445G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487762 | ||||||
chr8:24487765
|
G | A | 95 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(92): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1091+448G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487765 | ||||||
chr8:24487807
|
T | A | 1 | a0002c0003t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1091+490T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487807 | ||||||
chr8:24487827
|
G | A | 5 | a0005c0006t0001g0037a0005c0006t0001g0039a0005c0006t0001g0040others(2): Show | 5 | HG02451.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+510G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487827 | ||||||
chr8:24487884
|
G | A | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | NA18978.hp1 NA18999.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+567G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487884 | ||||||
chr8:24487899
|
A | C | 1 | a0001c0002t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1091+582A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487899 | ||||||
chr8:24488001
|
C | T | 1 | a0001c0008t0001g0297 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1091+684C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488001 | ||||||
chr8:24488043
|
C | G | 1 | a0002c0003t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1091+726C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488043 | ||||||
chr8:24488063
|
C | G | 11 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(8): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+746C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488063 | ||||||
chr8:24488131
|
C | T | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+814C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488131 | ||||||
chr8:24488237
|
C | T | 11 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(8): Show | 12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+920C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488237 | ||||||
chr8:24488412
|
A | G | 2 | a0002c0003t0001g0113a0002c0003t0001g0130 | 2 | HG00099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1092-747A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488412 | ||||||
chr8:24488446
|
A | G | 95 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(92): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1092-713A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488446 | ||||||
chr8:24488452
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1092-707A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488452 | ||||||
chr8:24488561
|
C | T | 1 | a0001c0004t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1092-598C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488561 | ||||||
chr8:24488564
|
A | G | 2 | a0005c0006t0001g0040a0005c0006t0001g0041 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1092-595A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488564 | ||||||
chr8:24488599
|
C | T | 95 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(92): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1092-560C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488599 | ||||||
chr8:24488631
|
G | A | 95 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(92): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1092-528G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488631 | ||||||
chr8:24489388
|
T | C | 4 | a0002c0007t0001g0035a0002c0007t0001g0036a0002c0007t0001g0112others(1): Show | 4 | HG00438.hp2 NA18962.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+55T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24489388 | ||||||
chr8:24489467
|
T | G | 2 | a0001c0002t0001g0025a0001c0028t0001g0204 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1266+134T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24489467 | ||||||
chr8:24490005
|
G | C | 1 | a0001c0002t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1266+672G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490005 | ||||||
chr8:24490021
|
G | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+688G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490021 | ||||||
chr8:24490133
|
T | G | 11 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0148others(8): Show | 13 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1267-666T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490133 | ||||||
chr8:24490163
|
A | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1267-636A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490163 | ||||||
chr8:24490386
|
T | C | 2 | a0001c0001t0002g0031a0001c0001t0002g0275 | 3 | HG01433.hp1 HG01934.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1267-413T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490386 | ||||||
chr8:24490608
|
C | A | 105 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(102): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1267-191C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490608 | ||||||
chr8:24490641
|
C | T | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1267-158C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490641 | ||||||
chr8:24490708
|
T | A | 268 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0029others(265): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-91T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490708 | ||||||
chr8:24490728
|
A | G | 84 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1267-71A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490728 | ||||||
chr8:24490756
|
A | T | 1 | a0001c0002t0001g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1267-43A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490756 | ||||||
chr8:24490774
|
ATC | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1267-19_1267-18del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 24490774 | |||||
chr8:24490912
|
G | GT | 9 | a0001c0001t0002g0048a0001c0001t0002g0217a0001c0002t0001g0296others(6): Show | 9 | HG01258.hp2 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1356+35dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 24490912 | |||||
chr8:24491116
|
G | C | 1 | a0001c0004t0003g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1356+228G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491116 | ||||||
chr8:24491192
|
T | C | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1356+304T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491192 | ||||||
chr8:24491217
|
G | T | 1 | a0002c0007t0001g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1356+329G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491217 | ||||||
chr8:24491241
|
G | C | 1 | a0001c0028t0001g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1356+353G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491241 | ||||||
chr8:24491277
|
C | G | 1 | a0001c0002t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1356+389C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491277 | ||||||
chr8:24491341
|
A | C | 120 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(117): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1356+453A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491341 | ||||||
chr8:24491422
|
T | G | 1 | a0001c0002t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1357-481T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491422 | ||||||
chr8:24491447
|
T | C | 1 | a0005c0006t0001g0042 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1357-456T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491447 | ||||||
chr8:24491466
|
A | G | 1 | a0003c0033t0004g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1357-437A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491466 | ||||||
chr8:24491643
|
G | A | 105 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(102): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1357-260G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491643 | ||||||
chr8:24491747
|
T | C | 4 | a0001c0002t0001g0033a0001c0002t0001g0290a0001c0002t0001g0301others(1): Show | 5 | HG01123.hp2 HG01175.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357-156T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491747 | ||||||
chr8:24491846
|
G | A | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357-57G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491846 | ||||||
chr8:24491867
|
T | C | 1 | a0002c0003t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1357-36T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491867 | ||||||
chr8:24491882
|
C | G | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1357-21C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491882 | ||||||
chr8:24492243
|
C | T | 1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1552+145C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492243 | ||||||
chr8:24492265
|
C | T | 33 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(30): Show | 37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1552+167C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492265 | ||||||
chr8:24492408
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1553-87G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492408 | ||||||
chr8:24492638
|
G | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1655+41G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492638 | ||||||
chr8:24492660
|
G | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1655+63G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492660 | ||||||
chr8:24492675
|
C | T | 105 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(102): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1655+78C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492675 | ||||||
chr8:24492694
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1655+97T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492694 | ||||||
chr8:24492861
|
C | T | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1656-182C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492861 | ||||||
chr8:24492862
|
G | A | 1 | a0002c0003t0012g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1656-181G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492862 | ||||||
chr8:24492900
|
T | A | 1 | a0004c0005t0001g0092 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1656-143T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492900 | ||||||
chr8:24492960
|
A | G | 1 | a0002c0012t0001g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1656-83A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492960 | ||||||
chr8:24492984
|
G | T | 14 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0234others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656-59G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492984 | ||||||
chr8:24493483
|
T | G | 115 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(112): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+254T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493483 | ||||||
chr8:24493484
|
AGACATG | A | 115 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(112): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+258_1842+263d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24493484 | |||||
chr8:24493491
|
G | A | 115 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(112): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+262G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493491 | ||||||
chr8:24493698
|
T | C | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1842+469T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493698 | ||||||
chr8:24493837
|
A | G | 3 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143 | 4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+608A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493837 | ||||||
chr8:24494170
|
A | G | 33 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(30): Show | 37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1842+941A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494170 | ||||||
chr8:24494300
|
A | T | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1842+1071A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494300 | ||||||
chr8:24494457
|
T | A | 1 | a0001c0004t0003g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1842+1228T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494457 | ||||||
chr8:24494459
|
C | G | 1 | a0001c0004t0003g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1842+1230C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494459 | ||||||
chr8:24494464
|
T | TGCTTCCT others(322): Show |
1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1842+1247_1842+124 others(333): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24494464 | |||||
chr8:24494484
|
G | T | 1 | a0001c0008t0001g0295 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1842+1255G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494484 | ||||||
chr8:24494712
|
GA | G | 98 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(95): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1842+1492delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24494712 | |||||
chr8:24494721
|
A | T | 103 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1842+1492A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494721 | ||||||
chr8:24494722
|
T | C | 103 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1842+1493T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494722 | ||||||
chr8:24494723
|
C | T | 103 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1842+1494C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494723 | ||||||
chr8:24494839
|
C | T | 1 | a0001c0002t0013g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1842+1610C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494839 | ||||||
chr8:24494846
|
G | T | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1842+1617G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494846 | ||||||
chr8:24494872
|
A | C | 5 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0001g0106others(2): Show | 5 | NA18943.hp1 NA18944.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+1643A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494872 | ||||||
chr8:24494949
|
C | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+1720C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494949 | ||||||
chr8:24494986
|
C | G | 1 | a0001c0002t0001g0025 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1842+1757C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494986 | ||||||
chr8:24495034
|
C | A | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+1805C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495034 | ||||||
chr8:24495398
|
G | GA | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2176dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24495398 | |||||
chr8:24495468
|
G | A | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2239G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495468 | ||||||
chr8:24495480
|
C | T | 1 | a0002c0022t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1842+2251C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495480 | ||||||
chr8:24495499
|
G | A | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1842+2270G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495499 | ||||||
chr8:24495563
|
A | G | 34 | a0001c0001t0002g0174a0001c0002t0001g0019a0001c0002t0001g0021others(31): Show | 38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1842+2334A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495563 | ||||||
chr8:24495704
|
T | A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 12 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1842+2475T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495704 | ||||||
chr8:24495722
|
AAG | A | 2 | a0003c0009t0005g0020a0003c0009t0005g0165 | 3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1842+2499_1842+250 others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24495722 | |||||
chr8:24495913
|
G | A | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2684G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495913 | ||||||
chr8:24496033
|
G | C | 7 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1842+2804G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496033 | ||||||
chr8:24496083
|
T | C | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2854T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496083 | ||||||
chr8:24496089
|
A | G | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1842+2860A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496089 | ||||||
chr8:24496254
|
G | A | 15 | a0001c0004t0003g0010a0001c0004t0003g0057a0001c0004t0003g0058others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1843-2982G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496254 | ||||||
chr8:24496368
|
C | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-2868C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496368 | ||||||
chr8:24496393
|
T | G | 2 | a0002c0003t0001g0131a0002c0003t0001g0140 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1843-2843T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496393 | ||||||
chr8:24496442
|
C | T | 84 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1843-2794C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496442 | ||||||
chr8:24496648
|
T | G | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1843-2588T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496648 | ||||||
chr8:24496668
|
C | T | 3 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143 | 4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843-2568C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496668 | ||||||
chr8:24496745
|
C | G | 1 | a0002c0003t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1843-2491C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496745 | ||||||
chr8:24496767
|
G | A | 101 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(98): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1843-2469G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496767 | ||||||
chr8:24496959
|
C | T | 84 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1843-2277C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496959 | ||||||
chr8:24497049
|
A | G | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-2187A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497049 | ||||||
chr8:24497050
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1843-2186T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497050 | ||||||
chr8:24497062
|
C | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-2174C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497062 | ||||||
chr8:24497080
|
T | C | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1843-2156T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497080 | ||||||
chr8:24497102
|
G | C | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1843-2134G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497102 | ||||||
chr8:24497269
|
G | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1967G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497269 | ||||||
chr8:24497308
|
G | A | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1928G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497308 | ||||||
chr8:24497342
|
T | C | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1843-1894T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497342 | ||||||
chr8:24497456
|
T | C | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1780T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497456 | ||||||
chr8:24497571
|
A | C | 1 | a0015c0035t0008g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1843-1665A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497571 | ||||||
chr8:24497620
|
G | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1616G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497620 | ||||||
chr8:24497830
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1843-1406C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497830 | ||||||
chr8:24498032
|
T | C | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-1204T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498032 | ||||||
chr8:24498054
|
A | C | 1 | a0001c0001t0002g0266 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1843-1182A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498054 | ||||||
chr8:24498300
|
G | A | 1 | a0002c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1843-936G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498300 | ||||||
chr8:24498409
|
T | C | 18 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(15): Show | 22 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1843-827T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498409 | ||||||
chr8:24498543
|
C | G | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-693C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498543 | ||||||
chr8:24498549
|
G | GTA | 4 | a0003c0011t0001g0011a0003c0011t0001g0074a0003c0011t0001g0143others(1): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-673_1843-672d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24498549 | |||||
chr8:24498549
|
G | GTATA | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1843-675_1843-672d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24498549 | |||||
chr8:24498552
|
T | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0269 | 3 | HG03834.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1843-684T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498552 | ||||||
chr8:24498651
|
T | A | 3 | a0003c0009t0005g0034a0003c0009t0005g0317a0003c0009t0005g0318 | 4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843-585T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498651 | ||||||
chr8:24498714
|
C | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-522C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498714 | ||||||
chr8:24498751
|
G | C | 1 | a0001c0004t0003g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1843-485G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498751 | ||||||
chr8:24498806
|
T | C | 8 | a0001c0001t0002g0218a0001c0001t0002g0234a0001c0001t0002g0244others(5): Show | 8 | HG00408.hp1 HG02132.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843-430T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498806 | ||||||
chr8:24498848
|
T | C | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-388T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498848 | ||||||
chr8:24499120
|
A | C | 3 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289 | 3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1843-116A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499120 | ||||||
chr8:24499212
|
C | G | 1 | a0002c0003t0001g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1843-24C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499212 | ||||||
chr8:24499233
|
T | C | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1843-3T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499233 | ||||||
chr8:24499414
|
T | G | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1923+98T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499414 | ||||||
chr8:24499650
|
C | T | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1923+334C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499650 | ||||||
chr8:24499729
|
A | G | 106 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(103): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1923+413A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499729 | ||||||
chr8:24499758
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG00558.hp1 HG02027.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-420G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499758 | ||||||
chr8:24499771
|
G | A | 3 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289 | 3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1924-407G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499771 | ||||||
chr8:24499797
|
T | TAC | 36 | a0001c0001t0002g0024a0001c0001t0002g0049a0001c0001t0002g0174others(33): Show | 40 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1924-351_1924-350d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
T | TACAC | 6 | a0001c0002t0001g0168a0001c0002t0001g0179a0001c0002t0001g0207others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1924-353_1924-350d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
TAC | T | 53 | a0001c0001t0002g0146a0001c0001t0002g0236a0001c0001t0002g0239others(50): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1924-351_1924-350d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
TACAC | T | 5 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0002t0001g0304others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-353_1924-350d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
TACACACA others(1): Show |
T | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1924-357_1924-350d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
TACACACA others(3): Show |
T | 3 | a0003c0032t0001g0216a0005c0006t0001g0008a0005c0006t0001g0038 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-359_1924-350d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499797
|
TACACACA others(5): Show |
T | 14 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(11): Show | 17 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1924-361_1924-350d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | |||||
chr8:24499822
|
A | T | 1 | a0002c0003t0012g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1924-356A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499822 | ||||||
chr8:24499827
|
C | T | 3 | a0003c0033t0004g0205a0016c0015t0004g0055a0017c0016t0008g0056 | 3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1924-351C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499827 | ||||||
chr8:24499836
|
TCA | T | 8 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(5): Show | 9 | HG02451.hp2 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1924-325_1924-324d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499836 | |||||
chr8:24499838
|
A | T | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1924-340A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499838 | ||||||
chr8:24499856
|
A | G | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-322A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499856 | ||||||
chr8:24499881
|
T | C | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-297T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499881 | ||||||
chr8:24499898
|
C | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-280C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499898 | ||||||
chr8:24499902
|
G | GA | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-273dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499902 | |||||
chr8:24499953
|
A | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-225A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499953 | ||||||
chr8:24499997
|
A | G | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1924-181A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499997 | ||||||
chr8:24500047
|
A | T | 16 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(13): Show | 20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-131A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24500047 | ||||||
chr8:24500137
|
A | T | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1924-41A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24500137 | ||||||
chr8:24500311
|
A | G | 2 | a0005c0006t0001g0008a0005c0006t0001g0038 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2002+55A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500311 | ||||||
chr8:24500404
|
G | T | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2002+148G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500404 | ||||||
chr8:24500557
|
T | C | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2003-233T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500557 | ||||||
chr8:24500706
|
A | G | 87 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(84): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2003-84A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500706 | ||||||
chr8:24500977
|
A | G | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108+82A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24500977 | ||||||
chr8:24501117
|
A | T | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2108+222A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501117 | ||||||
chr8:24501161
|
T | C | 1 | a0002c0003t0001g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2108+266T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501161 | ||||||
chr8:24501179
|
T | C | 86 | a0001c0013t0001g0053a0002c0003t0001g0001a0002c0003t0001g0012others(83): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2108+284T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501179 | ||||||
chr8:24501337
|
C | G | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2109-140C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501337 | ||||||
chr8:24501612
|
A | AT | 14 | a0001c0002t0001g0294a0003c0009t0005g0020a0003c0009t0005g0034others(11): Show | 18 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2208+48dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24501612 | |||||
chr8:24501612
|
ATT | A | 84 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(81): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+47_2208+48del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24501612 | |||||
chr8:24501735
|
A | G | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+159A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501735 | ||||||
chr8:24501743
|
G | A | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+167G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501743 | ||||||
chr8:24501766
|
G | A | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+190G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501766 | ||||||
chr8:24501792
|
T | C | 1 | a0002c0003t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2208+216T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501792 | ||||||
chr8:24501825
|
C | T | 102 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(99): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2208+249C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501825 | ||||||
chr8:24501827
|
A | G | 1 | a0010c0021t0001g0123 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2208+251A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501827 | ||||||
chr8:24501837
|
C | G | 1 | a0001c0002t0001g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2208+261C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501837 | ||||||
chr8:24501856
|
G | A | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+280G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501856 | ||||||
chr8:24501857
|
C | A | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+281C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501857 | ||||||
chr8:24501896
|
A | T | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+320A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501896 | ||||||
chr8:24501930
|
G | A | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2208+354G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501930 | ||||||
chr8:24501958
|
G | A | 60 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(57): Show | 66 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2208+382G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501958 | ||||||
chr8:24502028
|
TAA | T | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+454_2208+455d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502028 | |||||
chr8:24502159
|
G | C | 1 | a0002c0012t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2208+583G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502159 | ||||||
chr8:24502210
|
A | G | 2 | a0003c0033t0004g0205a0016c0015t0004g0055 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2208+634A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502210 | ||||||
chr8:24502227
|
GA | G | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+655delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502227 | |||||
chr8:24502254
|
T | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2208+678T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502254 | ||||||
chr8:24502569
|
A | T | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+993A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502569 | ||||||
chr8:24502625
|
T | A | 102 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(99): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2208+1049T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502625 | ||||||
chr8:24502661
|
T | C | 7 | a0001c0002t0004g0155a0001c0002t0004g0157a0001c0002t0004g0158others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2208+1085T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502661 | ||||||
chr8:24502919
|
GAA | G | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2208+1347_2208+134 others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502919 | |||||
chr8:24502941
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2208+1365C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502941 | ||||||
chr8:24503028
|
G | A | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+1452G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503028 | ||||||
chr8:24503100
|
G | T | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+1524G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503100 | ||||||
chr8:24503129
|
T | C | 1 | a0002c0020t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2208+1553T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503129 | ||||||
chr8:24503146
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2208+1570A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503146 | ||||||
chr8:24503208
|
C | G | 9 | a0001c0002t0001g0006a0001c0002t0001g0033a0001c0002t0001g0290others(6): Show | 12 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2208+1632C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503208 | ||||||
chr8:24503301
|
A | G | 1 | a0001c0002t0001g0294 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2208+1725A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503301 | ||||||
chr8:24503306
|
G | A | 23 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(20): Show | 30 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2208+1730G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503306 | ||||||
chr8:24503362
|
A | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2208+1786A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503362 | ||||||
chr8:24503431
|
G | C | 3 | a0001c0001t0002g0028a0001c0001t0002g0313a0001c0001t0011g0247 | 4 | HG00609.hp2 HG02132.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.2208+1855G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503431 | ||||||
chr8:24503550
|
C | A | 85 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2208+1974C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503550 | ||||||
chr8:24503577
|
G | A | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2208+2001G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503577 | ||||||
chr8:24503581
|
G | A | 1 | a0002c0003t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2208+2005G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503581 | ||||||
chr8:24503587
|
C | T | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+2011C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503587 | ||||||
chr8:24503616
|
G | T | 1 | a0001c0002t0001g0306 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2208+2040G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503616 | ||||||
chr8:24503639
|
A | G | 28 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(25): Show | 35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2063A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503639 | ||||||
chr8:24503850
|
A | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+2274A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503850 | ||||||
chr8:24503866
|
A | G | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+2290A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503866 | ||||||
chr8:24504023
|
A | AAAAAT | 12 | a0001c0001t0002g0023a0001c0001t0002g0075a0001c0001t0002g0185others(9): Show | 13 | HG02630.hp1 NA18612.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.2208+2486_2208+249 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | |||||
chr8:24504023
|
AAAAAT | A | 41 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(38): Show | 43 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2208+2486_2208+249 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | |||||
chr8:24504023
|
AAAAATAA others(3): Show |
A | 2 | a0001c0010t0001g0009a0001c0010t0001g0054 | 3 | HG02109.hp2 HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2208+2481_2208+249 others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | |||||
chr8:24504023
|
AAAAATAA others(8): Show |
A | 81 | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(78): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2208+2476_2208+249 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | |||||
chr8:24504062
|
A | T | 28 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(25): Show | 35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2486A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504062 | ||||||
chr8:24504063
|
T | A | 28 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(25): Show | 35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2487T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504063 | ||||||
chr8:24504063
|
T | TA | 12 | a0003c0009t0005g0020a0003c0009t0005g0165a0003c0009t0005g0317others(9): Show | 13 | HG00733.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2208+2490dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | |||||
chr8:24504063
|
T | TAAAATA | 4 | a0001c0001t0002g0246a0003c0009t0005g0034a0003c0009t0005g0318others(1): Show | 6 | HG00738.hp2 HG02145.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+2490_2208+249 others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | |||||
chr8:24504063
|
T | TAAAATAA others(4): Show |
2 | a0005c0006t0001g0038a0006c0014t0005g0026 | 3 | HG02647.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2208+2490_2208+249 others(15): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | |||||
chr8:24504072
|
T | A | 1 | a0001c0001t0002g0246 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2208+2496T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504072 | ||||||
chr8:24504165
|
C | G | 18 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(15): Show | 22 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2208+2589C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504165 | ||||||
chr8:24504171
|
C | T | 1 | a0002c0003t0001g0013 | 2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2208+2595C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504171 | ||||||
chr8:24504191
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2208+2615G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504191 | ||||||
chr8:24504260
|
G | A | 23 | a0001c0001t0002g0174a0001c0002t0001g0027a0001c0002t0001g0166others(20): Show | 25 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2208+2684G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504260 | ||||||
chr8:24504382
|
T | A | 103 | a0001c0013t0001g0053a0002c0003t0001g0001a0002c0003t0001g0012others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2208+2806T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504382 | ||||||
chr8:24504389
|
C | A | 103 | a0001c0013t0001g0053a0002c0003t0001g0001a0002c0003t0001g0012others(100): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2208+2813C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504389 | ||||||
chr8:24504443
|
TA | T | 107 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(104): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2208+2878delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504443 | |||||
chr8:24504547
|
A | G | 1 | a0002c0003t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2209-2933A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504547 | ||||||
chr8:24504572
|
T | C | 8 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(5): Show | 11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2908T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504572 | ||||||
chr8:24504578
|
G | A | 1 | a0001c0001t0002g0310 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2209-2902G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504578 | ||||||
chr8:24504599
|
C | T | 2 | a0005c0006t0001g0008a0005c0006t0001g0038 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2209-2881C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504599 | ||||||
chr8:24504700
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG00558.hp1 HG02027.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2209-2780G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504700 | ||||||
chr8:24504755
|
AC | A | 8 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(5): Show | 11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2720delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504755 | |||||
chr8:24505010
|
C | T | 2 | a0003c0033t0004g0205a0016c0015t0004g0055 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2209-2470C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505010 | ||||||
chr8:24505013
|
A | G | 8 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(5): Show | 11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2467A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505013 | ||||||
chr8:24505024
|
G | A | 1 | a0001c0002t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2209-2456G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505024 | ||||||
chr8:24505177
|
C | A | 1 | a0001c0002t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2209-2303C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505177 | ||||||
chr8:24505190
|
G | A | 91 | a0001c0001t0002g0174a0001c0002t0001g0005a0001c0002t0001g0006others(88): Show | 104 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.2209-2290G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505190 | ||||||
chr8:24505269
|
G | A | 3 | a0004c0005t0001g0002a0004c0005t0001g0111a0004c0005t0001g0129 | 5 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2209-2211G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505269 | ||||||
chr8:24505276
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2209-2204A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505276 | ||||||
chr8:24505297
|
C | T | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2209-2183C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505297 | ||||||
chr8:24505358
|
A | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2209-2122A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505358 | ||||||
chr8:24505383
|
G | C | 1 | a0001c0002t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2209-2097G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505383 | ||||||
chr8:24505585
|
C | T | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2209-1895C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505585 | ||||||
chr8:24505621
|
T | C | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2209-1859T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505621 | ||||||
chr8:24505669
|
T | G | 205 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(202): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2209-1811T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505669 | ||||||
chr8:24505720
|
A | G | 1 | a0002c0003t0001g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2209-1760A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505720 | ||||||
chr8:24505872
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-1608C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505872 | ||||||
chr8:24505934
|
T | C | 204 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2209-1546T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505934 | ||||||
chr8:24506086
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2209-1394A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506086 | ||||||
chr8:24506161
|
G | A | 17 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(14): Show | 21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2209-1319G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506161 | ||||||
chr8:24506230
|
T | C | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-1250T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506230 | ||||||
chr8:24506250
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2209-1230G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506250 | ||||||
chr8:24506279
|
G | A | 195 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(192): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2209-1201G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506279 | ||||||
chr8:24506353
|
G | T | 1 | a0001c0001t0002g0238 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2209-1127G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506353 | ||||||
chr8:24506404
|
T | C | 1 | a0001c0004t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2209-1076T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506404 | ||||||
chr8:24506476
|
C | T | 7 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(4): Show | 10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209-1004C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506476 | ||||||
chr8:24506495
|
T | C | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-985T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506495 | ||||||
chr8:24506592
|
A | G | 21 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0033others(18): Show | 28 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2209-888A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506592 | ||||||
chr8:24506753
|
G | GCA | 28 | a0001c0001t0002g0095a0001c0001t0002g0193a0001c0001t0002g0195others(25): Show | 34 | HG00280.hp1 HG00558.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2209-690_2209-689d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
G | GCACA | 7 | a0001c0001t0002g0233a0001c0001t0002g0314a0001c0001t0002g0315others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2209-692_2209-689d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
G | GCACACAC others(3): Show |
1 | a0003c0032t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2209-698_2209-689d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
GCA | G | 141 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0029others(138): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2209-690_2209-689d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
GCACA | G | 25 | a0001c0001t0002g0214a0001c0001t0002g0217a0001c0001t0002g0218others(22): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.2209-692_2209-689d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
GCACACA | G | 27 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(24): Show | 30 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2209-694_2209-689d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
GCACACAC others(3): Show |
G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-698_2209-689d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506753
|
GCACACAC others(5): Show |
G | 1 | a0001c0001t0002g0242 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2209-700_2209-689d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | |||||
chr8:24506896
|
C | T | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2209-584C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506896 | ||||||
chr8:24506967
|
C | T | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2209-513C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506967 | ||||||
chr8:24507021
|
C | A | 9 | a0005c0006t0001g0008a0005c0006t0001g0037a0005c0006t0001g0038others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2209-459C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507021 | ||||||
chr8:24507169
|
C | G | 2 | a0015c0035t0008g0045a0017c0016t0008g0056 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-311C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507169 | ||||||
chr8:24507182
|
T | TGAAAATC others(24): Show |
1 | a0009c0019t0001g0122 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2209-295_2209-265d others(33): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24507182 | |||||
chr8:24507220
|
C | T | 8 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-260C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507220 | ||||||
chr8:24507644
|
TCA | T | 198 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0019others(195): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2264+112_2264+113d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507644 | |||||
chr8:24507662
|
G | A | 1 | a0002c0022t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2264+127G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24507662 | ||||||
chr8:24507668
|
AT | A | 171 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0019others(168): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.2264+148delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507668 | |||||
chr8:24507668
|
ATTTT | A | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2264+145_2264+148d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507668 | |||||
chr8:24507878
|
T | C | 6 | a0003c0009t0005g0020a0003c0009t0005g0034a0003c0009t0005g0165others(3): Show | 9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2264+343T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24507878 | ||||||
chr8:24508450
|
G | T | 1 | a0001c0028t0001g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2265-96G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508450 | ||||||
chr8:24508507
|
T | C | 92 | a0001c0010t0001g0009a0001c0010t0001g0050a0001c0010t0001g0051others(89): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.2265-39T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508507 | ||||||
chr8:24508514
|
C | T | 1 | a0001c0027t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2265-32C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508514 |