geneid | 10863 |
---|---|
ensemblid | ENSG00000042980.14 |
hgncid | 206 |
symbol | ADAM28 |
name | ADAM metallopeptidase domain 28 |
refseq_nuc | NM_014265.6 |
refseq_prot | NP_055080.2 |
ensembl_nuc | ENST00000265769.9 |
ensembl_prot | ENSP00000265769.4 |
mane_status | MANE Select |
chr | chr8 |
start | 24294069 |
end | 24359014 |
strand | + |
ver | v1.2 |
region | chr8:24294069-24359014 |
region5000 | chr8:24289069-24364014 |
regionname0 | ADAM28_chr8_24294069_24359014 |
regionname5000 | ADAM28_chr8_24289069_24364014 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 775 | 264 | 44 | 46 | 135 | 11 | 27 | 93 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002 | 0/0 | 775 | 34 | 3 | 4 | 21 | 0 | 6 | 19 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003 | 0/0 | 775 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0004 | 1/0 | 775 | 9 | 5 | 0 | 0 | 0 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0005 | 0/0 | 775 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0006 | 0/0 | 775 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007 | 0/0 | 775 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0008 | 0/0 | 775 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0009 | 0/0 | 775 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0010 | 0/0 | 775 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0011 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0012 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0013 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0014 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0015 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0016 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0017 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0018 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0019 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0020 | 0/0 | 775 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0021 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2328 | 210 | 41 | 36 | 98 | 7 | 27 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0002 | 0/0 | 2328 | 48 | 0 | 9 | 36 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0003 | 0/0 | 2328 | 27 | 1 | 1 | 20 | 0 | 5 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0004 | 1/0 | 2328 | 9 | 5 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0005 | 0/0 | 2328 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0006 | 0/0 | 2328 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0007 | 0/0 | 2328 | 4 | 2 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0008 | 0/0 | 2328 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0009 | 0/0 | 2328 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0010 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0011 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0012 | 0/0 | 2328 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0013 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0014 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0015 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0016 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0017 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0018 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0019 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0020 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0021 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0022 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0023 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0024 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0025 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0026 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0027 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0028 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0029 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0030 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0031 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0032 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0033 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
c0034 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4705 | 93 | 8 | 6 | 69 | 5 | 5 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0002 | 0/0 | 4705 | 81 | 35 | 13 | 17 | 2 | 14 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0003 | 0/1 | 4705 | 58 | 4 | 14 | 24 | 3 | 12 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0004 | 0/0 | 4706 | 18 | 0 | 0 | 18 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0005 | 0/0 | 4706 | 14 | 3 | 2 | 9 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0006 | 0/0 | 4705 | 11 | 8 | 3 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0007 | 1/0 | 4692 | 8 | 4 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0008 | 0/0 | 4705 | 6 | 0 | 0 | 6 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0009 | 0/0 | 4705 | 5 | 0 | 4 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0010 | 0/0 | 4681 | 5 | 0 | 5 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0011 | 0/0 | 4710 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0012 | 0/0 | 4706 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0013 | 0/0 | 4706 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0014 | 0/0 | 4705 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0015 | 0/0 | 4706 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0016 | 0/0 | 4705 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0017 | 0/0 | 4703 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0018 | 0/0 | 4705 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0019 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0020 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0021 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0022 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0023 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0024 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0025 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0026 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0027 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0028 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0029 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0030 | 0/0 | 4722 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0031 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0032 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0033 | 0/0 | 4707 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0034 | 0/0 | 4706 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0035 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0036 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0037 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0038 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0039 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0040 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0041 | 0/0 | 4707 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0042 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0043 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0044 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0045 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0046 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
t0047 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2328 | 210 | 41 | 36 | 98 | 7 | 27 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002 | 0/0 | 2328 | 48 | 0 | 9 | 36 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0013 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0017 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0025 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0026 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0034 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003 | 0/0 | 2328 | 27 | 1 | 1 | 20 | 0 | 5 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0007 | 0/0 | 2328 | 4 | 2 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0019 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0031 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0033 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0005 | 0/0 | 2328 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0006 | 0/0 | 2328 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0004c0004 | 1/0 | 2328 | 9 | 5 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0005c0008 | 0/0 | 2328 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0006c0010 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0006c0028 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007c0011 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007c0020 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0008c0009 | 0/0 | 2328 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0009c0012 | 0/0 | 2328 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0010c0014 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0011c0027 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0012c0024 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0013c0021 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0014c0022 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0015c0023 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0016c0029 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0017c0030 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0018c0018 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0019c0032 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0020c0016 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0021c0015 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7032 | 59 | 7 | 5 | 42 | 1 | 4 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0002 | 0/0 | 7032 | 55 | 20 | 6 | 14 | 2 | 13 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0003 | 0/1 | 7032 | 38 | 4 | 11 | 12 | 3 | 7 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0004 | 0/0 | 7033 | 7 | 0 | 0 | 7 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0005 | 0/0 | 7033 | 9 | 1 | 2 | 6 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0006 | 0/0 | 7032 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0008 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0009 | 0/0 | 7032 | 5 | 0 | 4 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0010 | 0/0 | 7008 | 4 | 0 | 4 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0011 | 0/0 | 7037 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0012 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0015 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0016 | 0/0 | 7032 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0017 | 0/0 | 7030 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0018 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0019 | 0/0 | 7033 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0021 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0022 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0025 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0027 | 0/0 | 7028 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0030 | 0/0 | 7049 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0032 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0034 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0036 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0037 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0038 | 0/0 | 7030 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0039 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0040 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0043 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0044 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0001t0047 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0001 | 0/0 | 7032 | 22 | 0 | 1 | 18 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0002 | 0/0 | 7032 | 6 | 0 | 6 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0003 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0004 | 0/0 | 7033 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0005 | 0/0 | 7033 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0008 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0010 | 0/0 | 7008 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0012 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0002t0014 | 0/0 | 7032 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0013t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0013t0013 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0017t0002 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0025t0042 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0026t0001 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0001c0034t0024 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0001 | 0/0 | 7032 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0003 | 0/0 | 7032 | 11 | 0 | 0 | 7 | 0 | 4 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0004 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0008 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0029 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0031 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0045 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0003t0046 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0007t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0007t0003 | 0/0 | 7032 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0007t0026 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0019t0006 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0031t0002 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0002c0033t0008 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0005t0005 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0005t0006 | 0/0 | 7032 | 5 | 3 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0006t0001 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0006t0002 | 0/0 | 7032 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0003c0006t0013 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0004c0004t0007 | 1/0 | 7019 | 7 | 3 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0004c0004t0020 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0004c0004t0041 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0005c0008t0002 | 0/0 | 7032 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0006c0010t0002 | 0/0 | 7032 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0006c0028t0006 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007c0011t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007c0011t0006 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0007c0020t0023 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0008c0009t0003 | 0/0 | 7032 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0009c0012t0001 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0009c0012t0003 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0010c0014t0028 | 0/0 | 7024 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0011c0027t0007 | 0/0 | 7019 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0012c0024t0003 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0013c0021t0001 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0014c0022t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0015c0023t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0016c0029t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0017c0030t0004 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0018c0018t0035 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0019c0032t0033 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0020c0016t0003 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
a0021c0015t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | copy fasta | chr8 | 24289069 | 24364014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0015g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0016g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0018g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0019g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0021g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0022g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0025g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0027g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0030g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0032g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0034g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0036g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0037g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0038g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0039g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0040g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0043g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0044g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0047g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0008g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0010g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0012g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0012g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0014g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0014g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0014g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0013t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0013t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0017t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0025t0042g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0026t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0034t0024g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0029g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0031g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0045g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0046g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0026g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0019t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0031t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0033t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0013g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0020g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0041g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0010t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0010t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0028t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0011t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0011t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0020t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0009t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0009t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0009t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0009c0012t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0009c0012t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0010c0014t0028g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0011c0027t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0012c0024t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0013c0021t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0014c0022t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0015c0023t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0016c0029t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0017c0030t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0018c0018t0035g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0019c0032t0033g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0020c0016t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0021c0015t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0287 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0218 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00140 | hp1 | a0010 | c0014 | t0028 | g0168 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | FIN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0060 | EUR | FIN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0319 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00438 | hp2 | a0001 | c0001 | t0022 | g0093 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00609 | hp2 | a0001 | c0002 | t0012 | g0323 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0017 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0090 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00673 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00733 | hp2 | a0003 | c0005 | t0006 | g0242 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00738 | hp2 | a0003 | c0005 | t0006 | g0240 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0214 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01074 | hp2 | a0001 | c0001 | t0043 | g0022 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01081 | hp1 | a0001 | c0001 | t0009 | g0134 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0169 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0195 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0221 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01167 | hp1 | a0002 | c0007 | t0003 | g0271 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01169 | hp1 | a0002 | c0007 | t0003 | g0272 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01192 | hp2 | a0001 | c0017 | t0002 | g0130 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01258 | hp1 | a0001 | c0001 | t0037 | g0088 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0303 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01261 | hp2 | a0002 | c0019 | t0006 | g0226 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01346 | hp2 | a0001 | c0001 | t0009 | g0135 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0312 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0296 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0289 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01516 | hp2 | a0001 | c0026 | t0001 | g0114 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0305 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0080 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01884 | hp1 | a0004 | c0004 | t0007 | g0109 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01891 | hp1 | a0005 | c0008 | t0002 | g0327 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01891 | hp2 | a0001 | c0001 | t0038 | g0129 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01934 | hp1 | a0001 | c0002 | t0010 | g0282 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01943 | hp1 | a0002 | c0003 | t0029 | g0261 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02015 | hp2 | a0009 | c0012 | t0003 | g0212 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02027 | hp1 | a0001 | c0001 | t0025 | g0219 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02040 | hp1 | a0001 | c0002 | t0004 | g0286 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0234 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02055 | hp1 | a0019 | c0032 | t0033 | g0248 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02055 | hp2 | a0003 | c0006 | t0002 | g0278 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0307 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02071 | hp2 | a0002 | c0033 | t0008 | g0267 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02074 | hp2 | a0013 | c0021 | t0001 | g0057 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02080 | hp1 | a0012 | c0024 | t0003 | g0045 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02080 | hp2 | a0008 | c0009 | t0003 | g0189 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02083 | hp1 | a0001 | c0001 | t0015 | g0150 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0299 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02145 | hp1 | a0001 | c0001 | t0027 | g0187 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02145 | hp2 | a0003 | c0005 | t0006 | g0243 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02155 | hp1 | a0001 | c0034 | t0024 | g0304 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02257 | hp1 | a0004 | c0004 | t0007 | g0128 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02257 | hp2 | a0007 | c0020 | t0023 | g0247 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02258 | hp1 | a0001 | c0001 | t0044 | g0227 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02258 | hp2 | a0003 | c0006 | t0002 | g0276 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02280 | hp1 | a0004 | c0004 | t0020 | g0229 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02572 | hp1 | a0003 | c0006 | t0002 | g0275 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02615 | hp1 | a0015 | c0023 | t0002 | g0126 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02615 | hp2 | a0003 | c0005 | t0005 | g0245 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02630 | hp1 | a0021 | c0015 | t0002 | g0225 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02630 | hp2 | a0004 | c0004 | t0007 | g0081 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02698 | hp2 | a0002 | c0003 | t0046 | g0259 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02735 | hp2 | a0001 | c0001 | t0036 | g0216 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02809 | hp1 | a0002 | c0007 | t0026 | g0102 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02809 | hp2 | a0001 | c0013 | t0002 | g0173 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02895 | hp1 | a0007 | c0011 | t0002 | g0019 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02895 | hp2 | a0003 | c0006 | t0001 | g0279 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02922 | hp1 | a0005 | c0008 | t0002 | g0328 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02922 | hp2 | a0003 | c0006 | t0013 | g0274 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02965 | hp1 | a0001 | c0025 | t0042 | g0249 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02965 | hp2 | a0002 | c0007 | t0002 | g0124 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03130 | hp1 | a0004 | c0004 | t0041 | g0078 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03195 | hp1 | a0005 | c0008 | t0002 | g0326 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03195 | hp2 | a0011 | c0027 | t0007 | g0018 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03453 | hp1 | a0003 | c0005 | t0006 | g0239 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03486 | hp2 | a0003 | c0006 | t0013 | g0277 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03490 | hp1 | a0020 | c0016 | t0003 | g0178 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03491 | hp1 | a0002 | c0003 | t0003 | g0014 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03492 | hp1 | a0002 | c0003 | t0003 | g0014 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03540 | hp1 | a0006 | c0010 | t0002 | g0238 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03540 | hp2 | a0005 | c0008 | t0002 | g0325 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03579 | hp1 | a0003 | c0005 | t0005 | g0246 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03579 | hp2 | a0001 | c0001 | t0040 | g0115 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03669 | hp2 | a0002 | c0003 | t0003 | g0263 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03688 | hp1 | a0002 | c0003 | t0003 | g0264 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03831 | hp1 | a0004 | c0004 | t0007 | g0039 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03831 | hp2 | a0009 | c0012 | t0001 | g0118 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03834 | hp1 | a0001 | c0001 | t0039 | g0104 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03942 | hp1 | a0004 | c0004 | t0007 | g0116 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03942 | hp2 | a0004 | c0004 | t0007 | g0107 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG04204 | hp2 | a0002 | c0031 | t0002 | g0256 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18906 | hp2 | a0003 | c0005 | t0006 | g0241 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18943 | hp1 | a0002 | c0003 | t0003 | g0268 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18943 | hp2 | a0001 | c0001 | t0018 | g0052 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18944 | hp2 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18945 | hp2 | a0002 | c0003 | t0008 | g0260 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18946 | hp2 | a0016 | c0029 | t0002 | g0295 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18948 | hp2 | a0001 | c0002 | t0005 | g0302 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0159 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18954 | hp2 | a0001 | c0001 | t0032 | g0006 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18961 | hp1 | a0001 | c0001 | t0030 | g0006 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18963 | hp1 | a0002 | c0003 | t0004 | g0254 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18965 | hp1 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18965 | hp2 | a0001 | c0001 | t0034 | g0197 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18967 | hp1 | a0002 | c0003 | t0002 | g0265 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18968 | hp1 | a0014 | c0022 | t0002 | g0185 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18969 | hp2 | a0001 | c0002 | t0004 | g0314 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18970 | hp2 | a0008 | c0009 | t0003 | g0182 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18971 | hp2 | a0001 | c0001 | t0011 | g0119 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0235 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18979 | hp2 | a0001 | c0002 | t0008 | g0016 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18982 | hp2 | a0002 | c0003 | t0003 | g0252 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18986 | hp1 | a0001 | c0001 | t0011 | g0106 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18988 | hp1 | a0001 | c0001 | t0021 | g0157 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18989 | hp1 | a0001 | c0002 | t0005 | g0308 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18989 | hp2 | a0001 | c0001 | t0047 | g0036 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18993 | hp2 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18995 | hp1 | a0001 | c0001 | t0015 | g0174 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19005 | hp1 | a0001 | c0002 | t0014 | g0301 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19030 | hp2 | a0006 | c0028 | t0006 | g0244 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19054 | hp1 | a0001 | c0002 | t0014 | g0288 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19057 | hp2 | a0001 | c0002 | t0014 | g0306 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19060 | hp2 | a0018 | c0018 | t0035 | g0183 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19062 | hp1 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19062 | hp2 | a0002 | c0003 | t0031 | g0236 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19064 | hp2 | a0002 | c0003 | t0004 | g0251 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19067 | hp2 | a0002 | c0003 | t0003 | g0253 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19070 | hp2 | a0001 | c0002 | t0008 | g0016 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19074 | hp2 | a0008 | c0009 | t0003 | g0011 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19080 | hp1 | a0017 | c0030 | t0004 | g0315 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19080 | hp2 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19086 | hp2 | a0001 | c0002 | t0012 | g0322 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19087 | hp1 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19091 | hp2 | a0001 | c0001 | t0018 | g0067 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | TSI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | GIH | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20905 | hp2 | a0001 | c0001 | t0019 | g0089 | SAS | GIH | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02109 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02486 | hp1 | a0006 | c0010 | t0002 | g0237 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03471 | hp1 | a0003 | c0006 | t0002 | g0280 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG06807 | hp1 | a0001 | c0013 | t0013 | g0172 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA21309 | hp1 | a0002 | c0003 | t0045 | g0273 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA21309 | hp2 | a0007 | c0011 | t0006 | g0097 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0166 | REF | REF | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
homoSapiens_grch38 | hp1 | a0004 | c0004 | t0007 | g0079 | REF | REF | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24294172
|
T | A | 1 | a0010 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.23T>A | p.Val8Asp | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/23 | 104/7019 | 23/2328 | 8/775 | chr8 | 24294172 | ||
chr8:24311367
|
T | A | 1 | a0021 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.313T>A | p.Cys105Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/23 | 394/7019 | 313/2328 | 105/775 | chr8 | 24311367 | ||
chr8:24313423
|
T | C | 1 | a0020 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.419T>C | p.Ile140Thr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 500/7019 | 419/2328 | 140/775 | chr8 | 24313423 | ||
chr8:24313447
|
G | T | 1 | a0005 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.443G>T | p.Arg148Leu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 524/7019 | 443/2328 | 148/775 | chr8 | 24313447 | ||
chr8:24313470
|
T | C | 1 | a0008 | 3 | HG02080.hp2 NA18970.hp2 NA19074.hp2 |
missense_variant | MODERATE | c.466T>C | p.Phe156Leu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 547/7019 | 466/2328 | 156/775 | chr8 | 24313470 | ||
chr8:24321225
|
G | T | 3 | a0003a0006a0011 | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
missense_variant | MODERATE | c.656G>T | p.Arg219Met | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/23 | 737/7019 | 656/2328 | 219/775 | chr8 | 24321225 | ||
chr8:24335552
|
A | G | 2 | a0005a0019 | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.1478A>G | p.Asn493Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/23 | 1559/7019 | 1478/2328 | 493/775 | chr8 | 24335552 | ||
chr8:24339500
|
G | C | 1 | a0018 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1602G>C | p.Arg534Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1683/7019 | 1602/2328 | 534/775 | chr8 | 24339500 | ||
chr8:24339504
|
G | A | 2 | a0016a0017 | 2 | NA18946.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.1606G>A | p.Glu536Lys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1687/7019 | 1606/2328 | 536/775 | chr8 | 24339504 | ||
chr8:24339531
|
C | T | 1 | a0012 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.1633C>T | p.Arg545Cys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1714/7019 | 1633/2328 | 545/775 | chr8 | 24339531 | ||
chr8:24341705
|
C | A | 4 | a0002a0005a0006others(1): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
missense_variant | MODERATE | c.1778C>A | p.Thr593Lys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/23 | 1859/7019 | 1778/2328 | 593/775 | chr8 | 24341705 | ||
chr8:24349882
|
G | A | 1 | a0013 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2009G>A | p.Gly670Glu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2090/7019 | 2009/2328 | 670/775 | chr8 | 24349882 | ||
chr8:24349923
|
A | G | 1 | a0015 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2050A>G | p.Met684Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2131/7019 | 2050/2328 | 684/775 | chr8 | 24349923 | ||
chr8:24349925
|
G | A | 6 | a0002a0006a0009others(3): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
missense_variant | MODERATE | c.2052G>A | p.Met684Ile | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2133/7019 | 2052/2328 | 684/775 | chr8 | 24349925 | ||
chr8:24349959
|
A | C | 1 | a0005 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2086A>C | p.Lys696Gln | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2167/7019 | 2086/2328 | 696/775 | chr8 | 24349959 | ||
chr8:24352045
|
C | T | 1 | a0014 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.2237C>T | p.Ala746Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/23 | 2318/7019 | 2237/2328 | 746/775 | chr8 | 24352045 | ||
chr8:24353818
|
G | A | 19 | a0001a0002a0003others(16): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
missense_variant | MODERATE | c.2293G>A | p.Val765Met | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/23 | 2374/7019 | 2293/2328 | 765/775 | chr8 | 24353818 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24310238
|
T | C | 1 | a0006c0010 | 2 | HG02486.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.303T>C | p.Ile101Ile | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/23 | 384/7019 | 303/2328 | 101/775 | chr8 | 24310238 | ||
chr8:24313472
|
C | T | 1 | a0001c0034 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.468C>T | p.Phe156Phe | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 549/7019 | 468/2328 | 156/775 | chr8 | 24313472 | ||
chr8:24313538
|
C | T | 10 | a0001c0002a0001c0034a0002c0003others(7): Show | 92 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.534C>T | p.His178His | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 615/7019 | 534/2328 | 178/775 | chr8 | 24313538 | ||
chr8:24323926
|
C | T | 1 | a0001c0026 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.813C>T | p.Phe271Phe | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/23 | 894/7019 | 813/2328 | 271/775 | chr8 | 24323926 | ||
chr8:24326575
|
G | T | 1 | a0001c0025 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.912G>T | p.Thr304Thr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/23 | 993/7019 | 912/2328 | 304/775 | chr8 | 24326575 | ||
chr8:24330044
|
C | T | 1 | a0002c0033 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.1032C>T | p.Asn344Asn | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/23 | 1113/7019 | 1032/2328 | 344/775 | chr8 | 24330044 | ||
chr8:24331291
|
G | A | 6 | a0001c0017a0003c0005a0003c0006others(3): Show | 22 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(19): Show |
synonymous_variant | LOW | c.1245G>A | p.Val415Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/23 | 1326/7019 | 1245/2328 | 415/775 | chr8 | 24331291 | ||
chr8:24339521
|
C | T | 4 | a0001c0013a0003c0005a0003c0006others(1): Show | 17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.1623C>T | p.Tyr541Tyr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1704/7019 | 1623/2328 | 541/775 | chr8 | 24339521 | ||
chr8:24343562
|
C | T | 1 | a0019c0032 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1968C>T | p.Cys656Cys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/23 | 2049/7019 | 1968/2328 | 656/775 | chr8 | 24343562 | ||
chr8:24349886
|
G | C | 9 | a0002c0003a0002c0019a0002c0033others(6): Show | 36 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(33): Show |
synonymous_variant | LOW | c.2013G>C | p.Val671Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2094/7019 | 2013/2328 | 671/775 | chr8 | 24349886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24354444
|
T | G | 1 | a0001c0001t0019 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 40 | chr8 | 24354444 | |||||
chr8:24354480
|
ACTAT | A | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*83_*86delATCT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 83 | INFO_REALIGN_3_PRIME | chr8 | 24354480 | ||||
chr8:24354495
|
A | T | 1 | a0001c0001t0047 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 91 | chr8 | 24354495 | |||||
chr8:24354507
|
C | T | 1 | a0002c0003t0046 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 103 | chr8 | 24354507 | |||||
chr8:24354527
|
T | C | 17 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(14): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*123T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 123 | chr8 | 24354527 | |||||
chr8:24354541
|
T | A | 3 | a0001c0013t0013a0002c0007t0026a0003c0006t0013 | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 137 | chr8 | 24354541 | |||||
chr8:24354632
|
A | G | 1 | a0001c0001t0018 | 2 | NA18943.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 228 | chr8 | 24354632 | |||||
chr8:24354695
|
T | G | 1 | a0001c0001t0015 | 2 | HG02083.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*291T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 291 | chr8 | 24354695 | |||||
chr8:24354863
|
A | C | 4 | a0001c0013t0013a0002c0003t0045a0002c0007t0026others(1): Show | 5 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 459 | chr8 | 24354863 | |||||
chr8:24354951
|
G | A | 21 | a0001c0001t0003a0001c0001t0008a0001c0001t0016others(18): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 547 | chr8 | 24354951 | |||||
chr8:24355057
|
G | A | 3 | a0001c0013t0013a0002c0007t0026a0003c0006t0013 | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 653 | chr8 | 24355057 | |||||
chr8:24355087
|
T | G | 1 | a0001c0001t0021 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 683 | chr8 | 24355087 | |||||
chr8:24355221
|
T | A | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*817T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 817 | chr8 | 24355221 | |||||
chr8:24355259
|
T | A | 1 | a0002c0007t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 855 | chr8 | 24355259 | |||||
chr8:24355392
|
C | CCTAT | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*992_*995dupTCTA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 996 | INFO_REALIGN_3_PRIME | chr8 | 24355392 | ||||
chr8:24355409
|
T | G | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*1005T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1005 | chr8 | 24355409 | |||||
chr8:24355517
|
C | CT | 9 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(6): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1124dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1125 | INFO_REALIGN_3_PRIME | chr8 | 24355517 | ||||
chr8:24355533
|
G | T | 1 | a0001c0001t0044 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1129 | chr8 | 24355533 | |||||
chr8:24355662
|
A | AAGATAGA others(1): Show |
87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*1262_*1269dupTAGA others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1270 | INFO_REALIGN_3_PRIME | chr8 | 24355662 | ||||
chr8:24355675
|
C | T | 1 | a0001c0001t0043 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1271 | chr8 | 24355675 | |||||
chr8:24355935
|
G | T | 1 | a0001c0025t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1531 | chr8 | 24355935 | |||||
chr8:24356052
|
C | G | 5 | a0001c0001t0006a0002c0019t0006a0003c0005t0006others(2): Show | 11 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1648 | chr8 | 24356052 | |||||
chr8:24356091
|
T | C | 1 | a0018c0018t0035 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1687T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1687 | chr8 | 24356091 | |||||
chr8:24356241
|
T | A | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*1837T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1837 | chr8 | 24356241 | |||||
chr8:24356248
|
G | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*1844G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1844 | chr8 | 24356248 | |||||
chr8:24356409
|
A | G | 1 | a0001c0001t0009 | 5 | HG00323.hp2 HG00741.hp1 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2005 | chr8 | 24356409 | |||||
chr8:24356539
|
T | C | 1 | a0002c0003t0029 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2135 | chr8 | 24356539 | |||||
chr8:24356562
|
C | G | 1 | a0001c0001t0025 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2158 | chr8 | 24356562 | |||||
chr8:24356613
|
C | T | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2209C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2209 | chr8 | 24356613 | |||||
chr8:24356658
|
C | T | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*2254C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2254 | chr8 | 24356658 | |||||
chr8:24356686
|
G | A | 3 | a0001c0013t0013a0002c0007t0026a0003c0006t0013 | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2282G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2282 | chr8 | 24356686 | |||||
chr8:24356870
|
C | CCTTTGGG others(30): Show |
1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2467_*2503dupCTTT others(33): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2504 | INFO_REALIGN_3_PRIME | chr8 | 24356870 | ||||
chr8:24356921
|
G | C | 1 | a0002c0003t0031 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2517 | chr8 | 24356921 | |||||
chr8:24357097
|
A | G | 1 | a0001c0001t0039 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2693A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2693 | chr8 | 24357097 | |||||
chr8:24357128
|
ATT | A | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*2727_*2728delTT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2727 | INFO_REALIGN_3_PRIME | chr8 | 24357128 | ||||
chr8:24357212
|
T | C | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*2808T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2808 | chr8 | 24357212 | |||||
chr8:24357247
|
G | A | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*2843G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2843 | chr8 | 24357247 | |||||
chr8:24357334
|
A | G | 1 | a0001c0025t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2930 | chr8 | 24357334 | |||||
chr8:24357422
|
C | A | 21 | a0001c0001t0003a0001c0001t0008a0001c0001t0016others(18): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3018C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3018 | chr8 | 24357422 | |||||
chr8:24357488
|
A | G | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*3084A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3084 | chr8 | 24357488 | |||||
chr8:24357562
|
G | A | 1 | a0001c0001t0022 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3158 | chr8 | 24357562 | |||||
chr8:24357662
|
G | C | 1 | a0002c0003t0029 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3258G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3258 | chr8 | 24357662 | |||||
chr8:24357713
|
G | T | 1 | a0001c0034t0024 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3309G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3309 | chr8 | 24357713 | |||||
chr8:24357755
|
C | T | 2 | a0001c0001t0030a0001c0001t0032 | 2 | NA18954.hp2 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3351C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3351 | chr8 | 24357755 | |||||
chr8:24357775
|
T | TTCTC | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*3372_*3373insCTCT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3373 | INFO_REALIGN_3_PRIME | chr8 | 24357775 | ||||
chr8:24357865
|
C | T | 1 | a0001c0034t0024 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3461C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3461 | chr8 | 24357865 | |||||
chr8:24357914
|
A | T | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*3510A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3510 | chr8 | 24357914 | |||||
chr8:24357984
|
TTATAGTT others(18): Show |
T | 2 | a0001c0001t0010a0001c0002t0010 | 5 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3606_*3630delTATA others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3606 | INFO_REALIGN_3_PRIME | chr8 | 24357984 | ||||
chr8:24358101
|
A | C | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*3697A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3697 | chr8 | 24358101 | |||||
chr8:24358112
|
T | TATG | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*3710_*3711insGAT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3711 | INFO_REALIGN_3_PRIME | chr8 | 24358112 | ||||
chr8:24358137
|
G | A | 1 | a0007c0020t0023 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3733G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3733 | chr8 | 24358137 | |||||
chr8:24358137
|
G | T | 1 | a0001c0001t0011 | 3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3733G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3733 | chr8 | 24358137 | |||||
chr8:24358150
|
T | C | 1 | a0001c0001t0037 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3746T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3746 | chr8 | 24358150 | |||||
chr8:24358178
|
G | C | 2 | a0001c0001t0030a0001c0001t0032 | 2 | NA18954.hp2 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3774G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3774 | chr8 | 24358178 | |||||
chr8:24358224
|
T | A | 1 | a0001c0002t0014 | 3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3820T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3820 | chr8 | 24358224 | |||||
chr8:24358284
|
T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3880T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3880 | chr8 | 24358284 | |||||
chr8:24358293
|
G | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3889 | chr8 | 24358293 | |||||
chr8:24358303
|
T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3899T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3899 | chr8 | 24358303 | |||||
chr8:24358306
|
T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3902T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3902 | chr8 | 24358306 | |||||
chr8:24358311
|
C | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3907C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3907 | chr8 | 24358311 | |||||
chr8:24358317
|
T | TATAGAAT others(8): Show |
1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3913_*3914insATAG others(11): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3914 | chr8 | 24358317 | |||||
chr8:24358318
|
C | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3914C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3914 | chr8 | 24358318 | |||||
chr8:24358318
|
CATT | C | 2 | a0001c0001t0017a0001c0001t0038 | 3 | HG01891.hp2 HG02109.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3915_*3917delATT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3915 | chr8 | 24358318 | |||||
chr8:24358326
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3922A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3922 | chr8 | 24358326 | |||||
chr8:24358327
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3923A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3923 | chr8 | 24358327 | |||||
chr8:24358332
|
T | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3928T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3928 | chr8 | 24358332 | |||||
chr8:24358355
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3951A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3951 | chr8 | 24358355 | |||||
chr8:24358366
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3962A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3962 | chr8 | 24358366 | |||||
chr8:24358371
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3967A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3967 | chr8 | 24358371 | |||||
chr8:24358372
|
G | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3968G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3968 | chr8 | 24358372 | |||||
chr8:24358374
|
A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3970A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3970 | chr8 | 24358374 | |||||
chr8:24358376
|
C | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3972 | chr8 | 24358376 | |||||
chr8:24358379
|
G | T | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*3975G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3975 | chr8 | 24358379 | |||||
chr8:24358382
|
G | C | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3978G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3978 | chr8 | 24358382 | |||||
chr8:24358383
|
T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3979T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3979 | chr8 | 24358383 | |||||
chr8:24358387
|
A | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3983A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3983 | chr8 | 24358387 | |||||
chr8:24358404
|
T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4000T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4000 | chr8 | 24358404 | |||||
chr8:24358502
|
T | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4098T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4098 | chr8 | 24358502 | |||||
chr8:24358505
|
GCTCCACC others(28): Show |
G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4102_*4136delCTCC others(31): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4102 | chr8 | 24358505 | |||||
chr8:24358543
|
A | C | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4139A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4139 | chr8 | 24358543 | |||||
chr8:24358553
|
C | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4149C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4149 | chr8 | 24358553 | |||||
chr8:24358563
|
A | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4159A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4159 | chr8 | 24358563 | |||||
chr8:24358568
|
C | T | 3 | a0001c0013t0013a0002c0007t0026a0003c0006t0013 | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4164C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4164 | chr8 | 24358568 | |||||
chr8:24358648
|
C | CT | 12 | a0001c0001t0005a0001c0001t0015a0001c0001t0017others(9): Show | 26 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4249dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4250 | INFO_REALIGN_3_PRIME | chr8 | 24358648 | ||||
chr8:24358711
|
T | A | 1 | a0001c0001t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4307T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4307 | chr8 | 24358711 | |||||
chr8:24358734
|
A | C | 1 | a0001c0001t0047 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4330A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4330 | chr8 | 24358734 | |||||
chr8:24358755
|
A | T | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*4351A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4351 | chr8 | 24358755 | |||||
chr8:24358818
|
C | T | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*4414C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4414 | chr8 | 24358818 | |||||
chr8:24358856
|
T | C | 4 | a0001c0001t0008a0001c0002t0008a0002c0003t0008others(1): Show | 6 | HG00673.hp1 HG02071.hp2 NA18945.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4452T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4452 | chr8 | 24358856 | |||||
chr8:24358878
|
A | G | 9 | a0001c0001t0005a0001c0001t0015a0001c0001t0017others(6): Show | 22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4474A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4474 | chr8 | 24358878 | |||||
chr8:24358935
|
A | AAAACT | 1 | a0001c0001t0011 | 3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4533_*4537dupAACT others(1): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4538 | INFO_REALIGN_3_PRIME | chr8 | 24358935 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24294203
|
T | C | 1 | a0001c0001t0010g0017 | 1 | HG00639.hp2 | splice_region_variant&intron_variant | LOW | c.46+8T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294203 | ||||||
chr8:24294636
|
GTTTGAGT others(7): Show |
G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+446_46+459delAG others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24294636 | |||||
chr8:24294678
|
T | C | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.46+483T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294678 | ||||||
chr8:24294725
|
C | T | 101 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0002t0001g0281others(98): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.46+530C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294725 | ||||||
chr8:24295115
|
T | G | 2 | a0001c0002t0004g0235a0001c0002t0005g0234 | 2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.46+920T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295115 | ||||||
chr8:24295155
|
T | C | 2 | a0002c0003t0003g0013a0002c0003t0031g0236 | 3 | NA18993.hp2 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.46+960T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295155 | ||||||
chr8:24295305
|
C | G | 1 | a0001c0001t0005g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.46+1110C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295305 | ||||||
chr8:24295469
|
GT | G | 41 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0025t0042g0249others(38): Show | 46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.46+1281delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24295469 | |||||
chr8:24295683
|
G | A | 2 | a0006c0010t0002g0237a0006c0010t0002g0238 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.46+1488G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295683 | ||||||
chr8:24295685
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.46+1490C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295685 | ||||||
chr8:24295689
|
G | A | 1 | a0001c0001t0016g0004 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.46+1494G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295689 | ||||||
chr8:24295788
|
G | A | 1 | a0007c0011t0002g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.46+1593G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295788 | ||||||
chr8:24296145
|
G | T | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.46+1950G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296145 | ||||||
chr8:24296176
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.46+1981G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296176 | ||||||
chr8:24296268
|
A | C | 1 | a0001c0001t0002g0231 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.46+2073A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296268 | ||||||
chr8:24296312
|
G | GT | 7 | a0001c0001t0002g0224a0001c0001t0002g0228a0001c0001t0002g0230others(4): Show | 7 | HG01261.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+2123dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24296312 | |||||
chr8:24296346
|
C | T | 1 | a0001c0002t0008g0016 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.46+2151C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296346 | ||||||
chr8:24296427
|
A | T | 25 | a0001c0001t0003g0269a0001c0001t0003g0270a0002c0003t0001g0001others(22): Show | 30 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.46+2232A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296427 | ||||||
chr8:24296433
|
C | T | 48 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(45): Show | 50 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.46+2238C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296433 | ||||||
chr8:24296641
|
A | G | 2 | a0001c0002t0001g0324a0001c0002t0008g0016 | 3 | NA18969.hp1 NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.46+2446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296641 | ||||||
chr8:24296645
|
T | C | 49 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.46+2450T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296645 | ||||||
chr8:24296685
|
C | A | 1 | a0001c0001t0012g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.46+2490C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296685 | ||||||
chr8:24296803
|
T | C | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+2608T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296803 | ||||||
chr8:24296884
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.46+2689C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296884 | ||||||
chr8:24296936
|
G | A | 60 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(57): Show | 62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.46+2741G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296936 | ||||||
chr8:24297075
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.46+2880G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297075 | ||||||
chr8:24297141
|
C | T | 41 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0025t0042g0249others(38): Show | 46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-2833C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297141 | ||||||
chr8:24297159
|
G | GTTT | 45 | a0001c0002t0001g0281a0001c0002t0001g0287a0001c0002t0001g0289others(42): Show | 47 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.47-2808_47-2806dup others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297159 | |||||
chr8:24297159
|
G | GTTTTT | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-2810_47-2806dup others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297159 | |||||
chr8:24297162
|
T | G | 1 | a0001c0001t0043g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47-2812T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297162 | ||||||
chr8:24297166
|
TTTG | T | 40 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0025t0042g0249others(37): Show | 45 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.47-2793_47-2791del others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297166 | |||||
chr8:24297169
|
G | T | 163 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(160): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.47-2805G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297169 | ||||||
chr8:24297380
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0003g0023a0001c0001t0003g0025 | 3 | HG00323.hp1 HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.47-2594T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297380 | ||||||
chr8:24297445
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0087a0001c0001t0002g0086others(1): Show | 5 | HG01433.hp2 HG01934.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-2529T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297445 | ||||||
chr8:24297474
|
C | T | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-2500C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297474 | ||||||
chr8:24297641
|
T | G | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-2333T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297641 | ||||||
chr8:24297652
|
A | G | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-2322A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297652 | ||||||
chr8:24297679
|
G | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-2295G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297679 | ||||||
chr8:24297910
|
G | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-2064G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297910 | ||||||
chr8:24298155
|
G | A | 60 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(57): Show | 62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.47-1819G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298155 | ||||||
chr8:24298242
|
A | T | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.47-1732A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298242 | ||||||
chr8:24298252
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.47-1722T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298252 | ||||||
chr8:24298419
|
T | A | 99 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0002t0001g0281others(96): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.47-1555T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298419 | ||||||
chr8:24298552
|
G | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.47-1422G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298552 | ||||||
chr8:24298607
|
T | C | 2 | a0001c0001t0019g0089a0001c0001t0037g0088 | 2 | HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.47-1367T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298607 | ||||||
chr8:24298691
|
C | T | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(105): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.47-1283C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298691 | ||||||
chr8:24298874
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.47-1100G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298874 | ||||||
chr8:24298892
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47-1082T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298892 | ||||||
chr8:24298893
|
C | A | 1 | a0001c0001t0010g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47-1081C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298893 | ||||||
chr8:24298959
|
A | G | 50 | a0001c0001t0003g0080a0001c0002t0001g0281a0001c0002t0001g0283others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.47-1015A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298959 | ||||||
chr8:24299031
|
G | GA | 8 | a0001c0001t0002g0091a0001c0001t0002g0137a0001c0001t0002g0224others(5): Show | 8 | HG02886.hp1 HG03486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-928dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299031 | |||||
chr8:24299031
|
GAA | G | 12 | a0001c0025t0042g0249a0003c0005t0005g0245a0003c0005t0005g0246others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-929_47-928delAA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299031 | |||||
chr8:24299069
|
T | G | 1 | a0001c0001t0003g0138 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.47-905T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299069 | ||||||
chr8:24299297
|
G | T | 41 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0025t0042g0249others(38): Show | 46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-677G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299297 | ||||||
chr8:24299462
|
GT | G | 287 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.47-503delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299462 | |||||
chr8:24299511
|
T | A | 41 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0025t0042g0249others(38): Show | 46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-463T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299511 | ||||||
chr8:24299528
|
A | G | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0009g0134others(1): Show | 4 | HG00733.hp1 HG01081.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299528 | ||||||
chr8:24299553
|
A | T | 1 | a0001c0001t0003g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-421A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299553 | ||||||
chr8:24299558
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18963.hp2 NA18994.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.47-416A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299558 | ||||||
chr8:24299634
|
C | T | 102 | a0001c0001t0003g0080a0001c0001t0003g0269a0001c0001t0003g0270others(99): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.47-340C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299634 | ||||||
chr8:24299692
|
G | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-282G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299692 | ||||||
chr8:24299891
|
T | C | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.47-83T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299891 | ||||||
chr8:24300130
|
CAT | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+62_150+63delAT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24300130 | |||||
chr8:24300149
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.150+72G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300149 | ||||||
chr8:24300317
|
C | T | 1 | a0001c0001t0009g0222 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150+240C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300317 | ||||||
chr8:24300411
|
T | C | 1 | a0001c0001t0043g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.150+334T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300411 | ||||||
chr8:24300480
|
G | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+403G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300480 | ||||||
chr8:24300517
|
C | T | 8 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+440C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300517 | ||||||
chr8:24300527
|
C | T | 1 | a0001c0001t0010g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+450C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300527 | ||||||
chr8:24300561
|
G | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+484G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300561 | ||||||
chr8:24300705
|
C | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+628C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300705 | ||||||
chr8:24300814
|
T | C | 1 | a0001c0002t0010g0282 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.150+737T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300814 | ||||||
chr8:24300838
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.150+761T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300838 | ||||||
chr8:24300842
|
G | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+765G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300842 | ||||||
chr8:24300960
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+883C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300960 | ||||||
chr8:24301104
|
A | G | 2 | a0003c0006t0001g0279a0003c0006t0002g0280 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.150+1027A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301104 | ||||||
chr8:24301136
|
T | G | 1 | a0001c0001t0003g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150+1059T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301136 | ||||||
chr8:24301326
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0005g0095others(1): Show | 4 | HG00438.hp2 HG00558.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+1249G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301326 | ||||||
chr8:24301329
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.150+1252T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301329 | ||||||
chr8:24301362
|
T | C | 99 | a0001c0001t0003g0080a0001c0002t0001g0027a0001c0002t0001g0281others(96): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.150+1285T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301362 | ||||||
chr8:24301446
|
G | T | 40 | a0001c0025t0042g0249a0002c0003t0001g0001a0002c0003t0001g0250others(37): Show | 45 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.150+1369G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301446 | ||||||
chr8:24301725
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0030 | 3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.150+1648G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301725 | ||||||
chr8:24301968
|
T | C | 1 | a0007c0011t0006g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+1891T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301968 | ||||||
chr8:24302012
|
G | C | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+1935G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302012 | ||||||
chr8:24302054
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+1977C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302054 | ||||||
chr8:24302071
|
A | G | 3 | a0003c0005t0005g0245a0003c0005t0005g0246a0006c0028t0006g0244 | 3 | HG02615.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.150+1994A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302071 | ||||||
chr8:24302229
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+2152C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302229 | ||||||
chr8:24302295
|
A | G | 1 | a0001c0001t0004g0131 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.150+2218A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302295 | ||||||
chr8:24302376
|
C | A | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.150+2299C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302376 | ||||||
chr8:24302503
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+2426G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302503 | ||||||
chr8:24302547
|
G | A | 59 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(56): Show | 61 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.150+2470G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302547 | ||||||
chr8:24302734
|
T | C | 49 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.150+2657T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302734 | ||||||
chr8:24302755
|
C | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2678C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302755 | ||||||
chr8:24302768
|
C | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.150+2691C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302768 | ||||||
chr8:24302770
|
C | CT | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2701dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24302770 | |||||
chr8:24302778
|
T | A | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+2701T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302778 | ||||||
chr8:24302791
|
T | C | 49 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.150+2714T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302791 | ||||||
chr8:24302817
|
C | T | 35 | a0001c0025t0042g0249a0002c0003t0001g0001a0002c0003t0001g0250others(32): Show | 40 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.150+2740C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302817 | ||||||
chr8:24302918
|
C | G | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2841C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302918 | ||||||
chr8:24302939
|
G | A | 1 | a0001c0001t0043g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.150+2862G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302939 | ||||||
chr8:24302973
|
T | C | 50 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.150+2896T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302973 | ||||||
chr8:24303010
|
A | G | 23 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(20): Show | 28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.150+2933A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303010 | ||||||
chr8:24303019
|
T | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2942T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303019 | ||||||
chr8:24303541
|
C | T | 23 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(20): Show | 28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.150+3464C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303541 | ||||||
chr8:24303715
|
C | G | 50 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.150+3638C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303715 | ||||||
chr8:24304047
|
A | G | 39 | a0001c0025t0042g0249a0002c0003t0001g0001a0002c0003t0001g0250others(36): Show | 44 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.150+3970A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304047 | ||||||
chr8:24304053
|
G | A | 1 | a0001c0002t0004g0286 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.150+3976G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304053 | ||||||
chr8:24304148
|
C | T | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+4071C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304148 | ||||||
chr8:24304234
|
A | C | 39 | a0001c0025t0042g0249a0002c0003t0001g0001a0002c0003t0001g0250others(36): Show | 44 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.150+4157A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304234 | ||||||
chr8:24304251
|
T | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0098a0001c0001t0002g0099 | 3 | HG02004.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.150+4174T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304251 | ||||||
chr8:24304487
|
G | C | 2 | a0001c0001t0002g0100a0001c0001t0006g0101 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.150+4410G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304487 | ||||||
chr8:24304526
|
G | A | 2 | a0002c0003t0001g0250a0002c0003t0004g0251 | 2 | NA18985.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.150+4449G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304526 | ||||||
chr8:24304587
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.150+4510T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304587 | ||||||
chr8:24304590
|
G | T | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4513G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304590 | ||||||
chr8:24304603
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.150+4526C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304603 | ||||||
chr8:24304701
|
T | C | 101 | a0001c0001t0003g0080a0001c0002t0001g0027a0001c0002t0001g0281others(98): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.150+4624T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304701 | ||||||
chr8:24304738
|
T | TACCTCTA others(42): Show |
1 | a0002c0003t0045g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+4711_150+4759d others(51): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304738 | |||||
chr8:24304875
|
A | C | 1 | a0001c0001t0017g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.150+4798A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304875 | ||||||
chr8:24304881
|
A | T | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4804A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304881 | ||||||
chr8:24304916
|
C | CA | 36 | a0001c0001t0001g0032a0001c0001t0001g0075a0001c0001t0001g0143others(33): Show | 41 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(38): Show |
intron_variant | MODIFIER | c.150+4854dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304916 | |||||
chr8:24304916
|
CA | C | 17 | a0001c0001t0001g0073a0001c0001t0002g0072a0001c0001t0002g0074others(14): Show | 17 | HG01192.hp2 HG01891.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.150+4854delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304916 | |||||
chr8:24304930
|
A | AAAAATAG | 57 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(54): Show | 59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.150+4854_150+4855i others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304930 | |||||
chr8:24304932
|
T | G | 61 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(58): Show | 63 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+4855T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304932 | ||||||
chr8:24305063
|
T | G | 1 | a0001c0002t0012g0322 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.151-4831T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305063 | ||||||
chr8:24305110
|
TG | T | 16 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(13): Show | 16 | HG00733.hp2 HG00738.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-4783delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305110 | ||||||
chr8:24305117
|
T | A | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-4777T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305117 | ||||||
chr8:24305174
|
T | G | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.151-4720T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305174 | ||||||
chr8:24305264
|
C | T | 24 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(21): Show | 29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-4630C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305264 | ||||||
chr8:24305268
|
C | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-4626C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305268 | ||||||
chr8:24305269
|
G | A | 4 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0019t0006g0226others(1): Show | 4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-4625G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305269 | ||||||
chr8:24305355
|
AGTGTGTG others(7): Show |
A | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4531_151-4518d others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305355 | |||||
chr8:24305451
|
C | CT | 27 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0070others(24): Show | 28 | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-4417dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305451
|
C | CTT | 14 | a0001c0001t0038g0129a0001c0002t0001g0281a0001c0002t0001g0287others(11): Show | 14 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-4418_151-4417d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305451
|
C | CTTT | 42 | a0001c0001t0003g0080a0001c0002t0001g0283a0001c0002t0001g0290others(39): Show | 44 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.151-4419_151-4417d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305451
|
C | CTTTT | 26 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0285others(23): Show | 30 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-4420_151-4417d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305451
|
C | CTTTTT | 5 | a0001c0002t0001g0027a0002c0003t0002g0265a0002c0003t0003g0014others(2): Show | 6 | HG02071.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-4421_151-4417d others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305451
|
CT | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0148others(24): Show | 28 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.151-4417delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | |||||
chr8:24305468
|
TTTTTTTT others(3): Show |
T | 1 | a0005c0008t0002g0325 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151-4425_151-4416d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305468 | ||||||
chr8:24305477
|
T | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 15 | HG00438.hp1 HG02074.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-4417T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305477 | ||||||
chr8:24305478
|
A | T | 97 | a0001c0001t0002g0224a0001c0001t0002g0228a0001c0001t0002g0230others(94): Show | 104 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.151-4416A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305478 | ||||||
chr8:24305641
|
A | G | 74 | a0001c0001t0003g0080a0001c0002t0001g0027a0001c0002t0001g0281others(71): Show | 81 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.151-4253A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305641 | ||||||
chr8:24305654
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.151-4240G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305654 | ||||||
chr8:24305691
|
C | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4203C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305691 | ||||||
chr8:24305767
|
A | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4127A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305767 | ||||||
chr8:24305852
|
TA | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(87): Show | 99 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.151-4041delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305852 | ||||||
chr8:24306006
|
G | A | 2 | a0006c0010t0002g0237a0006c0010t0002g0238 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.151-3888G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306006 | ||||||
chr8:24306061
|
A | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3833A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306061 | ||||||
chr8:24306064
|
C | T | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-3830C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306064 | ||||||
chr8:24306117
|
G | C | 15 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0019t0006g0226others(12): Show | 15 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.151-3777G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306117 | ||||||
chr8:24306156
|
G | T | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3738G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306156 | ||||||
chr8:24306190
|
C | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3704C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306190 | ||||||
chr8:24306213
|
C | A | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.151-3681C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306213 | ||||||
chr8:24306213
|
C | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.151-3681C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306213 | ||||||
chr8:24306214
|
G | A | 11 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3680G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306214 | ||||||
chr8:24306280
|
G | T | 1 | a0001c0001t0004g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.151-3614G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306280 | ||||||
chr8:24306349
|
CAAATAAA others(5): Show |
C | 22 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(19): Show | 27 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.151-3539_151-3528d others(14): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306349 | |||||
chr8:24306351
|
A | AATATATA others(3): Show |
3 | a0001c0002t0004g0292a0001c0002t0010g0282a0005c0008t0002g0327 | 3 | HG01891.hp1 HG01934.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(5): Show |
7 | a0001c0002t0001g0283a0001c0002t0001g0311a0001c0002t0001g0316others(4): Show | 7 | HG00423.hp2 HG00741.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(14): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(7): Show |
2 | a0001c0025t0042g0249a0005c0008t0002g0326 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(9): Show |
5 | a0001c0002t0001g0281a0001c0002t0001g0317a0001c0002t0008g0016others(2): Show | 6 | HG00408.hp1 HG02165.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(18): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(11): Show |
7 | a0001c0002t0001g0027a0001c0002t0001g0293a0001c0002t0001g0294others(4): Show | 7 | HG00558.hp2 HG01496.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(20): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(53): Show |
4 | a0003c0005t0006g0240a0003c0005t0006g0241a0003c0005t0006g0242others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(62): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(13): Show |
1 | a0001c0002t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(22): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(87): Show |
1 | a0003c0005t0005g0245 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.151-3540_151-3539i others(96): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(15): Show |
8 | a0001c0002t0001g0298a0001c0002t0001g0300a0001c0002t0001g0318others(5): Show | 8 | HG00621.hp1 HG00673.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(24): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(89): Show |
1 | a0003c0005t0005g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(98): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(17): Show |
4 | a0001c0002t0002g0303a0001c0002t0002g0320a0001c0002t0004g0286others(1): Show | 4 | HG01256.hp1 HG01258.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(19): Show |
4 | a0001c0002t0001g0285a0001c0002t0001g0305a0001c0002t0014g0306others(1): Show | 4 | HG01517.hp1 HG02155.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(28): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(21): Show |
3 | a0001c0002t0001g0309a0001c0002t0004g0307a0001c0002t0005g0308 | 3 | HG02056.hp2 NA18971.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(75): Show |
1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151-3540_151-3539i others(84): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(31): Show |
2 | a0001c0002t0004g0235a0003c0006t0002g0275 | 2 | HG02572.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(40): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(67): Show |
1 | a0006c0010t0002g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(76): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | AATATATA others(17): Show |
2 | a0001c0002t0001g0313a0001c0002t0001g0321 | 2 | NA18951.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306351
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0004g0314 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.151-3543_151-3542i others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | ||||||
chr8:24306351
|
A | ATATATAT others(16): Show |
1 | a0017c0030t0004g0315 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.151-3543_151-3542i others(25): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | ||||||
chr8:24306351
|
A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0289 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.151-3543_151-3542i others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | ||||||
chr8:24306351
|
AATAAATA others(35): Show |
A | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3539_151-3498d others(44): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | |||||
chr8:24306353
|
TAAATAAA others(3): Show |
T | 5 | a0001c0002t0001g0287a0001c0002t0002g0015a0001c0002t0002g0312others(2): Show | 6 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-3539_151-3530d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306353 | |||||
chr8:24306355
|
A | T | 66 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(63): Show | 67 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.151-3539A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306355 | ||||||
chr8:24306356
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0044g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306356 | |||||
chr8:24306357
|
T | TATATATA others(23): Show |
1 | a0002c0019t0006g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.151-3536_151-3535i others(32): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | |||||
chr8:24306357
|
T | TATATATA others(55): Show |
1 | a0021c0015t0002g0225 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(64): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | |||||
chr8:24306357
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | |||||
chr8:24306359
|
A | T | 67 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(64): Show | 68 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.151-3535A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306359 | ||||||
chr8:24306361
|
T | A | 4 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0019t0006g0226others(1): Show | 4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3533T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306361 | ||||||
chr8:24306361
|
T | TAAATATA others(21): Show |
3 | a0001c0001t0002g0155a0001c0001t0003g0184a0001c0001t0005g0034 | 3 | HG02083.hp2 HG03209.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.151-3516_151-3489d others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306361 | |||||
chr8:24306363
|
A | AAT | 11 | a0001c0001t0001g0066a0001c0001t0002g0002a0001c0001t0002g0091others(8): Show | 13 | HG00408.hp2 HG02004.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.151-3510_151-3509d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306363 | |||||
chr8:24306363
|
A | T | 71 | a0001c0001t0009g0214a0001c0002t0001g0027a0001c0002t0001g0281others(68): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.151-3531A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306363 | ||||||
chr8:24306365
|
T | A | 1 | a0001c0001t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151-3529T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306365 | ||||||
chr8:24306367
|
T | A | 1 | a0001c0001t0002g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.151-3527T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306367 | ||||||
chr8:24306367
|
T | TATATAAA others(87): Show |
1 | a0006c0028t0006g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-3522_151-3521i others(96): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306367 | |||||
chr8:24306369
|
T | A | 6 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0240others(3): Show | 6 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-3525T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306369 | ||||||
chr8:24306369
|
T | TAAATATA others(85): Show |
1 | a0003c0005t0006g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151-3524_151-3523i others(94): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306369 | |||||
chr8:24306371
|
T | TATATATA others(69): Show |
1 | a0006c0010t0002g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.151-3511_151-3510i others(78): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306371 | |||||
chr8:24306373
|
T | A | 1 | a0006c0010t0002g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151-3521T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306373 | ||||||
chr8:24306385
|
TTTAAAA | T | 2 | a0001c0002t0002g0015a0001c0002t0002g0312 | 3 | HG01069.hp1 HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.151-3508_151-3503d others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306385 | ||||||
chr8:24306386
|
T | A | 82 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(79): Show | 88 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.151-3508T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306386 | ||||||
chr8:24306389
|
A | T | 58 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(55): Show | 59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.151-3505A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306389 | ||||||
chr8:24306391
|
A | T | 5 | a0001c0002t0001g0311a0001c0002t0001g0324a0001c0002t0002g0310others(2): Show | 5 | HG00609.hp2 HG00741.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-3503A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306391 | ||||||
chr8:24306393
|
T | A | 15 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0019t0006g0226others(12): Show | 15 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.151-3501T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306393 | ||||||
chr8:24306716
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.151-3178C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306716 | ||||||
chr8:24306813
|
C | A | 1 | a0001c0001t0002g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.151-3081C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306813 | ||||||
chr8:24306890
|
C | A | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-3004C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306890 | ||||||
chr8:24306922
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.151-2972A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306922 | ||||||
chr8:24306989
|
T | C | 1 | a0014c0022t0002g0185 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.151-2905T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306989 | ||||||
chr8:24307025
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.151-2869T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307025 | ||||||
chr8:24307147
|
C | T | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-2747C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307147 | ||||||
chr8:24307180
|
T | A | 1 | a0004c0004t0007g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-2714T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307180 | ||||||
chr8:24307193
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-2701C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307193 | ||||||
chr8:24307236
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-2658T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307236 | ||||||
chr8:24307245
|
C | A | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151-2649C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307245 | ||||||
chr8:24307380
|
G | T | 1 | a0001c0001t0002g0123 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.151-2514G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307380 | ||||||
chr8:24307647
|
A | G | 8 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0007t0003g0271others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-2247A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307647 | ||||||
chr8:24307898
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-1996C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307898 | ||||||
chr8:24307965
|
G | A | 1 | a0002c0003t0003g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151-1929G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307965 | ||||||
chr8:24308001
|
C | G | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1893C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308001 | ||||||
chr8:24308042
|
G | A | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1852G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308042 | ||||||
chr8:24308187
|
G | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-1707G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308187 | ||||||
chr8:24308193
|
TCTTA | T | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-1697_151-1694d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24308193 | |||||
chr8:24308259
|
C | G | 1 | a0001c0001t0005g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.151-1635C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308259 | ||||||
chr8:24308312
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.151-1582A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308312 | ||||||
chr8:24308356
|
ATCTTTCC others(14): Show |
A | 58 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(55): Show | 60 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.151-1536_151-1516d others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24308356 | |||||
chr8:24308536
|
A | G | 1 | a0001c0002t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-1358A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308536 | ||||||
chr8:24308583
|
G | A | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1311G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308583 | ||||||
chr8:24308774
|
G | A | 4 | a0001c0001t0002g0103a0001c0001t0002g0108a0001c0001t0039g0104others(1): Show | 4 | HG03704.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1120G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308774 | ||||||
chr8:24308786
|
T | A | 1 | a0002c0003t0003g0253 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.151-1108T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308786 | ||||||
chr8:24308824
|
G | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.151-1070G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308824 | ||||||
chr8:24308869
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.151-1025C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308869 | ||||||
chr8:24308875
|
C | T | 98 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(95): Show | 105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.151-1019C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308875 | ||||||
chr8:24308907
|
G | A | 24 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(21): Show | 29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-987G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308907 | ||||||
chr8:24308914
|
G | T | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-980G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308914 | ||||||
chr8:24308967
|
A | C | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-927A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308967 | ||||||
chr8:24309000
|
T | C | 61 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(58): Show | 63 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-894T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309000 | ||||||
chr8:24309037
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151-857A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309037 | ||||||
chr8:24309128
|
G | C | 2 | a0002c0007t0003g0271a0002c0007t0003g0272 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.151-766G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309128 | ||||||
chr8:24309135
|
A | G | 3 | a0001c0001t0002g0091a0001c0001t0002g0098a0001c0001t0002g0099 | 3 | HG02004.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.151-759A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309135 | ||||||
chr8:24309270
|
A | G | 82 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(79): Show | 89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.151-624A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309270 | ||||||
chr8:24309324
|
T | C | 100 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(97): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.151-570T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309324 | ||||||
chr8:24309543
|
T | C | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-351T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309543 | ||||||
chr8:24309566
|
C | G | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0007c0011t0006g0097 | 3 | HG02717.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.151-328C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309566 | ||||||
chr8:24309694
|
G | C | 2 | a0003c0006t0013g0274a0003c0006t0013g0277 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.151-200G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309694 | ||||||
chr8:24309760
|
G | A | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-134G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309760 | ||||||
chr8:24309776
|
T | C | 87 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-118T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309776 | ||||||
chr8:24309803
|
G | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-91G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309803 | ||||||
chr8:24309979
|
C | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.227+9C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 3/22 | chr8 | 24309979 | ||||||
chr8:24310096
|
T | A | 1 | a0001c0001t0002g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.228-67T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 3/22 | chr8 | 24310096 | ||||||
chr8:24310545
|
A | ATT | 73 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(70): Show | 80 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.306+306_306+307dup others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 24310545 | |||||
chr8:24310551
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+310A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310551 | ||||||
chr8:24310569
|
T | C | 4 | a0001c0001t0002g0228a0001c0001t0044g0227a0002c0019t0006g0226others(1): Show | 4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+328T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310569 | ||||||
chr8:24310938
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.307-423A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310938 | ||||||
chr8:24310945
|
A | T | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-416A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310945 | ||||||
chr8:24311010
|
G | A | 5 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-351G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311010 | ||||||
chr8:24311014
|
T | G | 1 | a0004c0004t0007g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307-347T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311014 | ||||||
chr8:24311025
|
A | T | 5 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-336A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311025 | ||||||
chr8:24311042
|
T | C | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.307-319T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311042 | ||||||
chr8:24311048
|
T | C | 5 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-313T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311048 | ||||||
chr8:24311126
|
C | A | 1 | a0001c0002t0004g0307 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.307-235C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311126 | ||||||
chr8:24311134
|
A | G | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-227A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311134 | ||||||
chr8:24311228
|
T | A | 4 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-133T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311228 | ||||||
chr8:24311310
|
C | T | 1 | a0001c0001t0009g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.307-51C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311310 | ||||||
chr8:24311311
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-50G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311311 | ||||||
chr8:24311564
|
C | A | 5 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+127C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311564 | ||||||
chr8:24311614
|
T | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+177T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311614 | ||||||
chr8:24311677
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+240A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311677 | ||||||
chr8:24311754
|
G | A | 5 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+317G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311754 | ||||||
chr8:24311863
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+426C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311863 | ||||||
chr8:24311886
|
C | T | 1 | a0009c0012t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.383+449C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311886 | ||||||
chr8:24312141
|
A | C | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383+704A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312141 | ||||||
chr8:24312327
|
T | C | 12 | a0001c0025t0042g0249a0003c0005t0005g0245a0003c0005t0005g0246others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.383+890T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312327 | ||||||
chr8:24312330
|
A | G | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383+893A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312330 | ||||||
chr8:24312412
|
T | C | 1 | a0001c0001t0003g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.383+975T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312412 | ||||||
chr8:24312444
|
A | G | 12 | a0001c0025t0042g0249a0003c0005t0005g0245a0003c0005t0005g0246others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.384-944A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312444 | ||||||
chr8:24312637
|
A | G | 1 | a0002c0003t0001g0262 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.384-751A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312637 | ||||||
chr8:24312669
|
G | A | 1 | a0002c0003t0002g0265 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.384-719G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312669 | ||||||
chr8:24312681
|
T | C | 1 | a0003c0006t0002g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.384-707T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312681 | ||||||
chr8:24312745
|
G | T | 11 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-643G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312745 | ||||||
chr8:24312746
|
C | CT | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-641dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr8 | 24312746 | |||||
chr8:24312757
|
T | C | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.384-631T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312757 | ||||||
chr8:24312911
|
T | C | 111 | a0001c0001t0002g0228a0001c0001t0038g0129a0001c0001t0044g0227others(108): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.384-477T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312911 | ||||||
chr8:24313225
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.384-163A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313225 | ||||||
chr8:24313292
|
T | C | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-96T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313292 | ||||||
chr8:24313375
|
C | A | 1 | a0001c0001t0047g0036 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.384-13C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313375 | ||||||
chr8:24313609
|
C | T | 6 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG00597.hp2 HG00609.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+29C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313609 | ||||||
chr8:24313757
|
T | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0069 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.576+177T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313757 | ||||||
chr8:24313758
|
A | AT | 60 | a0001c0001t0002g0155a0001c0001t0003g0207a0001c0002t0001g0027others(57): Show | 62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.576+194dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24313758 | |||||
chr8:24313758
|
A | T | 23 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(20): Show | 28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.576+178A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313758 | ||||||
chr8:24313758
|
AT | A | 11 | a0001c0001t0002g0110a0001c0001t0006g0038a0003c0005t0006g0239others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+194delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24313758 | |||||
chr8:24313856
|
T | C | 328 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.576+276T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313856 | ||||||
chr8:24313919
|
A | G | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+339A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313919 | ||||||
chr8:24314026
|
A | G | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314026 | ||||||
chr8:24314049
|
A | G | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+469A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314049 | ||||||
chr8:24314131
|
G | C | 6 | a0001c0017t0002g0130a0005c0008t0002g0325a0005c0008t0002g0326others(3): Show | 6 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+551G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314131 | ||||||
chr8:24314157
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+577C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314157 | ||||||
chr8:24314190
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.576+610A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314190 | ||||||
chr8:24314340
|
A | T | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.576+760A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314340 | ||||||
chr8:24314408
|
T | C | 4 | a0001c0001t0002g0103a0001c0001t0002g0108a0001c0001t0039g0104others(1): Show | 4 | HG03704.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+828T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314408 | ||||||
chr8:24314414
|
T | C | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.576+834T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314414 | ||||||
chr8:24314515
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.576+935A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314515 | ||||||
chr8:24314534
|
C | G | 1 | a0020c0016t0003g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.576+954C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314534 | ||||||
chr8:24314667
|
T | C | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1087T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314667 | ||||||
chr8:24314822
|
T | G | 1 | a0001c0001t0002g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.576+1242T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314822 | ||||||
chr8:24314924
|
C | CA | 39 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0112others(36): Show | 39 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.576+1358dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24314924 | |||||
chr8:24314924
|
CAA | C | 84 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(81): Show | 91 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.576+1357_576+1358d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24314924 | |||||
chr8:24314998
|
A | G | 85 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(82): Show | 92 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.576+1418A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314998 | ||||||
chr8:24315229
|
T | A | 1 | a0001c0017t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.576+1649T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315229 | ||||||
chr8:24315271
|
C | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1691C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315271 | ||||||
chr8:24315358
|
A | G | 86 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+1778A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315358 | ||||||
chr8:24315489
|
C | T | 1 | a0007c0011t0002g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.576+1909C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315489 | ||||||
chr8:24315656
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.576+2076T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315656 | ||||||
chr8:24315723
|
C | G | 31 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(28): Show | 36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.576+2143C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315723 | ||||||
chr8:24315910
|
C | T | 1 | a0001c0001t0004g0131 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.576+2330C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315910 | ||||||
chr8:24315912
|
T | G | 6 | a0001c0017t0002g0130a0005c0008t0002g0325a0005c0008t0002g0326others(3): Show | 6 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+2332T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315912 | ||||||
chr8:24316053
|
A | G | 3 | a0003c0005t0005g0245a0003c0005t0005g0246a0006c0028t0006g0244 | 3 | HG02615.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.576+2473A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316053 | ||||||
chr8:24316060
|
CCATT | C | 45 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(42): Show | 47 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.576+2481_576+2484d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316060 | ||||||
chr8:24316061
|
C | CATTT | 21 | a0001c0001t0001g0062a0001c0001t0002g0072a0001c0001t0002g0105others(18): Show | 21 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.576+2512_576+2515d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316061 | |||||
chr8:24316061
|
C | CATTTATT others(1): Show |
3 | a0001c0017t0002g0130a0003c0005t0005g0246a0005c0008t0002g0326 | 3 | HG01192.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.576+2508_576+2515d others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316061 | |||||
chr8:24316061
|
C | T | 34 | a0001c0002t0014g0288a0001c0002t0014g0301a0001c0002t0014g0306others(31): Show | 39 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.576+2481C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316061 | ||||||
chr8:24316097
|
T | C | 2 | a0006c0010t0002g0237a0006c0010t0002g0238 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.576+2517T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316097 | ||||||
chr8:24316359
|
A | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.576+2779A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316359 | ||||||
chr8:24316369
|
T | C | 2 | a0001c0001t0003g0080a0001c0001t0009g0222 | 2 | HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.576+2789T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316369 | ||||||
chr8:24316426
|
T | C | 86 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+2846T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316426 | ||||||
chr8:24316532
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0030 | 3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.576+2952A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316532 | ||||||
chr8:24316753
|
A | C | 1 | a0001c0001t0038g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.576+3173A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316753 | ||||||
chr8:24316811
|
A | G | 91 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.576+3231A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316811 | ||||||
chr8:24316851
|
C | T | 86 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+3271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316851 | ||||||
chr8:24316858
|
G | A | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+3278G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316858 | ||||||
chr8:24316863
|
A | G | 1 | a0002c0003t0029g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.576+3283A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316863 | ||||||
chr8:24316916
|
C | T | 2 | a0001c0002t0004g0292a0001c0002t0004g0319 | 2 | HG00423.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.577-3320C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316916 | ||||||
chr8:24316998
|
A | AG | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.577-3236dupG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316998 | |||||
chr8:24317017
|
T | C | 90 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.577-3219T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317017 | ||||||
chr8:24317095
|
A | C | 2 | a0006c0010t0002g0237a0006c0010t0002g0238 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.577-3141A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317095 | ||||||
chr8:24317409
|
G | C | 31 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(28): Show | 36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2827G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317409 | ||||||
chr8:24317409
|
G | T | 49 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.577-2827G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317409 | ||||||
chr8:24317506
|
T | G | 31 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(28): Show | 36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2730T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317506 | ||||||
chr8:24317540
|
GA | G | 10 | a0001c0001t0002g0103a0001c0001t0002g0108a0001c0001t0011g0106others(7): Show | 10 | HG03704.hp2 HG03831.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2691delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24317540 | |||||
chr8:24317550
|
C | A | 3 | a0001c0002t0014g0288a0001c0002t0014g0301a0001c0002t0014g0306 | 3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.577-2686C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317550 | ||||||
chr8:24317591
|
A | G | 31 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(28): Show | 36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2645A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317591 | ||||||
chr8:24317694
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.577-2542C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317694 | ||||||
chr8:24317739
|
A | C | 50 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.577-2497A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317739 | ||||||
chr8:24317829
|
G | A | 31 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(28): Show | 36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2407G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317829 | ||||||
chr8:24317853
|
C | T | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.577-2383C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317853 | ||||||
chr8:24317924
|
A | C | 86 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.577-2312A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317924 | ||||||
chr8:24318010
|
T | C | 86 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.577-2226T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318010 | ||||||
chr8:24318013
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.577-2223C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318013 | ||||||
chr8:24318024
|
T | A | 55 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(52): Show | 57 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.577-2212T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318024 | ||||||
chr8:24318385
|
T | C | 1 | a0001c0002t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.577-1851T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318385 | ||||||
chr8:24318449
|
G | A | 1 | a0003c0005t0006g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.577-1787G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318449 | ||||||
chr8:24318475
|
T | C | 75 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(72): Show | 77 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.577-1761T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318475 | ||||||
chr8:24318653
|
T | C | 1 | a0020c0016t0003g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.577-1583T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318653 | ||||||
chr8:24318765
|
C | T | 25 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(22): Show | 30 | HG00621.hp2 HG01192.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.577-1471C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318765 | ||||||
chr8:24318809
|
C | T | 24 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(21): Show | 29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.577-1427C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318809 | ||||||
chr8:24318816
|
G | A | 32 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(29): Show | 37 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.577-1420G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318816 | ||||||
chr8:24318934
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0040others(4): Show | 8 | NA18939.hp1 NA18941.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-1302G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318934 | ||||||
chr8:24318965
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0002g0035a0001c0001t0002g0061 | 3 | NA18998.hp2 NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.577-1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318965 | ||||||
chr8:24319112
|
C | T | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.577-1124C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319112 | ||||||
chr8:24319146
|
T | C | 2 | a0006c0010t0002g0237a0006c0010t0002g0238 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.577-1090T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319146 | ||||||
chr8:24319168
|
C | T | 1 | a0002c0033t0008g0267 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.577-1068C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319168 | ||||||
chr8:24319495
|
CAT | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0030 | 3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.577-740_577-739del others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319495 | ||||||
chr8:24319535
|
G | A | 51 | a0001c0017t0002g0130a0001c0025t0042g0249a0002c0003t0001g0001others(48): Show | 56 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.577-701G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319535 | ||||||
chr8:24319551
|
C | T | 23 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(20): Show | 28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.577-685C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319551 | ||||||
chr8:24319730
|
G | C | 50 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(47): Show | 55 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.577-506G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319730 | ||||||
chr8:24319751
|
C | A | 3 | a0001c0002t0001g0293a0001c0002t0004g0314a0001c0002t0008g0016 | 4 | NA18967.hp2 NA18969.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-485C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319751 | ||||||
chr8:24319805
|
T | C | 50 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.577-431T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319805 | ||||||
chr8:24319893
|
T | A | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.577-343T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319893 | ||||||
chr8:24320041
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577-195G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24320041 | ||||||
chr8:24320206
|
G | A | 1 | a0001c0001t0021g0157 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.577-30G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24320206 | ||||||
chr8:24320322
|
T | C | 1 | a0001c0001t0027g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.648+15T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320322 | ||||||
chr8:24320409
|
T | C | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.648+102T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320409 | ||||||
chr8:24320429
|
A | C | 23 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0002g0020others(20): Show | 23 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.648+122A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320429 | ||||||
chr8:24320459
|
T | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+152T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320459 | ||||||
chr8:24320478
|
A | ATTT | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.648+171_648+172ins others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320478 | ||||||
chr8:24320574
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.648+267A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320574 | ||||||
chr8:24320814
|
A | G | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.649-404A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320814 | ||||||
chr8:24321150
|
G | A | 1 | a0004c0004t0007g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.649-68G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24321150 | ||||||
chr8:24321347
|
T | A | 1 | a0001c0001t0017g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.720+58T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321347 | ||||||
chr8:24321680
|
A | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+391A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321680 | ||||||
chr8:24321691
|
C | T | 51 | a0001c0017t0002g0130a0001c0025t0042g0249a0002c0003t0001g0001others(48): Show | 56 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.720+402C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321691 | ||||||
chr8:24321743
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+454A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321743 | ||||||
chr8:24321922
|
C | A | 50 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(47): Show | 55 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.720+633C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321922 | ||||||
chr8:24322073
|
A | G | 20 | a0002c0007t0002g0124a0002c0007t0026g0102a0003c0005t0005g0245others(17): Show | 20 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+784A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322073 | ||||||
chr8:24322116
|
A | G | 200 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(197): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.720+827A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322116 | ||||||
chr8:24322123
|
A | T | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+834A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322123 | ||||||
chr8:24322128
|
C | T | 1 | a0007c0011t0006g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+839C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322128 | ||||||
chr8:24322168
|
T | C | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.720+879T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322168 | ||||||
chr8:24322196
|
A | G | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+907A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322196 | ||||||
chr8:24322305
|
G | T | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+1016G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322305 | ||||||
chr8:24322355
|
G | A | 1 | a0001c0002t0004g0307 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.720+1066G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322355 | ||||||
chr8:24322382
|
T | C | 3 | a0001c0001t0006g0038a0004c0004t0007g0109a0007c0011t0006g0097 | 3 | HG01884.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.720+1093T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322382 | ||||||
chr8:24322389
|
G | A | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.720+1100G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322389 | ||||||
chr8:24322398
|
A | C | 2 | a0001c0001t0002g0205a0001c0001t0010g0017 | 2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.720+1109A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322398 | ||||||
chr8:24322509
|
C | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.720+1220C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322509 | ||||||
chr8:24322702
|
A | G | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-1132A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322702 | ||||||
chr8:24322802
|
T | A | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-1032T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322802 | ||||||
chr8:24322861
|
C | A | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0007c0020t0023g0247 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.721-973C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322861 | ||||||
chr8:24323145
|
G | A | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.721-689G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323145 | ||||||
chr8:24323184
|
A | G | 18 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-650A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323184 | ||||||
chr8:24323289
|
C | T | 26 | a0001c0025t0042g0249a0002c0007t0003g0271a0002c0007t0003g0272others(23): Show | 26 | HG00733.hp2 HG00738.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.721-545C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323289 | ||||||
chr8:24323415
|
C | A | 32 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(29): Show | 37 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.721-419C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323415 | ||||||
chr8:24323442
|
T | C | 1 | a0001c0001t0037g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.721-392T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323442 | ||||||
chr8:24323485
|
A | G | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.721-349A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323485 | ||||||
chr8:24323610
|
A | C | 24 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(21): Show | 29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.721-224A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323610 | ||||||
chr8:24323633
|
T | C | 1 | a0004c0004t0020g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.721-201T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323633 | ||||||
chr8:24324120
|
G | C | 2 | a0003c0006t0001g0279a0003c0006t0002g0280 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.890+117G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324120 | ||||||
chr8:24324166
|
T | A | 28 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(25): Show | 33 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.890+163T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324166 | ||||||
chr8:24324167
|
A | G | 2 | a0003c0006t0001g0279a0003c0006t0002g0280 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.890+164A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324167 | ||||||
chr8:24324167
|
A | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.890+164A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324167 | ||||||
chr8:24324231
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.890+228A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324231 | ||||||
chr8:24324381
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.890+378A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324381 | ||||||
chr8:24324405
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0003g0211 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.890+402G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324405 | ||||||
chr8:24324459
|
G | T | 1 | a0002c0003t0003g0266 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.890+456G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324459 | ||||||
chr8:24324653
|
G | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.890+650G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324653 | ||||||
chr8:24324670
|
T | C | 2 | a0004c0004t0007g0039a0004c0004t0007g0116 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.890+667T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324670 | ||||||
chr8:24324910
|
T | C | 1 | a0001c0001t0015g0174 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.890+907T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324910 | ||||||
chr8:24325132
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.890+1129A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325132 | ||||||
chr8:24325142
|
T | C | 17 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.890+1139T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325142 | ||||||
chr8:24325349
|
T | C | 1 | a0001c0001t0019g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.891-1205T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325349 | ||||||
chr8:24325574
|
T | C | 2 | a0001c0001t0002g0132a0001c0026t0001g0114 | 2 | HG01516.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.891-980T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325574 | ||||||
chr8:24325736
|
C | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-818C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325736 | ||||||
chr8:24325835
|
T | G | 17 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.891-719T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325835 | ||||||
chr8:24325871
|
C | CA | 16 | a0001c0001t0001g0042a0001c0001t0001g0076a0001c0001t0001g0087others(13): Show | 16 | HG00438.hp2 HG01081.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.891-654dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(3): Show |
1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-663_891-654dup others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(15): Show |
1 | a0003c0006t0013g0274 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.891-675_891-654dup others(22): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(16): Show |
1 | a0003c0006t0013g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.891-676_891-654dup others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(17): Show |
2 | a0003c0006t0002g0275a0003c0006t0002g0276 | 2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.891-677_891-654dup others(24): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(18): Show |
1 | a0003c0006t0001g0279 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.891-678_891-654dup others(25): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(19): Show |
1 | a0003c0006t0002g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.891-679_891-654dup others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
C | CAAAAAAA others(23): Show |
1 | a0003c0006t0002g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.891-654_891-653ins others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
CA | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(106): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.891-654delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325871
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | NA18944.hp1 NA18972.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.891-669_891-654del others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | |||||
chr8:24325882
|
A | AAAACAAA others(5): Show |
2 | a0001c0002t0004g0286a0001c0002t0005g0234 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.891-669_891-668ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325882 | |||||
chr8:24325883
|
A | AAAACAAA others(5): Show |
2 | a0001c0001t0001g0186a0001c0001t0004g0156 | 2 | HG02523.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.891-668_891-667ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | |||||
chr8:24325883
|
A | AAACAAAC others(4): Show |
44 | a0001c0002t0001g0027a0001c0002t0001g0281a0001c0002t0001g0283others(41): Show | 46 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.891-669_891-668ins others(11): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | |||||
chr8:24325883
|
A | AACAAACA others(3): Show |
1 | a0001c0002t0004g0292 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.891-670_891-669ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | |||||
chr8:24325884
|
A | AACAAACA others(3): Show |
2 | a0001c0002t0001g0298a0001c0002t0002g0310 | 2 | HG00673.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.891-669_891-668ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325884 | |||||
chr8:24325886
|
A | C | 2 | a0001c0002t0004g0286a0001c0002t0005g0234 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.891-668A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325886 | ||||||
chr8:24325887
|
A | AACAAACA others(3): Show |
3 | a0002c0003t0001g0255a0002c0003t0003g0253a0002c0003t0029g0261 | 3 | HG00621.hp2 HG01943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.891-666_891-665ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325887 | |||||
chr8:24325887
|
A | ACAAACAA others(2): Show |
22 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(19): Show | 27 | HG01192.hp2 HG02071.hp2 HG02698.hp2 others(24): Show |
intron_variant | MODIFIER | c.891-667_891-666ins others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325887 | ||||||
chr8:24325887
|
A | C | 47 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(44): Show | 49 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.891-667A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325887 | ||||||
chr8:24325888
|
A | C | 2 | a0001c0002t0001g0298a0001c0002t0002g0310 | 2 | HG00673.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.891-666A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325888 | ||||||
chr8:24325889
|
A | AAAAAAAA others(22): Show |
2 | a0003c0005t0005g0245a0003c0005t0005g0246 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.891-654_891-653ins others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325889 | |||||
chr8:24325889
|
A | C | 5 | a0003c0005t0006g0239a0003c0005t0006g0240a0003c0005t0006g0241others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-665A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325889 | ||||||
chr8:24325891
|
A | C | 27 | a0001c0002t0001g0300a0001c0002t0001g0311a0001c0017t0002g0130others(24): Show | 32 | HG00621.hp1 HG00621.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.891-663A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325891 | ||||||
chr8:24325893
|
A | C | 1 | a0001c0001t0003g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.891-661A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325893 | ||||||
chr8:24325904
|
A | C | 1 | a0001c0001t0006g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.891-650A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325904 | ||||||
chr8:24326005
|
T | C | 1 | a0003c0006t0002g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.891-549T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326005 | ||||||
chr8:24326059
|
C | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-495C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326059 | ||||||
chr8:24326132
|
C | G | 1 | a0001c0001t0003g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.891-422C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326132 | ||||||
chr8:24326257
|
A | G | 98 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(95): Show | 105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.891-297A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326257 | ||||||
chr8:24326305
|
T | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-249T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326305 | ||||||
chr8:24326386
|
C | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-168C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326386 | ||||||
chr8:24326543
|
C | T | 17 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.891-11C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326543 | ||||||
chr8:24326664
|
A | C | 2 | a0004c0004t0007g0039a0004c0004t0007g0116 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.972+29A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326664 | ||||||
chr8:24326754
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+119C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326754 | ||||||
chr8:24326804
|
A | T | 1 | a0001c0001t0001g0009 | 2 | NA18955.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.972+169A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326804 | ||||||
chr8:24326809
|
T | G | 18 | a0001c0025t0042g0249a0003c0005t0005g0245a0003c0005t0005g0246others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.972+174T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326809 | ||||||
chr8:24326893
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+258A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326893 | ||||||
chr8:24326978
|
G | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+343G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326978 | ||||||
chr8:24326979
|
A | C | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+344A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326979 | ||||||
chr8:24326982
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0087 | 3 | HG01433.hp2 HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.972+347G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326982 | ||||||
chr8:24327116
|
G | T | 48 | a0001c0017t0002g0130a0002c0003t0001g0001a0002c0003t0001g0250others(45): Show | 53 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.972+481G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327116 | ||||||
chr8:24327152
|
G | A | 8 | a0001c0025t0042g0249a0003c0006t0001g0279a0003c0006t0002g0275others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.972+517G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327152 | ||||||
chr8:24327154
|
A | C | 7 | a0003c0006t0001g0279a0003c0006t0002g0275a0003c0006t0002g0276others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.972+519A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327154 | ||||||
chr8:24327236
|
C | T | 3 | a0001c0001t0011g0106a0001c0001t0011g0117a0001c0001t0011g0119 | 3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.972+601C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327236 | ||||||
chr8:24327312
|
C | T | 1 | a0001c0017t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.972+677C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327312 | ||||||
chr8:24327421
|
T | C | 1 | a0001c0002t0002g0312 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.972+786T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327421 | ||||||
chr8:24327425
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0069 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.972+790G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327425 | ||||||
chr8:24327444
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+809C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327444 | ||||||
chr8:24327448
|
G | A | 5 | a0001c0025t0042g0249a0005c0008t0002g0325a0005c0008t0002g0326others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+813G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327448 | ||||||
chr8:24327621
|
G | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+986G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327621 | ||||||
chr8:24327661
|
A | T | 3 | a0001c0001t0002g0133a0001c0001t0009g0134a0001c0001t0009g0135 | 3 | HG00733.hp1 HG01081.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.972+1026A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327661 | ||||||
chr8:24327667
|
G | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1032G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327667 | ||||||
chr8:24327711
|
A | G | 1 | a0004c0004t0007g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972+1076A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327711 | ||||||
chr8:24327740
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.972+1105A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327740 | ||||||
chr8:24327822
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1187A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327822 | ||||||
chr8:24327986
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.972+1351A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327986 | ||||||
chr8:24328006
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.972+1371T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328006 | ||||||
chr8:24328008
|
A | G | 1 | a0001c0001t0015g0174 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.972+1373A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328008 | ||||||
chr8:24328018
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1383C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328018 | ||||||
chr8:24328027
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.972+1392C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328027 | ||||||
chr8:24328114
|
T | C | 1 | a0001c0001t0002g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.972+1479T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328114 | ||||||
chr8:24328148
|
A | G | 2 | a0001c0001t0005g0195a0001c0001t0005g0196 | 2 | HG01109.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.972+1513A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328148 | ||||||
chr8:24328150
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1515A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328150 | ||||||
chr8:24328183
|
A | C | 1 | a0002c0003t0045g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.972+1548A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328183 | ||||||
chr8:24328444
|
G | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0144a0001c0001t0001g0148others(9): Show | 13 | HG00558.hp2 HG02074.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.973-1541G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328444 | ||||||
chr8:24328465
|
A | C | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.973-1520A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328465 | ||||||
chr8:24328484
|
A | T | 1 | a0001c0001t0006g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.973-1501A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328484 | ||||||
chr8:24328488
|
T | G | 4 | a0001c0002t0001g0318a0001c0002t0005g0302a0001c0002t0005g0308others(1): Show | 4 | HG02155.hp1 NA18948.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1497T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328488 | ||||||
chr8:24328500
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0062a0013c0021t0001g0057 | 3 | HG02074.hp2 HG02165.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.973-1485C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328500 | ||||||
chr8:24328577
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.973-1408G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328577 | ||||||
chr8:24328607
|
C | G | 101 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(98): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.973-1378C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328607 | ||||||
chr8:24328615
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.973-1370C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328615 | ||||||
chr8:24328671
|
T | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1314T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328671 | ||||||
chr8:24328853
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.973-1132G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328853 | ||||||
chr8:24328894
|
T | C | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-1091T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328894 | ||||||
chr8:24328921
|
C | CA | 92 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0004g0156others(89): Show | 99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.973-1052dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24328921 | |||||
chr8:24328929
|
A | AG | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1056_973-1055i others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328929 | ||||||
chr8:24328976
|
G | C | 1 | a0001c0001t0003g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.973-1009G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328976 | ||||||
chr8:24329129
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-856A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329129 | ||||||
chr8:24329200
|
T | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-785T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329200 | ||||||
chr8:24329349
|
T | C | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-636T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329349 | ||||||
chr8:24329383
|
T | C | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-602T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329383 | ||||||
chr8:24329436
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-549C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329436 | ||||||
chr8:24329595
|
G | GAGCTTGT others(5): Show |
1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-390_973-389ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329595 | ||||||
chr8:24329596
|
G | C | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-389G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329596 | ||||||
chr8:24329614
|
A | C | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-371A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329614 | ||||||
chr8:24329615
|
T | A | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-370T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329615 | ||||||
chr8:24329616
|
C | T | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-369C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329616 | ||||||
chr8:24329654
|
A | G | 1 | a0018c0018t0035g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.973-331A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329654 | ||||||
chr8:24329769
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-216C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329769 | ||||||
chr8:24329807
|
A | G | 2 | a0001c0002t0002g0303a0001c0002t0002g0320 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.973-178A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329807 | ||||||
chr8:24329830
|
ACT | A | 3 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0017g0028 | 3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.973-144_973-143del others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329830 | |||||
chr8:24329847
|
C | CTG | 6 | a0001c0001t0003g0223a0001c0001t0005g0195a0001c0002t0002g0015others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.973-118_973-117dup others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329847 | |||||
chr8:24329859
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-116_973-107del others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329859 | |||||
chr8:24329867
|
G | T | 1 | a0015c0023t0002g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.973-118G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329867 | ||||||
chr8:24329869
|
T | G | 2 | a0011c0027t0007g0018a0015c0023t0002g0126 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.973-116T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329869 | ||||||
chr8:24329869
|
TTG | T | 3 | a0001c0001t0003g0207a0002c0007t0002g0124a0002c0007t0026g0102 | 3 | HG02809.hp1 HG02965.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.973-99_973-98delTG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329869 | |||||
chr8:24329871
|
G | T | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.973-114G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329871 | ||||||
chr8:24329880
|
TGTGTGTG others(1): Show |
T | 16 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(13): Show | 16 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.973-103_973-96delT others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329880 | |||||
chr8:24329882
|
TGTGTGAG others(1): Show |
T | 3 | a0001c0017t0002g0130a0002c0007t0003g0271a0002c0007t0003g0272 | 3 | HG01167.hp1 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.973-101_973-94delT others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329882 | |||||
chr8:24329882
|
TGTGTGAG others(3): Show |
T | 28 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(25): Show | 33 | HG00621.hp2 HG01891.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.973-101_973-92delT others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329882 | |||||
chr8:24329884
|
T | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0002g0020others(3): Show | 6 | HG01106.hp2 HG02300.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-101T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329884 | ||||||
chr8:24329884
|
T | TGA | 21 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0076others(18): Show | 21 | HG00140.hp1 HG00733.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.973-100_973-99insA others(1): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | |||||
chr8:24329884
|
TGTGA | T | 6 | a0001c0001t0002g0161a0001c0001t0005g0034a0001c0001t0021g0157others(3): Show | 6 | HG02074.hp2 HG02083.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-99_973-96delTG others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | |||||
chr8:24329884
|
TGTGAGAG others(3): Show |
T | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.973-99_973-90delTG others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | |||||
chr8:24329886
|
T | A | 262 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(259): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.973-99T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329886 | ||||||
chr8:24329897
|
G | T | 50 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.973-88G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329897 | ||||||
chr8:24329908
|
A | G | 7 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-77A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329908 | ||||||
chr8:24329929
|
T | C | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-56T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329929 | ||||||
chr8:24329932
|
T | A | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-53T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329932 | ||||||
chr8:24330203
|
C | T | 1 | a0001c0001t0009g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1103+88C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330203 | ||||||
chr8:24330374
|
G | A | 1 | a0001c0017t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1103+259G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330374 | ||||||
chr8:24330394
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1103+279C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330394 | ||||||
chr8:24330559
|
C | T | 50 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(47): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1103+444C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330559 | ||||||
chr8:24330744
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1104-406T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330744 | ||||||
chr8:24330750
|
A | C | 51 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1104-400A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330750 | ||||||
chr8:24330834
|
A | G | 101 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(98): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1104-316A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330834 | ||||||
chr8:24331007
|
G | A | 1 | a0001c0002t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1104-143G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24331007 | ||||||
chr8:24331331
|
T | C | 104 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0186others(101): Show | 111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
splice_region_variant&intron_variant | LOW | c.1281+4T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331331 | ||||||
chr8:24331445
|
C | T | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1281+118C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331445 | ||||||
chr8:24331537
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1281+210A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331537 | ||||||
chr8:24331588
|
G | A | 1 | a0001c0001t0043g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1281+261G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331588 | ||||||
chr8:24331636
|
A | G | 100 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(97): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1281+309A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331636 | ||||||
chr8:24331675
|
C | T | 82 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(79): Show | 89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1281+348C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331675 | ||||||
chr8:24331687
|
T | C | 82 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(79): Show | 89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1281+360T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331687 | ||||||
chr8:24331735
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+408A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331735 | ||||||
chr8:24331770
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1281+443C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331770 | ||||||
chr8:24332024
|
C | A | 1 | a0001c0001t0040g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1282-636C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332024 | ||||||
chr8:24332142
|
A | C | 1 | a0002c0003t0045g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1282-518A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332142 | ||||||
chr8:24332376
|
T | C | 5 | a0002c0007t0002g0124a0002c0007t0026g0102a0006c0028t0006g0244others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-284T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332376 | ||||||
chr8:24332406
|
A | C | 1 | a0001c0001t0006g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1282-254A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332406 | ||||||
chr8:24332414
|
T | C | 1 | a0004c0004t0007g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1282-246T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332414 | ||||||
chr8:24332499
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1282-161C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332499 | ||||||
chr8:24332537
|
A | G | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1282-123A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332537 | ||||||
chr8:24332544
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1282-116C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332544 | ||||||
chr8:24332624
|
A | G | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-36A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332624 | ||||||
chr8:24332779
|
TATG | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+33_1371+35del others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24332779 | |||||
chr8:24332866
|
A | G | 1 | a0001c0001t0037g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1371+117A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332866 | ||||||
chr8:24332921
|
T | G | 2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | NA18955.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1371+172T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332921 | ||||||
chr8:24332982
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+233A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332982 | ||||||
chr8:24333002
|
T | C | 1 | a0001c0002t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1371+253T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333002 | ||||||
chr8:24333050
|
C | G | 102 | a0001c0001t0001g0186a0001c0001t0004g0156a0001c0002t0001g0027others(99): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1371+301C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333050 | ||||||
chr8:24333099
|
G | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+350G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333099 | ||||||
chr8:24333155
|
A | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+406A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333155 | ||||||
chr8:24333170
|
C | T | 3 | a0001c0002t0014g0288a0001c0002t0014g0301a0001c0002t0014g0306 | 3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1371+421C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333170 | ||||||
chr8:24333691
|
G | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+942G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333691 | ||||||
chr8:24333713
|
G | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+964G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333713 | ||||||
chr8:24333781
|
C | G | 1 | a0001c0001t0006g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1371+1032C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333781 | ||||||
chr8:24333815
|
T | C | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1371+1066T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333815 | ||||||
chr8:24333970
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+1221C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333970 | ||||||
chr8:24333983
|
GTT | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+1237_1371+123 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24333983 | |||||
chr8:24334065
|
G | A | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1371+1316G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334065 | ||||||
chr8:24334247
|
G | A | 1 | a0010c0014t0028g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1372-1199G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334247 | ||||||
chr8:24334271
|
A | G | 5 | a0003c0005t0006g0239a0003c0005t0006g0240a0003c0005t0006g0241others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372-1175A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334271 | ||||||
chr8:24334325
|
T | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-1121T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334325 | ||||||
chr8:24334398
|
C | T | 1 | a0006c0010t0002g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1372-1048C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334398 | ||||||
chr8:24334447
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-999A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334447 | ||||||
chr8:24334493
|
CT | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-951delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24334493 | |||||
chr8:24334615
|
T | G | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-831T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334615 | ||||||
chr8:24334616
|
C | G | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-830C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334616 | ||||||
chr8:24334868
|
G | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-578G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334868 | ||||||
chr8:24335166
|
G | GT | 13 | a0001c0001t0044g0227a0003c0005t0005g0245a0003c0005t0005g0246others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372-268dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24335166 | |||||
chr8:24335309
|
A | C | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-137A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24335309 | ||||||
chr8:24335344
|
T | C | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1372-102T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24335344 | ||||||
chr8:24335675
|
C | T | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+34C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335675 | ||||||
chr8:24335749
|
T | C | 1 | a0009c0012t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1567+108T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335749 | ||||||
chr8:24335751
|
T | C | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1567+110T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335751 | ||||||
chr8:24335835
|
C | T | 1 | a0001c0001t0009g0214 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1567+194C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335835 | ||||||
chr8:24335839
|
A | G | 1 | a0001c0001t0005g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1567+198A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335839 | ||||||
chr8:24335948
|
T | C | 1 | a0001c0001t0015g0174 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1567+307T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335948 | ||||||
chr8:24336039
|
G | GGT | 4 | a0001c0001t0003g0203a0001c0001t0006g0141a0001c0001t0010g0017others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+418_1567+419d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336039 | |||||
chr8:24336039
|
GGT | G | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+418_1567+419d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336039 | |||||
chr8:24336043
|
T | G | 5 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+402T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336043 | ||||||
chr8:24336137
|
G | A | 1 | a0001c0001t0006g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1567+496G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336137 | ||||||
chr8:24336301
|
T | C | 9 | a0001c0013t0002g0173a0001c0013t0013g0172a0003c0006t0001g0279others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+660T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336301 | ||||||
chr8:24336349
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1567+708T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336349 | ||||||
chr8:24336366
|
G | T | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1567+725G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336366 | ||||||
chr8:24336411
|
G | T | 2 | a0002c0003t0003g0253a0002c0003t0029g0261 | 2 | HG01943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1567+770G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336411 | ||||||
chr8:24336443
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0029others(44): Show | 48 | HG00323.hp1 HG01074.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1567+802C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336443 | ||||||
chr8:24336512
|
G | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+871G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336512 | ||||||
chr8:24336580
|
C | CA | 61 | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0186others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1567+958dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | |||||
chr8:24336580
|
CA | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0112others(5): Show | 8 | HG00558.hp1 HG03041.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+958delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | |||||
chr8:24336580
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1567+945_1567+958d others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | |||||
chr8:24336580
|
CAAAAAAA others(10): Show |
C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+942_1567+958d others(19): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | |||||
chr8:24336590
|
AAAAAAAA others(3): Show |
A | 5 | a0003c0005t0006g0239a0003c0005t0006g0240a0003c0005t0006g0241others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+965_1567+974d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336590 | |||||
chr8:24336599
|
AG | A | 4 | a0001c0001t0002g0063a0001c0001t0002g0091a0001c0001t0002g0098others(1): Show | 4 | HG02004.hp1 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+959delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336599 | ||||||
chr8:24336646
|
T | C | 1 | a0002c0031t0002g0256 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+1005T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336646 | ||||||
chr8:24336669
|
A | G | 109 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(106): Show | 116 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1567+1028A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336669 | ||||||
chr8:24336697
|
G | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+1056G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336697 | ||||||
chr8:24336756
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567+1115C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336756 | ||||||
chr8:24336956
|
G | A | 10 | a0001c0002t0001g0287a0001c0002t0001g0289a0001c0002t0001g0297others(7): Show | 11 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567+1315G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336956 | ||||||
chr8:24337035
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1567+1394A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337035 | ||||||
chr8:24337166
|
C | G | 87 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(84): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1567+1525C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337166 | ||||||
chr8:24337191
|
A | G | 92 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(89): Show | 99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1567+1550A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337191 | ||||||
chr8:24337206
|
G | C | 90 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1567+1565G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337206 | ||||||
chr8:24337253
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1567+1612T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337253 | ||||||
chr8:24337522
|
G | T | 1 | a0015c0023t0002g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1567+1881G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337522 | ||||||
chr8:24337538
|
T | C | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1567+1897T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337538 | ||||||
chr8:24337606
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1860A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337606 | ||||||
chr8:24337614
|
G | A | 1 | a0001c0001t0010g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1568-1852G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337614 | ||||||
chr8:24337707
|
G | C | 1 | a0009c0012t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1568-1759G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337707 | ||||||
chr8:24337963
|
T | G | 3 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0017g0028 | 3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1568-1503T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337963 | ||||||
chr8:24337976
|
A | C | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1568-1490A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337976 | ||||||
chr8:24337978
|
G | C | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1568-1488G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337978 | ||||||
chr8:24338036
|
G | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1430G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338036 | ||||||
chr8:24338167
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1299A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338167 | ||||||
chr8:24338170
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1296A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338170 | ||||||
chr8:24338195
|
C | T | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338195 | ||||||
chr8:24338227
|
ATTAG | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1235_1568-123 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338227 | |||||
chr8:24338243
|
G | A | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1568-1223G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338243 | ||||||
chr8:24338314
|
A | G | 51 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1568-1152A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338314 | ||||||
chr8:24338368
|
A | G | 1 | a0002c0003t0008g0260 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1568-1098A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338368 | ||||||
chr8:24338380
|
A | C | 5 | a0003c0005t0006g0239a0003c0005t0006g0240a0003c0005t0006g0241others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-1086A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338380 | ||||||
chr8:24338399
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1067A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338399 | ||||||
chr8:24338406
|
A | C | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1060A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338406 | ||||||
chr8:24338426
|
CTCCCTGA others(54): Show |
C | 1 | a0001c0001t0003g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1568-995_1568-935d others(63): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338426 | |||||
chr8:24338433
|
A | C | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1033A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338433 | ||||||
chr8:24338435
|
T | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1031T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338435 | ||||||
chr8:24338533
|
T | C | 1 | a0002c0003t0045g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1568-933T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338533 | ||||||
chr8:24338577
|
A | T | 51 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1568-889A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338577 | ||||||
chr8:24338579
|
TAAA | T | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-884_1568-882d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338579 | |||||
chr8:24338607
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-859A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338607 | ||||||
chr8:24338701
|
A | T | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-765A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338701 | ||||||
chr8:24338779
|
G | C | 5 | a0002c0007t0002g0124a0002c0007t0026g0102a0006c0028t0006g0244others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-687G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338779 | ||||||
chr8:24338834
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0002g0035a0001c0001t0002g0061 | 3 | NA18998.hp2 NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1568-632G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338834 | ||||||
chr8:24338844
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-622A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338844 | ||||||
chr8:24339118
|
G | A | 328 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1568-348G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339118 | ||||||
chr8:24339202
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-264A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339202 | ||||||
chr8:24339225
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-241A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339225 | ||||||
chr8:24339277
|
T | C | 1 | a0001c0001t0043g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1568-189T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339277 | ||||||
chr8:24339368
|
G | A | 4 | a0003c0005t0006g0240a0003c0005t0006g0241a0003c0005t0006g0242others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-98G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339368 | ||||||
chr8:24339385
|
C | T | 89 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(86): Show | 96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1568-81C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339385 | ||||||
chr8:24339419
|
T | C | 1 | a0002c0019t0006g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1568-47T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339419 | ||||||
chr8:24339424
|
A | G | 8 | a0001c0001t0001g0073a0001c0001t0002g0155a0001c0001t0002g0165others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568-42A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339424 | ||||||
chr8:24339837
|
G | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+269G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339837 | ||||||
chr8:24339857
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1670+289A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339857 | ||||||
chr8:24339983
|
T | C | 1 | a0001c0017t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1670+415T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339983 | ||||||
chr8:24340020
|
T | A | 1 | a0007c0020t0023g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1670+452T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340020 | ||||||
chr8:24340056
|
A | T | 19 | a0001c0013t0002g0173a0001c0013t0013g0172a0001c0017t0002g0130others(16): Show | 19 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670+488A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340056 | ||||||
chr8:24340134
|
G | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+566G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340134 | ||||||
chr8:24340168
|
T | A | 1 | a0001c0001t0003g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1670+600T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340168 | ||||||
chr8:24340322
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1670+754C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340322 | ||||||
chr8:24340383
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1670+815G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340383 | ||||||
chr8:24340438
|
T | C | 2 | a0003c0005t0005g0245a0003c0005t0005g0246 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1670+870T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340438 | ||||||
chr8:24340442
|
G | A | 35 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(32): Show | 40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1670+874G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340442 | ||||||
chr8:24340469
|
G | T | 2 | a0004c0004t0007g0039a0004c0004t0007g0116 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1670+901G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340469 | ||||||
chr8:24340656
|
A | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-942A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340656 | ||||||
chr8:24340717
|
G | T | 35 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(32): Show | 40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1671-881G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340717 | ||||||
chr8:24341001
|
G | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-597G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341001 | ||||||
chr8:24341011
|
G | C | 90 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1671-587G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341011 | ||||||
chr8:24341037
|
A | G | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1671-561A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341037 | ||||||
chr8:24341058
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1671-540T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341058 | ||||||
chr8:24341108
|
T | G | 5 | a0001c0001t0002g0072a0001c0001t0002g0074a0001c0001t0002g0125others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-490T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341108 | ||||||
chr8:24341117
|
C | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1671-481C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341117 | ||||||
chr8:24341194
|
T | C | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-404T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341194 | ||||||
chr8:24341309
|
C | A | 1 | a0006c0028t0006g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1671-289C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341309 | ||||||
chr8:24341346
|
A | G | 2 | a0003c0005t0005g0245a0003c0005t0005g0246 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1671-252A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341346 | ||||||
chr8:24341348
|
G | A | 3 | a0001c0001t0002g0155a0001c0001t0003g0223a0001c0001t0004g0082 | 3 | HG03688.hp2 HG04204.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1671-250G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341348 | ||||||
chr8:24341390
|
A | T | 30 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(27): Show | 35 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1671-208A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341390 | ||||||
chr8:24341401
|
A | G | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-197A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341401 | ||||||
chr8:24341496
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0002g0047 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1671-102C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341496 | ||||||
chr8:24341550
|
G | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-48G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341550 | ||||||
chr8:24341561
|
A | G | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1671-37A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341561 | ||||||
chr8:24341578
|
C | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1671-20C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341578 | ||||||
chr8:24341586
|
C | G | 3 | a0001c0002t0014g0288a0001c0002t0014g0301a0001c0002t0014g0306 | 3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1671-12C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341586 | ||||||
chr8:24341805
|
G | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+48G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341805 | ||||||
chr8:24341841
|
T | C | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+84T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341841 | ||||||
chr8:24341869
|
G | A | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+112G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341869 | ||||||
chr8:24341878
|
T | C | 1 | a0001c0002t0004g0292 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1830+121T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341878 | ||||||
chr8:24341904
|
G | T | 1 | a0002c0003t0003g0263 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1830+147G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341904 | ||||||
chr8:24341933
|
C | A | 5 | a0002c0007t0002g0124a0002c0007t0026g0102a0006c0028t0006g0244others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1830+176C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341933 | ||||||
chr8:24341958
|
G | T | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1830+201G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341958 | ||||||
chr8:24341998
|
A | C | 1 | a0011c0027t0007g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1830+241A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341998 | ||||||
chr8:24342040
|
G | A | 1 | a0002c0003t0001g0250 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1830+283G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342040 | ||||||
chr8:24342084
|
C | T | 1 | a0002c0003t0046g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1830+327C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342084 | ||||||
chr8:24342111
|
C | T | 1 | a0002c0003t0003g0258 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1830+354C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342111 | ||||||
chr8:24342440
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1831-661G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342440 | ||||||
chr8:24342481
|
A | G | 54 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(51): Show | 56 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1831-620A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342481 | ||||||
chr8:24342635
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1831-466C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342635 | ||||||
chr8:24342722
|
A | G | 89 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(86): Show | 96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1831-379A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342722 | ||||||
chr8:24342761
|
G | C | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1831-340G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342761 | ||||||
chr8:24342762
|
A | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1831-339A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342762 | ||||||
chr8:24342797
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0198 | 3 | HG03516.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1831-304G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342797 | ||||||
chr8:24342961
|
C | T | 49 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1831-140C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342961 | ||||||
chr8:24342978
|
T | G | 1 | a0003c0005t0006g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1831-123T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342978 | ||||||
chr8:24343261
|
A | G | 89 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(86): Show | 96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1911+80A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 17/22 | chr8 | 24343261 | ||||||
chr8:24343477
|
G | T | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1912-29G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 17/22 | chr8 | 24343477 | ||||||
chr8:24343761
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+177C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343761 | ||||||
chr8:24343762
|
G | A | 1 | a0001c0001t0038g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1990+178G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343762 | ||||||
chr8:24343805
|
T | A | 1 | a0019c0032t0033g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1990+221T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343805 | ||||||
chr8:24343911
|
C | G | 3 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0017g0028 | 3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1990+327C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343911 | ||||||
chr8:24343931
|
A | AT | 91 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1990+351dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24343931 | |||||
chr8:24344035
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0094a0001c0001t0001g0096others(21): Show | 24 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1990+451G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344035 | ||||||
chr8:24344087
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+503C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344087 | ||||||
chr8:24344175
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1990+591G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344175 | ||||||
chr8:24344241
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+657C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344241 | ||||||
chr8:24344263
|
AG | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0087others(41): Show | 46 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1990+682delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24344263 | |||||
chr8:24344334
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+750C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344334 | ||||||
chr8:24344385
|
A | C | 51 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1990+801A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344385 | ||||||
chr8:24344414
|
G | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+830G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344414 | ||||||
chr8:24344453
|
A | G | 3 | a0001c0001t0025g0219a0002c0007t0003g0271a0002c0007t0003g0272 | 3 | HG01167.hp1 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1990+869A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344453 | ||||||
chr8:24344465
|
A | G | 1 | a0015c0023t0002g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1990+881A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344465 | ||||||
chr8:24344481
|
G | A | 4 | a0001c0013t0002g0173a0001c0013t0013g0172a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990+897G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344481 | ||||||
chr8:24344514
|
G | C | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+930G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344514 | ||||||
chr8:24344546
|
T | G | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990+962T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344546 | ||||||
chr8:24344622
|
A | G | 1 | a0001c0025t0042g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1990+1038A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344622 | ||||||
chr8:24344669
|
T | C | 51 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1990+1085T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344669 | ||||||
chr8:24344724
|
CTT | C | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1142_1990+114 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24344724 | |||||
chr8:24344761
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1990+1177A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344761 | ||||||
chr8:24344828
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1990+1244T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344828 | ||||||
chr8:24344838
|
G | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1254G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344838 | ||||||
chr8:24345028
|
C | CA | 6 | a0001c0001t0001g0073a0001c0001t0002g0108a0001c0001t0002g0137others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1990+1458dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | |||||
chr8:24345028
|
CA | C | 57 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0186others(54): Show | 59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1990+1458delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | |||||
chr8:24345028
|
CAAAA | C | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1455_1990+145 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | |||||
chr8:24345079
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1990+1495T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345079 | ||||||
chr8:24345247
|
A | G | 110 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(107): Show | 117 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1990+1663A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345247 | ||||||
chr8:24345342
|
A | C | 5 | a0002c0007t0002g0124a0002c0007t0026g0102a0006c0028t0006g0244others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1990+1758A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345342 | ||||||
chr8:24345514
|
C | G | 1 | a0002c0003t0045g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1990+1930C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345514 | ||||||
chr8:24345578
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1990+1994A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345578 | ||||||
chr8:24345623
|
T | C | 9 | a0001c0013t0002g0173a0001c0013t0013g0172a0003c0006t0001g0279others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1990+2039T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345623 | ||||||
chr8:24345672
|
A | G | 28 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(25): Show | 33 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1990+2088A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345672 | ||||||
chr8:24345707
|
G | A | 3 | a0006c0028t0006g0244a0007c0011t0002g0019a0007c0011t0006g0097 | 3 | HG02895.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2123G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345707 | ||||||
chr8:24345751
|
T | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990+2167T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345751 | ||||||
chr8:24345816
|
G | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+2232G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345816 | ||||||
chr8:24345902
|
T | C | 40 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(37): Show | 45 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1990+2318T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345902 | ||||||
chr8:24346032
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1990+2448C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346032 | ||||||
chr8:24346098
|
G | A | 1 | a0001c0001t0011g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1990+2514G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346098 | ||||||
chr8:24346162
|
T | G | 9 | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(6): Show | 9 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1990+2578T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346162 | ||||||
chr8:24346354
|
G | T | 2 | a0007c0011t0002g0019a0007c0011t0006g0097 | 2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2770G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346354 | ||||||
chr8:24346366
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+2782C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346366 | ||||||
chr8:24346368
|
T | C | 2 | a0007c0011t0002g0019a0007c0011t0006g0097 | 2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2784T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346368 | ||||||
chr8:24346443
|
C | T | 2 | a0007c0011t0002g0019a0007c0011t0006g0097 | 2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2859C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346443 | ||||||
chr8:24346523
|
G | T | 3 | a0001c0001t0002g0205a0001c0001t0010g0017a0001c0001t0010g0221 | 3 | HG00639.hp2 HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1990+2939G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346523 | ||||||
chr8:24346571
|
T | G | 90 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1990+2987T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346571 | ||||||
chr8:24346614
|
C | G | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+3030C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346614 | ||||||
chr8:24346708
|
G | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+3124G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346708 | ||||||
chr8:24346712
|
A | G | 1 | a0007c0011t0006g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1990+3128A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346712 | ||||||
chr8:24346812
|
T | G | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-3052T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346812 | ||||||
chr8:24346827
|
C | T | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-3037C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346827 | ||||||
chr8:24346880
|
G | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-2984G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346880 | ||||||
chr8:24346997
|
C | T | 2 | a0007c0011t0002g0019a0007c0011t0006g0097 | 2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1991-2867C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346997 | ||||||
chr8:24347018
|
G | A | 108 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(105): Show | 115 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1991-2846G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347018 | ||||||
chr8:24347081
|
A | ATGCTTTC others(21): Show |
1 | a0001c0001t0025g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1991-2780_1991-275 others(32): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24347081 | |||||
chr8:24347130
|
C | G | 1 | a0001c0001t0027g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1991-2734C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347130 | ||||||
chr8:24347363
|
A | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-2501A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347363 | ||||||
chr8:24347435
|
C | T | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1991-2429C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347435 | ||||||
chr8:24347457
|
C | G | 1 | a0001c0017t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1991-2407C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347457 | ||||||
chr8:24347603
|
G | C | 2 | a0001c0001t0001g0056a0013c0021t0001g0057 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1991-2261G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347603 | ||||||
chr8:24347629
|
A | G | 30 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(27): Show | 35 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1991-2235A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347629 | ||||||
chr8:24347690
|
G | A | 2 | a0001c0017t0002g0130a0001c0025t0042g0249 | 2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1991-2174G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347690 | ||||||
chr8:24347690
|
G | T | 1 | a0002c0003t0003g0253 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1991-2174G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347690 | ||||||
chr8:24347724
|
T | G | 51 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(48): Show | 53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1991-2140T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347724 | ||||||
chr8:24347815
|
GACC | G | 3 | a0006c0028t0006g0244a0007c0011t0002g0019a0007c0011t0006g0097 | 3 | HG02895.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1991-2047_1991-204 others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24347815 | |||||
chr8:24347829
|
A | G | 19 | a0001c0013t0002g0173a0001c0013t0013g0172a0001c0017t0002g0130others(16): Show | 19 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1991-2035A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347829 | ||||||
chr8:24347838
|
G | C | 90 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1991-2026G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347838 | ||||||
chr8:24348011
|
G | A | 15 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0002g0103others(12): Show | 15 | HG00423.hp1 HG00733.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1991-1853G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348011 | ||||||
chr8:24348071
|
A | C | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-1793A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348071 | ||||||
chr8:24348102
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | NA18955.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1991-1762C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348102 | ||||||
chr8:24348219
|
A | T | 35 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(32): Show | 40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1991-1645A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348219 | ||||||
chr8:24348271
|
C | T | 1 | a0002c0019t0006g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1991-1593C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348271 | ||||||
chr8:24348301
|
C | T | 49 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1991-1563C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348301 | ||||||
chr8:24348314
|
A | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1550A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348314 | ||||||
chr8:24348357
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1991-1507T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348357 | ||||||
chr8:24348362
|
G | A | 49 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(46): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1991-1502G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348362 | ||||||
chr8:24348372
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1492C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348372 | ||||||
chr8:24348454
|
G | A | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1410G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348454 | ||||||
chr8:24348523
|
C | T | 39 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1341C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348523 | ||||||
chr8:24348524
|
A | G | 90 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1991-1340A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348524 | ||||||
chr8:24348560
|
T | G | 1 | a0001c0002t0004g0307 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1991-1304T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348560 | ||||||
chr8:24348616
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0040others(11): Show | 15 | HG02015.hp1 HG02056.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1991-1248C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348616 | ||||||
chr8:24348773
|
G | A | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1991-1091G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348773 | ||||||
chr8:24348780
|
T | C | 37 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(34): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-1084T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348780 | ||||||
chr8:24348791
|
G | C | 3 | a0001c0001t0001g0149a0001c0002t0012g0322a0001c0002t0012g0323 | 3 | HG00609.hp2 HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1991-1073G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348791 | ||||||
chr8:24348913
|
G | A | 88 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(85): Show | 95 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1991-951G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348913 | ||||||
chr8:24348933
|
C | A | 37 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(34): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-931C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348933 | ||||||
chr8:24348956
|
C | T | 37 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(34): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-908C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348956 | ||||||
chr8:24348996
|
G | A | 4 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-868G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348996 | ||||||
chr8:24349013
|
G | A | 18 | a0001c0013t0002g0173a0001c0013t0013g0172a0002c0003t0004g0254others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1991-851G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349013 | ||||||
chr8:24349068
|
C | A | 2 | a0002c0007t0002g0124a0002c0007t0026g0102 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1991-796C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349068 | ||||||
chr8:24349170
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1991-694C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349170 | ||||||
chr8:24349214
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1991-650C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349214 | ||||||
chr8:24349231
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1991-633T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349231 | ||||||
chr8:24349506
|
A | G | 1 | a0002c0003t0003g0264 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1991-358A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349506 | ||||||
chr8:24349520
|
A | T | 37 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(34): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-344A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349520 | ||||||
chr8:24349523
|
A | C | 1 | a0001c0001t0006g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1991-341A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349523 | ||||||
chr8:24349591
|
G | A | 37 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(34): Show | 42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-273G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349591 | ||||||
chr8:24349647
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0004g0156 | 2 | NA18972.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1991-217G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349647 | ||||||
chr8:24349710
|
A | G | 1 | a0001c0001t0004g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1991-154A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349710 | ||||||
chr8:24349718
|
A | G | 38 | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(35): Show | 43 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1991-146A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349718 | ||||||
chr8:24350101
|
G | A | 39 | a0001c0001t0003g0188a0001c0001t0003g0206a0001c0001t0008g0200others(36): Show | 45 | HG00621.hp2 HG00673.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.2099+129G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350101 | ||||||
chr8:24350160
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2099+188A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350160 | ||||||
chr8:24350161
|
T | C | 51 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(48): Show | 57 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2099+189T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350161 | ||||||
chr8:24350227
|
A | G | 2 | a0003c0006t0001g0279a0003c0006t0002g0280 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2099+255A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350227 | ||||||
chr8:24350381
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2099+409G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350381 | ||||||
chr8:24350426
|
A | G | 177 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 188 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2099+454A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350426 | ||||||
chr8:24350431
|
AG | A | 3 | a0001c0013t0013g0172a0003c0006t0013g0274a0003c0006t0013g0277 | 3 | HG02922.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2099+460delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350431 | ||||||
chr8:24350481
|
T | C | 92 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0142others(89): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2099+509T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350481 | ||||||
chr8:24350505
|
T | C | 95 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0142others(92): Show | 104 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2099+533T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350505 | ||||||
chr8:24350547
|
A | G | 9 | a0001c0001t0006g0141a0002c0019t0006g0226a0003c0005t0006g0239others(6): Show | 9 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2099+575A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350547 | ||||||
chr8:24350625
|
T | C | 2 | a0001c0001t0002g0220a0001c0001t0039g0104 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2100-607T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350625 | ||||||
chr8:24350674
|
C | T | 13 | a0001c0001t0006g0141a0001c0013t0013g0172a0002c0007t0026g0102others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2100-558C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350674 | ||||||
chr8:24350845
|
G | A | 2 | a0003c0005t0005g0245a0003c0005t0005g0246 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2100-387G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350845 | ||||||
chr8:24350858
|
AACG | A | 3 | a0001c0001t0003g0092a0001c0001t0003g0120a0001c0001t0047g0036 | 3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-373_2100-371d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350858 | ||||||
chr8:24350860
|
C | T | 313 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(310): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2100-372C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350860 | ||||||
chr8:24350864
|
GTT | G | 30 | a0001c0001t0004g0051a0001c0001t0004g0071a0001c0001t0004g0082others(27): Show | 30 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.2100-343_2100-342d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | |||||
chr8:24350864
|
GTTT | G | 85 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0002g0002others(82): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2100-344_2100-342d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | |||||
chr8:24350864
|
GTTTT | G | 26 | a0001c0001t0001g0058a0001c0001t0001g0204a0001c0001t0002g0132others(23): Show | 26 | HG00140.hp2 HG00597.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2100-345_2100-342d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | |||||
chr8:24350864
|
GTTTTT | G | 177 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 186 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2100-346_2100-342d others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | |||||
chr8:24350865
|
T | G | 3 | a0001c0001t0003g0092a0001c0001t0003g0120a0001c0001t0047g0036 | 3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-367T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350865 | ||||||
chr8:24350867
|
T | G | 3 | a0001c0001t0003g0092a0001c0001t0003g0120a0001c0001t0047g0036 | 3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-365T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350867 | ||||||
chr8:24350875
|
T | G | 26 | a0001c0001t0004g0051a0001c0001t0004g0071a0001c0001t0004g0082others(23): Show | 26 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.2100-357T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350875 | ||||||
chr8:24350876
|
T | C | 3 | a0001c0001t0001g0096a0001c0002t0001g0281a0001c0002t0001g0285 | 3 | HG00408.hp1 NA18612.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2100-356T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350876 | ||||||
chr8:24350876
|
T | G | 114 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0002g0002others(111): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2100-356T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350876 | ||||||
chr8:24350877
|
T | G | 113 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0122others(110): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2100-355T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350877 | ||||||
chr8:24350878
|
T | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 211 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2100-354T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350878 | ||||||
chr8:24350879
|
T | G | 175 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 184 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2100-353T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350879 | ||||||
chr8:24350949
|
A | G | 3 | a0001c0001t0008g0200a0001c0002t0008g0016a0002c0003t0008g0260 | 4 | HG00673.hp1 NA18945.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2100-283A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350949 | ||||||
chr8:24351081
|
A | G | 15 | a0001c0001t0005g0034a0001c0001t0005g0095a0001c0001t0005g0145others(12): Show | 15 | HG01109.hp1 HG02004.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2100-151A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351081 | ||||||
chr8:24351093
|
C | T | 75 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0002g0002others(72): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2100-139C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351093 | ||||||
chr8:24351136
|
C | T | 316 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(313): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2100-96C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351136 | ||||||
chr8:24351334
|
G | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 218 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2178+24G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351334 | ||||||
chr8:24351421
|
C | A | 75 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0161others(72): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2178+111C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351421 | ||||||
chr8:24351432
|
A | G | 1 | a0004c0004t0007g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178+122A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351432 | ||||||
chr8:24351478
|
C | T | 1 | a0001c0001t0011g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2178+168C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351478 | ||||||
chr8:24351498
|
T | A | 5 | a0001c0001t0002g0063a0001c0001t0002g0098a0001c0001t0002g0099others(2): Show | 5 | HG02004.hp1 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2178+188T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351498 | ||||||
chr8:24351541
|
C | G | 1 | a0001c0001t0017g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2178+231C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351541 | ||||||
chr8:24351567
|
G | A | 3 | a0003c0006t0002g0275a0003c0006t0002g0276a0003c0006t0002g0278 | 3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2178+257G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351567 | ||||||
chr8:24351596
|
A | T | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2178+286A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351596 | ||||||
chr8:24351759
|
A | ATCATTTA others(17): Show |
292 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2179-226_2179-203d others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 24351759 | |||||
chr8:24351772
|
T | C | 1 | a0001c0001t0004g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2179-215T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351772 | ||||||
chr8:24351834
|
C | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0123a0001c0001t0002g0205others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2179-153C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351834 | ||||||
chr8:24351969
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2179-18A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351969 | ||||||
chr8:24352093
|
C | T | 1 | a0001c0001t0006g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2244+41C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352093 | ||||||
chr8:24352378
|
C | T | 68 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0003g0003others(65): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.2244+326C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352378 | ||||||
chr8:24352379
|
T | C | 1 | a0001c0002t0001g0287 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2244+327T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352379 | ||||||
chr8:24352405
|
C | A | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+353C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352405 | ||||||
chr8:24352583
|
C | T | 3 | a0002c0007t0003g0271a0002c0007t0003g0272a0019c0032t0033g0248 | 3 | HG01167.hp1 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2244+531C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352583 | ||||||
chr8:24352612
|
T | C | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+560T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352612 | ||||||
chr8:24352679
|
T | C | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+627T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352679 | ||||||
chr8:24352809
|
G | A | 8 | a0002c0019t0006g0226a0003c0005t0006g0239a0003c0005t0006g0240others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244+757G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352809 | ||||||
chr8:24352844
|
T | A | 1 | a0001c0001t0003g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2244+792T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352844 | ||||||
chr8:24352871
|
A | G | 22 | a0001c0001t0005g0034a0001c0001t0005g0095a0001c0001t0005g0145others(19): Show | 22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2244+819A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352871 | ||||||
chr8:24352911
|
ATCT | A | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-854_2245-852d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24352911 | |||||
chr8:24352924
|
G | GTAAC | 22 | a0001c0001t0005g0034a0001c0001t0005g0095a0001c0001t0005g0145others(19): Show | 22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2245-843_2245-842i others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24352924 | |||||
chr8:24352928
|
G | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(314): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.2245-842G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352928 | ||||||
chr8:24352942
|
T | C | 3 | a0001c0013t0013g0172a0003c0006t0013g0274a0003c0006t0013g0277 | 3 | HG02922.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2245-828T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352942 | ||||||
chr8:24352960
|
C | G | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-810C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352960 | ||||||
chr8:24353038
|
C | A | 8 | a0001c0001t0002g0179a0001c0001t0002g0224a0001c0001t0002g0230others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2245-732C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353038 | ||||||
chr8:24353055
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2245-715A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353055 | ||||||
chr8:24353135
|
A | G | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-635A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353135 | ||||||
chr8:24353147
|
C | T | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-623C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353147 | ||||||
chr8:24353202
|
A | AAG | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-567_2245-566d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353202 | |||||
chr8:24353240
|
G | A | 320 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2245-530G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353240 | ||||||
chr8:24353285
|
G | C | 316 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(313): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2245-485G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353285 | ||||||
chr8:24353292
|
T | A | 4 | a0001c0013t0013g0172a0002c0007t0026g0102a0003c0006t0013g0274others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-478T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353292 | ||||||
chr8:24353309
|
T | TAAGAGTC others(11): Show |
1 | a0001c0001t0003g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2245-457_2245-440d others(20): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353309 | |||||
chr8:24353428
|
A | AT | 316 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(313): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2245-335dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353428 | |||||
chr8:24353579
|
T | C | 321 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.2245-191T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353579 | ||||||
chr8:24353598
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2245-172C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353598 | ||||||
chr8:24353656
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2245-114T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353656 | ||||||
chr8:24353681
|
A | T | 1 | a0002c0007t0026g0102 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2245-89A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353681 | ||||||
chr8:24353725
|
C | T | 1 | a0001c0002t0004g0299 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2245-45C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353725 | ||||||
chr8:24353765
|
C | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(316): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
splice_region_variant&intron_variant | LOW | c.2245-5C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353765 | ||||||
chr8:24353844
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2307+12A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24353844 | ||||||
chr8:24353916
|
A | AAAAACTT others(21): Show |
1 | a0001c0001t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2307+86_2307+113du others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 24353916 | |||||
chr8:24353983
|
G | A | 10 | a0001c0001t0006g0038a0001c0001t0006g0101a0002c0019t0006g0226others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2307+151G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24353983 | ||||||
chr8:24354045
|
C | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2307+213C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354045 | ||||||
chr8:24354175
|
C | T | 21 | a0001c0001t0005g0034a0001c0001t0005g0095a0001c0001t0005g0145others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.2308-209C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354175 | ||||||
chr8:24354203
|
G | A | 286 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2308-181G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354203 | ||||||
chr8:24354221
|
C | A | 1 | a0001c0002t0002g0310 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2308-163C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354221 | ||||||
chr8:24354221
|
C | G | 319 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(316): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2308-163C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354221 | ||||||
chr8:24354226
|
C | A | 320 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2308-158C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354226 | ||||||
chr8:24354247
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0232 | 2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2308-137G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354247 | ||||||
chr8:24354356
|
G | T | 33 | a0001c0001t0004g0051a0001c0001t0004g0071a0001c0001t0004g0082others(30): Show | 33 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2308-28G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354356 | ||||||
chr8:24354371
|
A | ATGTC | 321 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
splice_region_variant&intron_variant | LOW | c.2308-11_2308-8dupG others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 24354371 |