geneid | 8728 |
---|---|
ensemblid | ENSG00000135074.16 |
hgncid | 197 |
symbol | ADAM19 |
name | ADAM metallopeptidase domain 19 |
refseq_nuc | NM_033274.5 |
refseq_prot | NP_150377.1 |
ensembl_nuc | ENST00000257527.9 |
ensembl_prot | ENSP00000257527.5 |
mane_status | MANE Select |
chr | chr5 |
start | 157477304 |
end | 157575775 |
strand | - |
ver | v1.2 |
region | chr5:157477304-157575775 |
region5000 | chr5:157472304-157580775 |
regionname0 | ADAM19_chr5_157477304_157575775 |
regionname5000 | ADAM19_chr5_157472304_157580775 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 918 | 133 | 8 | 31 | 77 | 2 | 13 | 58 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002 | 0/0 | 918 | 103 | 33 | 23 | 24 | 6 | 17 | 17 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003 | 0/0 | 918 | 17 | 5 | 6 | 1 | 3 | 2 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004 | 0/0 | 918 | 14 | 11 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0005 | 0/0 | 918 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0006 | 0/0 | 918 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0007 | 0/0 | 918 | 5 | 2 | 1 | 0 | 2 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0008 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0009 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0010 | 0/0 | 918 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0011 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0012 | 0/0 | 918 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0013 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0014 | 0/0 | 918 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0015 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0016 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0017 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0018 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2757 | 132 | 8 | 30 | 77 | 2 | 13 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0002 | 0/0 | 2757 | 101 | 33 | 21 | 24 | 6 | 17 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0003 | 0/0 | 2757 | 17 | 5 | 6 | 1 | 3 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0004 | 0/0 | 2757 | 12 | 11 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0005 | 0/0 | 2757 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0006 | 0/0 | 2757 | 6 | 6 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0007 | 0/0 | 2757 | 5 | 2 | 1 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0008 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0009 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0010 | 0/0 | 2757 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0011 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0012 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0013 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0014 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0015 | 0/0 | 2757 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0016 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0017 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0018 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0019 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0020 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
c0021 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3725 | 68 | 7 | 12 | 41 | 2 | 5 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0002 | 1/0 | 3725 | 55 | 12 | 25 | 12 | 1 | 4 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0003 | 0/0 | 3724 | 22 | 2 | 4 | 4 | 4 | 8 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0004 | 0/0 | 3723 | 19 | 13 | 1 | 0 | 0 | 5 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0005 | 0/0 | 3727 | 18 | 0 | 0 | 16 | 0 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0006 | 0/0 | 3726 | 17 | 0 | 3 | 13 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0007 | 0/0 | 3724 | 14 | 5 | 6 | 0 | 2 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0008 | 0/0 | 3724 | 14 | 13 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0009 | 0/0 | 3726 | 9 | 1 | 1 | 5 | 0 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0010 | 0/0 | 3726 | 7 | 6 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0011 | 0/0 | 3724 | 5 | 2 | 0 | 1 | 1 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0012 | 0/0 | 3713 | 5 | 1 | 2 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0013 | 0/0 | 3713 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0014 | 0/0 | 3725 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0015 | 0/0 | 3724 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0016 | 0/0 | 3725 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0017 | 0/0 | 3723 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0018 | 0/0 | 3727 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0019 | 0/0 | 3725 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0020 | 0/0 | 3725 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0021 | 0/0 | 3724 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0022 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0023 | 0/0 | 3724 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0024 | 0/0 | 3725 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0025 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0026 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0027 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0028 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0029 | 0/0 | 3725 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0030 | 0/0 | 3725 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0031 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0032 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0033 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0034 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0035 | 0/0 | 3713 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0036 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0037 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0038 | 0/0 | 3724 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0039 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0040 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0041 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0042 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0043 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0044 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0045 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0046 | 0/0 | 3724 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
t0047 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2757 | 132 | 8 | 30 | 77 | 2 | 13 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0019 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002 | 0/0 | 2757 | 101 | 33 | 21 | 24 | 6 | 17 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0014 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003 | 0/0 | 2757 | 17 | 5 | 6 | 1 | 3 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0004 | 0/0 | 2757 | 12 | 11 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0013 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0005c0005 | 0/0 | 2757 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0006c0006 | 0/0 | 2757 | 6 | 6 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0007c0007 | 0/0 | 2757 | 5 | 2 | 1 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0008c0008 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0009c0009 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0010c0010 | 0/0 | 2757 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0011c0016 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0012c0015 | 0/0 | 2757 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0013c0011 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0014c0012 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0015c0021 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0016c0020 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0017c0018 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0018c0017 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6481 | 64 | 5 | 11 | 41 | 1 | 5 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0002 | 1/0 | 6481 | 19 | 1 | 12 | 3 | 1 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0003 | 0/0 | 6480 | 3 | 0 | 1 | 0 | 0 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0005 | 0/0 | 6483 | 18 | 0 | 0 | 16 | 0 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0006 | 0/0 | 6482 | 8 | 0 | 1 | 6 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0008 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0009 | 0/0 | 6482 | 9 | 1 | 1 | 5 | 0 | 2 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0017 | 0/0 | 6479 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0023 | 0/0 | 6480 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0027 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0029 | 0/0 | 6481 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0030 | 0/0 | 6481 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0033 | 0/0 | 6483 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0041 | 0/0 | 6481 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0042 | 0/0 | 6482 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0001t0043 | 0/0 | 6482 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0001c0019t0017 | 0/0 | 6479 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0001 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0002 | 0/0 | 6481 | 27 | 5 | 10 | 9 | 0 | 3 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0003 | 0/0 | 6480 | 18 | 1 | 3 | 4 | 4 | 6 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0004 | 0/0 | 6479 | 12 | 6 | 1 | 0 | 0 | 5 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0006 | 0/0 | 6482 | 9 | 0 | 2 | 7 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0007 | 0/0 | 6480 | 10 | 3 | 4 | 0 | 2 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0008 | 0/0 | 6480 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0014 | 0/0 | 6481 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0019 | 0/0 | 6481 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0020 | 0/0 | 6481 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0031 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0036 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0037 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0038 | 0/0 | 6480 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0039 | 0/0 | 6479 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0040 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0044 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0045 | 0/0 | 6481 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0046 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0002t0047 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0002c0014t0007 | 0/0 | 6480 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0004 | 0/0 | 6479 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0007 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0011 | 0/0 | 6480 | 5 | 2 | 0 | 1 | 1 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0015 | 0/0 | 6480 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0016 | 0/0 | 6481 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0021 | 0/0 | 6480 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0003c0003t0022 | 0/0 | 6479 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0004t0010 | 0/0 | 6482 | 7 | 6 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0004t0018 | 0/0 | 6483 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0004t0032 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0004t0034 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0004c0013t0012 | 0/0 | 6469 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0005c0005t0008 | 0/0 | 6480 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0006c0006t0001 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0006c0006t0013 | 0/0 | 6469 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0006c0006t0023 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0007c0007t0012 | 0/0 | 6469 | 3 | 1 | 0 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0007c0007t0025 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0007c0007t0035 | 0/0 | 6469 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0008c0008t0004 | 0/0 | 6479 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0009c0009t0002 | 0/0 | 6481 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0010c0010t0001 | 0/0 | 6481 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0010c0010t0002 | 0/0 | 6481 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0010c0010t0004 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0011c0016t0003 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0011c0016t0007 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0012c0015t0024 | 0/0 | 6481 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0013c0011t0026 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0013c0011t0028 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0014c0012t0002 | 0/0 | 6481 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0015c0021t0002 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0016c0020t0001 | 0/0 | 6481 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0017c0018t0002 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
a0018c0017t0022 | 0/0 | 6479 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | copy fasta | chr5 | 157472304 | 157580775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0002g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0017g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0017g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0023g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0033g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0041g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0042g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0001t0043g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0001c0019t0017g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0014g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0014g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0020g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0020g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0020g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0031g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0036g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0037g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0038g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0039g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0040g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0044g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0045g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0046g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0002t0047g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0014t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0002c0014t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0011g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0011g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0011g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0015g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0015g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0015g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0016g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0016g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0016g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0021g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0021g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0003c0003t0022g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0018g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0018g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0018g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0032g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0004t0034g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0013t0012g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0004c0013t0012g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0005c0005t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0006c0006t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0007c0007t0012g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0007c0007t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0007c0007t0012g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0007c0007t0025g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0007c0007t0035g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0008c0008t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0008c0008t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0008c0008t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0008c0008t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0009c0009t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0009c0009t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0009c0009t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0010c0010t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0010c0010t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0010c0010t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0011c0016t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0011c0016t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0012c0015t0024g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0012c0015t0024g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0013c0011t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0013c0011t0028g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0014c0012t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0014c0012t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0015c0021t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0016c0020t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0017c0018t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
a0018c0017t0022g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0021 | g0215 | EUR | GBR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00099 | hp2 | a0016 | c0020 | t0001 | g0094 | EUR | GBR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00140 | hp1 | a0002 | c0002 | t0007 | g0254 | EUR | GBR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00280 | hp1 | a0007 | c0007 | t0012 | g0022 | EUR | FIN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00280 | hp2 | a0003 | c0003 | t0011 | g0213 | EUR | FIN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0162 | EUR | FIN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00323 | hp2 | a0003 | c0003 | t0021 | g0216 | EUR | FIN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0111 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00621 | hp1 | a0001 | c0001 | t0030 | g0129 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00639 | hp1 | a0003 | c0003 | t0022 | g0218 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00639 | hp2 | a0018 | c0017 | t0022 | g0024 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00673 | hp1 | a0002 | c0002 | t0006 | g0190 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00735 | hp1 | a0003 | c0003 | t0016 | g0217 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0063 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00738 | hp1 | a0010 | c0010 | t0002 | g0009 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0153 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01069 | hp2 | a0001 | c0001 | t0017 | g0262 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01070 | hp1 | a0002 | c0014 | t0007 | g0269 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01071 | hp1 | a0001 | c0001 | t0017 | g0259 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01074 | hp2 | a0007 | c0007 | t0035 | g0020 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01081 | hp2 | a0003 | c0003 | t0015 | g0211 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01099 | hp2 | a0002 | c0002 | t0006 | g0187 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01106 | hp2 | a0002 | c0002 | t0007 | g0253 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01109 | hp2 | a0002 | c0002 | t0045 | g0147 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01168 | hp1 | a0002 | c0002 | t0007 | g0267 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01169 | hp2 | a0002 | c0014 | t0007 | g0268 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01175 | hp2 | a0002 | c0002 | t0007 | g0250 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01192 | hp1 | a0003 | c0003 | t0015 | g0289 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01243 | hp1 | a0012 | c0015 | t0024 | g0272 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01243 | hp2 | a0004 | c0004 | t0010 | g0294 | AMR | PUR | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01256 | hp1 | a0003 | c0003 | t0016 | g0209 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0159 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01258 | hp1 | a0003 | c0003 | t0016 | g0210 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01261 | hp1 | a0010 | c0010 | t0001 | g0019 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01261 | hp2 | a0004 | c0013 | t0012 | g0248 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01361 | hp1 | a0014 | c0012 | t0002 | g0089 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01433 | hp1 | a0004 | c0013 | t0012 | g0122 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01433 | hp2 | a0014 | c0012 | t0002 | g0090 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01496 | hp2 | a0002 | c0002 | t0006 | g0200 | AMR | CLM | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01515 | hp1 | a0002 | c0002 | t0007 | g0031 | EUR | IBS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0005 | EUR | IBS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01517 | hp2 | a0002 | c0002 | t0003 | g0005 | EUR | IBS | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01884 | hp1 | a0005 | c0005 | t0008 | g0274 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01884 | hp2 | a0001 | c0001 | t0027 | g0102 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01891 | hp1 | a0003 | c0003 | t0011 | g0286 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01891 | hp2 | a0002 | c0002 | t0007 | g0256 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01934 | hp2 | a0002 | c0002 | t0007 | g0116 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01943 | hp1 | a0001 | c0019 | t0017 | g0240 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01943 | hp2 | a0002 | c0002 | t0003 | g0084 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01952 | hp1 | a0001 | c0001 | t0041 | g0062 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0182 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01981 | hp1 | a0002 | c0002 | t0004 | g0241 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02015 | hp2 | a0002 | c0002 | t0046 | g0284 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02027 | hp2 | a0002 | c0002 | t0006 | g0188 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02040 | hp1 | a0001 | c0001 | t0042 | g0138 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02055 | hp1 | a0005 | c0005 | t0008 | g0276 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02055 | hp2 | a0004 | c0004 | t0018 | g0255 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0069 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02129 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02145 | hp1 | a0002 | c0002 | t0044 | g0282 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02145 | hp2 | a0004 | c0004 | t0010 | g0237 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0074 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | CDX | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02257 | hp1 | a0008 | c0008 | t0004 | g0227 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02257 | hp2 | a0002 | c0002 | t0004 | g0251 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02258 | hp1 | a0011 | c0016 | t0003 | g0301 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02258 | hp2 | a0006 | c0006 | t0001 | g0010 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02280 | hp1 | a0002 | c0002 | t0014 | g0008 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02300 | hp1 | a0001 | c0001 | t0023 | g0050 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0079 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02572 | hp1 | a0008 | c0008 | t0004 | g0226 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0025 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02622 | hp1 | a0004 | c0004 | t0034 | g0279 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02622 | hp2 | a0002 | c0002 | t0007 | g0285 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02630 | hp1 | a0002 | c0002 | t0014 | g0008 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02630 | hp2 | a0004 | c0004 | t0010 | g0296 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02647 | hp1 | a0009 | c0009 | t0002 | g0006 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02647 | hp2 | a0004 | c0004 | t0010 | g0265 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02683 | hp1 | a0002 | c0002 | t0004 | g0207 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0141 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0178 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02698 | hp2 | a0002 | c0002 | t0004 | g0206 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02717 | hp1 | a0004 | c0004 | t0010 | g0273 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02717 | hp2 | a0009 | c0009 | t0002 | g0123 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02723 | hp1 | a0004 | c0004 | t0032 | g0080 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02723 | hp2 | a0006 | c0006 | t0013 | g0015 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02735 | hp1 | a0002 | c0002 | t0038 | g0169 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0192 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02738 | hp1 | a0002 | c0002 | t0004 | g0203 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02738 | hp2 | a0002 | c0002 | t0003 | g0143 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02809 | hp1 | a0006 | c0006 | t0013 | g0013 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0258 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02818 | hp1 | a0015 | c0021 | t0002 | g0299 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02818 | hp2 | a0005 | c0005 | t0008 | g0275 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02886 | hp1 | a0002 | c0002 | t0008 | g0264 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02886 | hp2 | a0006 | c0006 | t0013 | g0012 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0260 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02896 | hp2 | a0009 | c0009 | t0002 | g0006 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02922 | hp1 | a0002 | c0002 | t0019 | g0027 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02965 | hp1 | a0006 | c0006 | t0023 | g0017 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02965 | hp2 | a0005 | c0005 | t0008 | g0001 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02970 | hp1 | a0003 | c0003 | t0004 | g0222 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02970 | hp2 | a0002 | c0002 | t0037 | g0257 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03017 | hp1 | a0003 | c0003 | t0015 | g0214 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03098 | hp1 | a0002 | c0002 | t0040 | g0266 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0028 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03130 | hp1 | a0002 | c0002 | t0008 | g0291 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03130 | hp2 | a0005 | c0005 | t0008 | g0001 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03139 | hp1 | a0002 | c0002 | t0047 | g0283 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03139 | hp2 | a0009 | c0009 | t0002 | g0154 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03195 | hp1 | a0002 | c0002 | t0004 | g0238 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03195 | hp2 | a0004 | c0004 | t0010 | g0252 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03209 | hp1 | a0005 | c0005 | t0008 | g0001 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0281 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03225 | hp2 | a0007 | c0007 | t0025 | g0011 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03453 | hp2 | a0002 | c0002 | t0004 | g0198 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03486 | hp2 | a0004 | c0004 | t0018 | g0295 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03516 | hp1 | a0002 | c0002 | t0008 | g0076 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03516 | hp2 | a0002 | c0002 | t0014 | g0026 | AFR | ESN | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03540 | hp1 | a0008 | c0008 | t0004 | g0225 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03540 | hp2 | a0011 | c0016 | t0007 | g0300 | AFR | GWD | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0261 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0091 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0161 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0180 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0119 | SAS | PJL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | BEB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03927 | hp2 | a0002 | c0002 | t0004 | g0202 | SAS | BEB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0140 | SAS | BEB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04115 | hp2 | a0002 | c0002 | t0004 | g0205 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0185 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04199 | hp2 | a0002 | c0002 | t0007 | g0127 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04228 | hp1 | a0003 | c0003 | t0011 | g0288 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0040 | SAS | STU | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18522 | hp1 | a0006 | c0006 | t0013 | g0014 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18522 | hp2 | a0017 | c0018 | t0002 | g0016 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18906 | hp1 | a0005 | c0005 | t0008 | g0293 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18906 | hp2 | a0002 | c0002 | t0007 | g0270 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18942 | hp1 | a0001 | c0001 | t0043 | g0135 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18946 | hp2 | a0002 | c0002 | t0020 | g0163 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18967 | hp1 | a0002 | c0002 | t0006 | g0191 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18971 | hp2 | a0002 | c0002 | t0020 | g0183 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18974 | hp1 | a0001 | c0001 | t0009 | g0113 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18974 | hp2 | a0002 | c0002 | t0020 | g0148 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18979 | hp1 | a0001 | c0001 | t0009 | g0037 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0068 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18986 | hp2 | a0003 | c0003 | t0011 | g0212 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18991 | hp1 | a0001 | c0001 | t0009 | g0046 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18998 | hp2 | a0002 | c0002 | t0006 | g0171 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19000 | hp1 | a0001 | c0001 | t0033 | g0219 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19000 | hp2 | a0001 | c0001 | t0009 | g0045 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19004 | hp2 | a0002 | c0002 | t0006 | g0177 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19005 | hp1 | a0001 | c0001 | t0029 | g0193 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19030 | hp1 | a0008 | c0008 | t0004 | g0228 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19030 | hp2 | a0004 | c0004 | t0018 | g0278 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19043 | hp1 | a0010 | c0010 | t0004 | g0023 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19043 | hp2 | a0003 | c0003 | t0007 | g0221 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19058 | hp1 | a0002 | c0002 | t0006 | g0189 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19079 | hp2 | a0002 | c0002 | t0006 | g0165 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19240 | hp1 | a0002 | c0002 | t0019 | g0197 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA19240 | hp2 | a0005 | c0005 | t0008 | g0277 | AFR | YRI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20129 | hp1 | a0005 | c0005 | t0008 | g0246 | AFR | ASW | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20129 | hp2 | a0002 | c0002 | t0019 | g0196 | AFR | ASW | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20805 | hp1 | a0007 | c0007 | t0012 | g0018 | EUR | TSI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0181 | EUR | TSI | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20905 | hp2 | a0002 | c0002 | t0039 | g0208 | SAS | GIH | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02109 | hp2 | a0013 | c0011 | t0026 | g0280 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02486 | hp1 | a0003 | c0003 | t0011 | g0287 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02486 | hp2 | a0012 | c0015 | t0024 | g0271 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0186 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG02559 | hp2 | a0004 | c0004 | t0010 | g0088 | AFR | ACB | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03471 | hp1 | a0002 | c0002 | t0036 | g0243 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG03471 | hp2 | a0013 | c0011 | t0028 | g0239 | AFR | MSL | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG06807 | hp1 | a0003 | c0003 | t0004 | g0290 | AFR | USA | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
HG06807 | hp2 | a0002 | c0002 | t0014 | g0292 | AFR | USA | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA20300 | hp2 | a0002 | c0002 | t0008 | g0263 | AFR | USA | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA21309 | hp1 | a0007 | c0007 | t0012 | g0021 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
NA21309 | hp2 | a0002 | c0002 | t0031 | g0204 | AFR | LWK | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0174 | REF | REF | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0298 | REF | REF | ADAM19_chr5_157472304_157580775 | ADAM19 | chr5 | 157472304 | 157580775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157488402
|
C | T | 1 | a0005 | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
missense_variant | MODERATE | c.2413G>A | p.Ala805Thr | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/23 | 2492/6481 | 2413/2757 | 805/918 | chr5 | 157488402 | ||
chr5:157490332
|
A | C | 6 | a0003a0004a0007others(3): Show | 43 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
missense_variant | MODERATE | c.2218T>G | p.Ser740Ala | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/23 | 2297/6481 | 2218/2757 | 740/918 | chr5 | 157490332 | ||
chr5:157491842
|
C | T | 3 | a0003a0008a0018 | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
missense_variant | MODERATE | c.1979G>A | p.Gly660Asp | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 17/23 | 2058/6481 | 1979/2757 | 660/918 | chr5 | 157491842 | ||
chr5:157496966
|
C | T | 1 | a0016 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.1522G>A | p.Gly508Ser | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/23 | 1601/6481 | 1522/2757 | 508/918 | chr5 | 157496966 | ||
chr5:157499598
|
T | C | 1 | a0012 | 2 | HG01243.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.1373A>G | p.His458Arg | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/23 | 1452/6481 | 1373/2757 | 458/918 | chr5 | 157499598 | ||
chr5:157502808
|
C | T | 1 | a0014 | 2 | HG01361.hp1 HG01433.hp2 |
missense_variant | MODERATE | c.1303G>A | p.Glu435Lys | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/23 | 1382/6481 | 1303/2757 | 435/918 | chr5 | 157502808 | ||
chr5:157509356
|
T | C | 9 | a0002a0004a0005others(6): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
missense_variant | MODERATE | c.850A>G | p.Ser284Gly | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/23 | 929/6481 | 850/2757 | 284/918 | chr5 | 157509356 | ||
chr5:157537936
|
G | C | 4 | a0008a0009a0015others(1): Show | 10 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.307C>G | p.Gln103Glu | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/23 | 386/6481 | 307/2757 | 103/918 | chr5 | 157537936 | ||
chr5:157575620
|
C | A | 1 | a0011 | 2 | HG02258.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.77G>T | p.Arg26Leu | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/23 | 156/6481 | 77/2757 | 26/918 | chr5 | 157575620 | ||
chr5:157575687
|
C | T | 5 | a0006a0007a0010others(2): Show | 16 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(13): Show |
missense_variant | MODERATE | c.10G>A | p.Gly4Ser | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/23 | 89/6481 | 10/2757 | 4/918 | chr5 | 157575687 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157488289
|
G | A | 1 | a0004c0004 | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
synonymous_variant | LOW | c.2526C>T | p.Pro842Pro | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/23 | 2605/6481 | 2526/2757 | 842/918 | chr5 | 157488289 | ||
chr5:157491877
|
G | A | 1 | a0002c0014 | 2 | HG01070.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1944C>T | p.Phe648Phe | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 17/23 | 2023/6481 | 1944/2757 | 648/918 | chr5 | 157491877 | ||
chr5:157519932
|
C | T | 2 | a0001c0019a0013c0011 | 3 | HG01943.hp1 HG02109.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.507G>A | p.Pro169Pro | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/23 | 586/6481 | 507/2757 | 169/918 | chr5 | 157519932 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157477448
|
C | T | 1 | a0004c0004t0032 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3501G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3501 | chr5 | 157477448 | |||||
chr5:157477534
|
C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3415G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3415 | chr5 | 157477534 | |||||
chr5:157477536
|
C | T | 1 | a0002c0002t0038 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3413G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3413 | chr5 | 157477536 | |||||
chr5:157477625
|
C | T | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0023others(11): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3324G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3324 | chr5 | 157477625 | |||||
chr5:157477626
|
G | A | 3 | a0001c0001t0017a0001c0019t0017a0002c0002t0031 | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3323C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3323 | chr5 | 157477626 | |||||
chr5:157477641
|
T | C | 1 | a0001c0001t0029 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3308A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3308 | chr5 | 157477641 | |||||
chr5:157477668
|
C | T | 1 | a0002c0002t0019 | 3 | HG02922.hp1 NA19240.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3281G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3281 | chr5 | 157477668 | |||||
chr5:157477682
|
T | C | 1 | a0001c0001t0030 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3267A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3267 | chr5 | 157477682 | |||||
chr5:157477765
|
G | C | 1 | a0004c0004t0034 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3184C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3184 | chr5 | 157477765 | |||||
chr5:157477773
|
A | G | 3 | a0001c0001t0017a0001c0019t0017a0002c0002t0031 | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3176T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3176 | chr5 | 157477773 | |||||
chr5:157477821
|
G | T | 3 | a0001c0001t0017a0001c0019t0017a0002c0002t0031 | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3128C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 3128 | chr5 | 157477821 | |||||
chr5:157478290
|
C | CA | 10 | a0001c0001t0006a0001c0001t0009a0001c0001t0042others(7): Show | 39 | HG00673.hp1 HG00735.hp2 HG01099.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2658dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2658 | chr5 | 157478290 | |||||
chr5:157478290
|
C | CAA | 3 | a0001c0001t0005a0001c0001t0033a0004c0004t0018 | 22 | HG00544.hp1 HG02055.hp2 HG02129.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2658dupTT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2658 | chr5 | 157478290 | |||||
chr5:157478290
|
CA | C | 22 | a0001c0001t0003a0001c0001t0008a0001c0001t0023others(19): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2658delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2658 | chr5 | 157478290 | |||||
chr5:157478290
|
CAA | C | 11 | a0001c0001t0017a0001c0019t0017a0002c0002t0004others(8): Show | 27 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2658delTT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2657 | chr5 | 157478290 | |||||
chr5:157478290
|
CAAAAAAA others(5): Show |
C | 4 | a0004c0013t0012a0006c0006t0013a0007c0007t0012others(1): Show | 10 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2647_*2658delTTTT others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2647 | chr5 | 157478290 | |||||
chr5:157478392
|
C | G | 13 | a0002c0002t0004a0002c0002t0007a0002c0002t0036others(10): Show | 38 | HG00140.hp1 HG01070.hp1 HG01106.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2557G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2557 | chr5 | 157478392 | |||||
chr5:157478430
|
G | A | 1 | a0001c0001t0042 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2519C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2519 | chr5 | 157478430 | |||||
chr5:157478509
|
G | A | 34 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(31): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2440 | chr5 | 157478509 | |||||
chr5:157478532
|
T | C | 1 | a0002c0002t0039 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2417A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2417 | chr5 | 157478532 | |||||
chr5:157478577
|
T | C | 4 | a0003c0003t0015a0003c0003t0016a0003c0003t0022others(1): Show | 8 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2372A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2372 | chr5 | 157478577 | |||||
chr5:157478680
|
G | A | 1 | a0002c0002t0019 | 3 | HG02922.hp1 NA19240.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2269C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2269 | chr5 | 157478680 | |||||
chr5:157478722
|
C | T | 1 | a0001c0001t0041 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2227G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2227 | chr5 | 157478722 | |||||
chr5:157478842
|
G | A | 1 | a0001c0001t0043 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2107 | chr5 | 157478842 | |||||
chr5:157478947
|
G | A | 1 | a0002c0002t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2002C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 2002 | chr5 | 157478947 | |||||
chr5:157478991
|
A | C | 3 | a0007c0007t0025a0013c0011t0026a0013c0011t0028 | 3 | HG02109.hp2 HG03225.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1958T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1958 | chr5 | 157478991 | |||||
chr5:157479149
|
A | C | 1 | a0002c0002t0037 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1800 | chr5 | 157479149 | |||||
chr5:157479304
|
G | C | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1645C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1645 | chr5 | 157479304 | |||||
chr5:157479319
|
G | A | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1630 | chr5 | 157479319 | |||||
chr5:157479453
|
C | G | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1496 | chr5 | 157479453 | |||||
chr5:157479454
|
G | A | 1 | a0002c0002t0044 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1495C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1495 | chr5 | 157479454 | |||||
chr5:157479563
|
C | T | 1 | a0002c0002t0036 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1386 | chr5 | 157479563 | |||||
chr5:157479571
|
A | T | 1 | a0012c0015t0024 | 2 | HG01243.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1378T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1378 | chr5 | 157479571 | |||||
chr5:157479694
|
G | A | 1 | a0004c0004t0034 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1255C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1255 | chr5 | 157479694 | |||||
chr5:157479802
|
G | A | 1 | a0007c0007t0035 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1147 | chr5 | 157479802 | |||||
chr5:157479811
|
C | T | 13 | a0002c0002t0004a0002c0002t0007a0002c0002t0036others(10): Show | 38 | HG00140.hp1 HG01070.hp1 HG01106.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1138G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 1138 | chr5 | 157479811 | |||||
chr5:157479978
|
A | G | 34 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(31): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*971T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 971 | chr5 | 157479978 | |||||
chr5:157480102
|
G | T | 6 | a0003c0003t0011a0003c0003t0015a0003c0003t0016others(3): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 847 | chr5 | 157480102 | |||||
chr5:157480163
|
G | A | 5 | a0001c0001t0003a0002c0002t0003a0002c0002t0045others(2): Show | 24 | HG00323.hp1 HG00544.hp2 HG00738.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 786 | chr5 | 157480163 | |||||
chr5:157480368
|
G | A | 1 | a0002c0002t0019 | 3 | HG02922.hp1 NA19240.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 581 | chr5 | 157480368 | |||||
chr5:157480485
|
G | A | 1 | a0002c0002t0020 | 3 | NA18946.hp2 NA18971.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*464C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 464 | chr5 | 157480485 | |||||
chr5:157480601
|
T | C | 1 | a0002c0002t0046 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 348 | chr5 | 157480601 | |||||
chr5:157480642
|
G | T | 2 | a0007c0007t0025a0013c0011t0026 | 2 | HG02109.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*307C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 307 | chr5 | 157480642 | |||||
chr5:157480670
|
A | C | 1 | a0003c0003t0021 | 2 | HG00099.hp1 HG00323.hp2 |
3_prime_UTR_variant | MODIFIER | c.*279T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 279 | chr5 | 157480670 | |||||
chr5:157480769
|
C | A | 2 | a0002c0002t0014a0002c0002t0047 | 5 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*180G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 23/23 | 180 | chr5 | 157480769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157481114
|
A | G | 1 | a0002c0002t0003g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2704-112T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481114 | ||||||
chr5:157481193
|
C | T | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2704-191G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481193 | ||||||
chr5:157481236
|
C | T | 3 | a0002c0002t0008g0076a0002c0002t0008g0263a0002c0002t0008g0264 | 3 | HG02886.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2704-234G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481236 | ||||||
chr5:157481278
|
G | A | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2704-276C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481278 | ||||||
chr5:157481309
|
C | T | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2704-307G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481309 | ||||||
chr5:157481593
|
A | T | 3 | a0001c0001t0005g0104a0001c0001t0005g0107a0001c0001t0005g0150 | 3 | NA18981.hp2 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2703+198T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481593 | ||||||
chr5:157481645
|
C | T | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2703+146G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 22/22 | chr5 | 157481645 | ||||||
chr5:157482215
|
C | T | 7 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(4): Show | 7 | HG02257.hp1 HG02572.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2551-272G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482215 | ||||||
chr5:157482306
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2551-363G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482306 | ||||||
chr5:157482308
|
C | T | 1 | a0002c0002t0008g0264 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2551-365G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482308 | ||||||
chr5:157482428
|
T | C | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2551-485A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482428 | ||||||
chr5:157482583
|
G | C | 1 | a0002c0002t0044g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2551-640C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482583 | ||||||
chr5:157482604
|
T | C | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2551-661A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482604 | ||||||
chr5:157482757
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2551-814C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482757 | ||||||
chr5:157482867
|
T | C | 2 | a0013c0011t0026g0280a0013c0011t0028g0239 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2551-924A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482867 | ||||||
chr5:157482876
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(87): Show | 93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2551-933T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482876 | ||||||
chr5:157482899
|
C | A | 1 | a0004c0004t0010g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2551-956G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482899 | ||||||
chr5:157482919
|
C | T | 22 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2551-976G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157482919 | ||||||
chr5:157483016
|
C | T | 3 | a0007c0007t0025g0011a0013c0011t0026g0280a0013c0011t0028g0239 | 3 | HG02109.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2551-1073G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483016 | ||||||
chr5:157483086
|
G | C | 2 | a0002c0002t0008g0291a0009c0009t0002g0006 | 3 | HG02647.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2551-1143C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483086 | ||||||
chr5:157483115
|
C | T | 31 | a0002c0002t0004g0025a0002c0002t0004g0079a0002c0002t0004g0198others(28): Show | 31 | HG00140.hp1 HG01070.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.2551-1172G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483115 | ||||||
chr5:157483146
|
A | G | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2551-1203T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483146 | ||||||
chr5:157483157
|
T | C | 1 | a0002c0002t0007g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2551-1214A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483157 | ||||||
chr5:157483192
|
C | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2551-1249G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483192 | ||||||
chr5:157483209
|
TA | T | 34 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2551-1267delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483209 | ||||||
chr5:157483291
|
C | A | 3 | a0001c0001t0005g0104a0001c0001t0005g0107a0001c0001t0005g0150 | 3 | NA18981.hp2 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2551-1348G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483291 | ||||||
chr5:157483304
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0009g0028 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2551-1361G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483304 | ||||||
chr5:157483525
|
G | A | 1 | a0002c0002t0003g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2551-1582C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483525 | ||||||
chr5:157483612
|
G | A | 2 | a0009c0009t0002g0123a0009c0009t0002g0154 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2551-1669C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483612 | ||||||
chr5:157483637
|
A | AT | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(131): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2551-1695dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483637 | ||||||
chr5:157483756
|
C | T | 1 | a0002c0002t0006g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2551-1813G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483756 | ||||||
chr5:157483779
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(88): Show | 94 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2551-1836T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483779 | ||||||
chr5:157483791
|
G | A | 8 | a0001c0001t0002g0093a0001c0001t0002g0097a0001c0001t0002g0101others(5): Show | 8 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2551-1848C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483791 | ||||||
chr5:157483806
|
G | C | 1 | a0002c0002t0003g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2551-1863C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483806 | ||||||
chr5:157483822
|
C | T | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2551-1879G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483822 | ||||||
chr5:157483854
|
G | A | 2 | a0002c0002t0002g0195a0002c0002t0002g0242 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2551-1911C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483854 | ||||||
chr5:157483944
|
C | CT | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(89): Show | 95 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2551-2002dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157483944 | ||||||
chr5:157484231
|
T | G | 1 | a0003c0003t0015g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2551-2288A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157484231 | ||||||
chr5:157484435
|
C | T | 5 | a0002c0002t0004g0202a0002c0002t0004g0203a0002c0002t0004g0205others(2): Show | 5 | HG02683.hp1 HG02698.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2551-2492G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157484435 | ||||||
chr5:157484441
|
G | A | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2551-2498C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157484441 | ||||||
chr5:157484462
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2551-2519C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157484462 | ||||||
chr5:157484811
|
A | T | 6 | a0006c0006t0001g0010a0006c0006t0013g0012a0006c0006t0013g0013others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2551-2868T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157484811 | ||||||
chr5:157485198
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 41 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.2550+3067A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157485198 | ||||||
chr5:157485970
|
C | T | 1 | a0002c0002t0004g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2550+2295G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157485970 | ||||||
chr5:157485994
|
G | A | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2550+2271C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157485994 | ||||||
chr5:157485995
|
C | A | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2550+2270G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157485995 | ||||||
chr5:157486120
|
G | T | 12 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0252others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2550+2145C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486120 | ||||||
chr5:157486143
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2550+2122G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486143 | ||||||
chr5:157486146
|
T | A | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2550+2119A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486146 | ||||||
chr5:157486179
|
C | T | 1 | a0002c0002t0006g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2550+2086G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486179 | ||||||
chr5:157486235
|
G | T | 1 | a0008c0008t0004g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2550+2030C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486235 | ||||||
chr5:157486344
|
A | G | 4 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2550+1921T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486344 | ||||||
chr5:157486445
|
C | T | 34 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2550+1820G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486445 | ||||||
chr5:157486464
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2550+1801G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486464 | ||||||
chr5:157486570
|
G | A | 1 | a0002c0002t0004g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2550+1695C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486570 | ||||||
chr5:157486670
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0027g0102a0007c0007t0025g0011others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2550+1595C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486670 | ||||||
chr5:157486703
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(289): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2550+1562A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486703 | ||||||
chr5:157486794
|
TA | T | 10 | a0001c0001t0006g0030a0002c0002t0006g0189a0004c0004t0010g0088others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2550+1470delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486794 | ||||||
chr5:157486872
|
A | T | 34 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2550+1393T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486872 | ||||||
chr5:157486921
|
C | T | 2 | a0009c0009t0002g0123a0009c0009t0002g0154 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2550+1344G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486921 | ||||||
chr5:157486923
|
TAAG | T | 26 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(23): Show | 27 | HG00544.hp1 HG01496.hp2 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.2550+1339_2550+134 others(7): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157486923 | ||||||
chr5:157487459
|
C | G | 4 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2550+806G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487459 | ||||||
chr5:157487529
|
C | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2550+736G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487529 | ||||||
chr5:157487533
|
C | T | 1 | a0001c0001t0043g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2550+732G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487533 | ||||||
chr5:157487662
|
T | TG | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(95): Show | 101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2550+602dupC | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487662 | ||||||
chr5:157487665
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2550+600A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487665 | ||||||
chr5:157487665
|
T | G | 4 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2550+600A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487665 | ||||||
chr5:157487845
|
CA | C | 5 | a0005c0005t0008g0001a0005c0005t0008g0274a0005c0005t0008g0275others(2): Show | 7 | HG01884.hp1 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2550+419delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487845 | ||||||
chr5:157487907
|
C | A | 1 | a0002c0002t0006g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2550+358G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487907 | ||||||
chr5:157487920
|
A | G | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2550+345T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487920 | ||||||
chr5:157487974
|
C | T | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2550+291G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157487974 | ||||||
chr5:157488080
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(95): Show | 101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2550+185A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157488080 | ||||||
chr5:157488125
|
G | A | 27 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(24): Show | 28 | HG00544.hp1 HG01496.hp2 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.2550+140C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 21/22 | chr5 | 157488125 | ||||||
chr5:157488549
|
G | C | 4 | a0004c0004t0010g0252a0004c0004t0010g0273a0004c0004t0018g0255others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2326-60C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488549 | ||||||
chr5:157488572
|
C | T | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2326-83G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488572 | ||||||
chr5:157488796
|
C | T | 1 | a0002c0002t0002g0157 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2325+306G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488796 | ||||||
chr5:157488813
|
C | T | 1 | a0006c0006t0013g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2325+289G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488813 | ||||||
chr5:157488866
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.2325+236A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488866 | ||||||
chr5:157488964
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2325+138T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157488964 | ||||||
chr5:157489029
|
C | CAAAAAGA others(1): Show |
138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2325+65_2325+72dup others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 20/22 | chr5 | 157489029 | ||||||
chr5:157489271
|
GC | G | 21 | a0001c0001t0003g0073a0002c0002t0003g0005a0002c0002t0003g0040others(18): Show | 22 | HG00323.hp1 HG00544.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2241-86delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489271 | ||||||
chr5:157489294
|
C | T | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2241-108G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489294 | ||||||
chr5:157489444
|
G | C | 7 | a0002c0002t0007g0031a0002c0002t0007g0116a0002c0002t0007g0250others(4): Show | 7 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241-258C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489444 | ||||||
chr5:157489547
|
A | G | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2241-361T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489547 | ||||||
chr5:157489581
|
A | G | 22 | a0003c0003t0004g0222a0003c0003t0004g0290a0003c0003t0007g0221others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2241-395T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489581 | ||||||
chr5:157489603
|
C | A | 38 | a0001c0001t0027g0102a0003c0003t0004g0222a0003c0003t0004g0290others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.2241-417G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489603 | ||||||
chr5:157489628
|
A | C | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2241-442T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489628 | ||||||
chr5:157489632
|
G | A | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2241-446C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489632 | ||||||
chr5:157489634
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(86): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2241-448C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489634 | ||||||
chr5:157489783
|
C | T | 19 | a0001c0001t0003g0073a0002c0002t0003g0005a0002c0002t0003g0040others(16): Show | 20 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2240+527G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489783 | ||||||
chr5:157489881
|
G | A | 1 | a0001c0001t0006g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2240+429C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489881 | ||||||
chr5:157489884
|
C | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2240+426G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489884 | ||||||
chr5:157489914
|
G | T | 2 | a0002c0002t0004g0241a0010c0010t0004g0023 | 2 | HG01981.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2240+396C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489914 | ||||||
chr5:157489917
|
G | C | 26 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(23): Show | 27 | HG00544.hp1 HG01496.hp2 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.2240+393C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489917 | ||||||
chr5:157489919
|
G | A | 1 | a0008c0008t0004g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2240+391C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489919 | ||||||
chr5:157489979
|
C | A | 15 | a0003c0003t0011g0212a0003c0003t0011g0213a0003c0003t0011g0286others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.2240+331G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157489979 | ||||||
chr5:157490108
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2240+202A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157490108 | ||||||
chr5:157490294
|
T | C | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2240+16A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 19/22 | chr5 | 157490294 | ||||||
chr5:157490504
|
A | AGCAGATT others(335): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0156 | 2 | HG02080.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2096-51_2096-50ins others(342): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490504 | ||||||
chr5:157490548
|
G | T | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2096-94C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490548 | ||||||
chr5:157490662
|
G | A | 1 | a0011c0016t0007g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2096-208C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490662 | ||||||
chr5:157490747
|
C | A | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2096-293G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490747 | ||||||
chr5:157490817
|
G | A | 19 | a0001c0001t0003g0073a0002c0002t0003g0005a0002c0002t0003g0040others(16): Show | 20 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2096-363C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490817 | ||||||
chr5:157490824
|
G | A | 1 | a0002c0002t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2096-370C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490824 | ||||||
chr5:157490891
|
C | CA | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2096-438dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490891 | ||||||
chr5:157490917
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2096-463C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157490917 | ||||||
chr5:157491034
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2096-580C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491034 | ||||||
chr5:157491104
|
G | A | 1 | a0001c0001t0041g0062 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2095+511C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491104 | ||||||
chr5:157491130
|
A | AT | 10 | a0004c0004t0010g0088a0004c0004t0010g0252a0004c0004t0010g0265others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2095+484dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491130 | ||||||
chr5:157491138
|
T | A | 8 | a0001c0001t0027g0102a0004c0013t0012g0122a0004c0013t0012g0248others(5): Show | 8 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095+477A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491138 | ||||||
chr5:157491139
|
A | T | 25 | a0001c0001t0001g0033a0001c0001t0001g0134a0002c0002t0019g0196others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2095+476T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491139 | ||||||
chr5:157491154
|
G | T | 2 | a0015c0021t0002g0299a0017c0018t0002g0016 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2095+461C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491154 | ||||||
chr5:157491317
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0099 | 2 | HG00438.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.2095+298G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491317 | ||||||
chr5:157491373
|
C | A | 12 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0252others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2095+242G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491373 | ||||||
chr5:157491473
|
G | T | 1 | a0003c0003t0004g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2095+142C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491473 | ||||||
chr5:157491584
|
C | T | 1 | a0002c0002t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2095+31G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 18/22 | chr5 | 157491584 | ||||||
chr5:157491979
|
G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(81): Show | 86 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1909-67C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157491979 | ||||||
chr5:157491981
|
T | A | 1 | a0001c0001t0009g0113 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1909-69A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157491981 | ||||||
chr5:157492223
|
C | G | 3 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265 | 3 | HG02145.hp2 HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1909-311G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492223 | ||||||
chr5:157492435
|
G | A | 27 | a0002c0002t0004g0025a0002c0002t0004g0079a0002c0002t0004g0198others(24): Show | 27 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909-523C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492435 | ||||||
chr5:157492436
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | NA18949.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1909-524T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492436 | ||||||
chr5:157492456
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1908+517A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492456 | ||||||
chr5:157492472
|
A | G | 2 | a0013c0011t0026g0280a0013c0011t0028g0239 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1908+501T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492472 | ||||||
chr5:157492704
|
A | T | 1 | a0001c0001t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1908+269T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492704 | ||||||
chr5:157492798
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1908+175G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492798 | ||||||
chr5:157492824
|
C | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1908+149G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492824 | ||||||
chr5:157492875
|
G | A | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1908+98C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 16/22 | chr5 | 157492875 | ||||||
chr5:157493281
|
G | A | 25 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(22): Show | 26 | HG00544.hp1 HG02040.hp1 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.1704-104C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493281 | ||||||
chr5:157493313
|
T | A | 1 | a0005c0005t0008g0276 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1704-136A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493313 | ||||||
chr5:157493659
|
T | C | 2 | a0003c0003t0015g0289a0003c0003t0022g0218 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1704-482A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493659 | ||||||
chr5:157493748
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1704-571C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493748 | ||||||
chr5:157493878
|
T | C | 1 | a0001c0001t0009g0113 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1704-701A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493878 | ||||||
chr5:157493903
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1704-726G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493903 | ||||||
chr5:157493906
|
T | C | 2 | a0012c0015t0024g0271a0012c0015t0024g0272 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1704-729A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157493906 | ||||||
chr5:157494161
|
C | T | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1703+526G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494161 | ||||||
chr5:157494166
|
AGATG | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(106): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1703+517_1703+520d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494166 | ||||||
chr5:157494223
|
T | C | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1703+464A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494223 | ||||||
chr5:157494263
|
A | AGATG | 77 | a0001c0001t0002g0067a0001c0001t0002g0078a0001c0001t0006g0066others(74): Show | 79 | HG00673.hp1 HG00741.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.1703+420_1703+423d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494263 | ||||||
chr5:157494263
|
A | AGATGGAT others(1): Show |
3 | a0002c0002t0002g0056a0002c0002t0007g0254a0002c0002t0007g0267 | 3 | HG00140.hp1 HG01168.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1703+416_1703+423d others(10): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494263 | ||||||
chr5:157494571
|
T | C | 2 | a0001c0001t0001g0036a0002c0002t0008g0291 | 2 | HG03130.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1703+116A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494571 | ||||||
chr5:157494643
|
G | A | 14 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0001t0027g0102others(11): Show | 14 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1703+44C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 15/22 | chr5 | 157494643 | ||||||
chr5:157494878
|
G | C | 3 | a0006c0006t0013g0013a0006c0006t0013g0014a0006c0006t0013g0015 | 3 | HG02723.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1595-83C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157494878 | ||||||
chr5:157494916
|
C | T | 4 | a0003c0003t0004g0290a0008c0008t0004g0225a0008c0008t0004g0226others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-121G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157494916 | ||||||
chr5:157494947
|
A | G | 47 | a0001c0001t0002g0067a0001c0001t0002g0078a0001c0001t0006g0066others(44): Show | 47 | HG00673.hp1 HG00741.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1595-152T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157494947 | ||||||
chr5:157495076
|
G | A | 1 | a0004c0004t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1595-281C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495076 | ||||||
chr5:157495114
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1595-319C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495114 | ||||||
chr5:157495121
|
T | C | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1595-326A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495121 | ||||||
chr5:157495129
|
CA | C | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595-335delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495129 | ||||||
chr5:157495175
|
A | T | 1 | a0002c0002t0004g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1595-380T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495175 | ||||||
chr5:157495245
|
C | A | 1 | a0004c0004t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1595-450G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495245 | ||||||
chr5:157495260
|
C | G | 1 | a0002c0002t0004g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1595-465G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495260 | ||||||
chr5:157495362
|
A | G | 1 | a0002c0002t0004g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1595-567T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495362 | ||||||
chr5:157495700
|
C | T | 24 | a0001c0001t0003g0073a0002c0002t0001g0086a0002c0002t0003g0005others(21): Show | 26 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1595-905G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495700 | ||||||
chr5:157495764
|
G | A | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1595-969C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495764 | ||||||
chr5:157495780
|
T | A | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595-985A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495780 | ||||||
chr5:157495782
|
CA | C | 4 | a0004c0004t0010g0252a0004c0004t0010g0273a0004c0004t0018g0255others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-988delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495782 | ||||||
chr5:157495846
|
C | T | 2 | a0009c0009t0002g0123a0009c0009t0002g0154 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1594+1048G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495846 | ||||||
chr5:157495933
|
C | CT | 31 | a0001c0001t0002g0083a0001c0001t0002g0093a0001c0001t0002g0118others(28): Show | 31 | HG00738.hp1 HG01099.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1594+960dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
C | CTT | 33 | a0001c0001t0002g0067a0001c0001t0002g0078a0001c0001t0003g0230others(30): Show | 33 | HG00673.hp1 HG01069.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1594+959_1594+960d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
C | CTTT | 13 | a0001c0001t0006g0066a0002c0002t0002g0153a0002c0002t0002g0158others(10): Show | 13 | HG00741.hp2 HG01070.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1594+958_1594+960d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
CT | C | 19 | a0001c0001t0003g0073a0001c0001t0005g0032a0002c0002t0003g0005others(16): Show | 20 | HG00323.hp1 HG01257.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1594+960delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
CTT | C | 16 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(13): Show | 16 | HG00280.hp1 HG00544.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1594+959_1594+960d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
CTTT | C | 17 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0071others(14): Show | 17 | HG00621.hp1 HG00621.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1594+958_1594+960d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
CTTTT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1594+957_1594+960d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495933
|
CTTTTTTT others(4): Show |
C | 5 | a0002c0002t0001g0086a0002c0002t0014g0008a0002c0002t0014g0026others(2): Show | 6 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1594+950_1594+960d others(13): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495933 | ||||||
chr5:157495934
|
T | A | 1 | a0002c0002t0004g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1594+960A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157495934 | ||||||
chr5:157496158
|
T | C | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1594+736A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496158 | ||||||
chr5:157496195
|
AT | A | 7 | a0005c0005t0008g0001a0005c0005t0008g0246a0005c0005t0008g0274others(4): Show | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1594+698delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496195 | ||||||
chr5:157496197
|
T | C | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+697A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496197 | ||||||
chr5:157496318
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0096others(1): Show | 4 | NA18961.hp1 NA18984.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594+576C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496318 | ||||||
chr5:157496430
|
T | C | 2 | a0001c0001t0005g0179a0001c0001t0006g0178 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1594+464A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496430 | ||||||
chr5:157496597
|
G | T | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+297C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496597 | ||||||
chr5:157496632
|
T | A | 1 | a0002c0002t0002g0260 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1594+262A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496632 | ||||||
chr5:157496695
|
G | T | 2 | a0002c0014t0007g0268a0002c0014t0007g0269 | 2 | HG01070.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1594+199C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496695 | ||||||
chr5:157496754
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0099 | 2 | HG00438.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1594+140A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496754 | ||||||
chr5:157496857
|
G | A | 1 | a0001c0001t0005g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1594+37C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 14/22 | chr5 | 157496857 | ||||||
chr5:157497570
|
T | TAC | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(106): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1399-483_1399-482d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497570 | ||||||
chr5:157497570
|
T | TACAC | 11 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0146others(8): Show | 12 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1399-485_1399-482d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497570 | ||||||
chr5:157497570
|
T | TACACACA others(11): Show |
1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1399-499_1399-482d others(20): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497570 | ||||||
chr5:157497570
|
T | TATACACA others(17): Show |
1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1399-482_1399-481i others(26): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497570 | ||||||
chr5:157497590
|
C | CACACACA others(11): Show |
3 | a0002c0002t0045g0147a0007c0007t0012g0021a0011c0016t0003g0301 | 3 | HG01109.hp2 HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1399-502_1399-501i others(20): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497590 | ||||||
chr5:157497590
|
C | CACACACA others(9): Show |
5 | a0002c0002t0008g0263a0004c0013t0012g0122a0007c0007t0012g0018others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399-502_1399-501i others(18): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497590 | ||||||
chr5:157497590
|
C | CACACACA others(7): Show |
60 | a0002c0002t0002g0047a0002c0002t0002g0055a0002c0002t0002g0153others(57): Show | 62 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1399-502_1399-501i others(16): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497590 | ||||||
chr5:157497590
|
C | CACACACA others(5): Show |
37 | a0002c0002t0002g0056a0002c0002t0002g0057a0002c0002t0002g0167others(34): Show | 37 | HG00140.hp1 HG01069.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1399-502_1399-501i others(14): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497590 | ||||||
chr5:157497590
|
C | CACACACA others(3): Show |
6 | a0002c0002t0007g0031a0002c0002t0007g0116a0002c0002t0007g0250others(3): Show | 6 | HG01106.hp2 HG01175.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1399-502_1399-501i others(12): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497590 | ||||||
chr5:157497849
|
C | T | 2 | a0002c0002t0004g0241a0010c0010t0004g0023 | 2 | HG01981.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1399-760G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157497849 | ||||||
chr5:157498185
|
G | T | 13 | a0002c0002t0019g0027a0002c0002t0019g0196a0002c0002t0019g0197others(10): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1399-1096C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498185 | ||||||
chr5:157498208
|
ACT | A | 117 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(117): Show |
intron_variant | MODIFIER | c.1399-1121_1399-112 others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498208 | ||||||
chr5:157498519
|
G | A | 6 | a0006c0006t0001g0010a0006c0006t0013g0012a0006c0006t0013g0013others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+1054C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498519 | ||||||
chr5:157498686
|
A | ATG | 15 | a0001c0001t0003g0073a0002c0002t0003g0040a0002c0002t0003g0044others(12): Show | 15 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1398+885_1398+886d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498686 | ||||||
chr5:157498688
|
G | GTA | 69 | a0001c0001t0002g0117a0001c0001t0002g0151a0001c0001t0002g0235others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1398+883_1398+884d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATA | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0075others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1398+881_1398+884d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATA | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0082others(17): Show | 21 | HG00741.hp2 HG01257.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1398+879_1398+884d others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(1): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0035others(36): Show | 40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1398+877_1398+884d others(10): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(3): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(10): Show | 14 | HG00673.hp2 HG02080.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1398+875_1398+884d others(12): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(5): Show |
11 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0051others(8): Show | 11 | HG02523.hp2 HG03017.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1398+873_1398+884d others(14): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(7): Show |
7 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG00621.hp2 NA18946.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398+871_1398+884d others(16): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0109 | 2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1398+867_1398+884d others(20): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1398+865_1398+884d others(22): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTGTA | 4 | a0002c0002t0003g0005a0002c0002t0003g0091a0002c0002t0003g0141others(1): Show | 5 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398+884_1398+885i others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1398+884_1398+885i others(12): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
GTA | G | 29 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1398+883_1398+884d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498688
|
GTATA | G | 3 | a0001c0001t0002g0092a0002c0002t0002g0242a0004c0004t0034g0279 | 3 | HG01928.hp1 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1398+881_1398+884d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498688 | ||||||
chr5:157498690
|
A | ATG | 7 | a0005c0005t0008g0001a0005c0005t0008g0246a0005c0005t0008g0274others(4): Show | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1398+882_1398+883i others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498690 | ||||||
chr5:157498861
|
T | A | 1 | a0002c0002t0002g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1398+712A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498861 | ||||||
chr5:157498879
|
T | C | 1 | a0002c0002t0036g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1398+694A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157498879 | ||||||
chr5:157499097
|
T | C | 1 | a0002c0002t0008g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1398+476A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499097 | ||||||
chr5:157499119
|
C | T | 1 | a0002c0002t0002g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1398+454G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499119 | ||||||
chr5:157499205
|
T | G | 3 | a0004c0004t0010g0252a0004c0004t0010g0273a0004c0004t0018g0255 | 3 | HG02055.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1398+368A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499205 | ||||||
chr5:157499219
|
C | G | 2 | a0001c0001t0005g0232a0001c0001t0006g0229 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1398+354G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499219 | ||||||
chr5:157499359
|
G | A | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1398+214C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499359 | ||||||
chr5:157499422
|
C | G | 2 | a0012c0015t0024g0271a0012c0015t0024g0272 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1398+151G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499422 | ||||||
chr5:157499434
|
T | C | 139 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0001g0086others(136): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1398+139A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499434 | ||||||
chr5:157499437
|
G | A | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1398+136C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499437 | ||||||
chr5:157499500
|
C | T | 1 | a0008c0008t0004g0226 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1398+73G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499500 | ||||||
chr5:157499526
|
C | T | 22 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0003g0005others(19): Show | 23 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1398+47G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499526 | ||||||
chr5:157499548
|
A | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1398+25T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499548 | ||||||
chr5:157499551
|
C | T | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1398+22G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 13/22 | chr5 | 157499551 | ||||||
chr5:157499732
|
G | T | 1 | a0002c0002t0019g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1309-70C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499732 | ||||||
chr5:157499767
|
CTA | C | 5 | a0002c0002t0014g0008a0002c0002t0014g0026a0002c0002t0014g0292others(2): Show | 6 | HG01070.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-107_1309-106d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499767 | ||||||
chr5:157499769
|
A | C | 132 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0001g0086others(129): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1309-107T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499769 | ||||||
chr5:157499773
|
CT | C | 108 | a0001c0001t0001g0096a0001c0001t0002g0297a0001c0019t0017g0240others(105): Show | 110 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.1309-112delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499773 | ||||||
chr5:157499775
|
T | C | 5 | a0002c0002t0014g0008a0002c0002t0014g0026a0002c0002t0014g0292others(2): Show | 6 | HG01070.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-113A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499775 | ||||||
chr5:157499835
|
G | A | 7 | a0005c0005t0008g0001a0005c0005t0008g0246a0005c0005t0008g0274others(4): Show | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309-173C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499835 | ||||||
chr5:157499874
|
T | G | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(229): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1309-212A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499874 | ||||||
chr5:157499975
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(81): Show | 86 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1309-313G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157499975 | ||||||
chr5:157500021
|
C | T | 1 | a0003c0003t0015g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1309-359G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500021 | ||||||
chr5:157500069
|
G | A | 1 | a0016c0020t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1309-407C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500069 | ||||||
chr5:157500079
|
T | C | 1 | a0016c0020t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1309-417A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500079 | ||||||
chr5:157500153
|
T | C | 1 | a0002c0002t0002g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1309-491A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500153 | ||||||
chr5:157500202
|
T | G | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1309-540A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500202 | ||||||
chr5:157500249
|
G | A | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1309-587C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500249 | ||||||
chr5:157500439
|
T | C | 7 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-777A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500439 | ||||||
chr5:157500603
|
T | C | 3 | a0001c0001t0027g0102a0013c0011t0026g0280a0013c0011t0028g0239 | 3 | HG01884.hp2 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1309-941A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500603 | ||||||
chr5:157500641
|
T | C | 33 | a0002c0002t0004g0025a0002c0002t0004g0079a0002c0002t0004g0198others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1309-979A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500641 | ||||||
chr5:157500694
|
C | T | 1 | a0002c0002t0002g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1309-1032G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500694 | ||||||
chr5:157500867
|
C | T | 111 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(108): Show | 114 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(111): Show |
intron_variant | MODIFIER | c.1309-1205G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157500867 | ||||||
chr5:157501000
|
C | T | 26 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0003g0005others(23): Show | 27 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1309-1338G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501000 | ||||||
chr5:157501213
|
C | T | 4 | a0003c0003t0004g0290a0008c0008t0004g0225a0008c0008t0004g0226others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-1551G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501213 | ||||||
chr5:157501262
|
C | T | 33 | a0002c0002t0004g0025a0002c0002t0004g0079a0002c0002t0004g0198others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1308+1541G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501262 | ||||||
chr5:157501434
|
T | C | 1 | a0007c0007t0012g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1308+1369A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501434 | ||||||
chr5:157501696
|
C | G | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+1107G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501696 | ||||||
chr5:157501782
|
C | CTCACGCC others(1): Show |
25 | a0001c0001t0003g0073a0002c0002t0003g0005a0002c0002t0003g0040others(22): Show | 26 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1308+1013_1308+102 others(12): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501782 | ||||||
chr5:157501786
|
C | T | 2 | a0003c0003t0004g0222a0003c0003t0007g0221 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1308+1017G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501786 | ||||||
chr5:157501815
|
G | A | 124 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0001g0086others(121): Show | 128 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1308+988C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501815 | ||||||
chr5:157501894
|
C | A | 5 | a0002c0002t0007g0270a0002c0002t0007g0285a0002c0014t0007g0268others(2): Show | 5 | HG01070.hp1 HG01169.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+909G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501894 | ||||||
chr5:157501894
|
C | CA | 28 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0003g0040others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1308+908dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501894 | ||||||
chr5:157501971
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1308+832G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157501971 | ||||||
chr5:157502069
|
A | AT | 24 | a0001c0001t0003g0073a0001c0001t0027g0102a0002c0002t0003g0005others(21): Show | 25 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1308+733dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157502069 | ||||||
chr5:157502247
|
G | A | 3 | a0002c0002t0019g0027a0002c0002t0019g0196a0002c0002t0019g0197 | 3 | HG02922.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1308+556C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157502247 | ||||||
chr5:157502274
|
A | G | 2 | a0004c0004t0018g0278a0007c0007t0025g0011 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+529T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157502274 | ||||||
chr5:157502393
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1308+410T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 12/22 | chr5 | 157502393 | ||||||
chr5:157503261
|
A | C | 1 | a0002c0002t0044g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1131-281T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503261 | ||||||
chr5:157503292
|
T | C | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1131-312A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503292 | ||||||
chr5:157503398
|
C | T | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131-418G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503398 | ||||||
chr5:157503489
|
T | TA | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(92): Show | 97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1131-510dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503489 | ||||||
chr5:157503620
|
G | C | 1 | a0001c0001t0001g0065 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1131-640C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503620 | ||||||
chr5:157503644
|
G | A | 12 | a0002c0002t0008g0291a0002c0002t0031g0204a0004c0004t0010g0088others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-664C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503644 | ||||||
chr5:157503776
|
C | G | 118 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.1131-796G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503776 | ||||||
chr5:157503832
|
G | A | 8 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131-852C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503832 | ||||||
chr5:157503865
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1131-885G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157503865 | ||||||
chr5:157504266
|
C | T | 119 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.1131-1286G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504266 | ||||||
chr5:157504344
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(90): Show | 95 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1130+1325C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504344 | ||||||
chr5:157504499
|
C | T | 16 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.1130+1170G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504499 | ||||||
chr5:157504629
|
T | A | 7 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1130+1040A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504629 | ||||||
chr5:157504843
|
A | AGCCGG | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1130+825_1130+826i others(7): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504843 | ||||||
chr5:157504845
|
C | T | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1130+824G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504845 | ||||||
chr5:157504890
|
C | A | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1130+779G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504890 | ||||||
chr5:157504975
|
C | T | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1130+694G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504975 | ||||||
chr5:157504988
|
A | G | 1 | a0003c0003t0011g0213 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1130+681T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504988 | ||||||
chr5:157504999
|
T | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1130+670A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157504999 | ||||||
chr5:157505034
|
G | T | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1130+635C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505034 | ||||||
chr5:157505116
|
C | T | 1 | a0001c0001t0006g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1130+553G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505116 | ||||||
chr5:157505118
|
C | CA | 14 | a0001c0001t0001g0061a0001c0001t0001g0099a0001c0001t0001g0142others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1130+550dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505118 | ||||||
chr5:157505118
|
C | CAA | 81 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1130+549_1130+550d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505118 | ||||||
chr5:157505118
|
C | CAAA | 45 | a0002c0002t0002g0057a0002c0002t0002g0164a0002c0002t0002g0172others(42): Show | 47 | HG00280.hp1 HG01069.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1130+548_1130+550d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505118 | ||||||
chr5:157505140
|
T | A | 119 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.1130+529A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505140 | ||||||
chr5:157505299
|
C | T | 1 | a0002c0002t0044g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1130+370G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505299 | ||||||
chr5:157505357
|
T | C | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1130+312A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505357 | ||||||
chr5:157505368
|
A | C | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1130+301T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505368 | ||||||
chr5:157505388
|
A | C | 1 | a0002c0002t0003g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1130+281T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505388 | ||||||
chr5:157505404
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0009g0028 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1130+265T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505404 | ||||||
chr5:157505564
|
A | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1130+105T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 11/22 | chr5 | 157505564 | ||||||
chr5:157505851
|
T | A | 18 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(15): Show | 19 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.991-43A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157505851 | ||||||
chr5:157505946
|
G | C | 119 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.991-138C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157505946 | ||||||
chr5:157505976
|
A | T | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.991-168T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157505976 | ||||||
chr5:157506174
|
G | T | 34 | a0002c0002t0002g0281a0002c0002t0004g0025a0002c0002t0004g0079others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.991-366C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506174 | ||||||
chr5:157506267
|
T | C | 18 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(15): Show | 19 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.991-459A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506267 | ||||||
chr5:157506335
|
C | G | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.991-527G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506335 | ||||||
chr5:157506450
|
A | C | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.990+606T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506450 | ||||||
chr5:157506484
|
T | A | 4 | a0002c0002t0014g0008a0002c0002t0014g0026a0002c0002t0014g0292others(1): Show | 5 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.990+572A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506484 | ||||||
chr5:157506559
|
A | C | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.990+497T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506559 | ||||||
chr5:157506756
|
C | A | 1 | a0002c0002t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.990+300G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506756 | ||||||
chr5:157506930
|
C | T | 1 | a0002c0002t0006g0165 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.990+126G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 10/22 | chr5 | 157506930 | ||||||
chr5:157507147
|
G | T | 8 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.906-7C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507147 | ||||||
chr5:157507169
|
G | C | 1 | a0002c0002t0038g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.906-29C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507169 | ||||||
chr5:157507254
|
T | A | 1 | a0003c0003t0011g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.906-114A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507254 | ||||||
chr5:157507299
|
C | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.906-159G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507299 | ||||||
chr5:157507340
|
C | G | 4 | a0001c0001t0002g0067a0001c0001t0002g0078a0001c0001t0006g0066others(1): Show | 4 | HG02083.hp2 HG02523.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-200G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507340 | ||||||
chr5:157507379
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(90): Show | 95 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.906-239G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507379 | ||||||
chr5:157507386
|
C | T | 2 | a0004c0004t0018g0278a0007c0007t0025g0011 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.906-246G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507386 | ||||||
chr5:157507666
|
A | G | 1 | a0002c0002t0008g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906-526T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507666 | ||||||
chr5:157507721
|
G | T | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.906-581C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507721 | ||||||
chr5:157507964
|
A | G | 2 | a0015c0021t0002g0299a0017c0018t0002g0016 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.906-824T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157507964 | ||||||
chr5:157508068
|
T | C | 1 | a0001c0001t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.906-928A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508068 | ||||||
chr5:157508270
|
G | C | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.905+1031C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508270 | ||||||
chr5:157508271
|
T | G | 1 | a0001c0001t0002g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.905+1030A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508271 | ||||||
chr5:157508423
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.905+878T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508423 | ||||||
chr5:157508426
|
T | A | 17 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(14): Show | 17 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.905+875A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508426 | ||||||
chr5:157508516
|
C | T | 136 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(133): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.905+785G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508516 | ||||||
chr5:157508604
|
GA | G | 8 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(5): Show | 8 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.905+696delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508604 | ||||||
chr5:157508688
|
A | C | 1 | a0001c0001t0002g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.905+613T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508688 | ||||||
chr5:157508900
|
C | T | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.905+401G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508900 | ||||||
chr5:157508949
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.905+352G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508949 | ||||||
chr5:157508965
|
A | C | 6 | a0004c0013t0012g0122a0004c0013t0012g0248a0007c0007t0012g0018others(3): Show | 6 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+336T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157508965 | ||||||
chr5:157509055
|
G | A | 6 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0173others(3): Show | 6 | HG01106.hp1 HG01928.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.905+246C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 9/22 | chr5 | 157509055 | ||||||
chr5:157509541
|
G | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(232): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.739-74C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509541 | ||||||
chr5:157509582
|
A | G | 1 | a0001c0001t0005g0220 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.739-115T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509582 | ||||||
chr5:157509595
|
T | A | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.739-128A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509595 | ||||||
chr5:157509596
|
A | T | 4 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-129T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509596 | ||||||
chr5:157509665
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.739-198G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509665 | ||||||
chr5:157509678
|
G | C | 1 | a0001c0001t0005g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.739-211C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509678 | ||||||
chr5:157509721
|
C | T | 17 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(14): Show | 18 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.739-254G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509721 | ||||||
chr5:157509758
|
A | G | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.739-291T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509758 | ||||||
chr5:157509767
|
G | A | 1 | a0004c0004t0010g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.739-300C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509767 | ||||||
chr5:157509952
|
A | G | 8 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-485T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509952 | ||||||
chr5:157509995
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.739-528C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157509995 | ||||||
chr5:157510035
|
A | G | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.739-568T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510035 | ||||||
chr5:157510051
|
T | C | 3 | a0001c0001t0017g0259a0001c0001t0017g0262a0001c0019t0017g0240 | 3 | HG01069.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.739-584A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510051 | ||||||
chr5:157510131
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.739-664A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510131 | ||||||
chr5:157510334
|
C | T | 119 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(116): Show | 123 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.739-867G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510334 | ||||||
chr5:157510342
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0144 | 2 | NA18945.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.739-875G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510342 | ||||||
chr5:157510503
|
G | A | 1 | a0004c0004t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.739-1036C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510503 | ||||||
chr5:157510527
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.739-1060A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510527 | ||||||
chr5:157510763
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.739-1296C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510763 | ||||||
chr5:157510774
|
C | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(226): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.739-1307G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510774 | ||||||
chr5:157510962
|
T | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(226): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.739-1495A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510962 | ||||||
chr5:157510996
|
G | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG00673.hp2 NA18957.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-1529C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157510996 | ||||||
chr5:157511013
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0099 | 2 | HG00438.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.739-1546G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511013 | ||||||
chr5:157511247
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.739-1780A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511247 | ||||||
chr5:157511262
|
T | C | 2 | a0002c0002t0003g0044a0002c0002t0003g0111 | 2 | HG00544.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.739-1795A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511262 | ||||||
chr5:157511319
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(106): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.739-1852C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511319 | ||||||
chr5:157511513
|
T | C | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.738+1921A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511513 | ||||||
chr5:157511792
|
C | T | 1 | a0002c0002t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.738+1642G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511792 | ||||||
chr5:157511822
|
G | A | 3 | a0002c0002t0031g0204a0002c0002t0045g0147a0011c0016t0003g0301 | 3 | HG01109.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.738+1612C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511822 | ||||||
chr5:157511843
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0023g0050 | 2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.738+1591G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157511843 | ||||||
chr5:157512242
|
A | C | 2 | a0002c0002t0002g0247a0010c0010t0001g0019 | 2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.738+1192T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512242 | ||||||
chr5:157512259
|
A | G | 1 | a0001c0001t0005g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.738+1175T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512259 | ||||||
chr5:157512466
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.738+968C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512466 | ||||||
chr5:157512477
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+957G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512477 | ||||||
chr5:157512490
|
T | G | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.738+944A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512490 | ||||||
chr5:157512591
|
T | C | 2 | a0009c0009t0002g0123a0009c0009t0002g0154 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.738+843A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512591 | ||||||
chr5:157512597
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.738+837T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512597 | ||||||
chr5:157512644
|
C | T | 3 | a0002c0002t0004g0261a0002c0002t0008g0291a0002c0002t0040g0266 | 3 | HG03098.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.738+790G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512644 | ||||||
chr5:157512678
|
G | A | 1 | a0002c0002t0003g0111 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.738+756C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512678 | ||||||
chr5:157512872
|
G | A | 137 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(134): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.738+562C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157512872 | ||||||
chr5:157513195
|
T | C | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.738+239A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 8/22 | chr5 | 157513195 | ||||||
chr5:157513749
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.667-244G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157513749 | ||||||
chr5:157513752
|
A | G | 18 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(15): Show | 19 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.667-247T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157513752 | ||||||
chr5:157513813
|
T | C | 2 | a0001c0001t0017g0259a0001c0001t0017g0262 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.667-308A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157513813 | ||||||
chr5:157513865
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(89): Show | 94 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.667-360G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157513865 | ||||||
chr5:157514150
|
G | A | 2 | a0002c0002t0002g0047a0002c0002t0002g0055 | 2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.667-645C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514150 | ||||||
chr5:157514326
|
C | CT | 11 | a0002c0002t0002g0182a0002c0002t0008g0291a0002c0002t0019g0027others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-822dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514326 | ||||||
chr5:157514329
|
TC | T | 3 | a0002c0002t0006g0177a0015c0021t0002g0299a0017c0018t0002g0016 | 3 | HG02818.hp1 NA18522.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.667-825delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514329 | ||||||
chr5:157514330
|
C | T | 134 | a0001c0001t0027g0102a0002c0002t0001g0086a0002c0002t0002g0047others(131): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.667-825G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514330 | ||||||
chr5:157514345
|
T | C | 1 | a0002c0002t0040g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667-840A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514345 | ||||||
chr5:157514508
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.667-1003C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514508 | ||||||
chr5:157514611
|
G | A | 3 | a0004c0004t0018g0278a0004c0004t0034g0279a0007c0007t0025g0011 | 3 | HG02622.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.667-1106C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514611 | ||||||
chr5:157514699
|
G | GA | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.667-1195dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514699 | ||||||
chr5:157514942
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.667-1437G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514942 | ||||||
chr5:157514943
|
G | A | 2 | a0002c0002t0004g0198a0003c0003t0004g0222 | 2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.667-1438C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514943 | ||||||
chr5:157514967
|
A | G | 1 | a0002c0002t0036g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.667-1462T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157514967 | ||||||
chr5:157515211
|
A | T | 5 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0173others(2): Show | 5 | HG01106.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-1706T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157515211 | ||||||
chr5:157515265
|
C | A | 1 | a0001c0001t0002g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.667-1760G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157515265 | ||||||
chr5:157515269
|
G | A | 1 | a0001c0001t0030g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.667-1764C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157515269 | ||||||
chr5:157515277
|
A | G | 17 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(14): Show | 17 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.667-1772T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157515277 | ||||||
chr5:157515667
|
A | C | 18 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(15): Show | 19 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.667-2162T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157515667 | ||||||
chr5:157516276
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0128 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.666+2547G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516276 | ||||||
chr5:157516277
|
G | A | 117 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(114): Show | 121 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.666+2546C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516277 | ||||||
chr5:157516733
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0128 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.666+2090A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516733 | ||||||
chr5:157516827
|
G | A | 2 | a0002c0002t0002g0195a0002c0002t0002g0242 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.666+1996C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516827 | ||||||
chr5:157516935
|
A | AAC | 60 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0002g0235others(57): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.666+1886_666+1887d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516935 | ||||||
chr5:157516935
|
A | AACAC | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0245 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.666+1884_666+1887d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516935 | ||||||
chr5:157516935
|
AAC | A | 121 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0057others(118): Show | 124 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.666+1886_666+1887d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516935 | ||||||
chr5:157516935
|
AACAC | A | 5 | a0002c0002t0001g0086a0002c0002t0014g0008a0002c0002t0014g0026others(2): Show | 6 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+1884_666+1887d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516935 | ||||||
chr5:157516936
|
A | G | 2 | a0002c0002t0002g0047a0002c0002t0037g0257 | 2 | HG02970.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.666+1887T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516936 | ||||||
chr5:157516938
|
A | G | 111 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0057others(108): Show | 114 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.666+1885T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516938 | ||||||
chr5:157516940
|
A | G | 5 | a0002c0002t0001g0086a0002c0002t0014g0008a0002c0002t0014g0026others(2): Show | 6 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+1883T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157516940 | ||||||
chr5:157517090
|
C | A | 1 | a0004c0004t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.666+1733G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517090 | ||||||
chr5:157517182
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.666+1641G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517182 | ||||||
chr5:157517191
|
C | A | 135 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(132): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.666+1632G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517191 | ||||||
chr5:157517196
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.666+1627T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517196 | ||||||
chr5:157517428
|
T | C | 20 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(17): Show | 21 | HG00323.hp1 HG00544.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.666+1395A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517428 | ||||||
chr5:157517467
|
G | T | 135 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(132): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.666+1356C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517467 | ||||||
chr5:157517629
|
T | G | 1 | a0002c0002t0003g0084 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.666+1194A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517629 | ||||||
chr5:157517663
|
C | T | 118 | a0002c0002t0001g0086a0002c0002t0002g0047a0002c0002t0002g0055others(115): Show | 122 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.666+1160G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517663 | ||||||
chr5:157517779
|
G | A | 1 | a0002c0002t0004g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666+1044C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517779 | ||||||
chr5:157517887
|
A | G | 52 | a0001c0001t0001g0121a0001c0001t0002g0235a0001c0001t0003g0230others(49): Show | 54 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.666+936T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517887 | ||||||
chr5:157517969
|
G | A | 1 | a0006c0006t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.666+854C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517969 | ||||||
chr5:157517992
|
G | A | 1 | a0008c0008t0004g0226 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666+831C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157517992 | ||||||
chr5:157518030
|
G | A | 20 | a0002c0002t0003g0005a0002c0002t0003g0040a0002c0002t0003g0044others(17): Show | 21 | HG00323.hp1 HG00544.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.666+793C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518030 | ||||||
chr5:157518045
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.666+778C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518045 | ||||||
chr5:157518077
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.666+746A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518077 | ||||||
chr5:157518140
|
T | C | 17 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(14): Show | 17 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.666+683A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518140 | ||||||
chr5:157518168
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0156 | 2 | HG02080.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.666+655T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518168 | ||||||
chr5:157518475
|
C | A | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.666+348G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518475 | ||||||
chr5:157518558
|
AT | A | 6 | a0001c0001t0001g0059a0001c0001t0001g0194a0001c0001t0002g0067others(3): Show | 6 | HG02083.hp2 HG02523.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+264delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518558 | ||||||
chr5:157518626
|
C | T | 98 | a0001c0001t0001g0174a0002c0002t0002g0047a0002c0002t0002g0055others(95): Show | 101 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.666+197G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518626 | ||||||
chr5:157518649
|
G | C | 52 | a0001c0001t0001g0121a0001c0001t0002g0235a0001c0001t0003g0230others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.666+174C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518649 | ||||||
chr5:157518712
|
G | C | 1 | a0001c0001t0009g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.666+111C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 7/22 | chr5 | 157518712 | ||||||
chr5:157518911
|
C | T | 9 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-23G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157518911 | ||||||
chr5:157518943
|
T | A | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601-55A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157518943 | ||||||
chr5:157519041
|
A | G | 189 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0156others(186): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.601-153T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519041 | ||||||
chr5:157519070
|
T | G | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.601-182A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519070 | ||||||
chr5:157519198
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.601-310C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519198 | ||||||
chr5:157519218
|
C | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601-330G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519218 | ||||||
chr5:157519219
|
C | A | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.601-331G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519219 | ||||||
chr5:157519260
|
A | G | 22 | a0002c0002t0031g0204a0002c0002t0045g0147a0003c0003t0004g0222others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.601-372T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519260 | ||||||
chr5:157519272
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601-384A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519272 | ||||||
chr5:157519283
|
C | G | 3 | a0002c0002t0001g0086a0002c0002t0002g0195a0002c0002t0002g0242 | 3 | HG02109.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.601-395G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519283 | ||||||
chr5:157519288
|
C | G | 31 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(28): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.601-400G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519288 | ||||||
chr5:157519299
|
A | G | 182 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(179): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.601-411T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519299 | ||||||
chr5:157519371
|
C | A | 1 | a0002c0002t0003g0084 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.600+468G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519371 | ||||||
chr5:157519445
|
C | T | 42 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.600+394G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519445 | ||||||
chr5:157519451
|
A | G | 2 | a0002c0002t0004g0202a0002c0002t0004g0205 | 2 | HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.600+388T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519451 | ||||||
chr5:157519795
|
C | A | 33 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(30): Show | 35 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.600+44G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 6/22 | chr5 | 157519795 | ||||||
chr5:157520195
|
A | G | 5 | a0002c0002t0001g0086a0002c0002t0002g0195a0002c0002t0002g0242others(2): Show | 5 | HG02109.hp1 HG03225.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-164T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520195 | ||||||
chr5:157520243
|
G | T | 1 | a0003c0003t0022g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.408-212C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520243 | ||||||
chr5:157520260
|
T | A | 32 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(29): Show | 34 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.408-229A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520260 | ||||||
chr5:157520428
|
T | A | 1 | a0002c0002t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.408-397A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520428 | ||||||
chr5:157520618
|
TC | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0105a0001c0001t0005g0136others(1): Show | 4 | NA18942.hp2 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-588delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520618 | ||||||
chr5:157520777
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0155 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.408-746C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520777 | ||||||
chr5:157520792
|
G | A | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-761C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520792 | ||||||
chr5:157520880
|
C | T | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.408-849G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520880 | ||||||
chr5:157520981
|
C | T | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.408-950G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157520981 | ||||||
chr5:157521039
|
T | C | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.408-1008A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521039 | ||||||
chr5:157521048
|
G | A | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.408-1017C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521048 | ||||||
chr5:157521169
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.408-1138C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521169 | ||||||
chr5:157521286
|
T | C | 184 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(181): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.408-1255A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521286 | ||||||
chr5:157521310
|
T | G | 24 | a0001c0019t0017g0240a0002c0002t0045g0147a0003c0003t0004g0222others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.408-1279A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521310 | ||||||
chr5:157521427
|
G | C | 43 | a0001c0001t0001g0174a0002c0002t0001g0086a0002c0002t0002g0047others(40): Show | 43 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.408-1396C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521427 | ||||||
chr5:157521670
|
C | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.408-1639G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521670 | ||||||
chr5:157521720
|
G | T | 1 | a0003c0003t0011g0288 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.408-1689C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521720 | ||||||
chr5:157521838
|
C | T | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.408-1807G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157521838 | ||||||
chr5:157522187
|
T | C | 1 | a0001c0001t0005g0220 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.408-2156A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522187 | ||||||
chr5:157522308
|
C | CTTTTA | 184 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(181): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.408-2282_408-2278d others(7): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522308 | ||||||
chr5:157522539
|
A | C | 1 | a0008c0008t0004g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.408-2508T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522539 | ||||||
chr5:157522550
|
C | A | 3 | a0001c0001t0006g0103a0002c0002t0003g0064a0002c0002t0003g0070 | 3 | NA18957.hp1 NA19058.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.408-2519G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522550 | ||||||
chr5:157522667
|
T | G | 1 | a0002c0002t0002g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.408-2636A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522667 | ||||||
chr5:157522741
|
G | A | 6 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0173others(3): Show | 6 | HG01106.hp1 HG01928.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-2710C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522741 | ||||||
chr5:157522924
|
G | A | 7 | a0005c0005t0008g0001a0005c0005t0008g0246a0005c0005t0008g0274others(4): Show | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.408-2893C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157522924 | ||||||
chr5:157523290
|
C | T | 13 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(10): Show | 14 | HG02602.hp2 HG02698.hp1 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.408-3259G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523290 | ||||||
chr5:157523408
|
T | G | 1 | a0001c0001t0043g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.408-3377A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523408 | ||||||
chr5:157523671
|
C | T | 1 | a0001c0001t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.408-3640G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523671 | ||||||
chr5:157523672
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408-3641C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523672 | ||||||
chr5:157523785
|
C | A | 5 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0173others(2): Show | 5 | HG01106.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.408-3754G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523785 | ||||||
chr5:157523792
|
C | A | 4 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-3761G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157523792 | ||||||
chr5:157524002
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.408-3971C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524002 | ||||||
chr5:157524026
|
C | T | 2 | a0001c0001t0005g0179a0001c0001t0006g0178 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.408-3995G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524026 | ||||||
chr5:157524114
|
G | C | 2 | a0002c0002t0002g0153a0002c0002t0038g0169 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.408-4083C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524114 | ||||||
chr5:157524234
|
T | C | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.408-4203A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524234 | ||||||
chr5:157524342
|
C | T | 3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.408-4311G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524342 | ||||||
chr5:157524366
|
G | A | 1 | a0002c0002t0046g0284 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.408-4335C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524366 | ||||||
chr5:157524556
|
C | T | 1 | a0002c0002t0003g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.408-4525G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524556 | ||||||
chr5:157524587
|
C | T | 1 | a0002c0002t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408-4556G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524587 | ||||||
chr5:157524873
|
C | T | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.408-4842G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157524873 | ||||||
chr5:157525141
|
G | A | 10 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.408-5110C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525141 | ||||||
chr5:157525255
|
A | C | 1 | a0002c0002t0008g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.408-5224T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525255 | ||||||
chr5:157525400
|
C | G | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.408-5369G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525400 | ||||||
chr5:157525590
|
C | A | 1 | a0002c0002t0004g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.407+5217G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525590 | ||||||
chr5:157525606
|
C | T | 117 | a0001c0001t0001g0174a0001c0001t0002g0235a0001c0001t0003g0230others(114): Show | 121 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.407+5201G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525606 | ||||||
chr5:157525896
|
G | A | 1 | a0003c0003t0011g0288 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.407+4911C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525896 | ||||||
chr5:157525905
|
A | G | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.407+4902T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525905 | ||||||
chr5:157525912
|
C | T | 2 | a0002c0002t0045g0147a0011c0016t0003g0301 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.407+4895G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525912 | ||||||
chr5:157525913
|
G | A | 1 | a0002c0002t0007g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.407+4894C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525913 | ||||||
chr5:157525939
|
G | A | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+4868C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157525939 | ||||||
chr5:157526029
|
C | T | 7 | a0001c0019t0017g0240a0002c0002t0004g0198a0002c0002t0014g0026others(4): Show | 7 | HG01943.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+4778G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526029 | ||||||
chr5:157526030
|
G | A | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.407+4777C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526030 | ||||||
chr5:157526159
|
CAT | C | 93 | a0001c0001t0001g0174a0001c0001t0001g0233a0001c0001t0017g0259others(90): Show | 95 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.407+4646_407+4647d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526159 | ||||||
chr5:157526171
|
T | C | 5 | a0003c0003t0004g0290a0008c0008t0004g0225a0008c0008t0004g0226others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.407+4636A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526171 | ||||||
chr5:157526171
|
TATAC | T | 7 | a0002c0002t0014g0008a0002c0002t0014g0292a0002c0002t0038g0169others(4): Show | 9 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.407+4632_407+4635d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526171 | ||||||
chr5:157526173
|
T | C | 43 | a0001c0001t0001g0054a0001c0001t0001g0144a0001c0001t0001g0174others(40): Show | 44 | HG01070.hp1 HG01169.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.407+4634A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526173 | ||||||
chr5:157526173
|
T | TAC | 21 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0002g0097others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.407+4632_407+4633d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526173 | ||||||
chr5:157526173
|
TAC | T | 4 | a0002c0002t0014g0026a0002c0002t0037g0257a0004c0004t0018g0278others(1): Show | 4 | HG02622.hp1 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+4632_407+4633d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526173 | ||||||
chr5:157526173
|
TACAC | T | 7 | a0001c0019t0017g0240a0004c0004t0010g0237a0007c0007t0025g0011others(4): Show | 7 | HG01943.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.407+4630_407+4633d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526173 | ||||||
chr5:157526177
|
C | T | 1 | a0004c0004t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.407+4630G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526177 | ||||||
chr5:157526294
|
A | G | 1 | a0002c0002t0003g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.407+4513T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526294 | ||||||
chr5:157526332
|
C | T | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.407+4475G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526332 | ||||||
chr5:157526373
|
G | A | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+4434C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526373 | ||||||
chr5:157526403
|
A | G | 1 | a0007c0007t0035g0020 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.407+4404T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526403 | ||||||
chr5:157526404
|
A | T | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.407+4403T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526404 | ||||||
chr5:157526410
|
A | T | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.407+4397T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526410 | ||||||
chr5:157526456
|
C | A | 1 | a0002c0002t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.407+4351G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526456 | ||||||
chr5:157526464
|
T | TAC | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.407+4341_407+4342d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526464 | ||||||
chr5:157526585
|
C | T | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+4222G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526585 | ||||||
chr5:157526618
|
G | C | 3 | a0002c0002t0014g0026a0013c0011t0026g0280a0013c0011t0028g0239 | 3 | HG02109.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.407+4189C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526618 | ||||||
chr5:157526624
|
A | AT | 67 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.407+4182dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526624 | ||||||
chr5:157526624
|
A | ATT | 9 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.407+4181_407+4182d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526624 | ||||||
chr5:157526624
|
AT | A | 36 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0174others(33): Show | 36 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.407+4182delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526624 | ||||||
chr5:157526660
|
G | A | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+4147C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526660 | ||||||
chr5:157526722
|
A | T | 11 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(8): Show | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.407+4085T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526722 | ||||||
chr5:157526732
|
T | C | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.407+4075A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526732 | ||||||
chr5:157526741
|
C | T | 2 | a0002c0002t0002g0153a0002c0002t0038g0169 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.407+4066G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526741 | ||||||
chr5:157526863
|
T | C | 147 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.407+3944A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526863 | ||||||
chr5:157526872
|
CG | C | 4 | a0001c0019t0017g0240a0002c0002t0014g0026a0013c0011t0026g0280others(1): Show | 4 | HG01943.hp1 HG02109.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+3934delC | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157526872 | ||||||
chr5:157527019
|
G | A | 10 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.407+3788C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527019 | ||||||
chr5:157527092
|
T | C | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.407+3715A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527092 | ||||||
chr5:157527111
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.407+3696G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527111 | ||||||
chr5:157527157
|
C | T | 19 | a0002c0002t0045g0147a0003c0003t0004g0222a0003c0003t0007g0221others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+3650G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527157 | ||||||
chr5:157527318
|
C | G | 19 | a0002c0002t0045g0147a0003c0003t0004g0222a0003c0003t0007g0221others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+3489G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527318 | ||||||
chr5:157527355
|
T | C | 147 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.407+3452A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527355 | ||||||
chr5:157527357
|
C | T | 117 | a0001c0001t0001g0174a0001c0001t0002g0235a0001c0001t0003g0230others(114): Show | 121 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.407+3450G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527357 | ||||||
chr5:157527614
|
C | T | 1 | a0002c0002t0004g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.407+3193G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527614 | ||||||
chr5:157527635
|
T | C | 1 | a0002c0002t0006g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.407+3172A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527635 | ||||||
chr5:157527903
|
A | G | 1 | a0006c0006t0013g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.407+2904T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157527903 | ||||||
chr5:157528089
|
G | A | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.407+2718C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528089 | ||||||
chr5:157528180
|
C | A | 1 | a0002c0002t0008g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.407+2627G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528180 | ||||||
chr5:157528415
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.407+2392C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528415 | ||||||
chr5:157528705
|
T | G | 1 | a0018c0017t0022g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.407+2102A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528705 | ||||||
chr5:157528795
|
A | G | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.407+2012T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528795 | ||||||
chr5:157528798
|
A | T | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+2009T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528798 | ||||||
chr5:157528809
|
G | T | 4 | a0002c0002t0014g0026a0004c0004t0034g0279a0013c0011t0026g0280others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+1998C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528809 | ||||||
chr5:157528865
|
T | C | 1 | a0011c0016t0007g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.407+1942A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528865 | ||||||
chr5:157528960
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.407+1847G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157528960 | ||||||
chr5:157529092
|
A | G | 1 | a0001c0019t0017g0240 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.407+1715T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529092 | ||||||
chr5:157529120
|
C | T | 7 | a0005c0005t0008g0001a0005c0005t0008g0246a0005c0005t0008g0274others(4): Show | 9 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.407+1687G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529120 | ||||||
chr5:157529177
|
G | A | 1 | a0013c0011t0026g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.407+1630C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529177 | ||||||
chr5:157529182
|
A | T | 183 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.407+1625T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529182 | ||||||
chr5:157529321
|
C | CA | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.407+1485dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529321 | ||||||
chr5:157529460
|
T | C | 183 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.407+1347A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529460 | ||||||
chr5:157529504
|
G | T | 183 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.407+1303C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529504 | ||||||
chr5:157529628
|
C | A | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.407+1179G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529628 | ||||||
chr5:157529825
|
T | C | 1 | a0001c0001t0009g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.407+982A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529825 | ||||||
chr5:157529870
|
G | A | 19 | a0002c0002t0045g0147a0003c0003t0004g0222a0003c0003t0007g0221others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+937C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529870 | ||||||
chr5:157529881
|
T | C | 117 | a0001c0001t0001g0174a0001c0001t0002g0235a0001c0001t0003g0230others(114): Show | 121 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.407+926A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529881 | ||||||
chr5:157529917
|
T | C | 2 | a0014c0012t0002g0089a0014c0012t0002g0090 | 2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.407+890A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529917 | ||||||
chr5:157529933
|
ACT | A | 7 | a0001c0019t0017g0240a0002c0002t0014g0026a0004c0004t0034g0279others(4): Show | 7 | HG01943.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+872_407+873del others(2): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157529933 | ||||||
chr5:157530053
|
T | A | 1 | a0003c0003t0011g0212 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.407+754A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530053 | ||||||
chr5:157530105
|
T | C | 117 | a0001c0001t0001g0174a0001c0001t0002g0235a0001c0001t0003g0230others(114): Show | 121 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.407+702A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530105 | ||||||
chr5:157530229
|
GC | G | 147 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.407+577delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530229 | ||||||
chr5:157530231
|
A | G | 147 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.407+576T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530231 | ||||||
chr5:157530246
|
G | C | 4 | a0002c0002t0014g0026a0004c0004t0034g0279a0013c0011t0026g0280others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.407+561C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530246 | ||||||
chr5:157530408
|
G | A | 102 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(99): Show | 105 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.407+399C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530408 | ||||||
chr5:157530428
|
A | G | 147 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.407+379T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530428 | ||||||
chr5:157530433
|
C | A | 15 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.407+374G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530433 | ||||||
chr5:157530488
|
G | A | 30 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(27): Show | 32 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+319C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530488 | ||||||
chr5:157530576
|
A | G | 2 | a0001c0001t0005g0112a0001c0001t0006g0114 | 2 | NA18973.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.407+231T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530576 | ||||||
chr5:157530733
|
C | T | 176 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(173): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.407+74G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530733 | ||||||
chr5:157530776
|
C | A | 45 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(42): Show | 48 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.407+31G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 5/22 | chr5 | 157530776 | ||||||
chr5:157531090
|
A | G | 1 | a0003c0003t0021g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.331-207T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531090 | ||||||
chr5:157531119
|
C | T | 22 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(19): Show | 23 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.331-236G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531119 | ||||||
chr5:157531138
|
T | C | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.331-255A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531138 | ||||||
chr5:157531282
|
T | C | 19 | a0002c0002t0045g0147a0003c0003t0004g0222a0003c0003t0007g0221others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.331-399A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531282 | ||||||
chr5:157531471
|
G | A | 17 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.331-588C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531471 | ||||||
chr5:157531524
|
G | A | 100 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(97): Show | 103 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.331-641C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531524 | ||||||
chr5:157531536
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.331-653C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531536 | ||||||
chr5:157531549
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.331-666G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531549 | ||||||
chr5:157531580
|
T | C | 10 | a0003c0003t0011g0212a0003c0003t0011g0213a0003c0003t0015g0211others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.331-697A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531580 | ||||||
chr5:157531676
|
G | GA | 24 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(21): Show | 25 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.331-794dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531676 | ||||||
chr5:157531916
|
G | T | 22 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(19): Show | 23 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.331-1033C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157531916 | ||||||
chr5:157532021
|
T | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0077a0001c0001t0001g0095others(4): Show | 7 | HG00438.hp2 HG02056.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.331-1138A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532021 | ||||||
chr5:157532112
|
T | G | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331-1229A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532112 | ||||||
chr5:157532254
|
C | T | 1 | a0003c0003t0015g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.331-1371G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532254 | ||||||
chr5:157532269
|
A | G | 4 | a0004c0004t0010g0088a0004c0004t0010g0237a0004c0004t0010g0265others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-1386T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532269 | ||||||
chr5:157532325
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0099a0001c0001t0009g0081 | 3 | HG00438.hp1 HG02129.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.331-1442T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532325 | ||||||
chr5:157532512
|
A | G | 1 | a0001c0001t0009g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.331-1629T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532512 | ||||||
chr5:157532519
|
T | A | 23 | a0001c0001t0002g0235a0001c0001t0003g0230a0001c0001t0005g0007others(20): Show | 25 | HG02083.hp1 HG02129.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.331-1636A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532519 | ||||||
chr5:157532559
|
C | T | 1 | a0002c0002t0002g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.331-1676G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532559 | ||||||
chr5:157532965
|
C | T | 100 | a0001c0001t0001g0174a0001c0001t0017g0259a0001c0001t0017g0262others(97): Show | 103 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.331-2082G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157532965 | ||||||
chr5:157533157
|
G | A | 3 | a0002c0002t0004g0261a0002c0002t0007g0256a0002c0002t0040g0266 | 3 | HG01891.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.331-2274C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533157 | ||||||
chr5:157533213
|
C | T | 1 | a0002c0002t0004g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.331-2330G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533213 | ||||||
chr5:157533573
|
G | A | 43 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.331-2690C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533573 | ||||||
chr5:157533693
|
G | A | 2 | a0015c0021t0002g0299a0017c0018t0002g0016 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.331-2810C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533693 | ||||||
chr5:157533786
|
G | A | 3 | a0002c0002t0002g0158a0002c0002t0006g0177a0004c0004t0010g0237 | 3 | HG02145.hp2 NA19001.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.331-2903C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533786 | ||||||
chr5:157533872
|
G | A | 22 | a0002c0002t0001g0086a0002c0002t0002g0195a0002c0002t0002g0242others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.331-2989C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533872 | ||||||
chr5:157533954
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.331-3071C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157533954 | ||||||
chr5:157534019
|
C | T | 2 | a0002c0002t0019g0196a0002c0002t0019g0197 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.331-3136G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534019 | ||||||
chr5:157534089
|
C | T | 4 | a0002c0002t0008g0291a0004c0004t0010g0294a0004c0004t0010g0296others(1): Show | 4 | HG01243.hp2 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-3206G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534089 | ||||||
chr5:157534130
|
C | T | 24 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(21): Show | 25 | HG00323.hp1 HG00544.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.331-3247G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534130 | ||||||
chr5:157534329
|
G | A | 5 | a0003c0003t0011g0286a0003c0003t0011g0287a0003c0003t0011g0288others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-3446C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534329 | ||||||
chr5:157534333
|
T | C | 45 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.331-3450A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534333 | ||||||
chr5:157534337
|
G | A | 8 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0237others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-3454C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534337 | ||||||
chr5:157534413
|
A | G | 1 | a0007c0007t0012g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.330+3500T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534413 | ||||||
chr5:157534493
|
C | A | 3 | a0002c0002t0020g0148a0002c0002t0020g0163a0002c0002t0020g0183 | 3 | NA18946.hp2 NA18971.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.330+3420G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534493 | ||||||
chr5:157534820
|
C | A | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.330+3093G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534820 | ||||||
chr5:157534876
|
C | T | 8 | a0003c0003t0004g0290a0008c0008t0004g0225a0008c0008t0004g0226others(5): Show | 9 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+3037G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534876 | ||||||
chr5:157534885
|
C | G | 8 | a0003c0003t0004g0290a0008c0008t0004g0225a0008c0008t0004g0226others(5): Show | 9 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+3028G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534885 | ||||||
chr5:157534948
|
G | A | 3 | a0006c0006t0013g0013a0006c0006t0013g0014a0006c0006t0013g0015 | 3 | HG02723.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.330+2965C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534948 | ||||||
chr5:157534994
|
C | T | 1 | a0016c0020t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.330+2919G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157534994 | ||||||
chr5:157535011
|
T | A | 1 | a0001c0001t0009g0113 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.330+2902A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535011 | ||||||
chr5:157535040
|
T | TAAA | 45 | a0001c0001t0001g0166a0001c0001t0001g0174a0002c0002t0002g0153others(42): Show | 46 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.330+2870_330+2872d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535040 | ||||||
chr5:157535045
|
T | A | 45 | a0001c0001t0001g0166a0001c0001t0001g0174a0002c0002t0002g0153others(42): Show | 46 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.330+2868A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535045 | ||||||
chr5:157535046
|
G | A | 45 | a0001c0001t0001g0166a0001c0001t0001g0174a0002c0002t0002g0153others(42): Show | 46 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.330+2867C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535046 | ||||||
chr5:157535047
|
T | A | 45 | a0001c0001t0001g0166a0001c0001t0001g0174a0002c0002t0002g0153others(42): Show | 46 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.330+2866A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535047 | ||||||
chr5:157535061
|
T | A | 162 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(159): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.330+2852A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535061 | ||||||
chr5:157535136
|
G | C | 178 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(175): Show | 184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.330+2777C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535136 | ||||||
chr5:157535270
|
C | G | 1 | a0002c0002t0007g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.330+2643G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535270 | ||||||
chr5:157535282
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.330+2631G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535282 | ||||||
chr5:157535392
|
C | T | 2 | a0001c0001t0005g0179a0001c0001t0006g0178 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.330+2521G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535392 | ||||||
chr5:157535393
|
A | G | 31 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(28): Show | 32 | HG00323.hp1 HG01109.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.330+2520T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535393 | ||||||
chr5:157535468
|
A | T | 9 | a0008c0008t0004g0225a0008c0008t0004g0226a0008c0008t0004g0227others(6): Show | 10 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.330+2445T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535468 | ||||||
chr5:157535473
|
G | A | 2 | a0002c0002t0019g0196a0002c0002t0019g0197 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+2440C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535473 | ||||||
chr5:157535491
|
C | T | 16 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.330+2422G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535491 | ||||||
chr5:157535569
|
T | C | 2 | a0015c0021t0002g0299a0017c0018t0002g0016 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.330+2344A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535569 | ||||||
chr5:157535577
|
G | A | 43 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(40): Show | 44 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+2336C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535577 | ||||||
chr5:157535592
|
A | G | 1 | a0002c0002t0002g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.330+2321T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535592 | ||||||
chr5:157535650
|
C | T | 47 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.330+2263G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535650 | ||||||
chr5:157535655
|
T | C | 22 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(19): Show | 23 | HG01243.hp2 HG02083.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.330+2258A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157535655 | ||||||
chr5:157536002
|
A | T | 14 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(11): Show | 15 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.330+1911T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536002 | ||||||
chr5:157536187
|
C | A | 1 | a0001c0001t0005g0007 | 2 | NA18982.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.330+1726G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536187 | ||||||
chr5:157536292
|
G | A | 7 | a0002c0002t0008g0291a0004c0004t0010g0088a0004c0004t0010g0265others(4): Show | 7 | HG01243.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+1621C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536292 | ||||||
chr5:157536350
|
G | A | 2 | a0001c0001t0017g0259a0001c0001t0017g0262 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.330+1563C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536350 | ||||||
chr5:157536624
|
T | TCA | 5 | a0001c0001t0001g0004a0002c0002t0019g0197a0002c0002t0045g0147others(2): Show | 6 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+1287_330+1288d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536624 | ||||||
chr5:157536624
|
T | TCACA | 14 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0156others(11): Show | 14 | HG02015.hp2 HG02056.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.330+1285_330+1288d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536624 | ||||||
chr5:157536858
|
C | T | 4 | a0002c0002t0014g0026a0004c0004t0034g0279a0013c0011t0026g0280others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+1055G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536858 | ||||||
chr5:157536940
|
C | T | 22 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(19): Show | 23 | HG01943.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.330+973G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157536940 | ||||||
chr5:157537269
|
T | C | 2 | a0003c0003t0016g0209a0003c0003t0016g0210 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.330+644A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537269 | ||||||
chr5:157537370
|
G | A | 1 | a0007c0007t0025g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.330+543C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537370 | ||||||
chr5:157537490
|
G | T | 6 | a0004c0013t0012g0248a0007c0007t0012g0018a0007c0007t0012g0021others(3): Show | 6 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+423C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537490 | ||||||
chr5:157537490
|
GCA | G | 3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.330+421_330+422del others(2): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537490 | ||||||
chr5:157537536
|
G | C | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.330+377C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537536 | ||||||
chr5:157537586
|
C | T | 174 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(171): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.330+327G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537586 | ||||||
chr5:157537613
|
T | G | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.330+300A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 4/22 | chr5 | 157537613 | ||||||
chr5:157538031
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.252-40A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538031 | ||||||
chr5:157538084
|
T | C | 1 | a0002c0002t0004g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.252-93A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538084 | ||||||
chr5:157538152
|
A | G | 2 | a0002c0002t0019g0196a0002c0002t0019g0197 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-161T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538152 | ||||||
chr5:157538273
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252-282C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538273 | ||||||
chr5:157538292
|
T | C | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252-301A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538292 | ||||||
chr5:157538326
|
AC | A | 18 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG02015.hp2 HG02056.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.252-336delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538326 | ||||||
chr5:157538587
|
G | A | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252-596C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538587 | ||||||
chr5:157538627
|
G | A | 1 | a0002c0002t0006g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.252-636C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538627 | ||||||
chr5:157538712
|
C | T | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252-721G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538712 | ||||||
chr5:157538794
|
A | T | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.252-803T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157538794 | ||||||
chr5:157539007
|
T | A | 72 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(69): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.252-1016A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539007 | ||||||
chr5:157539153
|
CA | C | 67 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(64): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.252-1163delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539153 | ||||||
chr5:157539217
|
G | A | 46 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.252-1226C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539217 | ||||||
chr5:157539399
|
G | C | 1 | a0004c0013t0012g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.252-1408C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539399 | ||||||
chr5:157539490
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252-1499C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539490 | ||||||
chr5:157539556
|
C | T | 105 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0005g0170others(102): Show | 109 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.252-1565G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539556 | ||||||
chr5:157539559
|
T | A | 46 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.252-1568A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539559 | ||||||
chr5:157539568
|
C | T | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.252-1577G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539568 | ||||||
chr5:157539587
|
A | C | 46 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.252-1596T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539587 | ||||||
chr5:157539589
|
A | G | 1 | a0002c0002t0007g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.252-1598T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539589 | ||||||
chr5:157539765
|
A | AG | 105 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0005g0170others(102): Show | 109 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.252-1775dupC | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539765 | ||||||
chr5:157539829
|
T | C | 1 | a0004c0004t0032g0080 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.252-1838A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539829 | ||||||
chr5:157539840
|
G | A | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.252-1849C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539840 | ||||||
chr5:157539922
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.252-1931C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539922 | ||||||
chr5:157539974
|
C | T | 3 | a0002c0002t0014g0008a0002c0002t0014g0292a0002c0002t0047g0283 | 4 | HG02280.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-1983G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157539974 | ||||||
chr5:157540143
|
G | A | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.252-2152C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540143 | ||||||
chr5:157540265
|
G | A | 2 | a0001c0001t0005g0179a0001c0001t0006g0178 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.252-2274C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540265 | ||||||
chr5:157540271
|
T | A | 1 | a0002c0002t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.252-2280A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540271 | ||||||
chr5:157540359
|
A | C | 18 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG02015.hp2 HG02056.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.252-2368T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540359 | ||||||
chr5:157540574
|
G | A | 1 | a0002c0002t0036g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.252-2583C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540574 | ||||||
chr5:157540636
|
A | G | 185 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(182): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.252-2645T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540636 | ||||||
chr5:157540882
|
A | C | 15 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-2891T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540882 | ||||||
chr5:157540893
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0009g0028 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-2902G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540893 | ||||||
chr5:157540973
|
C | T | 9 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(6): Show | 9 | HG01943.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.252-2982G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540973 | ||||||
chr5:157540988
|
A | T | 1 | a0002c0002t0037g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.252-2997T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157540988 | ||||||
chr5:157541082
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252-3091C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541082 | ||||||
chr5:157541128
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.252-3137C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541128 | ||||||
chr5:157541174
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.252-3183G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541174 | ||||||
chr5:157541478
|
T | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-3487A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541478 | ||||||
chr5:157541564
|
C | A | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG02145.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-3573G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541564 | ||||||
chr5:157541583
|
T | C | 7 | a0002c0002t0019g0027a0008c0008t0004g0225a0008c0008t0004g0226others(4): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-3592A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541583 | ||||||
chr5:157541597
|
G | A | 1 | a0002c0002t0008g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.252-3606C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541597 | ||||||
chr5:157541699
|
TC | T | 29 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 30 | HG02015.hp2 HG02056.hp1 HG02080.hp1 others(27): Show |
intron_variant | MODIFIER | c.252-3709delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541699 | ||||||
chr5:157541784
|
G | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-3793C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541784 | ||||||
chr5:157541867
|
C | T | 11 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(8): Show | 11 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3876G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541867 | ||||||
chr5:157541917
|
C | A | 11 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(8): Show | 11 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3926G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157541917 | ||||||
chr5:157542098
|
C | G | 39 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(36): Show | 40 | HG00544.hp1 HG00621.hp2 HG01975.hp2 others(37): Show |
intron_variant | MODIFIER | c.252-4107G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542098 | ||||||
chr5:157542259
|
GT | G | 78 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.252-4269delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542259 | ||||||
chr5:157542259
|
GTT | G | 14 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0233others(11): Show | 15 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-4270_252-4269d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542259 | ||||||
chr5:157542260
|
T | A | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.252-4269A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542260 | ||||||
chr5:157542290
|
G | A | 5 | a0002c0002t0002g0195a0002c0002t0019g0196a0002c0002t0019g0197others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-4299C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542290 | ||||||
chr5:157542497
|
T | C | 1 | a0002c0002t0006g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252-4506A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542497 | ||||||
chr5:157542514
|
C | A | 2 | a0001c0001t0002g0117a0001c0001t0002g0151 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.252-4523G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542514 | ||||||
chr5:157542548
|
C | T | 11 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(8): Show | 12 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-4557G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542548 | ||||||
chr5:157542582
|
A | G | 2 | a0003c0003t0004g0222a0003c0003t0007g0221 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.252-4591T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542582 | ||||||
chr5:157542675
|
C | T | 38 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-4684G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542675 | ||||||
chr5:157542742
|
C | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-4751G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542742 | ||||||
chr5:157542768
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.252-4777C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542768 | ||||||
chr5:157542817
|
T | C | 1 | a0001c0001t0006g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.252-4826A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542817 | ||||||
chr5:157542865
|
G | A | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-4874C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542865 | ||||||
chr5:157542899
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.252-4908C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157542899 | ||||||
chr5:157543136
|
A | C | 6 | a0004c0013t0012g0248a0007c0007t0012g0018a0007c0007t0012g0021others(3): Show | 6 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-5145T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543136 | ||||||
chr5:157543139
|
G | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.252-5148C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543139 | ||||||
chr5:157543143
|
C | A | 7 | a0002c0002t0002g0153a0002c0002t0003g0005a0002c0002t0003g0159others(4): Show | 8 | HG00741.hp2 HG01257.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.252-5152G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543143 | ||||||
chr5:157543151
|
C | T | 1 | a0002c0002t0004g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252-5160G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543151 | ||||||
chr5:157543152
|
G | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-5161C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543152 | ||||||
chr5:157543205
|
C | G | 40 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(37): Show | 41 | HG00544.hp1 HG00621.hp2 HG01975.hp2 others(38): Show |
intron_variant | MODIFIER | c.252-5214G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543205 | ||||||
chr5:157543241
|
C | T | 1 | a0002c0002t0006g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.252-5250G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543241 | ||||||
chr5:157543343
|
A | C | 70 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(67): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.252-5352T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543343 | ||||||
chr5:157543475
|
C | T | 2 | a0002c0002t0002g0056a0002c0002t0002g0057 | 2 | HG01069.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.252-5484G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543475 | ||||||
chr5:157543560
|
G | A | 39 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.252-5569C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543560 | ||||||
chr5:157543719
|
ATTT | A | 37 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-5731_252-5729d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543719 | ||||||
chr5:157543788
|
G | A | 142 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(139): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.252-5797C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543788 | ||||||
chr5:157543835
|
GA | G | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-5845delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543835 | ||||||
chr5:157543870
|
A | C | 15 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-5879T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543870 | ||||||
chr5:157543942
|
G | A | 40 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(37): Show | 41 | HG00544.hp1 HG00621.hp2 HG01975.hp2 others(38): Show |
intron_variant | MODIFIER | c.252-5951C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543942 | ||||||
chr5:157543944
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.252-5953C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157543944 | ||||||
chr5:157544371
|
C | G | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-6380G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544371 | ||||||
chr5:157544380
|
C | A | 1 | a0001c0001t0002g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.252-6389G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544380 | ||||||
chr5:157544412
|
C | A | 3 | a0004c0004t0018g0278a0004c0004t0034g0279a0013c0011t0026g0280 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.252-6421G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544412 | ||||||
chr5:157544485
|
A | G | 1 | a0002c0002t0004g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.252-6494T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544485 | ||||||
chr5:157544493
|
C | T | 1 | a0003c0003t0015g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252-6502G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544493 | ||||||
chr5:157544597
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.252-6606A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544597 | ||||||
chr5:157544655
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0002c0002t0004g0202 | 3 | HG02602.hp1 HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.252-6664C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544655 | ||||||
chr5:157544752
|
A | T | 82 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(79): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.252-6761T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544752 | ||||||
chr5:157544882
|
T | C | 1 | a0002c0002t0004g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.252-6891A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157544882 | ||||||
chr5:157545069
|
C | A | 1 | a0003c0003t0016g0217 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.252-7078G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545069 | ||||||
chr5:157545095
|
C | A | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.252-7104G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545095 | ||||||
chr5:157545098
|
T | G | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.252-7107A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545098 | ||||||
chr5:157545286
|
A | G | 70 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(67): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.252-7295T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545286 | ||||||
chr5:157545294
|
A | T | 9 | a0002c0002t0044g0282a0004c0004t0010g0273a0005c0005t0008g0001others(6): Show | 11 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.252-7303T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545294 | ||||||
chr5:157545604
|
C | T | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.252-7613G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545604 | ||||||
chr5:157545700
|
C | T | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.252-7709G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545700 | ||||||
chr5:157545784
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.252-7793T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157545784 | ||||||
chr5:157546008
|
C | T | 144 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(141): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.252-8017G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546008 | ||||||
chr5:157546256
|
G | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-8265C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546256 | ||||||
chr5:157546280
|
C | T | 40 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(37): Show | 41 | HG00544.hp1 HG00621.hp2 HG01975.hp2 others(38): Show |
intron_variant | MODIFIER | c.252-8289G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546280 | ||||||
chr5:157546293
|
G | A | 1 | a0002c0002t0007g0267 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.252-8302C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546293 | ||||||
chr5:157546310
|
G | A | 1 | a0001c0001t0005g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.252-8319C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546310 | ||||||
chr5:157546315
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.252-8324G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546315 | ||||||
chr5:157546356
|
G | A | 1 | a0001c0001t0029g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.252-8365C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546356 | ||||||
chr5:157546551
|
A | C | 2 | a0001c0001t0001g0095a0001c0001t0029g0193 | 2 | NA18946.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.252-8560T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546551 | ||||||
chr5:157546873
|
C | T | 1 | a0004c0004t0010g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252-8882G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546873 | ||||||
chr5:157546949
|
A | G | 1 | a0002c0002t0046g0284 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252-8958T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157546949 | ||||||
chr5:157547089
|
T | A | 2 | a0002c0002t0045g0147a0009c0009t0002g0154 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.252-9098A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547089 | ||||||
chr5:157547146
|
G | A | 4 | a0008c0008t0004g0225a0008c0008t0004g0226a0008c0008t0004g0227others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-9155C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547146 | ||||||
chr5:157547292
|
C | T | 1 | a0001c0001t0006g0114 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252-9301G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547292 | ||||||
chr5:157547360
|
T | A | 1 | a0008c0008t0004g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.252-9369A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547360 | ||||||
chr5:157547409
|
G | A | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252-9418C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547409 | ||||||
chr5:157547467
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.252-9476C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547467 | ||||||
chr5:157547535
|
A | C | 2 | a0002c0002t0008g0291a0003c0003t0004g0290 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.252-9544T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547535 | ||||||
chr5:157547550
|
C | T | 1 | a0002c0002t0002g0258 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.252-9559G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547550 | ||||||
chr5:157547980
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0003g0125 | 3 | HG00738.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.252-9989T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157547980 | ||||||
chr5:157548008
|
T | G | 59 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0002g0201others(56): Show | 63 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.252-10017A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548008 | ||||||
chr5:157548183
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.252-10192G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548183 | ||||||
chr5:157548199
|
A | G | 1 | a0009c0009t0002g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.252-10208T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548199 | ||||||
chr5:157548355
|
C | T | 3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.252-10364G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548355 | ||||||
chr5:157548444
|
T | C | 5 | a0002c0002t0002g0195a0002c0002t0019g0196a0002c0002t0019g0197others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-10453A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548444 | ||||||
chr5:157548710
|
G | A | 6 | a0002c0002t0007g0270a0002c0002t0007g0285a0002c0014t0007g0268others(3): Show | 6 | HG01070.hp1 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-10719C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548710 | ||||||
chr5:157548783
|
G | C | 10 | a0001c0001t0006g0069a0002c0002t0044g0282a0004c0004t0010g0273others(7): Show | 12 | HG01884.hp1 HG02055.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-10792C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548783 | ||||||
chr5:157548838
|
C | T | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.252-10847G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548838 | ||||||
chr5:157548903
|
C | T | 5 | a0002c0002t0002g0247a0002c0002t0002g0249a0002c0002t0002g0258others(2): Show | 5 | HG01255.hp2 HG01256.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-10912G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548903 | ||||||
chr5:157548905
|
A | G | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252-10914T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157548905 | ||||||
chr5:157549374
|
T | C | 1 | a0005c0005t0008g0275 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.252-11383A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549374 | ||||||
chr5:157549423
|
A | G | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252-11432T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549423 | ||||||
chr5:157549589
|
C | A | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.252-11598G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549589 | ||||||
chr5:157549590
|
C | A | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.252-11599G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549590 | ||||||
chr5:157549607
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.252-11616C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549607 | ||||||
chr5:157549683
|
G | T | 1 | a0002c0002t0003g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.252-11692C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157549683 | ||||||
chr5:157550049
|
T | G | 1 | a0004c0004t0010g0296 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.252-12058A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550049 | ||||||
chr5:157550114
|
G | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(68): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.252-12123C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550114 | ||||||
chr5:157550261
|
G | GC | 298 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(295): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.252-12271dupG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550261 | ||||||
chr5:157550317
|
A | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(68): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.252-12326T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550317 | ||||||
chr5:157550385
|
G | A | 15 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-12394C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550385 | ||||||
chr5:157550407
|
A | G | 3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.252-12416T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550407 | ||||||
chr5:157550632
|
C | T | 4 | a0002c0002t0004g0203a0002c0002t0004g0205a0002c0002t0004g0206others(1): Show | 4 | HG02683.hp1 HG02698.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-12641G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550632 | ||||||
chr5:157550686
|
G | GA | 57 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(54): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.252-12696dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550686 | ||||||
chr5:157550686
|
GA | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(65): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.252-12696delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550686 | ||||||
chr5:157550759
|
T | A | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-12768A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550759 | ||||||
chr5:157550790
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(78): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.252-12799G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550790 | ||||||
chr5:157550845
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252-12854C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550845 | ||||||
chr5:157550914
|
A | G | 2 | a0002c0002t0002g0153a0002c0002t0038g0169 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.252-12923T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550914 | ||||||
chr5:157550991
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.252-13000G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157550991 | ||||||
chr5:157551032
|
C | T | 1 | a0011c0016t0007g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.252-13041G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551032 | ||||||
chr5:157551137
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.252-13146C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551137 | ||||||
chr5:157551197
|
G | A | 1 | a0004c0004t0018g0278 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+13176C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551197 | ||||||
chr5:157551276
|
C | A | 6 | a0002c0002t0007g0270a0002c0002t0007g0285a0002c0014t0007g0268others(3): Show | 6 | HG01070.hp1 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+13097G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551276 | ||||||
chr5:157551410
|
C | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251+12963G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551410 | ||||||
chr5:157551411
|
C | CAA | 17 | a0001c0001t0001g0087a0001c0001t0001g0233a0001c0001t0002g0235others(14): Show | 18 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.251+12961_251+1296 others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551411 | ||||||
chr5:157551411
|
C | CAAA | 50 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(47): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.251+12961_251+1296 others(7): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551411 | ||||||
chr5:157551411
|
C | CAAAA | 6 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0156others(3): Show | 6 | HG02080.hp1 HG02922.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+12961_251+1296 others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551411 | ||||||
chr5:157551412
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(78): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.251+12961G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551412 | ||||||
chr5:157551412
|
C | CA | 193 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0033others(190): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.251+12960dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551412 | ||||||
chr5:157551412
|
C | CAA | 15 | a0001c0001t0001g0035a0001c0001t0002g0126a0001c0001t0005g0136others(12): Show | 15 | HG01106.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.251+12959_251+1296 others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551412 | ||||||
chr5:157551413
|
A | C | 1 | a0001c0001t0006g0115 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.251+12960T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551413 | ||||||
chr5:157551432
|
G | A | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+12941C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551432 | ||||||
chr5:157551456
|
C | T | 1 | a0002c0002t0002g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.251+12917G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551456 | ||||||
chr5:157551468
|
A | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+12905T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551468 | ||||||
chr5:157551723
|
G | GA | 12 | a0001c0001t0002g0201a0002c0002t0003g0143a0002c0002t0006g0200others(9): Show | 14 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+12649dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551723 | ||||||
chr5:157551754
|
T | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+12619A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551754 | ||||||
chr5:157551870
|
C | T | 39 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.251+12503G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551870 | ||||||
chr5:157551871
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(141): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.251+12502T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551871 | ||||||
chr5:157551907
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.251+12466T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551907 | ||||||
chr5:157551945
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+12428A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551945 | ||||||
chr5:157551978
|
C | G | 16 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(13): Show | 17 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+12395G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157551978 | ||||||
chr5:157552019
|
C | T | 16 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(13): Show | 17 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+12354G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552019 | ||||||
chr5:157552057
|
T | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(196): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.251+12316A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552057 | ||||||
chr5:157552083
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(30): Show | 34 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.251+12290C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552083 | ||||||
chr5:157552090
|
G | T | 3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.251+12283C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552090 | ||||||
chr5:157552105
|
C | T | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.251+12268G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552105 | ||||||
chr5:157552202
|
C | T | 1 | a0009c0009t0002g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.251+12171G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552202 | ||||||
chr5:157552234
|
G | A | 1 | a0002c0002t0007g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.251+12139C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552234 | ||||||
chr5:157552371
|
G | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+12002C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552371 | ||||||
chr5:157552395
|
T | TA | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+11977dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552395 | ||||||
chr5:157552420
|
G | A | 57 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(54): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.251+11953C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552420 | ||||||
chr5:157552457
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.251+11916C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552457 | ||||||
chr5:157552506
|
C | T | 6 | a0002c0002t0002g0195a0002c0002t0019g0196a0002c0002t0019g0197others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+11867G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552506 | ||||||
chr5:157552567
|
T | A | 1 | a0007c0007t0012g0018 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.251+11806A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552567 | ||||||
chr5:157552569
|
C | T | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251+11804G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552569 | ||||||
chr5:157552571
|
C | T | 2 | a0006c0006t0013g0013a0006c0006t0013g0014 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.251+11802G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552571 | ||||||
chr5:157552636
|
G | A | 2 | a0006c0006t0013g0012a0017c0018t0002g0016 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251+11737C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552636 | ||||||
chr5:157552677
|
C | CA | 12 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0093others(9): Show | 12 | HG01109.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+11695dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552677 | ||||||
chr5:157552677
|
CA | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.251+11695delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552677 | ||||||
chr5:157552677
|
CAA | C | 15 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(12): Show | 16 | HG01081.hp2 HG02083.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.251+11694_251+1169 others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552677 | ||||||
chr5:157552677
|
CAAAAAAA | C | 6 | a0004c0004t0010g0273a0005c0005t0008g0001a0005c0005t0008g0274others(3): Show | 8 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.251+11689_251+1169 others(11): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552677 | ||||||
chr5:157552705
|
A | T | 1 | a0001c0001t0003g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.251+11668T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157552705 | ||||||
chr5:157553102
|
A | G | 16 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(13): Show | 17 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+11271T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553102 | ||||||
chr5:157553204
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0006g0103 | 3 | NA18949.hp1 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.251+11169G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553204 | ||||||
chr5:157553205
|
G | A | 1 | a0002c0002t0008g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251+11168C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553205 | ||||||
chr5:157553259
|
A | T | 16 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(13): Show | 17 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+11114T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553259 | ||||||
chr5:157553294
|
G | A | 2 | a0002c0002t0037g0257a0002c0002t0046g0284 | 2 | HG02015.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.251+11079C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553294 | ||||||
chr5:157553322
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(68): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.251+11051G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553322 | ||||||
chr5:157553332
|
T | A | 57 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(54): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.251+11041A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553332 | ||||||
chr5:157553376
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.251+10997G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553376 | ||||||
chr5:157553401
|
A | G | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.251+10972T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553401 | ||||||
chr5:157553423
|
A | T | 1 | a0002c0002t0004g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.251+10950T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553423 | ||||||
chr5:157553726
|
CCTAA | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0008c0008t0004g0225others(4): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.251+10643_251+1064 others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157553726 | ||||||
chr5:157554070
|
T | C | 1 | a0002c0002t0004g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.251+10303A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554070 | ||||||
chr5:157554106
|
A | G | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.251+10267T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554106 | ||||||
chr5:157554137
|
A | G | 1 | a0001c0001t0030g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.251+10236T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554137 | ||||||
chr5:157554147
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.251+10226A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554147 | ||||||
chr5:157554209
|
G | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+10164C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554209 | ||||||
chr5:157554330
|
G | C | 2 | a0002c0002t0007g0270a0002c0002t0007g0285 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.251+10043C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554330 | ||||||
chr5:157554403
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0156 | 2 | HG02080.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.251+9970C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554403 | ||||||
chr5:157554439
|
T | C | 1 | a0011c0016t0007g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.251+9934A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554439 | ||||||
chr5:157554541
|
G | A | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.251+9832C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554541 | ||||||
chr5:157554617
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.251+9756G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554617 | ||||||
chr5:157554663
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.251+9710G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554663 | ||||||
chr5:157554844
|
A | C | 1 | a0001c0001t0009g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.251+9529T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554844 | ||||||
chr5:157554855
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00621.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.251+9518C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554855 | ||||||
chr5:157554896
|
A | C | 2 | a0002c0002t0045g0147a0009c0009t0002g0154 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.251+9477T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554896 | ||||||
chr5:157554905
|
T | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251+9468A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554905 | ||||||
chr5:157554989
|
G | C | 16 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(13): Show | 17 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+9384C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157554989 | ||||||
chr5:157555051
|
A | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.251+9322T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555051 | ||||||
chr5:157555347
|
G | A | 1 | a0006c0006t0013g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.251+9026C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555347 | ||||||
chr5:157555348
|
T | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0124others(5): Show | 9 | HG02027.hp1 HG02080.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+9025A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555348 | ||||||
chr5:157555645
|
C | T | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.251+8728G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555645 | ||||||
chr5:157555757
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0005g0136others(3): Show | 6 | HG02040.hp1 NA18942.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+8616C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555757 | ||||||
chr5:157555869
|
A | G | 1 | a0002c0002t0006g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.251+8504T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555869 | ||||||
chr5:157555958
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(30): Show | 34 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.251+8415A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157555958 | ||||||
chr5:157556209
|
C | CT | 9 | a0001c0001t0001g0038a0001c0001t0001g0124a0003c0003t0004g0290others(6): Show | 9 | HG01243.hp2 HG02080.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+8163dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CT | C | 114 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0096others(111): Show | 116 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.251+8163delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CTT | C | 19 | a0001c0001t0001g0043a0001c0001t0006g0030a0001c0001t0017g0262others(16): Show | 22 | HG00140.hp2 HG01069.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.251+8162_251+8163d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CTTT | C | 15 | a0001c0001t0001g0233a0001c0001t0003g0230a0001c0001t0005g0007others(12): Show | 16 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.251+8161_251+8163d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CTTTT | C | 17 | a0001c0001t0002g0235a0001c0001t0005g0220a0003c0003t0004g0222others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.251+8160_251+8163d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CTTTTTTT | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+8157_251+8163d others(9): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556209
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0009c0009t0002g0123 | 3 | HG02717.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251+8154_251+8163d others(12): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556209 | ||||||
chr5:157556214
|
T | TC | 34 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(31): Show | 35 | HG00544.hp1 HG00621.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.251+8158_251+8159i others(3): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556214 | ||||||
chr5:157556215
|
T | C | 3 | a0002c0002t0008g0076a0002c0002t0031g0204a0009c0009t0002g0006 | 4 | HG02647.hp1 HG02896.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+8158A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556215 | ||||||
chr5:157556220
|
T | C | 26 | a0001c0019t0017g0240a0002c0002t0001g0086a0002c0002t0002g0242others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.251+8153A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556220 | ||||||
chr5:157556225
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251+8148A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556225 | ||||||
chr5:157556283
|
A | G | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+8090T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556283 | ||||||
chr5:157556995
|
T | C | 41 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(38): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.251+7378A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556995 | ||||||
chr5:157556996
|
A | T | 41 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(38): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.251+7377T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556996 | ||||||
chr5:157556997
|
A | C | 41 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(38): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.251+7376T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157556997 | ||||||
chr5:157557021
|
C | T | 2 | a0002c0002t0002g0164a0002c0002t0002g0184 | 2 | NA18949.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.251+7352G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557021 | ||||||
chr5:157557037
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.251+7336A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557037 | ||||||
chr5:157557060
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251+7313A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557060 | ||||||
chr5:157557071
|
T | G | 1 | a0007c0007t0012g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.251+7302A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557071 | ||||||
chr5:157557142
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | NA18949.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.251+7231C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557142 | ||||||
chr5:157557397
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.251+6976G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557397 | ||||||
chr5:157557419
|
G | T | 57 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(54): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.251+6954C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557419 | ||||||
chr5:157557444
|
C | T | 88 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.251+6929G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557444 | ||||||
chr5:157557446
|
T | C | 39 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.251+6927A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557446 | ||||||
chr5:157557595
|
C | T | 1 | a0003c0003t0011g0212 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.251+6778G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557595 | ||||||
chr5:157557599
|
G | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+6774C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557599 | ||||||
chr5:157557626
|
C | T | 1 | a0003c0003t0011g0212 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.251+6747G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557626 | ||||||
chr5:157557665
|
T | C | 88 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.251+6708A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557665 | ||||||
chr5:157557676
|
C | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+6697G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557676 | ||||||
chr5:157557763
|
C | G | 98 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(95): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.251+6610G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557763 | ||||||
chr5:157557868
|
A | G | 2 | a0001c0001t0027g0102a0002c0002t0004g0198 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.251+6505T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157557868 | ||||||
chr5:157558027
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.251+6346T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558027 | ||||||
chr5:157558073
|
A | G | 1 | a0009c0009t0002g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.251+6300T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558073 | ||||||
chr5:157558121
|
G | C | 15 | a0003c0003t0004g0222a0003c0003t0007g0221a0003c0003t0011g0212others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.251+6252C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558121 | ||||||
chr5:157558127
|
A | G | 5 | a0002c0002t0002g0195a0002c0002t0019g0196a0002c0002t0019g0197others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+6246T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558127 | ||||||
chr5:157558131
|
A | T | 106 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(103): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.251+6242T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558131 | ||||||
chr5:157558173
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0003g0125 | 3 | HG00738.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.251+6200T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558173 | ||||||
chr5:157558327
|
C | T | 1 | a0002c0002t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.251+6046G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558327 | ||||||
chr5:157558373
|
A | C | 1 | a0011c0016t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.251+6000T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558373 | ||||||
chr5:157558404
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.251+5969T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558404 | ||||||
chr5:157558521
|
G | A | 1 | a0003c0003t0022g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.251+5852C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558521 | ||||||
chr5:157558647
|
G | A | 4 | a0002c0002t0007g0250a0002c0002t0007g0253a0002c0002t0007g0254others(1): Show | 4 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5726C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558647 | ||||||
chr5:157558694
|
G | C | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251+5679C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558694 | ||||||
chr5:157558761
|
A | C | 106 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(103): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.251+5612T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558761 | ||||||
chr5:157558871
|
A | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0083a0001c0001t0002g0098others(6): Show | 10 | HG01074.hp1 HG01109.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+5502T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558871 | ||||||
chr5:157558910
|
C | T | 1 | a0002c0002t0031g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.251+5463G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558910 | ||||||
chr5:157558945
|
C | T | 1 | a0011c0016t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.251+5428G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157558945 | ||||||
chr5:157559121
|
C | T | 5 | a0002c0002t0008g0291a0003c0003t0004g0290a0004c0004t0010g0294others(2): Show | 5 | HG01243.hp2 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+5252G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559121 | ||||||
chr5:157559209
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(141): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.251+5164T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559209 | ||||||
chr5:157559497
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0128 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.251+4876A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559497 | ||||||
chr5:157559521
|
T | G | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+4852A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559521 | ||||||
chr5:157559568
|
T | C | 106 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(103): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.251+4805A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559568 | ||||||
chr5:157559701
|
A | AG | 31 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(28): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.251+4671dupC | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559701 | ||||||
chr5:157559834
|
C | G | 1 | a0001c0001t0003g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251+4539G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559834 | ||||||
chr5:157559988
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.251+4385C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157559988 | ||||||
chr5:157560096
|
T | G | 1 | a0001c0001t0030g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.251+4277A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560096 | ||||||
chr5:157560121
|
C | T | 2 | a0001c0001t0002g0097a0002c0002t0001g0086 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.251+4252G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560121 | ||||||
chr5:157560192
|
A | G | 98 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(95): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.251+4181T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560192 | ||||||
chr5:157560242
|
G | A | 32 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(29): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.251+4131C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560242 | ||||||
chr5:157560260
|
G | A | 1 | a0001c0001t0009g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.251+4113C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560260 | ||||||
chr5:157560264
|
C | CA | 33 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0085others(30): Show | 33 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.251+4108dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560264
|
CA | C | 42 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(39): Show | 42 | HG00544.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.251+4108delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560264
|
CAA | C | 20 | a0001c0001t0001g0223a0001c0001t0001g0224a0002c0002t0002g0281others(17): Show | 21 | HG01070.hp1 HG01169.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.251+4107_251+4108d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560264
|
CAAA | C | 60 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(57): Show | 64 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.251+4106_251+4108d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560264
|
CAAAA | C | 14 | a0001c0001t0006g0229a0003c0003t0011g0212a0003c0003t0011g0213others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+4105_251+4108d others(6): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560264
|
CAAAAAAA others(5): Show |
C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+4097_251+4108d others(14): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560264 | ||||||
chr5:157560350
|
G | C | 1 | a0016c0020t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.251+4023C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560350 | ||||||
chr5:157560370
|
G | A | 9 | a0002c0002t0004g0079a0002c0002t0008g0291a0002c0002t0014g0292others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.251+4003C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560370 | ||||||
chr5:157560423
|
T | C | 1 | a0002c0002t0008g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+3950A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560423 | ||||||
chr5:157560598
|
T | C | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.251+3775A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560598 | ||||||
chr5:157560667
|
T | C | 1 | a0002c0002t0002g0249 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.251+3706A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157560667 | ||||||
chr5:157561003
|
C | T | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0008c0008t0004g0225others(4): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.251+3370G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561003 | ||||||
chr5:157561134
|
G | A | 98 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(95): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.251+3239C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561134 | ||||||
chr5:157561167
|
G | A | 1 | a0005c0005t0008g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.251+3206C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561167 | ||||||
chr5:157561257
|
G | A | 1 | a0001c0001t0001g0004 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.251+3116C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561257 | ||||||
chr5:157561294
|
T | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+3079A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561294 | ||||||
chr5:157561426
|
C | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+2947G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561426 | ||||||
chr5:157561523
|
T | C | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+2850A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561523 | ||||||
chr5:157561579
|
G | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(199): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.251+2794C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561579 | ||||||
chr5:157561586
|
G | A | 2 | a0012c0015t0024g0271a0012c0015t0024g0272 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+2787C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561586 | ||||||
chr5:157561631
|
G | A | 94 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(91): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.251+2742C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561631 | ||||||
chr5:157561758
|
G | A | 1 | a0008c0008t0004g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251+2615C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561758 | ||||||
chr5:157561790
|
T | C | 56 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(53): Show | 59 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.251+2583A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561790 | ||||||
chr5:157561852
|
G | T | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.251+2521C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561852 | ||||||
chr5:157561926
|
T | TA | 13 | a0001c0001t0001g0085a0001c0001t0001g0132a0001c0001t0001g0144others(10): Show | 13 | HG00741.hp1 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+2446dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561926 | ||||||
chr5:157561926
|
TA | T | 7 | a0001c0001t0005g0220a0002c0002t0003g0084a0002c0002t0020g0163others(4): Show | 7 | HG01243.hp2 HG01943.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+2446delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157561926 | ||||||
chr5:157562018
|
T | A | 1 | a0002c0002t0002g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.251+2355A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562018 | ||||||
chr5:157562112
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(31): Show | 35 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.251+2261G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562112 | ||||||
chr5:157562266
|
G | C | 1 | a0002c0002t0040g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+2107C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562266 | ||||||
chr5:157562382
|
A | G | 1 | a0002c0002t0003g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.251+1991T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562382 | ||||||
chr5:157562395
|
A | G | 1 | a0017c0018t0002g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.251+1978T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562395 | ||||||
chr5:157562402
|
C | T | 3 | a0006c0006t0013g0013a0006c0006t0013g0014a0006c0006t0013g0015 | 3 | HG02723.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.251+1971G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562402 | ||||||
chr5:157562715
|
G | A | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+1658C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562715 | ||||||
chr5:157562749
|
C | T | 94 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(91): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.251+1624G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562749 | ||||||
chr5:157562857
|
G | A | 11 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(8): Show | 12 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+1516C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562857 | ||||||
chr5:157562897
|
C | T | 10 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.251+1476G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562897 | ||||||
chr5:157562949
|
G | A | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.251+1424C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562949 | ||||||
chr5:157562955
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251+1418G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157562955 | ||||||
chr5:157563044
|
C | T | 3 | a0004c0004t0018g0278a0004c0004t0034g0279a0013c0011t0026g0280 | 3 | HG02109.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.251+1329G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563044 | ||||||
chr5:157563105
|
A | C | 94 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(91): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.251+1268T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563105 | ||||||
chr5:157563130
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | NA18949.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.251+1243A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563130 | ||||||
chr5:157563135
|
GCTGCACT others(63): Show |
G | 1 | a0011c0016t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.251+1168_251+1237d others(72): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563135 | ||||||
chr5:157563165
|
G | A | 55 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(52): Show | 58 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.251+1208C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563165 | ||||||
chr5:157563249
|
C | A | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.251+1124G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563249 | ||||||
chr5:157563301
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.251+1072A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563301 | ||||||
chr5:157563573
|
G | A | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+800C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563573 | ||||||
chr5:157563842
|
A | G | 55 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(52): Show | 58 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.251+531T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563842 | ||||||
chr5:157563888
|
G | A | 55 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(52): Show | 58 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.251+485C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563888 | ||||||
chr5:157563894
|
C | T | 1 | a0006c0006t0013g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.251+479G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157563894 | ||||||
chr5:157564119
|
G | A | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.251+254C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157564119 | ||||||
chr5:157564122
|
G | A | 1 | a0002c0002t0006g0189 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.251+251C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 3/22 | chr5 | 157564122 | ||||||
chr5:157564500
|
G | A | 48 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(45): Show | 51 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-57C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564500 | ||||||
chr5:157564600
|
T | C | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.181-157A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564600 | ||||||
chr5:157564633
|
T | C | 1 | a0002c0002t0004g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.181-190A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564633 | ||||||
chr5:157564713
|
A | G | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.181-270T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564713 | ||||||
chr5:157564809
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0002c0002t0004g0025 | 3 | HG02451.hp1 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181-366C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564809 | ||||||
chr5:157564886
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0002c0002t0004g0202 | 3 | HG02602.hp1 HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.181-443A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564886 | ||||||
chr5:157564921
|
A | G | 3 | a0002c0002t0014g0026a0002c0002t0019g0027a0004c0004t0010g0237 | 3 | HG02145.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.181-478T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157564921 | ||||||
chr5:157565159
|
G | A | 1 | a0001c0001t0005g0236 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.181-716C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565159 | ||||||
chr5:157565207
|
G | A | 104 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(101): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.181-764C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565207 | ||||||
chr5:157565233
|
C | T | 10 | a0002c0002t0004g0079a0002c0002t0008g0291a0002c0002t0014g0292others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-790G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565233 | ||||||
chr5:157565346
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.181-903C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565346 | ||||||
chr5:157565402
|
C | T | 1 | a0002c0002t0046g0284 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.181-959G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565402 | ||||||
chr5:157565622
|
T | C | 12 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0133others(9): Show | 12 | HG01496.hp1 HG01943.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.181-1179A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565622 | ||||||
chr5:157565650
|
A | G | 1 | a0002c0002t0036g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.181-1207T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565650 | ||||||
chr5:157565701
|
ACT | A | 10 | a0002c0002t0004g0079a0002c0002t0008g0291a0002c0002t0014g0292others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-1260_181-1259d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565701 | ||||||
chr5:157565710
|
C | CA | 6 | a0001c0001t0001g0142a0001c0001t0001g0156a0002c0002t0003g0141others(3): Show | 6 | HG02683.hp2 HG02738.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-1268dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565710 | ||||||
chr5:157565710
|
CA | C | 12 | a0001c0001t0001g0233a0001c0001t0002g0235a0001c0001t0003g0230others(9): Show | 13 | HG02083.hp1 HG02129.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-1268delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565710 | ||||||
chr5:157565837
|
A | G | 104 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(101): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.181-1394T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565837 | ||||||
chr5:157565942
|
C | G | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.181-1499G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157565942 | ||||||
chr5:157566043
|
A | C | 1 | a0002c0002t0004g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.181-1600T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566043 | ||||||
chr5:157566070
|
C | T | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.181-1627G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566070 | ||||||
chr5:157566088
|
G | GACAGAGT others(220): Show |
1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1646_181-1645i others(229): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566088 | ||||||
chr5:157566095
|
C | A | 5 | a0002c0002t0002g0195a0002c0002t0019g0196a0002c0002t0019g0197others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-1652G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566095 | ||||||
chr5:157566096
|
G | A | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1653C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566096 | ||||||
chr5:157566101
|
T | C | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1658A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566101 | ||||||
chr5:157566103
|
T | C | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1660A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566103 | ||||||
chr5:157566104
|
G | A | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1661C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566104 | ||||||
chr5:157566108
|
C | CA | 10 | a0002c0002t0006g0190a0002c0002t0006g0191a0003c0003t0016g0209others(7): Show | 12 | HG00673.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.181-1666dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566108 | ||||||
chr5:157566108
|
C | CAA | 88 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.181-1667_181-1666d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566108 | ||||||
chr5:157566108
|
C | CAAA | 9 | a0001c0001t0005g0220a0001c0019t0017g0240a0002c0002t0002g0242others(6): Show | 9 | HG01943.hp1 HG01981.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-1668_181-1666d others(5): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566108 | ||||||
chr5:157566109
|
A | T | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1666T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566109 | ||||||
chr5:157566115
|
A | T | 1 | a0009c0009t0002g0006 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.181-1672T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566115 | ||||||
chr5:157566187
|
T | C | 1 | a0002c0002t0002g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.181-1744A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566187 | ||||||
chr5:157566488
|
CT | C | 6 | a0002c0002t0004g0203a0002c0002t0004g0205a0002c0002t0004g0206others(3): Show | 6 | HG02683.hp1 HG02698.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-2046delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566488 | ||||||
chr5:157566546
|
C | T | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.181-2103G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566546 | ||||||
chr5:157566724
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0144 | 2 | NA18945.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.181-2281A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566724 | ||||||
chr5:157566863
|
G | C | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.181-2420C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566863 | ||||||
chr5:157566869
|
A | T | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.181-2426T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157566869 | ||||||
chr5:157567023
|
C | T | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.181-2580G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567023 | ||||||
chr5:157567057
|
C | G | 105 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(102): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.181-2614G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567057 | ||||||
chr5:157567234
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.181-2791C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567234 | ||||||
chr5:157567324
|
G | A | 1 | a0010c0010t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181-2881C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567324 | ||||||
chr5:157567429
|
T | C | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.181-2986A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567429 | ||||||
chr5:157567458
|
A | G | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.181-3015T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567458 | ||||||
chr5:157567514
|
C | G | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-3071G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567514 | ||||||
chr5:157567525
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(35): Show | 39 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.181-3082G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567525 | ||||||
chr5:157567560
|
G | A | 1 | a0013c0011t0026g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.181-3117C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567560 | ||||||
chr5:157567784
|
C | T | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.180+3111G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567784 | ||||||
chr5:157567800
|
CA | C | 94 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0017g0259others(91): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.180+3094delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567800 | ||||||
chr5:157567807
|
A | T | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0016c0020t0001g0094 | 3 | HG00099.hp2 HG01175.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.180+3088T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567807 | ||||||
chr5:157567808
|
A | T | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+3087T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567808 | ||||||
chr5:157567819
|
A | C | 1 | a0002c0002t0003g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.180+3076T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567819 | ||||||
chr5:157567835
|
G | A | 2 | a0012c0015t0024g0271a0012c0015t0024g0272 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.180+3060C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567835 | ||||||
chr5:157567949
|
A | G | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.180+2946T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157567949 | ||||||
chr5:157568007
|
G | A | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2888C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568007 | ||||||
chr5:157568025
|
C | G | 105 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(102): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.180+2870G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568025 | ||||||
chr5:157568074
|
C | G | 1 | a0001c0001t0009g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.180+2821G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568074 | ||||||
chr5:157568129
|
T | C | 105 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(102): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.180+2766A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568129 | ||||||
chr5:157568189
|
T | C | 1 | a0002c0002t0020g0148 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.180+2706A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568189 | ||||||
chr5:157568192
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(203): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.180+2703A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568192 | ||||||
chr5:157568269
|
C | T | 1 | a0002c0002t0002g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.180+2626G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568269 | ||||||
chr5:157568684
|
T | C | 2 | a0003c0003t0004g0222a0003c0003t0007g0221 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.180+2211A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568684 | ||||||
chr5:157568854
|
T | C | 5 | a0006c0006t0013g0012a0006c0006t0013g0013a0006c0006t0013g0014others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+2041A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568854 | ||||||
chr5:157568861
|
G | A | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.180+2034C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157568861 | ||||||
chr5:157569014
|
A | T | 2 | a0014c0012t0002g0089a0014c0012t0002g0090 | 2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.180+1881T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569014 | ||||||
chr5:157569234
|
A | AT | 82 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(79): Show | 83 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.180+1660dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569234 | ||||||
chr5:157569234
|
A | ATT | 10 | a0001c0001t0009g0045a0002c0002t0003g0074a0002c0002t0004g0251others(7): Show | 10 | HG01070.hp1 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.180+1659_180+1660d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569234 | ||||||
chr5:157569234
|
AT | A | 79 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0152others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.180+1660delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569234 | ||||||
chr5:157569394
|
A | ACC | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.180+1499_180+1500d others(4): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569394 | ||||||
chr5:157569416
|
C | CT | 17 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0002g0083others(14): Show | 17 | HG00738.hp1 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.180+1478dupA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569416 | ||||||
chr5:157569416
|
CT | C | 52 | a0001c0001t0001g0039a0001c0001t0001g0155a0001c0001t0001g0223others(49): Show | 57 | HG01070.hp1 HG01169.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.180+1478delA | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569416 | ||||||
chr5:157569420
|
T | C | 1 | a0002c0002t0002g0281 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180+1475A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569420 | ||||||
chr5:157569459
|
T | C | 2 | a0001c0001t0001g0075a0002c0002t0003g0074 | 2 | HG02080.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.180+1436A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569459 | ||||||
chr5:157569541
|
G | A | 1 | a0002c0002t0044g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180+1354C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569541 | ||||||
chr5:157569582
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180+1313C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569582 | ||||||
chr5:157569750
|
C | G | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.180+1145G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569750 | ||||||
chr5:157569876
|
A | G | 1 | a0001c0001t0002g0078 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.180+1019T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569876 | ||||||
chr5:157569915
|
A | T | 1 | a0003c0003t0015g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.180+980T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157569915 | ||||||
chr5:157570075
|
C | T | 1 | a0002c0002t0003g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.180+820G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570075 | ||||||
chr5:157570124
|
G | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG00673.hp2 NA18957.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+771C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570124 | ||||||
chr5:157570193
|
G | A | 1 | a0002c0002t0047g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.180+702C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570193 | ||||||
chr5:157570238
|
C | T | 2 | a0003c0003t0016g0209a0003c0003t0016g0210 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.180+657G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570238 | ||||||
chr5:157570270
|
C | CAAACAAA others(1): Show |
3 | a0004c0004t0010g0294a0004c0004t0010g0296a0004c0004t0018g0295 | 3 | HG01243.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.180+617_180+624dup others(8): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570270 | ||||||
chr5:157570274
|
C | A | 1 | a0002c0002t0004g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+621G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570274 | ||||||
chr5:157570302
|
AC | A | 41 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0002g0201others(38): Show | 42 | HG00323.hp1 HG00673.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.180+592delG | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570302 | ||||||
chr5:157570315
|
C | G | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.180+580G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570315 | ||||||
chr5:157570396
|
A | G | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+499T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570396 | ||||||
chr5:157570406
|
T | C | 105 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(102): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.180+489A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570406 | ||||||
chr5:157570407
|
G | A | 1 | a0002c0002t0046g0284 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.180+488C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570407 | ||||||
chr5:157570438
|
C | A | 1 | a0002c0002t0008g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.180+457G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570438 | ||||||
chr5:157570442
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.180+453T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570442 | ||||||
chr5:157570709
|
G | A | 1 | a0011c0016t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.180+186C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570709 | ||||||
chr5:157570777
|
C | T | 104 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(101): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.180+118G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 2/22 | chr5 | 157570777 | ||||||
chr5:157571282
|
A | G | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.95-302T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571282 | ||||||
chr5:157571366
|
G | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(34): Show | 38 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.95-386C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571366 | ||||||
chr5:157571375
|
C | T | 6 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(3): Show | 6 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-395G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571375 | ||||||
chr5:157571538
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.95-558G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571538 | ||||||
chr5:157571578
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01496.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.95-598G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571578 | ||||||
chr5:157571676
|
C | T | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.95-696G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571676 | ||||||
chr5:157571730
|
T | G | 1 | a0001c0001t0029g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.95-750A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571730 | ||||||
chr5:157571827
|
A | T | 1 | a0002c0002t0004g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.95-847T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571827 | ||||||
chr5:157571938
|
G | A | 1 | a0018c0017t0022g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-958C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571938 | ||||||
chr5:157571997
|
T | A | 1 | a0001c0001t0001g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.95-1017A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157571997 | ||||||
chr5:157572085
|
C | T | 7 | a0001c0019t0017g0240a0002c0002t0002g0242a0002c0002t0004g0238others(4): Show | 7 | HG01943.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1105G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572085 | ||||||
chr5:157572088
|
G | GTT | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.95-1110_95-1109dup others(2): Show |
ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572088 | ||||||
chr5:157572090
|
T | G | 7 | a0007c0007t0012g0018a0007c0007t0012g0021a0007c0007t0012g0022others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1110A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572090 | ||||||
chr5:157572120
|
T | C | 1 | a0002c0002t0002g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.95-1140A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572120 | ||||||
chr5:157572154
|
C | T | 1 | a0002c0002t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.95-1174G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572154 | ||||||
chr5:157572179
|
G | A | 2 | a0002c0002t0019g0196a0002c0002t0019g0197 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.95-1199C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572179 | ||||||
chr5:157572210
|
C | T | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.95-1230G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572210 | ||||||
chr5:157572332
|
C | T | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.95-1352G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572332 | ||||||
chr5:157572337
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG00673.hp2 NA18957.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1357G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572337 | ||||||
chr5:157572804
|
C | A | 1 | a0002c0002t0007g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.95-1824G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572804 | ||||||
chr5:157572808
|
G | A | 1 | a0001c0001t0005g0236 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.95-1828C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572808 | ||||||
chr5:157572957
|
C | T | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.95-1977G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572957 | ||||||
chr5:157572958
|
G | A | 1 | a0002c0002t0004g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.95-1978C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157572958 | ||||||
chr5:157573250
|
C | T | 1 | a0002c0002t0007g0031 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-2270G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573250 | ||||||
chr5:157573351
|
T | C | 3 | a0001c0001t0002g0201a0002c0002t0002g0199a0002c0002t0006g0200 | 3 | HG01081.hp1 HG01496.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.94+2252A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573351 | ||||||
chr5:157573483
|
C | G | 3 | a0002c0002t0002g0247a0002c0002t0002g0249a0004c0013t0012g0248 | 3 | HG01255.hp2 HG01256.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.94+2120G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573483 | ||||||
chr5:157573517
|
G | A | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.94+2086C>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573517 | ||||||
chr5:157573683
|
C | T | 105 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(102): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.94+1920G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573683 | ||||||
chr5:157573704
|
C | G | 1 | a0005c0005t0008g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.94+1899G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573704 | ||||||
chr5:157573710
|
C | T | 1 | a0001c0001t0006g0030 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.94+1893G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573710 | ||||||
chr5:157573741
|
G | GA | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.94+1861dupT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573741 | ||||||
chr5:157573741
|
GA | G | 8 | a0001c0001t0001g0029a0002c0002t0008g0291a0002c0002t0014g0292others(5): Show | 8 | HG01243.hp2 HG02630.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+1861delT | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573741 | ||||||
chr5:157573786
|
A | T | 46 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.94+1817T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573786 | ||||||
chr5:157573819
|
T | C | 1 | a0002c0002t0004g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.94+1784A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573819 | ||||||
chr5:157573846
|
C | G | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.94+1757G>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573846 | ||||||
chr5:157573861
|
T | G | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.94+1742A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573861 | ||||||
chr5:157573942
|
C | T | 6 | a0002c0002t0004g0203a0002c0002t0004g0205a0002c0002t0004g0206others(3): Show | 6 | HG02683.hp1 HG02698.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1661G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157573942 | ||||||
chr5:157574168
|
A | G | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.94+1435T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574168 | ||||||
chr5:157574175
|
A | C | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.94+1428T>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574175 | ||||||
chr5:157574192
|
A | G | 1 | a0001c0001t0009g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+1411T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574192 | ||||||
chr5:157574294
|
C | T | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(36): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.94+1309G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574294 | ||||||
chr5:157574317
|
A | T | 104 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(101): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.94+1286T>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574317 | ||||||
chr5:157574664
|
C | T | 2 | a0002c0002t0014g0026a0002c0002t0019g0027 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.94+939G>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574664 | ||||||
chr5:157574727
|
T | G | 104 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0233others(101): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.94+876A>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574727 | ||||||
chr5:157574751
|
G | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0002c0002t0004g0025 | 3 | HG02451.hp1 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.94+852C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574751 | ||||||
chr5:157574945
|
T | A | 58 | a0001c0001t0017g0259a0001c0001t0017g0262a0002c0002t0002g0247others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.94+658A>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574945 | ||||||
chr5:157574996
|
G | T | 1 | a0002c0002t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+607C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157574996 | ||||||
chr5:157575048
|
A | G | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.94+555T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575048 | ||||||
chr5:157575087
|
C | A | 3 | a0003c0003t0011g0286a0003c0003t0011g0287a0003c0003t0011g0288 | 3 | HG01891.hp1 HG02486.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.94+516G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575087 | ||||||
chr5:157575208
|
G | C | 1 | a0003c0003t0015g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+395C>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575208 | ||||||
chr5:157575272
|
C | A | 7 | a0002c0002t0008g0291a0002c0002t0014g0292a0003c0003t0004g0290others(4): Show | 7 | HG01243.hp2 HG02630.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+331G>T | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575272 | ||||||
chr5:157575399
|
G | T | 2 | a0011c0016t0003g0301a0011c0016t0007g0300 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94+204C>A | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575399 | ||||||
chr5:157575544
|
A | G | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(296): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.94+59T>C | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575544 | ||||||
chr5:157575548
|
T | C | 1 | a0015c0021t0002g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.94+55A>G | ADAM19 | ENSG00000135074.16 | transcript | ENST00000257527.9 | protein_coding | 1/22 | chr5 | 157575548 |