geneid | 10666 |
---|---|
ensemblid | ENSG00000150637.9 |
hgncid | 16961 |
symbol | CD226 |
name | CD226 molecule |
refseq_nuc | NM_001303618.2 |
refseq_prot | NP_001290547.1 |
ensembl_nuc | ENST00000582621.6 |
ensembl_prot | ENSP00000461947.1 |
mane_status | MANE Select |
chr | chr18 |
start | 69853274 |
end | 69947873 |
strand | - |
ver | v1.2 |
region | chr18:69853274-69947873 |
region5000 | chr18:69848274-69952873 |
regionname0 | CD226_chr18_69853274_69947873 |
regionname5000 | CD226_chr18_69848274_69952873 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 336 | 134 | 55 | 24 | 34 | 3 | 17 | 22 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002 | 0/1 | 336 | 106 | 26 | 34 | 29 | 1 | 15 | 17 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003 | 0/0 | 336 | 12 | 4 | 4 | 2 | 0 | 2 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0004 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0005 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0006 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0007 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1011 | 134 | 55 | 24 | 34 | 3 | 17 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0002 | 0/1 | 1011 | 103 | 24 | 33 | 29 | 1 | 15 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0003 | 0/0 | 1011 | 12 | 4 | 4 | 2 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0004 | 0/0 | 1011 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0005 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0007 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
c0009 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 11518 | 16 | 0 | 2 | 12 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0002 | 0/0 | 11517 | 16 | 0 | 9 | 0 | 1 | 6 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0003 | 0/0 | 11516 | 7 | 2 | 3 | 0 | 1 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0004 | 0/0 | 11513 | 6 | 0 | 0 | 5 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0005 | 0/0 | 11511 | 5 | 4 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0006 | 0/0 | 11532 | 5 | 0 | 5 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0007 | 0/0 | 11534 | 5 | 1 | 3 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0008 | 0/0 | 11533 | 4 | 1 | 0 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0009 | 0/0 | 11531 | 4 | 0 | 3 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0010 | 0/0 | 11532 | 4 | 0 | 3 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0011 | 0/0 | 11518 | 4 | 0 | 0 | 3 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0012 | 1/0 | 11508 | 3 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0013 | 0/0 | 11530 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0014 | 0/0 | 11532 | 3 | 2 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0015 | 0/0 | 11534 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0016 | 0/0 | 11517 | 3 | 1 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0017 | 0/0 | 11513 | 3 | 0 | 2 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0018 | 0/0 | 11512 | 3 | 1 | 1 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0019 | 0/0 | 11533 | 3 | 0 | 2 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0020 | 0/0 | 11535 | 3 | 0 | 1 | 0 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0021 | 0/0 | 11518 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0022 | 0/0 | 11494 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0023 | 0/0 | 11512 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0024 | 0/0 | 11511 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0025 | 0/0 | 11508 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0026 | 0/0 | 11518 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0027 | 0/0 | 11535 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0028 | 0/0 | 11531 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0029 | 0/0 | 11535 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0030 | 0/0 | 11533 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0031 | 0/0 | 11517 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0032 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0033 | 0/0 | 11514 | 2 | 0 | 1 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0034 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0035 | 0/0 | 11535 | 2 | 0 | 0 | 0 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0036 | 0/0 | 11534 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0037 | 0/0 | 11536 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0038 | 0/0 | 11536 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0039 | 0/0 | 11537 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0040 | 0/0 | 11534 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0041 | 0/0 | 11518 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0042 | 0/0 | 11518 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0043 | 0/0 | 11515 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0044 | 0/0 | 11518 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0045 | 0/0 | 11517 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0046 | 0/0 | 11530 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0047 | 0/0 | 11530 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0048 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0049 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0050 | 0/0 | 11508 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0051 | 0/0 | 11530 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0052 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0053 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0054 | 0/0 | 11513 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0055 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0056 | 0/0 | 11512 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0057 | 0/0 | 11507 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0058 | 0/0 | 11506 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0059 | 0/0 | 11521 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0060 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0061 | 0/0 | 11515 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0062 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0063 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0064 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0065 | 0/0 | 11530 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0066 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0067 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0068 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0069 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0070 | 0/0 | 11530 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0071 | 0/0 | 11534 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0072 | 0/0 | 11537 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0073 | 0/0 | 11543 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0074 | 0/0 | 11539 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0075 | 0/0 | 11538 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0076 | 0/0 | 11530 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0077 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0078 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0079 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0080 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0081 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0082 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0083 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0084 | 0/0 | 11518 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0085 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0086 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0087 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0088 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0089 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0090 | 0/0 | 11515 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0091 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0092 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0093 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0094 | 0/0 | 11509 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0095 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0096 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0097 | 0/0 | 11530 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0098 | 0/1 | 11541 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0099 | 0/0 | 11535 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0100 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0101 | 0/0 | 11531 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0102 | 0/0 | 11528 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0103 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0104 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0105 | 0/0 | 11516 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0106 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0107 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0108 | 0/0 | 11536 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0109 | 0/0 | 11540 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0110 | 0/0 | 11540 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0111 | 0/0 | 11539 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0112 | 0/0 | 11538 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0113 | 0/0 | 11541 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0114 | 0/0 | 11542 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0115 | 0/0 | 11542 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0116 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0117 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0118 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0119 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0120 | 0/0 | 11533 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0121 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0122 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0123 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0124 | 0/0 | 11519 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0125 | 0/0 | 11519 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0126 | 0/0 | 11519 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0127 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0128 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0129 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0130 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0131 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0132 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0133 | 0/0 | 11519 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0134 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0135 | 0/0 | 11514 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0136 | 0/0 | 11514 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0137 | 0/0 | 11515 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0138 | 0/0 | 11510 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0139 | 0/0 | 11509 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0140 | 0/0 | 11530 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0141 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0142 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0143 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0144 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0145 | 0/0 | 11519 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0146 | 0/0 | 11519 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
t0147 | 0/0 | 11514 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1011 | 134 | 55 | 24 | 34 | 3 | 17 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002 | 0/1 | 1011 | 103 | 24 | 33 | 29 | 1 | 15 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0004 | 0/0 | 1011 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0009 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003 | 0/0 | 1011 | 12 | 4 | 4 | 2 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0004c0005 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0005c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0006c0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0007c0007 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 12528 | 16 | 0 | 2 | 12 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0002 | 0/0 | 12527 | 16 | 0 | 9 | 0 | 1 | 6 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0003 | 0/0 | 12526 | 7 | 2 | 3 | 0 | 1 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0004 | 0/0 | 12523 | 6 | 0 | 0 | 5 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0011 | 0/0 | 12528 | 3 | 0 | 0 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0012 | 1/0 | 12518 | 3 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0016 | 0/0 | 12527 | 3 | 1 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0021 | 0/0 | 12528 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0022 | 0/0 | 12504 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0023 | 0/0 | 12522 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0024 | 0/0 | 12521 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0025 | 0/0 | 12518 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0026 | 0/0 | 12528 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0031 | 0/0 | 12527 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0032 | 0/0 | 12526 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0033 | 0/0 | 12524 | 2 | 0 | 1 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0041 | 0/0 | 12528 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0042 | 0/0 | 12528 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0043 | 0/0 | 12525 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0044 | 0/0 | 12528 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0045 | 0/0 | 12527 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0048 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0049 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0050 | 0/0 | 12518 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0054 | 0/0 | 12523 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0055 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0057 | 0/0 | 12517 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0058 | 0/0 | 12516 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0060 | 0/0 | 12530 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0061 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0062 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0063 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0064 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0077 | 0/0 | 12521 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0078 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0079 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0080 | 0/0 | 12527 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0081 | 0/0 | 12527 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0082 | 0/0 | 12528 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0083 | 0/0 | 12528 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0084 | 0/0 | 12528 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0085 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0086 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0087 | 0/0 | 12526 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0088 | 0/0 | 12524 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0089 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0090 | 0/0 | 12525 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0091 | 0/0 | 12527 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0092 | 0/0 | 12523 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0094 | 0/0 | 12519 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0123 | 0/0 | 12530 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0124 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0125 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0126 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0127 | 0/0 | 12527 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0128 | 0/0 | 12526 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0129 | 0/0 | 12527 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0130 | 0/0 | 12526 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0131 | 0/0 | 12528 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0132 | 0/0 | 12530 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0133 | 0/0 | 12529 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0134 | 0/0 | 12527 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0135 | 0/0 | 12524 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0136 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0137 | 0/0 | 12525 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0138 | 0/0 | 12520 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0139 | 0/0 | 12519 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0142 | 0/0 | 12529 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0143 | 0/0 | 12528 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0145 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0146 | 0/0 | 12529 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0001c0001t0147 | 0/0 | 12524 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0006 | 0/0 | 12542 | 5 | 0 | 5 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0007 | 0/0 | 12544 | 5 | 1 | 3 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0008 | 0/0 | 12543 | 4 | 1 | 0 | 2 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0009 | 0/0 | 12541 | 4 | 0 | 3 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0010 | 0/0 | 12542 | 4 | 0 | 3 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0011 | 0/0 | 12528 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0013 | 0/0 | 12540 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0014 | 0/0 | 12542 | 3 | 2 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0015 | 0/0 | 12544 | 3 | 3 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0019 | 0/0 | 12543 | 3 | 0 | 2 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0020 | 0/0 | 12545 | 3 | 0 | 1 | 0 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0027 | 0/0 | 12545 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0028 | 0/0 | 12541 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0029 | 0/0 | 12545 | 2 | 1 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0030 | 0/0 | 12543 | 2 | 2 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0034 | 0/0 | 12542 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0035 | 0/0 | 12545 | 2 | 0 | 0 | 0 | 0 | 2 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0036 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0037 | 0/0 | 12546 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0038 | 0/0 | 12546 | 2 | 0 | 0 | 1 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0039 | 0/0 | 12547 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0040 | 0/0 | 12544 | 2 | 0 | 0 | 2 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0046 | 0/0 | 12540 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0047 | 0/0 | 12540 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0051 | 0/0 | 12540 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0052 | 0/0 | 12541 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0053 | 0/0 | 12541 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0059 | 0/0 | 12531 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0066 | 0/0 | 12541 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0067 | 0/0 | 12544 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0068 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0069 | 0/0 | 12541 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0070 | 0/0 | 12540 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0071 | 0/0 | 12544 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0072 | 0/0 | 12547 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0073 | 0/0 | 12553 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0074 | 0/0 | 12549 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0075 | 0/0 | 12548 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0076 | 0/0 | 12540 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0095 | 0/0 | 12542 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0096 | 0/0 | 12545 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0097 | 0/0 | 12540 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0098 | 0/1 | 12551 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0099 | 0/0 | 12545 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0101 | 0/0 | 12541 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0102 | 0/0 | 12538 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0103 | 0/0 | 12548 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0104 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0105 | 0/0 | 12526 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0106 | 0/0 | 12548 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0107 | 0/0 | 12547 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0108 | 0/0 | 12546 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0109 | 0/0 | 12550 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0110 | 0/0 | 12550 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0111 | 0/0 | 12549 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0112 | 0/0 | 12548 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0113 | 0/0 | 12551 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0114 | 0/0 | 12552 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0115 | 0/0 | 12552 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0116 | 0/0 | 12545 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0117 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0118 | 0/0 | 12545 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0119 | 0/0 | 12547 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0120 | 0/0 | 12543 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0121 | 0/0 | 12542 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0122 | 0/0 | 12542 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0002t0144 | 0/0 | 12544 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0004t0034 | 0/0 | 12542 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0004t0065 | 0/0 | 12540 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0002c0009t0140 | 0/0 | 12540 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003t0005 | 0/0 | 12521 | 4 | 3 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003t0017 | 0/0 | 12523 | 3 | 0 | 2 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003t0018 | 0/0 | 12522 | 3 | 1 | 1 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003t0056 | 0/0 | 12522 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0003c0003t0093 | 0/0 | 12521 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0004c0005t0100 | 0/0 | 12544 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0005c0006t0036 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0006c0008t0141 | 0/0 | 12522 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
a0007c0007t0005 | 0/0 | 12521 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | copy fasta | chr18 | 69848274 | 69952873 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0011g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0011g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0012g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0016g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0021g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0021g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0021g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0022g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0023g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0024g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0025g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0025g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0026g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0026g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0031g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0031g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0032g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0032g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0033g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0033g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0041g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0041g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0042g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0042g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0043g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0043g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0044g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0044g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0045g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0045g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0048g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0049g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0050g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0054g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0055g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0057g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0058g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0060g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0061g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0062g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0063g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0064g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0077g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0078g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0079g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0080g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0081g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0082g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0083g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0084g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0085g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0086g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0087g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0088g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0089g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0090g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0091g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0092g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0094g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0123g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0124g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0125g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0126g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0127g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0128g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0129g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0130g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0131g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0132g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0133g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0134g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0135g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0136g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0137g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0138g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0139g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0142g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0143g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0145g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0146g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0001c0001t0147g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0007g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0014g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0015g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0019g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0019g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0020g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0020g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0020g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0027g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0028g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0029g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0029g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0030g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0030g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0034g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0035g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0035g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0036g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0037g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0037g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0038g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0038g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0039g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0039g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0040g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0040g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0046g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0047g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0051g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0052g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0053g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0059g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0066g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0067g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0068g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0069g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0070g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0071g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0072g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0073g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0074g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0075g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0076g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0095g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0096g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0097g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0098g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0099g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0101g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0102g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0103g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0104g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0105g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0106g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0107g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0108g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0109g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0110g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0111g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0112g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0113g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0114g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0115g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0116g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0117g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0118g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0119g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0120g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0121g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0122g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0002t0144g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0004t0034g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0004t0065g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0002c0009t0140g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0017g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0017g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0018g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0018g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0018g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0056g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0003c0003t0093g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0004c0005t0100g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0005c0006t0036g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0006c0008t0141g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
a0007c0007t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0033 | g0083 | EUR | GBR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00280 | hp1 | a0002 | c0002 | t0099 | g0155 | EUR | FIN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0089 | EUR | FIN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0122 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00544 | hp1 | a0002 | c0002 | t0008 | g0039 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00544 | hp2 | a0002 | c0002 | t0068 | g0043 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00597 | hp1 | a0002 | c0002 | t0008 | g0041 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00597 | hp2 | a0001 | c0001 | t0031 | g0092 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00609 | hp1 | a0002 | c0002 | t0037 | g0115 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00621 | hp1 | a0002 | c0002 | t0105 | g0163 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00639 | hp1 | a0002 | c0002 | t0039 | g0156 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00639 | hp2 | a0001 | c0001 | t0033 | g0082 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00642 | hp1 | a0002 | c0002 | t0006 | g0217 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00673 | hp1 | a0002 | c0002 | t0011 | g0205 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00673 | hp2 | a0005 | c0006 | t0036 | g0210 | EAS | CHS | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00733 | hp1 | a0002 | c0002 | t0121 | g0200 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00733 | hp2 | a0001 | c0001 | t0133 | g0220 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00735 | hp1 | a0003 | c0003 | t0017 | g0201 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00735 | hp2 | a0002 | c0002 | t0019 | g0215 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG00738 | hp2 | a0002 | c0002 | t0009 | g0126 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01069 | hp1 | a0001 | c0001 | t0130 | g0109 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01071 | hp2 | a0002 | c0004 | t0034 | g0136 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01074 | hp2 | a0002 | c0002 | t0029 | g0040 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01081 | hp1 | a0002 | c0002 | t0006 | g0238 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01081 | hp2 | a0002 | c0002 | t0027 | g0027 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01106 | hp1 | a0002 | c0002 | t0006 | g0219 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01106 | hp2 | a0003 | c0003 | t0017 | g0221 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01109 | hp1 | a0002 | c0002 | t0071 | g0015 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01175 | hp1 | a0002 | c0002 | t0120 | g0235 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01175 | hp2 | a0002 | c0002 | t0034 | g0128 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01243 | hp1 | a0001 | c0001 | t0094 | g0135 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01243 | hp2 | a0003 | c0003 | t0056 | g0079 | AMR | PUR | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01255 | hp1 | a0001 | c0001 | t0129 | g0106 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01255 | hp2 | a0002 | c0002 | t0014 | g0065 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01256 | hp1 | a0002 | c0002 | t0009 | g0001 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01257 | hp1 | a0002 | c0002 | t0112 | g0119 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01257 | hp2 | a0001 | c0001 | t0128 | g0189 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01258 | hp1 | a0002 | c0002 | t0009 | g0001 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01261 | hp1 | a0002 | c0002 | t0076 | g0090 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01261 | hp2 | a0002 | c0002 | t0007 | g0153 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01346 | hp1 | a0001 | c0001 | t0135 | g0158 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01346 | hp2 | a0002 | c0002 | t0059 | g0070 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01358 | hp1 | a0001 | c0001 | t0042 | g0108 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01358 | hp2 | a0002 | c0002 | t0007 | g0145 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01361 | hp1 | a0002 | c0002 | t0110 | g0193 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01361 | hp2 | a0001 | c0001 | t0041 | g0129 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01433 | hp1 | a0002 | c0002 | t0019 | g0175 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01433 | hp2 | a0002 | c0002 | t0020 | g0152 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01496 | hp2 | a0002 | c0002 | t0113 | g0130 | AMR | CLM | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01884 | hp1 | a0002 | c0002 | t0144 | g0255 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01884 | hp2 | a0001 | c0001 | t0092 | g0057 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01891 | hp1 | a0001 | c0001 | t0044 | g0246 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01891 | hp2 | a0003 | c0003 | t0005 | g0074 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01952 | hp1 | a0002 | c0002 | t0052 | g0006 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01952 | hp2 | a0001 | c0001 | t0054 | g0004 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01978 | hp2 | a0002 | c0002 | t0006 | g0176 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01981 | hp1 | a0002 | c0002 | t0006 | g0140 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01981 | hp2 | a0002 | c0002 | t0066 | g0088 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG01993 | hp2 | a0002 | c0002 | t0010 | g0151 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02004 | hp1 | a0002 | c0002 | t0010 | g0150 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02004 | hp2 | a0002 | c0002 | t0007 | g0105 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02040 | hp1 | a0003 | c0003 | t0005 | g0045 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02040 | hp2 | a0002 | c0002 | t0037 | g0206 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02055 | hp1 | a0004 | c0005 | t0100 | g0104 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02055 | hp2 | a0003 | c0003 | t0005 | g0081 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02074 | hp1 | a0001 | c0001 | t0124 | g0169 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02074 | hp2 | a0002 | c0002 | t0096 | g0111 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02132 | hp1 | a0002 | c0002 | t0010 | g0184 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02135 | hp1 | a0002 | c0002 | t0038 | g0180 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02135 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02145 | hp1 | a0001 | c0001 | t0088 | g0100 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02145 | hp2 | a0001 | c0001 | t0064 | g0096 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02148 | hp1 | a0002 | c0002 | t0010 | g0165 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02148 | hp2 | a0003 | c0003 | t0018 | g0166 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02257 | hp1 | a0003 | c0003 | t0005 | g0078 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02257 | hp2 | a0001 | c0001 | t0080 | g0103 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02258 | hp1 | a0002 | c0004 | t0065 | g0091 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02258 | hp2 | a0001 | c0001 | t0025 | g0099 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02280 | hp1 | a0001 | c0001 | t0079 | g0030 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02280 | hp2 | a0002 | c0002 | t0007 | g0142 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02300 | hp1 | a0002 | c0002 | t0039 | g0186 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02451 | hp1 | a0001 | c0001 | t0055 | g0009 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02451 | hp2 | a0002 | c0002 | t0067 | g0028 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02523 | hp1 | a0001 | c0001 | t0132 | g0174 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02523 | hp2 | a0002 | c0002 | t0118 | g0179 | EAS | KHV | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02602 | hp2 | a0003 | c0003 | t0018 | g0218 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02615 | hp1 | a0001 | c0001 | t0090 | g0054 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02615 | hp2 | a0001 | c0001 | t0060 | g0029 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02630 | hp1 | a0001 | c0001 | t0044 | g0247 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02630 | hp2 | a0002 | c0002 | t0013 | g0101 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02647 | hp1 | a0001 | c0001 | t0087 | g0098 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02647 | hp2 | a0001 | c0001 | t0063 | g0046 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02717 | hp1 | a0001 | c0001 | t0023 | g0052 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02717 | hp2 | a0002 | c0002 | t0015 | g0072 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02723 | hp1 | a0002 | c0002 | t0074 | g0051 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02723 | hp2 | a0001 | c0001 | t0142 | g0243 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02738 | hp1 | a0002 | c0002 | t0035 | g0234 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0084 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02809 | hp1 | a0002 | c0002 | t0030 | g0053 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02809 | hp2 | a0002 | c0002 | t0030 | g0075 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02886 | hp1 | a0002 | c0002 | t0013 | g0022 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02886 | hp2 | a0001 | c0001 | t0050 | g0008 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02895 | hp1 | a0001 | c0001 | t0143 | g0241 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02895 | hp2 | a0001 | c0001 | t0057 | g0017 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02896 | hp1 | a0002 | c0002 | t0028 | g0050 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02896 | hp2 | a0001 | c0001 | t0021 | g0250 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02897 | hp1 | a0002 | c0002 | t0028 | g0032 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0016 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02922 | hp1 | a0002 | c0002 | t0029 | g0058 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0248 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0073 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02965 | hp2 | a0001 | c0001 | t0024 | g0067 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02976 | hp1 | a0001 | c0001 | t0045 | g0245 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02976 | hp2 | a0001 | c0001 | t0058 | g0033 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03017 | hp1 | a0001 | c0001 | t0134 | g0187 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03017 | hp2 | a0002 | c0002 | t0111 | g0196 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03041 | hp1 | a0001 | c0001 | t0077 | g0080 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03041 | hp2 | a0001 | c0001 | t0139 | g0240 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03098 | hp1 | a0001 | c0001 | t0061 | g0049 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0077 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03130 | hp1 | a0001 | c0001 | t0025 | g0069 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03130 | hp2 | a0002 | c0002 | t0013 | g0060 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0019 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03139 | hp2 | a0001 | c0001 | t0045 | g0244 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03195 | hp1 | a0006 | c0008 | t0141 | g0251 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03195 | hp2 | a0001 | c0001 | t0049 | g0010 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03209 | hp1 | a0001 | c0001 | t0032 | g0025 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03209 | hp2 | a0002 | c0009 | t0140 | g0242 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03225 | hp1 | a0002 | c0002 | t0075 | g0062 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0023 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03453 | hp1 | a0001 | c0001 | t0062 | g0018 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03453 | hp2 | a0002 | c0002 | t0015 | g0048 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03486 | hp1 | a0001 | c0001 | t0081 | g0047 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03486 | hp2 | a0001 | c0001 | t0089 | g0014 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03491 | hp2 | a0002 | c0002 | t0007 | g0228 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03492 | hp1 | a0002 | c0002 | t0035 | g0236 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03492 | hp2 | a0002 | c0002 | t0020 | g0229 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03516 | hp1 | a0002 | c0002 | t0015 | g0031 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03516 | hp2 | a0002 | c0002 | t0014 | g0059 | AFR | ESN | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03540 | hp1 | a0001 | c0001 | t0138 | g0239 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03540 | hp2 | a0001 | c0001 | t0086 | g0071 | AFR | GWD | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03579 | hp1 | a0002 | c0002 | t0072 | g0061 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0161 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03688 | hp1 | a0002 | c0002 | t0097 | g0131 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03688 | hp2 | a0002 | c0002 | t0114 | g0204 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03710 | hp1 | a0002 | c0002 | t0095 | g0191 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03710 | hp2 | a0003 | c0003 | t0017 | g0223 | SAS | PJL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03927 | hp1 | a0002 | c0002 | t0101 | g0237 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03927 | hp2 | a0002 | c0002 | t0051 | g0011 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04115 | hp1 | a0001 | c0001 | t0083 | g0087 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04115 | hp2 | a0002 | c0002 | t0038 | g0224 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04184 | hp2 | a0001 | c0001 | t0127 | g0197 | SAS | BEB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04199 | hp2 | a0002 | c0002 | t0108 | g0182 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04204 | hp1 | a0002 | c0002 | t0008 | g0037 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0042 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04228 | hp1 | a0002 | c0002 | t0019 | g0160 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG04228 | hp2 | a0002 | c0002 | t0020 | g0181 | SAS | STU | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18522 | hp1 | a0001 | c0001 | t0048 | g0007 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18522 | hp2 | a0002 | c0002 | t0070 | g0035 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18747 | hp1 | a0002 | c0002 | t0109 | g0118 | EAS | CHB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18906 | hp1 | a0001 | c0001 | t0026 | g0097 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18906 | hp2 | a0002 | c0002 | t0014 | g0020 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18940 | hp1 | a0002 | c0002 | t0103 | g0146 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18940 | hp2 | a0001 | c0001 | t0123 | g0194 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18941 | hp1 | a0002 | c0002 | t0009 | g0162 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18941 | hp2 | a0002 | c0002 | t0116 | g0110 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18945 | hp2 | a0002 | c0002 | t0036 | g0147 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18951 | hp1 | a0002 | c0002 | t0047 | g0002 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18951 | hp2 | a0002 | c0002 | t0046 | g0003 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18952 | hp1 | a0001 | c0001 | t0084 | g0038 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18952 | hp2 | a0002 | c0002 | t0122 | g0133 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18956 | hp2 | a0001 | c0001 | t0011 | g0192 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18960 | hp1 | a0002 | c0002 | t0102 | g0138 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18960 | hp2 | a0001 | c0001 | t0136 | g0121 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18962 | hp1 | a0001 | c0001 | t0145 | g0254 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18962 | hp2 | a0001 | c0001 | t0147 | g0253 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18966 | hp1 | a0002 | c0002 | t0040 | g0173 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18968 | hp1 | a0002 | c0002 | t0053 | g0005 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18968 | hp2 | a0002 | c0002 | t0106 | g0222 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18971 | hp1 | a0002 | c0002 | t0040 | g0171 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18971 | hp2 | a0003 | c0003 | t0093 | g0137 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18984 | hp1 | a0002 | c0002 | t0119 | g0233 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18990 | hp2 | a0001 | c0001 | t0146 | g0252 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18995 | hp1 | a0001 | c0001 | t0043 | g0159 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA18995 | hp2 | a0001 | c0001 | t0126 | g0209 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19003 | hp1 | a0001 | c0001 | t0043 | g0141 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19006 | hp1 | a0001 | c0001 | t0137 | g0208 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19010 | hp1 | a0002 | c0002 | t0107 | g0148 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19010 | hp2 | a0001 | c0001 | t0125 | g0177 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19060 | hp2 | a0002 | c0002 | t0104 | g0227 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19068 | hp1 | a0002 | c0002 | t0117 | g0117 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19090 | hp1 | a0002 | c0002 | t0115 | g0199 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19240 | hp1 | a0001 | c0001 | t0082 | g0013 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA19240 | hp2 | a0001 | c0001 | t0026 | g0066 | AFR | YRI | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20129 | hp1 | a0001 | c0001 | t0023 | g0021 | AFR | ASW | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20129 | hp2 | a0001 | c0001 | t0041 | g0134 | AFR | ASW | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20905 | hp1 | a0001 | c0001 | t0131 | g0202 | SAS | GIH | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | GIH | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02109 | hp1 | a0003 | c0003 | t0018 | g0226 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02109 | hp2 | a0001 | c0001 | t0032 | g0068 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02486 | hp1 | a0002 | c0002 | t0027 | g0026 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02486 | hp2 | a0002 | c0002 | t0008 | g0095 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0249 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG02559 | hp2 | a0001 | c0001 | t0091 | g0055 | AFR | ACB | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03471 | hp1 | a0001 | c0001 | t0085 | g0102 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG03471 | hp2 | a0007 | c0007 | t0005 | g0024 | AFR | MSL | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG06807 | hp1 | a0001 | c0001 | t0078 | g0064 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20300 | hp1 | a0002 | c0002 | t0069 | g0056 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA20300 | hp2 | a0001 | c0001 | t0042 | g0107 | AFR | USA | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA21309 | hp1 | a0002 | c0002 | t0073 | g0063 | AFR | LWK | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | LWK | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0098 | g0149 | REF | REF | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0076 | REF | REF | CD226_chr18_69848274_69952873 | CD226 | chr18 | 69848274 | 69952873 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:69864406
|
T | C | 3 | a0002a0004a0005 | 108 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(105): Show |
missense_variant | MODERATE | c.919A>G | p.Ser307Gly | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1386/12518 | 919/1011 | 307/336 | chr18 | 69864406 | ||
chr18:69867406
|
C | T | 2 | a0003a0007 | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
missense_variant | MODERATE | c.836G>A | p.Arg279Lys | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/6 | 1303/12518 | 836/1011 | 279/336 | chr18 | 69867406 | ||
chr18:69895704
|
C | T | 1 | a0006 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.724G>A | p.Glu242Lys | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/6 | 1191/12518 | 724/1011 | 242/336 | chr18 | 69895704 | ||
chr18:69895746
|
C | T | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.682G>A | p.Ala228Thr | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/6 | 1149/12518 | 682/1011 | 228/336 | chr18 | 69895746 | ||
chr18:69895916
|
C | T | 1 | a0005 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.512G>A | p.Arg171His | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/6 | 979/12518 | 512/1011 | 171/336 | chr18 | 69895916 | ||
chr18:69946843
|
C | T | 1 | a0004 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.273G>A | p.Met91Ile | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/6 | 740/12518 | 273/1011 | 91/336 | chr18 | 69946843 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:69867396
|
C | T | 1 | a0002c0004 | 2 | HG01071.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.846G>A | p.Glu282Glu | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/6 | 1313/12518 | 846/1011 | 282/336 | chr18 | 69867396 | ||
chr18:69895747
|
G | A | 1 | a0002c0009 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.681C>T | p.Ser227Ser | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/6 | 1148/12518 | 681/1011 | 227/336 | chr18 | 69895747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:69853369
|
A | G | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0135 | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10945T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10945 | chr18 | 69853369 | |||||
chr18:69853615
|
C | A | 2 | a0001c0001t0087a0001c0001t0089 | 2 | HG02647.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10699G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10699 | chr18 | 69853615 | |||||
chr18:69853631
|
G | A | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10683C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10683 | chr18 | 69853631 | |||||
chr18:69853761
|
T | C | 3 | a0001c0001t0025a0001c0001t0050a0001c0001t0094 | 4 | HG01243.hp1 HG02258.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10553A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10553 | chr18 | 69853761 | |||||
chr18:69853828
|
C | T | 1 | a0001c0001t0060 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10486G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10486 | chr18 | 69853828 | |||||
chr18:69853951
|
G | A | 15 | a0001c0001t0021a0001c0001t0026a0001c0001t0041others(12): Show | 21 | HG01081.hp2 HG01361.hp2 HG01891.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*10363C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10363 | chr18 | 69853951 | |||||
chr18:69853995
|
T | G | 1 | a0002c0002t0096 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10319A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10319 | chr18 | 69853995 | |||||
chr18:69854035
|
C | A | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10279G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10279 | chr18 | 69854035 | |||||
chr18:69854112
|
G | GA | 142 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(139): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*10201_*10202insT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 10201 | chr18 | 69854112 | |||||
chr18:69854518
|
T | C | 2 | a0001c0001t0077a0006c0008t0141 | 2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9796A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 9796 | chr18 | 69854518 | |||||
chr18:69854798
|
C | T | 136 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(133): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*9516G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 9516 | chr18 | 69854798 | |||||
chr18:69855122
|
C | CA | 68 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(65): Show | 103 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*9191dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 9191 | chr18 | 69855122 | |||||
chr18:69855196
|
G | T | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9118C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 9118 | chr18 | 69855196 | |||||
chr18:69855211
|
C | T | 2 | a0001c0001t0077a0006c0008t0141 | 2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9103G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 9103 | chr18 | 69855211 | |||||
chr18:69855500
|
T | A | 2 | a0001c0001t0045a0001c0001t0086 | 3 | HG02976.hp1 HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8814A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8814 | chr18 | 69855500 | |||||
chr18:69855585
|
C | T | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*8729G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8729 | chr18 | 69855585 | |||||
chr18:69855648
|
G | C | 14 | a0001c0001t0021a0001c0001t0026a0001c0001t0041others(11): Show | 20 | HG01081.hp2 HG01361.hp2 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8666C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8666 | chr18 | 69855648 | |||||
chr18:69855681
|
C | T | 1 | a0001c0001t0132 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8633G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8633 | chr18 | 69855681 | |||||
chr18:69855684
|
C | A | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8630G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8630 | chr18 | 69855684 | |||||
chr18:69855740
|
G | GAAGT | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8573_*8574insACTT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8573 | chr18 | 69855740 | |||||
chr18:69855740
|
G | GGAGT | 136 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(133): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*8573_*8574insACTC | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8573 | chr18 | 69855740 | |||||
chr18:69855883
|
A | G | 1 | a0002c0002t0071 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8431T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8431 | chr18 | 69855883 | |||||
chr18:69855900
|
C | T | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8414G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8414 | chr18 | 69855900 | |||||
chr18:69855969
|
C | T | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8345G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8345 | chr18 | 69855969 | |||||
chr18:69856017
|
A | G | 3 | a0002c0002t0068a0002c0002t0104a0002c0002t0115 | 3 | HG00544.hp2 NA19060.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8297T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8297 | chr18 | 69856017 | |||||
chr18:69856021
|
G | A | 2 | a0001c0001t0077a0006c0008t0141 | 2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8293C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8293 | chr18 | 69856021 | |||||
chr18:69856024
|
A | G | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*8290T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8290 | chr18 | 69856024 | |||||
chr18:69856038
|
C | T | 3 | a0001c0001t0061a0001c0001t0063a0001c0001t0064 | 3 | HG02145.hp2 HG02647.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8276G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8276 | chr18 | 69856038 | |||||
chr18:69856139
|
A | T | 1 | a0002c0002t0114 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8175T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8175 | chr18 | 69856139 | |||||
chr18:69856217
|
T | C | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 93 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*8097A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8097 | chr18 | 69856217 | |||||
chr18:69856278
|
A | G | 1 | a0001c0001t0092 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8036T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 8036 | chr18 | 69856278 | |||||
chr18:69856510
|
T | C | 1 | a0001c0001t0143 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7804A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7804 | chr18 | 69856510 | |||||
chr18:69856707
|
A | T | 1 | a0001c0001t0085 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7607T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7607 | chr18 | 69856707 | |||||
chr18:69856727
|
C | G | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7587G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7587 | chr18 | 69856727 | |||||
chr18:69856758
|
T | C | 1 | a0001c0001t0127 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7556A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7556 | chr18 | 69856758 | |||||
chr18:69856894
|
C | T | 1 | a0002c0002t0108 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7420G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7420 | chr18 | 69856894 | |||||
chr18:69857047
|
A | T | 142 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(139): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*7267T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7267 | chr18 | 69857047 | |||||
chr18:69857120
|
G | A | 69 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(66): Show | 105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*7194C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7194 | chr18 | 69857120 | |||||
chr18:69857147
|
C | T | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*7167G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7167 | chr18 | 69857147 | |||||
chr18:69857168
|
CA | C | 3 | a0001c0001t0061a0001c0001t0063a0001c0001t0064 | 3 | HG02145.hp2 HG02647.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7145delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 7145 | chr18 | 69857168 | |||||
chr18:69857332
|
C | A | 2 | a0001c0001t0023a0001c0001t0062 | 3 | HG02717.hp1 HG03453.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6982G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6982 | chr18 | 69857332 | |||||
chr18:69857397
|
C | T | 2 | a0001c0001t0077a0006c0008t0141 | 2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6917G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6917 | chr18 | 69857397 | |||||
chr18:69857410
|
G | T | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*6904C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6904 | chr18 | 69857410 | |||||
chr18:69857737
|
T | C | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*6577A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6577 | chr18 | 69857737 | |||||
chr18:69857737
|
T | G | 1 | a0002c0002t0112 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6577A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6577 | chr18 | 69857737 | |||||
chr18:69857894
|
A | G | 8 | a0001c0001t0033a0001c0001t0055a0001c0001t0087others(5): Show | 9 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6420T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6420 | chr18 | 69857894 | |||||
chr18:69857991
|
G | T | 1 | a0002c0002t0102 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6323C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6323 | chr18 | 69857991 | |||||
chr18:69858050
|
T | G | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*6264A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 6264 | chr18 | 69858050 | |||||
chr18:69858340
|
T | C | 1 | a0001c0001t0081 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5974A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5974 | chr18 | 69858340 | |||||
chr18:69858618
|
C | A | 1 | a0001c0001t0064 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5696G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5696 | chr18 | 69858618 | |||||
chr18:69858621
|
C | T | 75 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(72): Show | 117 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*5693G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5693 | chr18 | 69858621 | |||||
chr18:69858718
|
C | CT | 10 | a0001c0001t0083a0001c0001t0084a0001c0001t0124others(7): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5595dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTT | 10 | a0001c0001t0055a0001c0001t0089a0001c0001t0092others(7): Show | 17 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5594_*5595dupAA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTT | 9 | a0001c0001t0060a0001c0001t0088a0001c0001t0135others(6): Show | 9 | HG01346.hp1 HG01884.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5593_*5595dupAAA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTTT | 27 | a0001c0001t0033a0002c0002t0006a0002c0002t0007others(24): Show | 45 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*5592_*5595dupAAAA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTTTT | 14 | a0001c0001t0087a0001c0001t0090a0002c0002t0009others(11): Show | 23 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5591_*5595dupAAAA others(1): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTTTTT | 9 | a0002c0002t0034a0002c0002t0038a0002c0002t0047others(6): Show | 10 | HG01071.hp2 HG01175.hp2 HG01361.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5590_*5595dupAAAA others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTTTTTT | 5 | a0002c0002t0027a0002c0002t0076a0002c0002t0096others(2): Show | 6 | HG00280.hp1 HG01081.hp2 HG01261.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5589_*5595dupAAAA others(3): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0098 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5583_*5595dupAAAA others(9): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
CT | C | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 55 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*5595delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5595 | chr18 | 69858718 | |||||
chr18:69858718
|
CTT | C | 8 | a0001c0001t0024a0001c0001t0058a0001c0001t0063others(5): Show | 9 | HG01069.hp1 HG01257.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5594_*5595delAA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5594 | chr18 | 69858718 | |||||
chr18:69858718
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0105 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5582_*5595delAAAA others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5582 | chr18 | 69858718 | |||||
chr18:69858735
|
T | C | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5579A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5579 | chr18 | 69858735 | |||||
chr18:69858786
|
G | C | 1 | a0001c0001t0079 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5528C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5528 | chr18 | 69858786 | |||||
chr18:69858790
|
T | C | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*5524A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5524 | chr18 | 69858790 | |||||
chr18:69858976
|
T | C | 142 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(139): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*5338A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5338 | chr18 | 69858976 | |||||
chr18:69859051
|
T | C | 3 | a0001c0001t0042a0001c0001t0129a0001c0001t0130 | 4 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5263A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5263 | chr18 | 69859051 | |||||
chr18:69859130
|
T | A | 1 | a0001c0001t0032 | 2 | HG02109.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5184A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5184 | chr18 | 69859130 | |||||
chr18:69859167
|
C | T | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5147G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 5147 | chr18 | 69859167 | |||||
chr18:69859408
|
T | C | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*4906A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4906 | chr18 | 69859408 | |||||
chr18:69859489
|
T | A | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*4825A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4825 | chr18 | 69859489 | |||||
chr18:69859573
|
G | GA | 64 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(61): Show | 94 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*4740dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4740 | chr18 | 69859573 | |||||
chr18:69859713
|
AC | A | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0137others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4600delG | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4600 | chr18 | 69859713 | |||||
chr18:69859714
|
C | A | 1 | a0001c0001t0136 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4600G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4600 | chr18 | 69859714 | |||||
chr18:69859720
|
C | A | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0137others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4594G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4594 | chr18 | 69859720 | |||||
chr18:69859722
|
A | C | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0137others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4592T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4592 | chr18 | 69859722 | |||||
chr18:69859724
|
C | A | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0137others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4590G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4590 | chr18 | 69859724 | |||||
chr18:69859728
|
C | A | 4 | a0001c0001t0004a0001c0001t0043a0001c0001t0137others(1): Show | 10 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4586G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4586 | chr18 | 69859728 | |||||
chr18:69859884
|
C | T | 8 | a0001c0001t0001a0001c0001t0031a0001c0001t0054others(5): Show | 24 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4430G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4430 | chr18 | 69859884 | |||||
chr18:69859898
|
C | A | 14 | a0001c0001t0033a0001c0001t0055a0001c0001t0087others(11): Show | 22 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4416G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4416 | chr18 | 69859898 | |||||
chr18:69859944
|
T | C | 1 | a0002c0002t0105 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4370A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4370 | chr18 | 69859944 | |||||
chr18:69859997
|
G | T | 38 | a0001c0001t0021a0001c0001t0023a0001c0001t0024others(35): Show | 53 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4317C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4317 | chr18 | 69859997 | |||||
chr18:69860079
|
AT | A | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0135 | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4234delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4234 | chr18 | 69860079 | |||||
chr18:69860278
|
A | ATC | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4035_*4036insGA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 4035 | chr18 | 69860278 | |||||
chr18:69860346
|
G | A | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0135 | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3968C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3968 | chr18 | 69860346 | |||||
chr18:69860373
|
A | G | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3941T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3941 | chr18 | 69860373 | |||||
chr18:69860391
|
C | T | 1 | a0002c0002t0028 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3923G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3923 | chr18 | 69860391 | |||||
chr18:69860392
|
G | A | 1 | a0002c0002t0075 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3922C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3922 | chr18 | 69860392 | |||||
chr18:69860463
|
G | C | 142 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(139): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*3851C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3851 | chr18 | 69860463 | |||||
chr18:69860465
|
T | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3849A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3849 | chr18 | 69860465 | |||||
chr18:69860524
|
T | G | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3790A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3790 | chr18 | 69860524 | |||||
chr18:69860560
|
T | C | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3754A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3754 | chr18 | 69860560 | |||||
chr18:69860593
|
A | G | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0135 | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3721T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3721 | chr18 | 69860593 | |||||
chr18:69860686
|
G | GA | 3 | a0001c0001t0026a0001c0001t0044a0001c0001t0082 | 5 | HG01891.hp1 HG02630.hp1 NA18906.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3627dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3627 | chr18 | 69860686 | |||||
chr18:69860915
|
A | T | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 72 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*3399T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3399 | chr18 | 69860915 | |||||
chr18:69861194
|
C | T | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3120G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3120 | chr18 | 69861194 | |||||
chr18:69861195
|
A | G | 142 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(139): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*3119T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 3119 | chr18 | 69861195 | |||||
chr18:69861373
|
C | A | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2941G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2941 | chr18 | 69861373 | |||||
chr18:69861383
|
T | G | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2931A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2931 | chr18 | 69861383 | |||||
chr18:69861542
|
GTATATAT others(7): Show |
G | 1 | a0001c0001t0022 | 2 | HG03139.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2758_*2771delTACA others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2758 | chr18 | 69861542 | |||||
chr18:69861552
|
A | ATATG | 6 | a0001c0001t0060a0001c0001t0061a0001c0001t0062others(3): Show | 6 | HG01346.hp2 HG02145.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2761_*2762insCATA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2761 | chr18 | 69861552 | |||||
chr18:69861554
|
G | A | 9 | a0001c0001t0023a0001c0001t0024a0001c0001t0049others(6): Show | 11 | HG01346.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2760C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2760 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATA | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 69 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2756_*2759dupTATA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATA | 3 | a0001c0001t0123a0001c0001t0132a0001c0001t0133 | 3 | HG00733.hp2 HG02523.hp1 NA18940.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2754_*2759dupTATA others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(5): Show |
1 | a0002c0002t0076 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2748_*2759dupTATA others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(7): Show |
6 | a0002c0002t0009a0002c0002t0034a0002c0002t0047others(3): Show | 9 | HG00738.hp2 HG01071.hp2 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2746_*2759dupTATA others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(9): Show |
19 | a0002c0002t0006a0002c0002t0010a0002c0002t0019others(16): Show | 28 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2744_*2759dupTATA others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(11): Show |
14 | a0002c0002t0007a0002c0002t0008a0002c0002t0013others(11): Show | 28 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2742_*2759dupTATA others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(13): Show |
7 | a0002c0002t0014a0002c0002t0028a0002c0002t0029others(4): Show | 13 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(16): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(15): Show |
4 | a0002c0002t0015a0002c0002t0110a0002c0002t0111others(1): Show | 6 | HG01257.hp1 HG01361.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(17): Show |
2 | a0002c0002t0072a0002c0002t0113 | 2 | HG01496.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(20): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTATATAT others(19): Show |
5 | a0002c0002t0073a0002c0002t0074a0002c0002t0075others(2): Show | 5 | HG02723.hp1 HG03225.hp1 HG03688.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTA | 12 | a0001c0001t0021a0001c0001t0026a0001c0001t0041others(9): Show | 17 | HG01361.hp2 HG01891.hp1 HG02074.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTACA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAC others(11): Show |
2 | a0002c0002t0116a0002c0002t0117 | 2 | NA18941.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAT others(9): Show |
1 | a0002c0002t0096 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAT others(11): Show |
3 | a0002c0002t0035a0002c0002t0036a0005c0006t0036 | 4 | HG00673.hp2 HG02738.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAT others(13): Show |
2 | a0002c0002t0037a0002c0002t0103 | 3 | HG00609.hp1 HG02040.hp2 NA18940.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(16): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAT others(15): Show |
2 | a0002c0002t0106a0002c0002t0107 | 2 | NA18968.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
G | GTGTATAT others(17): Show |
2 | a0002c0002t0071a0002c0002t0109 | 2 | HG01109.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insTATA others(20): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2759 | chr18 | 69861554 | |||||
chr18:69861554
|
GTA | G | 17 | a0001c0001t0004a0001c0001t0033a0001c0001t0055others(14): Show | 30 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2758_*2759delTA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2758 | chr18 | 69861554 | |||||
chr18:69861556
|
A | G | 3 | a0001c0001t0023a0001c0001t0024a0001c0001t0049 | 5 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2758T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2758 | chr18 | 69861556 | |||||
chr18:69861558
|
A | G | 1 | a0001c0001t0048 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2756T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2756 | chr18 | 69861558 | |||||
chr18:69861594
|
T | G | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0135 | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2720A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2720 | chr18 | 69861594 | |||||
chr18:69861640
|
A | G | 1 | a0001c0001t0048 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2674T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2674 | chr18 | 69861640 | |||||
chr18:69861717
|
T | A | 8 | a0002c0002t0010a0002c0002t0040a0002c0002t0047others(5): Show | 12 | HG01952.hp1 HG01993.hp2 HG02004.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2597A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2597 | chr18 | 69861717 | |||||
chr18:69861778
|
A | G | 124 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(121): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*2536T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2536 | chr18 | 69861778 | |||||
chr18:69861981
|
G | A | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2333C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2333 | chr18 | 69861981 | |||||
chr18:69862069
|
T | TC | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2244dupG | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2244 | chr18 | 69862069 | |||||
chr18:69862247
|
G | A | 2 | a0002c0002t0120a0002c0002t0121 | 2 | HG00733.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2067C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2067 | chr18 | 69862247 | |||||
chr18:69862257
|
T | A | 1 | a0002c0002t0122 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2057A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 2057 | chr18 | 69862257 | |||||
chr18:69862565
|
C | T | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1749 | chr18 | 69862565 | |||||
chr18:69862625
|
C | T | 1 | a0001c0001t0123 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1689G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1689 | chr18 | 69862625 | |||||
chr18:69862728
|
TACTC | T | 70 | a0002c0002t0006a0002c0002t0007a0002c0002t0008others(67): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1582_*1585delGAGT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1582 | chr18 | 69862728 | |||||
chr18:69862861
|
A | G | 2 | a0001c0001t0055a0001c0001t0092 | 2 | HG01884.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1453T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1453 | chr18 | 69862861 | |||||
chr18:69862902
|
A | G | 1 | a0002c0002t0095 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1412T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1412 | chr18 | 69862902 | |||||
chr18:69862959
|
C | T | 8 | a0001c0001t0033a0001c0001t0055a0001c0001t0087others(5): Show | 9 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1355 | chr18 | 69862959 | |||||
chr18:69862991
|
C | A | 1 | a0002c0002t0076 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1323G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1323 | chr18 | 69862991 | |||||
chr18:69863175
|
T | C | 1 | a0002c0002t0053 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1139A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1139 | chr18 | 69863175 | |||||
chr18:69863203
|
G | A | 75 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(72): Show | 117 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1111 | chr18 | 69863203 | |||||
chr18:69863242
|
T | C | 1 | a0001c0001t0134 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 1072 | chr18 | 69863242 | |||||
chr18:69863375
|
C | G | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 939 | chr18 | 69863375 | |||||
chr18:69863416
|
G | A | 1 | a0001c0001t0044 | 2 | HG01891.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*898C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 898 | chr18 | 69863416 | |||||
chr18:69863546
|
T | C | 2 | a0001c0001t0077a0006c0008t0141 | 2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*768A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 768 | chr18 | 69863546 | |||||
chr18:69863560
|
G | A | 8 | a0001c0001t0033a0001c0001t0055a0001c0001t0087others(5): Show | 9 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*754C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 754 | chr18 | 69863560 | |||||
chr18:69863700
|
C | A | 1 | a0001c0001t0091 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*614G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 614 | chr18 | 69863700 | |||||
chr18:69863790
|
C | A | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 524 | chr18 | 69863790 | |||||
chr18:69863922
|
G | A | 2 | a0001c0001t0055a0001c0001t0092 | 2 | HG01884.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 392 | chr18 | 69863922 | |||||
chr18:69864269
|
G | C | 5 | a0001c0001t0004a0001c0001t0043a0001c0001t0136others(2): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*45C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 6/6 | 45 | chr18 | 69864269 | |||||
chr18:69947438
|
T | TA | 82 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(79): Show | 149 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(146): Show |
5_prime_UTR_variant | MODIFIER | c.-33dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/6 | 33 | chr18 | 69947438 | |||||
chr18:69947744
|
C | CA | 13 | a0001c0001t0021a0001c0001t0044a0001c0001t0045others(10): Show | 17 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-339dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/6 | 339 | chr18 | 69947744 | |||||
chr18:69947744
|
CA | C | 10 | a0001c0001t0048a0001c0001t0049a0001c0001t0050others(7): Show | 10 | HG01952.hp1 HG01952.hp2 HG02451.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-339delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/6 | 339 | chr18 | 69947744 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:69864531
|
A | C | 1 | a0001c0001t0125g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.886-92T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69864531 | ||||||
chr18:69864561
|
A | G | 99 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.886-122T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69864561 | ||||||
chr18:69864659
|
T | A | 117 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(114): Show | 118 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.886-220A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69864659 | ||||||
chr18:69864666
|
T | C | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.886-227A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69864666 | ||||||
chr18:69865054
|
G | A | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.886-615C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865054 | ||||||
chr18:69865056
|
A | G | 106 | a0002c0002t0006g0140a0002c0002t0006g0176a0002c0002t0006g0217others(103): Show | 107 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.886-617T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865056 | ||||||
chr18:69865069
|
T | C | 3 | a0001c0001t0087g0098a0001c0001t0088g0100a0001c0001t0089g0014 | 3 | HG02145.hp1 HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.886-630A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865069 | ||||||
chr18:69865097
|
A | G | 2 | a0001c0001t0077g0080a0006c0008t0141g0251 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.886-658T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865097 | ||||||
chr18:69865233
|
G | A | 3 | a0001c0001t0033g0083a0001c0001t0090g0054a0001c0001t0135g0158 | 3 | HG00099.hp1 HG01346.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.886-794C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865233 | ||||||
chr18:69865254
|
T | A | 1 | a0002c0002t0113g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.886-815A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865254 | ||||||
chr18:69865310
|
A | G | 99 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.886-871T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865310 | ||||||
chr18:69865431
|
T | TTCAAAAT others(2447): Show |
1 | a0001c0001t0004g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.886-993_886-992ins others(2454): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865431 | ||||||
chr18:69865431
|
T | TTCAAAAT others(2448): Show |
9 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0230others(6): Show | 9 | HG00438.hp1 HG00609.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.886-993_886-992ins others(2455): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865431 | ||||||
chr18:69865431
|
T | TTCAAAAT others(2448): Show |
1 | a0001c0001t0137g0208 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.886-993_886-992ins others(2455): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865431 | ||||||
chr18:69865514
|
CACA | C | 11 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.886-1078_886-1076d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865514 | ||||||
chr18:69865532
|
TA | T | 19 | a0002c0002t0013g0022a0002c0002t0013g0060a0002c0002t0013g0101others(16): Show | 19 | HG01255.hp2 HG01346.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.886-1094delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865532 | ||||||
chr18:69865597
|
G | A | 1 | a0001c0001t0077g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.886-1158C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865597 | ||||||
chr18:69865633
|
T | C | 4 | a0002c0002t0009g0001a0002c0002t0009g0126a0002c0002t0034g0128others(1): Show | 5 | HG00738.hp2 HG01175.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.886-1194A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865633 | ||||||
chr18:69865653
|
C | G | 4 | a0001c0001t0033g0082a0001c0001t0033g0083a0001c0001t0090g0054others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.886-1214G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865653 | ||||||
chr18:69865680
|
T | C | 11 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.886-1241A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865680 | ||||||
chr18:69865838
|
G | A | 216 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.886-1399C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69865838 | ||||||
chr18:69866018
|
GA | G | 178 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(175): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.885+1338delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866018 | ||||||
chr18:69866096
|
T | C | 56 | a0002c0002t0006g0140a0002c0002t0006g0176a0002c0002t0006g0217others(53): Show | 57 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.885+1261A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866096 | ||||||
chr18:69866158
|
C | T | 5 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(2): Show | 5 | HG01891.hp1 HG02630.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.885+1199G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866158 | ||||||
chr18:69866164
|
C | T | 116 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(113): Show | 117 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.885+1193G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866164 | ||||||
chr18:69866334
|
GAAGTA | G | 11 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.885+1018_885+1022d others(7): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866334 | ||||||
chr18:69866474
|
C | T | 1 | a0001c0001t0079g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.885+883G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866474 | ||||||
chr18:69866592
|
C | T | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.885+765G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866592 | ||||||
chr18:69866725
|
T | G | 119 | a0001c0001t0001g0212a0001c0001t0004g0113a0001c0001t0004g0116others(116): Show | 120 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.885+632A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866725 | ||||||
chr18:69866780
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.885+577C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69866780 | ||||||
chr18:69867121
|
G | A | 1 | a0002c0002t0029g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.885+236C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 5/5 | chr18 | 69867121 | ||||||
chr18:69867472
|
G | A | 4 | a0001c0001t0033g0082a0001c0001t0033g0083a0001c0001t0090g0054others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-61C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867472 | ||||||
chr18:69867474
|
A | G | 17 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(14): Show | 17 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.831-63T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867474 | ||||||
chr18:69867516
|
T | C | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.831-105A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867516 | ||||||
chr18:69867547
|
T | A | 1 | a0001c0001t0055g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.831-136A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867547 | ||||||
chr18:69867698
|
T | C | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.831-287A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867698 | ||||||
chr18:69867766
|
A | C | 22 | a0001c0001t0139g0240a0002c0002t0008g0095a0002c0002t0013g0022others(19): Show | 22 | HG01255.hp2 HG01346.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.831-355T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867766 | ||||||
chr18:69867815
|
T | TTA | 22 | a0001c0001t0139g0240a0002c0002t0008g0095a0002c0002t0013g0022others(19): Show | 22 | HG01255.hp2 HG01346.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.831-406_831-405dup others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867815 | ||||||
chr18:69867850
|
G | A | 3 | a0001c0001t0080g0103a0001c0001t0085g0102a0003c0003t0005g0045 | 3 | HG02040.hp1 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831-439C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867850 | ||||||
chr18:69867948
|
T | C | 151 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.831-537A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69867948 | ||||||
chr18:69868073
|
G | A | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.831-662C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868073 | ||||||
chr18:69868776
|
T | C | 22 | a0001c0001t0139g0240a0002c0002t0008g0095a0002c0002t0013g0022others(19): Show | 22 | HG01255.hp2 HG01346.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.831-1365A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868776 | ||||||
chr18:69868787
|
A | T | 1 | a0002c0002t0030g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.831-1376T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868787 | ||||||
chr18:69868796
|
C | T | 1 | a0001c0001t0016g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.831-1385G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868796 | ||||||
chr18:69868803
|
G | GCA | 37 | a0001c0001t0002g0211a0001c0001t0003g0093a0001c0001t0004g0113others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.831-1394_831-1393d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868803 | ||||||
chr18:69868803
|
G | GCACA | 103 | a0001c0001t0016g0077a0001c0001t0041g0129a0001c0001t0041g0134others(100): Show | 104 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.831-1396_831-1393d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868803 | ||||||
chr18:69868803
|
G | GCACACA | 67 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(64): Show | 67 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.831-1398_831-1393d others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868803 | ||||||
chr18:69868803
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0016g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.831-1402_831-1393d others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868803 | ||||||
chr18:69868803
|
GCA | G | 7 | a0001c0001t0033g0082a0001c0001t0033g0083a0001c0001t0081g0047others(4): Show | 7 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.831-1394_831-1393d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868803 | ||||||
chr18:69868807
|
A | G | 4 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0064g0096others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-1396T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868807 | ||||||
chr18:69868883
|
G | T | 2 | a0001c0001t0080g0103a0001c0001t0085g0102 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831-1472C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868883 | ||||||
chr18:69868951
|
T | G | 23 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(20): Show | 23 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.831-1540A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69868951 | ||||||
chr18:69869142
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.831-1731G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869142 | ||||||
chr18:69869238
|
G | T | 4 | a0003c0003t0017g0221a0003c0003t0018g0166a0003c0003t0018g0218others(1): Show | 4 | HG01106.hp2 HG02148.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1827C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869238 | ||||||
chr18:69869260
|
C | T | 82 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0176others(79): Show | 83 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.831-1849G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869260 | ||||||
chr18:69869306
|
T | C | 4 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0086g0071others(1): Show | 4 | HG02976.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1895A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869306 | ||||||
chr18:69869333
|
A | G | 23 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(20): Show | 23 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.831-1922T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869333 | ||||||
chr18:69869381
|
T | C | 118 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.831-1970A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869381 | ||||||
chr18:69869470
|
A | G | 1 | a0002c0002t0102g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.831-2059T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869470 | ||||||
chr18:69869731
|
C | T | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.831-2320G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869731 | ||||||
chr18:69869799
|
C | CT | 21 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(18): Show | 21 | HG00438.hp1 HG00609.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.831-2389dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869799 | ||||||
chr18:69869799
|
CT | C | 64 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.831-2389delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869799 | ||||||
chr18:69869802
|
T | TC | 4 | a0001c0001t0023g0021a0001c0001t0023g0052a0001c0001t0060g0029others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-2392_831-2391i others(3): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869802 | ||||||
chr18:69869803
|
T | C | 3 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0086g0071 | 3 | HG02976.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.831-2392A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869803 | ||||||
chr18:69869804
|
T | C | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.831-2393A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869804 | ||||||
chr18:69869925
|
T | A | 2 | a0001c0001t0045g0244a0001c0001t0045g0245 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.831-2514A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869925 | ||||||
chr18:69869975
|
T | G | 3 | a0002c0002t0019g0160a0002c0002t0038g0224a0002c0002t0112g0119 | 3 | HG01257.hp1 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.831-2564A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69869975 | ||||||
chr18:69870034
|
C | A | 108 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.831-2623G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870034 | ||||||
chr18:69870050
|
C | T | 3 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0086g0071 | 3 | HG02976.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.831-2639G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870050 | ||||||
chr18:69870100
|
C | G | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.831-2689G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870100 | ||||||
chr18:69870109
|
T | A | 1 | a0001c0001t0016g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.831-2698A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870109 | ||||||
chr18:69870115
|
T | C | 82 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0176others(79): Show | 83 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.831-2704A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870115 | ||||||
chr18:69870267
|
T | TC | 21 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(18): Show | 21 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.831-2857dupG | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870267 | ||||||
chr18:69870272
|
C | CT | 71 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.831-2862dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870272 | ||||||
chr18:69870272
|
C | CTT | 9 | a0001c0001t0002g0211a0001c0001t0003g0093a0001c0001t0011g0192others(6): Show | 9 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.831-2863_831-2862d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870272 | ||||||
chr18:69870272
|
CT | C | 13 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(10): Show | 13 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.831-2862delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870272 | ||||||
chr18:69870273
|
T | C | 6 | a0001c0001t0024g0067a0001c0001t0024g0073a0001c0001t0049g0010others(3): Show | 7 | HG00738.hp2 HG01175.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.831-2862A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870273 | ||||||
chr18:69870274
|
T | C | 11 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.831-2863A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870274 | ||||||
chr18:69870387
|
G | A | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.830+2757C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870387 | ||||||
chr18:69870567
|
G | C | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.830+2577C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870567 | ||||||
chr18:69870631
|
C | A | 2 | a0001c0001t0002g0188a0001c0001t0128g0189 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.830+2513G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870631 | ||||||
chr18:69870638
|
G | A | 22 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(19): Show | 22 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.830+2506C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870638 | ||||||
chr18:69870849
|
G | A | 3 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0077g0080 | 3 | HG02647.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.830+2295C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870849 | ||||||
chr18:69870955
|
G | C | 6 | a0002c0002t0006g0176a0002c0002t0019g0175a0002c0002t0066g0088others(3): Show | 6 | HG00733.hp1 HG01175.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+2189C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69870955 | ||||||
chr18:69871111
|
C | T | 1 | a0001c0001t0135g0158 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.830+2033G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871111 | ||||||
chr18:69871113
|
A | G | 1 | a0002c0002t0101g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.830+2031T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871113 | ||||||
chr18:69871345
|
G | A | 1 | a0001c0001t0083g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.830+1799C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871345 | ||||||
chr18:69871453
|
G | A | 242 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.830+1691C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871453 | ||||||
chr18:69871588
|
A | G | 159 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.830+1556T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871588 | ||||||
chr18:69871624
|
T | A | 105 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.830+1520A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871624 | ||||||
chr18:69871681
|
T | C | 3 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.830+1463A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871681 | ||||||
chr18:69871742
|
C | T | 1 | a0001c0001t0089g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.830+1402G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871742 | ||||||
chr18:69871827
|
T | G | 1 | a0002c0002t0007g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.830+1317A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69871827 | ||||||
chr18:69872027
|
G | A | 6 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+1117C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872027 | ||||||
chr18:69872054
|
A | ATGTGTGT others(9): Show |
1 | a0002c0002t0007g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.830+1089_830+1090i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872054 | ||||||
chr18:69872055
|
G | T | 1 | a0002c0002t0007g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.830+1089C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872055 | ||||||
chr18:69872057
|
G | GGT | 65 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(62): Show | 65 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.830+1085_830+1086d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGT | 29 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(26): Show | 30 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.830+1083_830+1086d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGT | 63 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0132others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.830+1081_830+1086d others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(1): Show |
15 | a0001c0001t0001g0207a0001c0001t0002g0188a0001c0001t0002g0216others(12): Show | 15 | HG00099.hp1 HG00639.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.830+1079_830+1086d others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(3): Show |
17 | a0001c0001t0001g0170a0001c0001t0002g0168a0001c0001t0021g0248others(14): Show | 17 | HG00621.hp2 HG01069.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.830+1077_830+1086d others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(5): Show |
16 | a0001c0001t0002g0198a0001c0001t0032g0025a0001c0001t0064g0096others(13): Show | 16 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.830+1075_830+1086d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(7): Show |
2 | a0002c0002t0014g0059a0002c0002t0069g0056 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.830+1073_830+1086d others(16): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.830+1069_830+1086d others(20): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GGTGTGTG others(13): Show |
1 | a0002c0002t0010g0150 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.830+1067_830+1086d others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GTGT | 3 | a0002c0002t0106g0222a0002c0002t0113g0130a0002c0002t0118g0179 | 3 | HG01496.hp2 HG02523.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.830+1086_830+1087i others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GTGTGTGT | 4 | a0001c0001t0002g0213a0001c0001t0031g0042a0001c0001t0042g0108others(1): Show | 4 | HG01069.hp2 HG01358.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.830+1086_830+1087i others(9): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | GTGTGTGT others(6): Show |
2 | a0001c0001t0002g0195a0002c0002t0013g0060 | 2 | HG01168.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.830+1086_830+1087i others(15): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
G | T | 1 | a0002c0002t0007g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.830+1087C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
GGT | G | 3 | a0002c0002t0006g0219a0002c0002t0019g0215a0002c0002t0108g0182 | 3 | HG00735.hp2 HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.830+1085_830+1086d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872057
|
GGTGTGT | G | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.830+1081_830+1086d others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872057 | ||||||
chr18:69872091
|
G | T | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01361.hp2 HG02074.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.830+1053C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872091 | ||||||
chr18:69872093
|
G | A | 2 | a0001c0001t0002g0188a0001c0001t0128g0189 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.830+1051C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872093 | ||||||
chr18:69872156
|
T | C | 82 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0176others(79): Show | 83 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.830+988A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872156 | ||||||
chr18:69872409
|
G | GTT | 41 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(38): Show | 41 | HG01255.hp2 HG01346.hp2 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.830+733_830+734dup others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872409 | ||||||
chr18:69872436
|
T | C | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.830+708A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872436 | ||||||
chr18:69872652
|
A | G | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.830+492T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872652 | ||||||
chr18:69872681
|
T | C | 1 | a0002c0002t0067g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.830+463A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69872681 | ||||||
chr18:69873132
|
T | G | 44 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(41): Show | 44 | HG01255.hp2 HG01346.hp2 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.830+12A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 4/5 | chr18 | 69873132 | ||||||
chr18:69873286
|
G | A | 4 | a0001c0001t0078g0064a0001c0001t0081g0047a0001c0001t0142g0243others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-40C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69873286 | ||||||
chr18:69873487
|
A | G | 159 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.728-241T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69873487 | ||||||
chr18:69873811
|
C | T | 2 | a0001c0001t0055g0009a0001c0001t0092g0057 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.728-565G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69873811 | ||||||
chr18:69873955
|
C | T | 242 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.728-709G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69873955 | ||||||
chr18:69874026
|
G | GA | 26 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0064g0096others(23): Show | 26 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.728-781dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874026 | ||||||
chr18:69874082
|
C | G | 23 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(20): Show | 23 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.728-836G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874082 | ||||||
chr18:69874203
|
G | A | 3 | a0002c0002t0006g0140a0002c0002t0007g0153a0002c0002t0020g0152 | 3 | HG01261.hp2 HG01433.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.728-957C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874203 | ||||||
chr18:69874352
|
T | C | 39 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0064g0096others(36): Show | 39 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.728-1106A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874352 | ||||||
chr18:69874389
|
G | C | 23 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(20): Show | 23 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.728-1143C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874389 | ||||||
chr18:69874397
|
C | T | 23 | a0001c0001t0064g0096a0001c0001t0139g0240a0002c0002t0008g0095others(20): Show | 23 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.728-1151G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874397 | ||||||
chr18:69874581
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.728-1335C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874581 | ||||||
chr18:69874759
|
CAAAT | C | 4 | a0003c0003t0017g0221a0003c0003t0018g0166a0003c0003t0018g0218others(1): Show | 4 | HG01106.hp2 HG02148.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-1517_728-1514d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874759 | ||||||
chr18:69874829
|
T | G | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-1583A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874829 | ||||||
chr18:69874884
|
C | G | 3 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086 | 3 | HG00738.hp1 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.728-1638G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69874884 | ||||||
chr18:69875046
|
G | A | 3 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0077g0080 | 3 | HG02647.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.728-1800C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875046 | ||||||
chr18:69875121
|
C | T | 241 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.728-1875G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875121 | ||||||
chr18:69875152
|
T | C | 1 | a0002c0002t0059g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.728-1906A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875152 | ||||||
chr18:69875234
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.728-1988C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875234 | ||||||
chr18:69875296
|
C | T | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-2050G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875296 | ||||||
chr18:69875483
|
T | C | 1 | a0002c0002t0109g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.728-2237A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875483 | ||||||
chr18:69875562
|
C | T | 157 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.728-2316G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875562 | ||||||
chr18:69875563
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.728-2317G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875563 | ||||||
chr18:69875668
|
A | G | 1 | a0002c0002t0096g0111 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.728-2422T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875668 | ||||||
chr18:69875778
|
G | T | 1 | a0002c0002t0034g0128 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.728-2532C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875778 | ||||||
chr18:69875911
|
G | T | 142 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.728-2665C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875911 | ||||||
chr18:69875929
|
G | A | 1 | a0002c0002t0108g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.728-2683C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69875929 | ||||||
chr18:69876027
|
T | C | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-2781A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876027 | ||||||
chr18:69876047
|
T | C | 3 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0077g0080 | 3 | HG02647.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.728-2801A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876047 | ||||||
chr18:69876161
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.728-2915C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876161 | ||||||
chr18:69876368
|
C | T | 3 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0086g0071 | 3 | HG02976.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.728-3122G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876368 | ||||||
chr18:69876452
|
C | T | 158 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.728-3206G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876452 | ||||||
chr18:69876550
|
G | C | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.728-3304C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876550 | ||||||
chr18:69876590
|
A | G | 13 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(10): Show | 13 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-3344T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876590 | ||||||
chr18:69876597
|
A | C | 11 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.728-3351T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876597 | ||||||
chr18:69876619
|
C | G | 1 | a0002c0002t0102g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.728-3373G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876619 | ||||||
chr18:69876714
|
G | A | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.728-3468C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876714 | ||||||
chr18:69876797
|
C | A | 16 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0077g0080others(13): Show | 16 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.728-3551G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876797 | ||||||
chr18:69876810
|
T | C | 130 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.728-3564A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876810 | ||||||
chr18:69876855
|
CT | C | 15 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0123others(12): Show | 15 | HG00438.hp1 HG00609.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.728-3610delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876855 | ||||||
chr18:69876855
|
CTT | C | 45 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0002g0139others(42): Show | 45 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.728-3611_728-3610d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876855 | ||||||
chr18:69876855
|
CTTT | C | 90 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0125others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.728-3612_728-3610d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876855 | ||||||
chr18:69876855
|
CTTTT | C | 89 | a0001c0001t0002g0154a0001c0001t0134g0187a0002c0002t0006g0140others(86): Show | 90 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.728-3613_728-3610d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876855 | ||||||
chr18:69876937
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.728-3691G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876937 | ||||||
chr18:69876959
|
G | A | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.728-3713C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69876959 | ||||||
chr18:69877008
|
C | T | 1 | a0001c0001t0129g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.728-3762G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877008 | ||||||
chr18:69877020
|
C | T | 63 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(60): Show | 63 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.728-3774G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877020 | ||||||
chr18:69877053
|
G | A | 21 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0002g0168others(18): Show | 21 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.728-3807C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877053 | ||||||
chr18:69877084
|
G | A | 2 | a0001c0001t0024g0073a0001c0001t0049g0010 | 2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.728-3838C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877084 | ||||||
chr18:69877115
|
C | T | 2 | a0002c0002t0030g0053a0002c0002t0070g0035 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.728-3869G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877115 | ||||||
chr18:69877191
|
G | T | 1 | a0002c0002t0008g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.728-3945C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877191 | ||||||
chr18:69877294
|
A | G | 1 | a0002c0002t0095g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.728-4048T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877294 | ||||||
chr18:69877401
|
T | A | 67 | a0001c0001t0004g0116a0002c0002t0006g0140a0002c0002t0006g0217others(64): Show | 68 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.728-4155A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877401 | ||||||
chr18:69877481
|
C | T | 71 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(68): Show | 71 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.728-4235G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877481 | ||||||
chr18:69877496
|
A | G | 17 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(14): Show | 17 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-4250T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877496 | ||||||
chr18:69877559
|
G | A | 1 | a0001c0001t0026g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.728-4313C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877559 | ||||||
chr18:69877661
|
G | A | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-4415C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877661 | ||||||
chr18:69877744
|
T | C | 1 | a0001c0001t0023g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.728-4498A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877744 | ||||||
chr18:69877765
|
G | A | 1 | a0002c0002t0072g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.728-4519C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877765 | ||||||
chr18:69877861
|
G | A | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.728-4615C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69877861 | ||||||
chr18:69878032
|
T | C | 1 | a0002c0002t0007g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.728-4786A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878032 | ||||||
chr18:69878044
|
G | A | 88 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.728-4798C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878044 | ||||||
chr18:69878056
|
G | A | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-4810C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878056 | ||||||
chr18:69878063
|
T | A | 15 | a0001c0001t0023g0021a0001c0001t0033g0082a0001c0001t0033g0083others(12): Show | 15 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.728-4817A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878063 | ||||||
chr18:69878175
|
T | C | 1 | a0001c0001t0084g0038 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.728-4929A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878175 | ||||||
chr18:69878239
|
T | C | 1 | a0001c0001t0016g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.728-4993A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878239 | ||||||
chr18:69878262
|
G | A | 76 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0217others(73): Show | 77 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.728-5016C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878262 | ||||||
chr18:69878288
|
A | ACTTTT | 128 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.728-5043_728-5042i others(7): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878288 | ||||||
chr18:69878300
|
A | G | 50 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(47): Show | 50 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.728-5054T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878300 | ||||||
chr18:69878511
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0183 | 2 | NA19003.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.728-5265A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878511 | ||||||
chr18:69878742
|
C | T | 74 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.728-5496G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878742 | ||||||
chr18:69878779
|
C | T | 10 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0170others(7): Show | 10 | HG00621.hp2 HG01109.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.728-5533G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878779 | ||||||
chr18:69878853
|
C | T | 1 | a0002c0002t0071g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.728-5607G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878853 | ||||||
chr18:69878854
|
G | A | 76 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0217others(73): Show | 77 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.728-5608C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878854 | ||||||
chr18:69878916
|
G | A | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-5670C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878916 | ||||||
chr18:69878949
|
A | G | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.728-5703T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69878949 | ||||||
chr18:69879140
|
C | T | 89 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.728-5894G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879140 | ||||||
chr18:69879163
|
T | C | 3 | a0002c0002t0027g0026a0002c0002t0027g0027a0002c0002t0067g0028 | 3 | HG01081.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.728-5917A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879163 | ||||||
chr18:69879367
|
T | C | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-6121A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879367 | ||||||
chr18:69879374
|
G | A | 2 | a0002c0002t0116g0110a0002c0002t0117g0117 | 2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.728-6128C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879374 | ||||||
chr18:69879433
|
T | G | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-6187A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879433 | ||||||
chr18:69879453
|
C | T | 15 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0002g0168others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.728-6207G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879453 | ||||||
chr18:69879454
|
G | A | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-6208C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879454 | ||||||
chr18:69879549
|
T | C | 128 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.728-6303A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879549 | ||||||
chr18:69879552
|
G | GA | 128 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.728-6307dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879552 | ||||||
chr18:69879583
|
C | T | 1 | a0001c0001t0133g0220 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.728-6337G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879583 | ||||||
chr18:69879595
|
T | C | 40 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.728-6349A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879595 | ||||||
chr18:69879603
|
A | G | 21 | a0001c0001t0064g0096a0001c0001t0079g0030a0001c0001t0139g0240others(18): Show | 21 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.728-6357T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879603 | ||||||
chr18:69879606
|
T | C | 128 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.728-6360A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879606 | ||||||
chr18:69879634
|
T | G | 1 | a0002c0002t0010g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.728-6388A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879634 | ||||||
chr18:69879743
|
C | T | 88 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.728-6497G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879743 | ||||||
chr18:69879805
|
C | A | 1 | a0001c0001t0145g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.728-6559G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69879805 | ||||||
chr18:69880024
|
T | A | 4 | a0001c0001t0062g0018a0001c0001t0078g0064a0001c0001t0142g0243others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-6778A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880024 | ||||||
chr18:69880033
|
G | A | 1 | a0002c0002t0030g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.728-6787C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880033 | ||||||
chr18:69880178
|
T | G | 242 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.728-6932A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880178 | ||||||
chr18:69880203
|
AAGGC | A | 132 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.728-6961_728-6958d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880203 | ||||||
chr18:69880256
|
C | T | 2 | a0001c0001t0032g0025a0001c0001t0032g0068 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.728-7010G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880256 | ||||||
chr18:69880257
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.728-7011C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880257 | ||||||
chr18:69880270
|
G | A | 1 | a0002c0002t0006g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.728-7024C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880270 | ||||||
chr18:69880272
|
GAGGGA | G | 17 | a0001c0001t0064g0096a0001c0001t0079g0030a0001c0001t0139g0240others(14): Show | 17 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-7031_728-7027d others(7): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880272 | ||||||
chr18:69880328
|
GAGAGAAA others(3): Show |
G | 1 | a0001c0001t0094g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.728-7092_728-7083d others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880328 | ||||||
chr18:69880330
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.728-7084C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
G | GAA | 5 | a0001c0001t0139g0240a0002c0002t0051g0011a0002c0002t0059g0070others(2): Show | 5 | HG01346.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-7085_728-7084i others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
G | GAAAGAA | 12 | a0001c0001t0064g0096a0001c0001t0079g0030a0002c0002t0008g0095others(9): Show | 12 | HG01255.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-7085_728-7084i others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
GAGAA | G | 19 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0045g0244others(16): Show | 19 | HG00733.hp1 HG01175.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.728-7088_728-7085d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
GAGAAAGA others(1): Show |
G | 8 | a0001c0001t0024g0067a0001c0001t0024g0073a0001c0001t0044g0246others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.728-7092_728-7085d others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
GAGAAAGA others(5): Show |
G | 12 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(9): Show | 12 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.728-7096_728-7085d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880330
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0147g0253 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.728-7100_728-7085d others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880330 | ||||||
chr18:69880349
|
A | AAAGG | 56 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(53): Show | 56 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.728-7104_728-7103i others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880349 | ||||||
chr18:69880349
|
A | AAAGGAAG others(1): Show |
7 | a0001c0001t0001g0212a0001c0001t0002g0168a0001c0001t0032g0025others(4): Show | 7 | HG02109.hp2 HG02698.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-7104_728-7103i others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880349 | ||||||
chr18:69880349
|
A | AAAGGAAG others(5): Show |
2 | a0001c0001t0048g0007a0002c0009t0140g0242 | 2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.728-7104_728-7103i others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880349 | ||||||
chr18:69880349
|
AAAGAAAG others(5): Show |
A | 1 | a0002c0002t0098g0149 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.728-7115_728-7104d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880349 | ||||||
chr18:69880353
|
A | AAAGGAAG others(5): Show |
9 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0002g0195others(6): Show | 9 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.728-7108_728-7107i others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880353 | ||||||
chr18:69880353
|
A | AAAGGAAG others(9): Show |
4 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(1): Show | 4 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-7108_728-7107i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880353 | ||||||
chr18:69880353
|
A | G | 95 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.728-7107T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880353 | ||||||
chr18:69880353
|
AAAGAAAG others(1): Show |
A | 81 | a0001c0001t0134g0187a0002c0002t0006g0140a0002c0002t0006g0217others(78): Show | 82 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.728-7115_728-7108d others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880353 | ||||||
chr18:69880353
|
AAAGAAAG others(5): Show |
A | 1 | a0002c0002t0035g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.728-7119_728-7108d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880353 | ||||||
chr18:69880357
|
A | G | 148 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.728-7111T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880357 | ||||||
chr18:69880361
|
G | A | 2 | a0001c0001t0025g0099a0001c0001t0094g0135 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.728-7115C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880361 | ||||||
chr18:69880382
|
G | A | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-7136C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880382 | ||||||
chr18:69880516
|
A | G | 2 | a0002c0002t0006g0217a0002c0002t0006g0238 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.728-7270T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880516 | ||||||
chr18:69880575
|
T | A | 2 | a0001c0001t0134g0187a0002c0002t0039g0156 | 2 | HG00639.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.728-7329A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880575 | ||||||
chr18:69880633
|
G | T | 2 | a0001c0001t0023g0052a0001c0001t0060g0029 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.728-7387C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880633 | ||||||
chr18:69880650
|
T | C | 17 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(14): Show | 17 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-7404A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880650 | ||||||
chr18:69880653
|
C | CT | 141 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.728-7408dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880653 | ||||||
chr18:69880653
|
C | CTT | 78 | a0001c0001t0002g0164a0001c0001t0011g0161a0001c0001t0016g0077others(75): Show | 79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.728-7409_728-7408d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880653 | ||||||
chr18:69880931
|
G | A | 14 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(11): Show | 14 | HG00438.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-7685C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880931 | ||||||
chr18:69880946
|
C | T | 16 | a0001c0001t0064g0096a0001c0001t0079g0030a0001c0001t0139g0240others(13): Show | 16 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.728-7700G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880946 | ||||||
chr18:69880947
|
A | G | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.728-7701T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880947 | ||||||
chr18:69880995
|
T | C | 1 | a0002c0002t0019g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.728-7749A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880995 | ||||||
chr18:69880998
|
T | C | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-7752A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69880998 | ||||||
chr18:69881246
|
A | G | 220 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.728-8000T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881246 | ||||||
chr18:69881320
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.728-8074G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881320 | ||||||
chr18:69881391
|
G | A | 157 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.728-8145C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881391 | ||||||
chr18:69881520
|
G | A | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.728-8274C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881520 | ||||||
chr18:69881529
|
A | G | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.728-8283T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881529 | ||||||
chr18:69881550
|
A | T | 203 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.728-8304T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881550 | ||||||
chr18:69881579
|
G | C | 10 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0230others(7): Show | 10 | HG00438.hp1 HG00609.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-8333C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881579 | ||||||
chr18:69881745
|
C | T | 3 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0086g0071 | 3 | HG02976.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.728-8499G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881745 | ||||||
chr18:69881865
|
C | T | 1 | a0001c0001t0023g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.728-8619G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881865 | ||||||
chr18:69881890
|
A | G | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.728-8644T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69881890 | ||||||
chr18:69882258
|
G | A | 3 | a0002c0002t0068g0043a0002c0002t0104g0227a0002c0002t0115g0199 | 3 | HG00544.hp2 NA19060.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.728-9012C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882258 | ||||||
chr18:69882332
|
A | G | 8 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.728-9086T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882332 | ||||||
chr18:69882358
|
C | T | 40 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.728-9112G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882358 | ||||||
chr18:69882370
|
A | G | 40 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.728-9124T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882370 | ||||||
chr18:69882398
|
T | A | 1 | a0001c0001t0137g0208 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-9152A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882398 | ||||||
chr18:69882450
|
C | T | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.728-9204G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882450 | ||||||
chr18:69882548
|
C | T | 1 | a0001c0001t0145g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.728-9302G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882548 | ||||||
chr18:69882564
|
A | G | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.728-9318T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882564 | ||||||
chr18:69882828
|
T | C | 1 | a0001c0001t0023g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.728-9582A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69882828 | ||||||
chr18:69883123
|
G | A | 160 | a0001c0001t0001g0132a0001c0001t0002g0124a0001c0001t0002g0139others(157): Show | 161 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.728-9877C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883123 | ||||||
chr18:69883170
|
A | C | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-9924T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883170 | ||||||
chr18:69883176
|
T | C | 147 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(144): Show | 148 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.728-9930A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883176 | ||||||
chr18:69883271
|
G | A | 3 | a0001c0001t0061g0049a0001c0001t0063g0046a0001c0001t0077g0080 | 3 | HG02647.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.728-10025C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883271 | ||||||
chr18:69883272
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-10026A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883272 | ||||||
chr18:69883350
|
T | C | 151 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(148): Show | 152 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.728-10104A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883350 | ||||||
chr18:69883539
|
G | T | 24 | a0001c0001t0023g0021a0001c0001t0026g0066a0001c0001t0026g0097others(21): Show | 24 | HG00733.hp1 HG01109.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.728-10293C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883539 | ||||||
chr18:69883564
|
A | G | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.728-10318T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883564 | ||||||
chr18:69883602
|
G | C | 5 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(2): Show | 5 | HG02647.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-10356C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883602 | ||||||
chr18:69883643
|
T | A | 133 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(130): Show | 134 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.728-10397A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883643 | ||||||
chr18:69883738
|
T | A | 224 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.728-10492A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883738 | ||||||
chr18:69883769
|
T | C | 1 | a0002c0002t0076g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.728-10523A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883769 | ||||||
chr18:69883829
|
G | A | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.728-10583C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883829 | ||||||
chr18:69883903
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.728-10657G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883903 | ||||||
chr18:69883916
|
G | C | 30 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(27): Show | 30 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.728-10670C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69883916 | ||||||
chr18:69884110
|
T | C | 98 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.728-10864A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884110 | ||||||
chr18:69884147
|
G | A | 2 | a0001c0001t0002g0188a0001c0001t0128g0189 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.728-10901C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884147 | ||||||
chr18:69884232
|
T | C | 17 | a0001c0001t0064g0096a0001c0001t0079g0030a0001c0001t0139g0240others(14): Show | 17 | HG01255.hp2 HG01346.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-10986A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884232 | ||||||
chr18:69884301
|
A | G | 2 | a0001c0001t0139g0240a0002c0002t0008g0095 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.728-11055T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884301 | ||||||
chr18:69884351
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0003g0086 | 2 | HG00738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.728-11105C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884351 | ||||||
chr18:69884398
|
CCA | C | 13 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.728-11154_728-1115 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884398 | ||||||
chr18:69884420
|
C | T | 1 | a0002c0002t0008g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.728-11174G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884420 | ||||||
chr18:69884425
|
T | C | 2 | a0002c0002t0059g0070a0002c0002t0076g0090 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.728-11179A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884425 | ||||||
chr18:69884545
|
A | G | 31 | a0001c0001t0023g0021a0001c0001t0026g0066a0001c0001t0026g0097others(28): Show | 31 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.727+11156T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884545 | ||||||
chr18:69884672
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.727+11029A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884672 | ||||||
chr18:69884743
|
A | G | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.727+10958T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69884743 | ||||||
chr18:69885102
|
T | C | 133 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(130): Show | 134 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.727+10599A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885102 | ||||||
chr18:69885122
|
T | C | 1 | a0002c0002t0008g0041 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.727+10579A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885122 | ||||||
chr18:69885140
|
T | C | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.727+10561A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885140 | ||||||
chr18:69885231
|
T | G | 3 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0091g0055 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.727+10470A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885231 | ||||||
chr18:69885353
|
A | G | 3 | a0001c0001t0041g0129a0001c0001t0041g0134a0001c0001t0124g0169 | 3 | HG01361.hp2 HG02074.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.727+10348T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885353 | ||||||
chr18:69885377
|
A | G | 1 | a0001c0001t0131g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.727+10324T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885377 | ||||||
chr18:69885655
|
G | A | 1 | a0002c0002t0119g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.727+10046C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885655 | ||||||
chr18:69885858
|
C | T | 4 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(1): Show | 4 | HG02647.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+9843G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885858 | ||||||
chr18:69885870
|
T | C | 1 | a0002c0002t0008g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.727+9831A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885870 | ||||||
chr18:69885961
|
GAC | G | 77 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(74): Show | 78 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.727+9738_727+9739d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69885961 | ||||||
chr18:69886274
|
C | T | 2 | a0001c0001t0032g0025a0001c0001t0032g0068 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.727+9427G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886274 | ||||||
chr18:69886373
|
G | C | 2 | a0002c0002t0020g0181a0002c0004t0034g0136 | 2 | HG01071.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.727+9328C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886373 | ||||||
chr18:69886398
|
T | C | 2 | a0002c0002t0028g0032a0002c0002t0028g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727+9303A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886398 | ||||||
chr18:69886482
|
G | T | 74 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.727+9219C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886482 | ||||||
chr18:69886667
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0133g0220 | 2 | HG00733.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.727+9034A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886667 | ||||||
chr18:69886687
|
C | G | 1 | a0001c0001t0092g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.727+9014G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886687 | ||||||
chr18:69886705
|
CA | C | 75 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.727+8995delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886705 | ||||||
chr18:69886722
|
T | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+8979A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886722 | ||||||
chr18:69886870
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.727+8831G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886870 | ||||||
chr18:69886905
|
T | C | 1 | a0001c0001t0132g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.727+8796A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69886905 | ||||||
chr18:69887040
|
A | T | 4 | a0003c0003t0005g0078a0003c0003t0005g0081a0003c0003t0056g0079others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+8661T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887040 | ||||||
chr18:69887162
|
A | G | 4 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(1): Show | 4 | HG02647.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+8539T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887162 | ||||||
chr18:69887172
|
T | C | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+8529A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887172 | ||||||
chr18:69887248
|
C | T | 76 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.727+8453G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887248 | ||||||
chr18:69887322
|
TAC | T | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.727+8377_727+8378d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887322 | ||||||
chr18:69887879
|
A | C | 1 | a0002c0002t0013g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.727+7822T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887879 | ||||||
chr18:69887936
|
G | C | 112 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.727+7765C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887936 | ||||||
chr18:69887965
|
T | G | 27 | a0001c0001t0023g0021a0001c0001t0026g0066a0001c0001t0026g0097others(24): Show | 27 | HG00733.hp1 HG01109.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.727+7736A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887965 | ||||||
chr18:69887985
|
C | T | 78 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(75): Show | 79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.727+7716G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69887985 | ||||||
chr18:69888106
|
G | A | 1 | a0002c0002t0119g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.727+7595C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888106 | ||||||
chr18:69888169
|
T | C | 1 | a0002c0002t0070g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.727+7532A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888169 | ||||||
chr18:69888182
|
T | C | 8 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.727+7519A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888182 | ||||||
chr18:69888208
|
T | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0190a0001c0001t0001g0203others(1): Show | 4 | HG02132.hp2 NA18966.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+7493A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888208 | ||||||
chr18:69888324
|
G | A | 45 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.727+7377C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888324 | ||||||
chr18:69888416
|
C | CT | 147 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0154others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.727+7284dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888416 | ||||||
chr18:69888416
|
C | CTT | 5 | a0002c0002t0009g0001a0002c0002t0020g0152a0002c0002t0034g0128others(2): Show | 6 | HG01175.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+7283_727+7284d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888416 | ||||||
chr18:69888416
|
CT | C | 14 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+7284delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888416 | ||||||
chr18:69888530
|
C | G | 1 | a0002c0002t0020g0181 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.727+7171G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888530 | ||||||
chr18:69888530
|
C | T | 1 | a0001c0001t0023g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727+7171G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888530 | ||||||
chr18:69888869
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.727+6832G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69888869 | ||||||
chr18:69889251
|
C | T | 2 | a0001c0001t0044g0246a0001c0001t0044g0247 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.727+6450G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889251 | ||||||
chr18:69889252
|
G | A | 2 | a0001c0001t0023g0052a0001c0001t0060g0029 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.727+6449C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889252 | ||||||
chr18:69889402
|
T | C | 75 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.727+6299A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889402 | ||||||
chr18:69889410
|
A | G | 75 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.727+6291T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889410 | ||||||
chr18:69889449
|
T | C | 79 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(76): Show | 80 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.727+6252A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889449 | ||||||
chr18:69889487
|
T | TA | 14 | a0001c0001t0088g0100a0001c0001t0138g0239a0003c0003t0005g0045others(11): Show | 14 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.727+6213dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889487 | ||||||
chr18:69889487
|
TA | T | 140 | a0001c0001t0001g0132a0001c0001t0002g0139a0001c0001t0002g0154others(137): Show | 141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.727+6213delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889487 | ||||||
chr18:69889487
|
TAAA | T | 75 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.727+6211_727+6213d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889487 | ||||||
chr18:69889489
|
A | T | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.727+6212T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889489 | ||||||
chr18:69889675
|
A | C | 2 | a0001c0001t0055g0009a0001c0001t0092g0057 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.727+6026T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889675 | ||||||
chr18:69889685
|
C | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.727+6016G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889685 | ||||||
chr18:69889705
|
T | C | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+5996A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889705 | ||||||
chr18:69889731
|
C | T | 12 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+5970G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889731 | ||||||
chr18:69889798
|
A | G | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.727+5903T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889798 | ||||||
chr18:69889817
|
C | A | 8 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.727+5884G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69889817 | ||||||
chr18:69890040
|
G | T | 27 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(24): Show | 27 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.727+5661C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890040 | ||||||
chr18:69890097
|
G | A | 2 | a0002c0002t0007g0153a0002c0002t0020g0152 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.727+5604C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890097 | ||||||
chr18:69890192
|
C | T | 12 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+5509G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890192 | ||||||
chr18:69890193
|
G | A | 30 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(27): Show | 30 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.727+5508C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890193 | ||||||
chr18:69890446
|
C | T | 1 | a0002c0002t0074g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.727+5255G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890446 | ||||||
chr18:69890447
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0133g0220 | 2 | HG00733.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.727+5254C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890447 | ||||||
chr18:69890567
|
T | C | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.727+5134A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890567 | ||||||
chr18:69890708
|
T | C | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.727+4993A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890708 | ||||||
chr18:69890922
|
T | C | 10 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0230others(7): Show | 10 | HG00438.hp1 HG00609.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+4779A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69890922 | ||||||
chr18:69891017
|
C | CA | 21 | a0001c0001t0024g0067a0001c0001t0061g0049a0001c0001t0063g0046others(18): Show | 21 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.727+4683dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891017 | ||||||
chr18:69891017
|
C | CAA | 83 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.727+4682_727+4683d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891017 | ||||||
chr18:69891017
|
C | CAAA | 55 | a0001c0001t0001g0132a0001c0001t0002g0139a0001c0001t0002g0154others(52): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.727+4681_727+4683d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891017 | ||||||
chr18:69891080
|
C | T | 83 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.727+4621G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891080 | ||||||
chr18:69891081
|
A | T | 1 | a0001c0001t0031g0092 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.727+4620T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891081 | ||||||
chr18:69891157
|
T | G | 1 | a0001c0001t0142g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.727+4544A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891157 | ||||||
chr18:69891174
|
A | G | 79 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(76): Show | 80 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.727+4527T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891174 | ||||||
chr18:69891288
|
T | TA | 83 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.727+4412dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891288 | ||||||
chr18:69891324
|
A | G | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.727+4377T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891324 | ||||||
chr18:69891491
|
T | C | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+4210A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891491 | ||||||
chr18:69891495
|
C | A | 12 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+4206G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891495 | ||||||
chr18:69891597
|
C | T | 2 | a0001c0001t0023g0052a0001c0001t0060g0029 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.727+4104G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891597 | ||||||
chr18:69891598
|
A | G | 220 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.727+4103T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891598 | ||||||
chr18:69891785
|
T | C | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+3916A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891785 | ||||||
chr18:69891889
|
T | C | 1 | a0002c0002t0095g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.727+3812A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69891889 | ||||||
chr18:69892083
|
G | A | 2 | a0001c0001t0043g0141a0001c0001t0043g0159 | 2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.727+3618C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892083 | ||||||
chr18:69892107
|
C | T | 238 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.727+3594G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892107 | ||||||
chr18:69892134
|
C | T | 16 | a0001c0001t0064g0096a0001c0001t0079g0030a0001c0001t0139g0240others(13): Show | 16 | HG01255.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.727+3567G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892134 | ||||||
chr18:69892149
|
A | G | 1 | a0001c0001t0061g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.727+3552T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892149 | ||||||
chr18:69892171
|
A | G | 221 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.727+3530T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892171 | ||||||
chr18:69892182
|
G | A | 2 | a0001c0001t0011g0192a0001c0001t0126g0209 | 2 | NA18956.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.727+3519C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892182 | ||||||
chr18:69892196
|
A | T | 79 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(76): Show | 80 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.727+3505T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892196 | ||||||
chr18:69892359
|
T | C | 1 | a0002c0002t0144g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727+3342A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892359 | ||||||
chr18:69892362
|
C | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+3339G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892362 | ||||||
chr18:69892403
|
T | A | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.727+3298A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892403 | ||||||
chr18:69892428
|
C | A | 1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727+3273G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892428 | ||||||
chr18:69892498
|
G | A | 3 | a0001c0001t0003g0012a0001c0001t0003g0085a0001c0001t0003g0089 | 3 | HG00280.hp2 HG02300.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.727+3203C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892498 | ||||||
chr18:69892535
|
T | G | 1 | a0001c0001t0004g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.727+3166A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892535 | ||||||
chr18:69892592
|
T | C | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.727+3109A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892592 | ||||||
chr18:69892751
|
C | CTG | 54 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(51): Show | 54 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.727+2948_727+2949d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892751 | ||||||
chr18:69892779
|
A | ATG | 12 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+2920_727+2921d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892779 | ||||||
chr18:69892816
|
ATC | A | 9 | a0001c0001t0090g0054a0001c0001t0135g0158a0002c0002t0006g0176others(6): Show | 9 | HG00733.hp1 HG01175.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+2883_727+2884d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69892816 | ||||||
chr18:69893156
|
T | C | 2 | a0001c0001t0045g0244a0001c0001t0045g0245 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.727+2545A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893156 | ||||||
chr18:69893261
|
C | A | 2 | a0001c0001t0023g0052a0001c0001t0060g0029 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.727+2440G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893261 | ||||||
chr18:69893470
|
T | C | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+2231A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893470 | ||||||
chr18:69893611
|
A | C | 85 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.727+2090T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893611 | ||||||
chr18:69893844
|
T | C | 181 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.727+1857A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893844 | ||||||
chr18:69893906
|
A | G | 1 | a0002c0002t0113g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.727+1795T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893906 | ||||||
chr18:69893930
|
A | C | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+1771T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69893930 | ||||||
chr18:69894272
|
G | T | 97 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(94): Show | 98 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.727+1429C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894272 | ||||||
chr18:69894282
|
G | A | 97 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(94): Show | 98 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.727+1419C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894282 | ||||||
chr18:69894376
|
GAGGA | G | 29 | a0001c0001t0001g0132a0001c0001t0002g0139a0001c0001t0002g0154others(26): Show | 29 | HG00280.hp2 HG00673.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.727+1321_727+1324d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894376 | ||||||
chr18:69894376
|
GAGGAAGG others(1): Show |
G | 109 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(106): Show | 110 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.727+1317_727+1324d others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894376 | ||||||
chr18:69894376
|
GAGGAAGG others(5): Show |
G | 5 | a0001c0001t0032g0025a0001c0001t0032g0068a0001c0001t0048g0007others(2): Show | 5 | HG00280.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+1313_727+1324d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894376 | ||||||
chr18:69894376
|
GAGGAAGG others(9): Show |
G | 11 | a0003c0003t0005g0045a0003c0003t0005g0078a0003c0003t0005g0081others(8): Show | 11 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.727+1309_727+1324d others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894376 | ||||||
chr18:69894404
|
A | G | 4 | a0001c0001t0002g0225a0001c0001t0041g0134a0001c0001t0078g0064others(1): Show | 4 | HG01168.hp1 HG06807.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+1297T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894404 | ||||||
chr18:69894408
|
A | G | 27 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(24): Show | 27 | HG00280.hp2 HG00673.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.727+1293T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894408 | ||||||
chr18:69894412
|
A | AAGGGAGG others(9): Show |
1 | a0001c0001t0092g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.727+1288_727+1289i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894412 | ||||||
chr18:69894412
|
A | G | 125 | a0001c0001t0001g0190a0001c0001t0002g0124a0001c0001t0002g0139others(122): Show | 126 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.727+1289T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894412 | ||||||
chr18:69894416
|
A | AAGGGAGG others(5): Show |
1 | a0002c0002t0071g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.727+1284_727+1285i others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894416 | ||||||
chr18:69894416
|
A | AAGGGAGG others(13): Show |
2 | a0001c0001t0055g0009a0002c0002t0070g0035 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.727+1284_727+1285i others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894416 | ||||||
chr18:69894416
|
A | G | 132 | a0001c0001t0001g0190a0001c0001t0002g0124a0001c0001t0002g0139others(129): Show | 133 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.727+1285T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894416 | ||||||
chr18:69894420
|
A | AAGGAAGG others(29): Show |
1 | a0001c0001t0132g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(38): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(25): Show |
1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(34): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(29): Show |
1 | a0001c0001t0001g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(38): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(33): Show |
1 | a0001c0001t0016g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(42): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(25): Show |
3 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0054g0004 | 3 | HG01109.hp2 HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(34): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(29): Show |
2 | a0001c0001t0080g0103a0001c0001t0085g0102 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(38): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(37): Show |
1 | a0001c0001t0089g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(46): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(9): Show |
1 | a0002c0002t0059g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(13): Show |
1 | a0001c0001t0026g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(17): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0203others(1): Show | 4 | HG00621.hp2 NA18747.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(26): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(21): Show |
3 | a0001c0001t0016g0094a0001c0001t0042g0108a0002c0002t0011g0205 | 3 | HG00673.hp1 HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(30): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(25): Show |
9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0033g0083others(6): Show | 9 | HG00099.hp1 HG01069.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(34): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(29): Show |
5 | a0001c0001t0011g0122a0001c0001t0016g0077a0001c0001t0087g0098others(2): Show | 5 | HG00438.hp2 HG01255.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(38): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(45): Show |
1 | a0001c0001t0049g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(54): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(5): Show |
1 | a0001c0001t0002g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(9): Show |
1 | a0001c0001t0026g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(13): Show |
5 | a0001c0001t0001g0120a0001c0001t0001g0172a0001c0001t0031g0042others(2): Show | 5 | HG00597.hp2 HG02132.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(17): Show |
2 | a0001c0001t0001g0212a0001c0001t0083g0087 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(26): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(25): Show |
2 | a0001c0001t0045g0245a0001c0001t0086g0071 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(34): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(21): Show |
9 | a0001c0001t0001g0207a0001c0001t0002g0211a0001c0001t0003g0093others(6): Show | 9 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(30): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(25): Show |
3 | a0001c0001t0011g0192a0001c0001t0033g0082a0001c0001t0090g0054 | 3 | HG00639.hp2 HG02615.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(34): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(45): Show |
1 | a0001c0001t0024g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(54): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(1): Show |
4 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0060g0029others(1): Show | 4 | HG01168.hp2 HG02615.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(9): Show |
1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(13): Show |
1 | a0001c0001t0001g0114 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.727+1280_727+1281i others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(17): Show |
7 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0003g0036others(4): Show | 7 | HG00099.hp2 HG01981.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1280_727+1281i others(26): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(21): Show |
2 | a0001c0001t0135g0158a0002c0002t0007g0105 | 2 | HG01346.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.727+1280_727+1281i others(30): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGAAGG others(33): Show |
1 | a0001c0001t0045g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.727+1280_727+1281i others(42): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | AAGGGAGG others(5): Show |
2 | a0002c0002t0028g0032a0002c0002t0028g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727+1269_727+1280d others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894420
|
A | G | 175 | a0001c0001t0001g0132a0001c0001t0001g0190a0001c0001t0002g0124others(172): Show | 176 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.727+1281T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894420 | ||||||
chr18:69894426
|
G | A | 12 | a0003c0003t0005g0045a0003c0003t0005g0074a0003c0003t0005g0078others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+1275C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894426 | ||||||
chr18:69894436
|
G | GAGGGAAG others(22): Show |
1 | a0001c0001t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.727+1236_727+1264d others(31): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894436 | ||||||
chr18:69894436
|
G | GAGGGAGG others(60): Show |
1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.727+1264_727+1265i others(69): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894436 | ||||||
chr18:69894442
|
A | G | 3 | a0001c0001t0078g0064a0002c0009t0140g0242a0006c0008t0141g0251 | 3 | HG03195.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.727+1259T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894442 | ||||||
chr18:69894452
|
GGGGAGGG others(12): Show |
G | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.727+1230_727+1248d others(21): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894452 | ||||||
chr18:69894479
|
GAGAGA | G | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+1217_727+1221d others(7): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894479 | ||||||
chr18:69894530
|
A | G | 3 | a0001c0001t0089g0014a0001c0001t0139g0240a0002c0002t0008g0095 | 3 | HG02486.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.727+1171T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894530 | ||||||
chr18:69894533
|
C | A | 208 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.727+1168G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894533 | ||||||
chr18:69894533
|
C | G | 3 | a0001c0001t0089g0014a0001c0001t0139g0240a0002c0002t0008g0095 | 3 | HG02486.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.727+1168G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894533 | ||||||
chr18:69894534
|
A | G | 33 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(30): Show | 33 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.727+1167T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894534 | ||||||
chr18:69894547
|
A | AGAGAAAG others(281): Show |
16 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(13): Show | 16 | HG00733.hp2 HG01168.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.727+1153_727+1154i others(290): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894547
|
A | AGAGAAAG others(286): Show |
2 | a0001c0001t0041g0134a0001c0001t0124g0169 | 2 | HG02074.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.727+1153_727+1154i others(295): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894547
|
A | AGAGAAAG others(272): Show |
5 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(2): Show | 5 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+1153_727+1154i others(281): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894547
|
A | AGAGAAAG others(268): Show |
1 | a0001c0001t0041g0129 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.727+1153_727+1154i others(277): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894547
|
A | AGAGAAAG others(300): Show |
1 | a0001c0001t0142g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.727+1153_727+1154i others(309): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894547
|
A | AGAGAAAG others(305): Show |
1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+1153_727+1154i others(314): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894547 | ||||||
chr18:69894549
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.727+1152C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894549 | ||||||
chr18:69894551
|
G | A | 29 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(26): Show | 29 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.727+1150C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894551 | ||||||
chr18:69894552
|
A | G | 3 | a0001c0001t0139g0240a0002c0002t0028g0032a0002c0002t0028g0050 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.727+1149T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894552 | ||||||
chr18:69894556
|
G | A | 201 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.727+1145C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894556 | ||||||
chr18:69894556
|
G | GA | 26 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(23): Show | 26 | HG00733.hp2 HG01168.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.727+1144_727+1145i others(3): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894556 | ||||||
chr18:69894556
|
G | GAGGGGAG others(223): Show |
1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.727+1144_727+1145i others(232): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894556 | ||||||
chr18:69894557
|
G | A | 10 | a0001c0001t0089g0014a0001c0001t0090g0054a0001c0001t0135g0158others(7): Show | 10 | HG00733.hp1 HG01175.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+1144C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894557 | ||||||
chr18:69894560
|
G | GGAGGGGA others(217): Show |
1 | a0001c0001t0088g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.727+1140_727+1141i others(226): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894560 | ||||||
chr18:69894560
|
G | GGGAGGGG others(216): Show |
1 | a0001c0001t0025g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.727+1140_727+1141i others(225): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894560 | ||||||
chr18:69894561
|
A | AG | 27 | a0001c0001t0002g0139a0001c0001t0002g0154a0001c0001t0002g0157others(24): Show | 27 | HG00733.hp2 HG01168.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.727+1139dupC | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGAAGG others(212): Show |
1 | a0001c0001t0089g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(221): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGAGGG others(232): Show |
1 | a0002c0002t0110g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(241): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(196): Show |
1 | a0003c0003t0017g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(205): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(199): Show |
1 | a0001c0001t0139g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(208): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(206): Show |
1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(215): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(250): Show |
1 | a0001c0001t0001g0112 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(259): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(253): Show |
2 | a0002c0002t0028g0032a0002c0002t0028g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(262): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(232): Show |
1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(241): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(204): Show |
6 | a0002c0002t0009g0001a0002c0002t0009g0126a0002c0002t0020g0181others(3): Show | 7 | HG00738.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(213): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(227): Show |
1 | a0002c0002t0071g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(236): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(196): Show |
9 | a0001c0001t0004g0113a0001c0001t0004g0116a0001c0001t0004g0230others(6): Show | 9 | HG00438.hp1 HG00609.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(205): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(256): Show |
1 | a0001c0001t0001g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(265): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(264): Show |
2 | a0001c0001t0003g0085a0001c0001t0003g0089 | 2 | HG00280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(273): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(214): Show |
4 | a0001c0001t0025g0069a0001c0001t0050g0008a0001c0001t0094g0135others(1): Show | 4 | HG01243.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(223): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(219): Show |
1 | a0002c0002t0014g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(228): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(210): Show |
1 | a0003c0003t0056g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(219): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(215): Show |
19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01106.hp2 HG01891.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(224): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(240): Show |
7 | a0001c0001t0026g0066a0001c0001t0026g0097a0001c0001t0044g0246others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(249): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(254): Show |
1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(263): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(232): Show |
1 | a0002c0002t0007g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(241): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(213): Show |
2 | a0001c0001t0061g0049a0001c0001t0063g0046 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(222): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(229): Show |
5 | a0001c0001t0045g0244a0001c0001t0045g0245a0001c0001t0055g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(238): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(218): Show |
1 | a0002c0002t0109g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(227): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(223): Show |
80 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(77): Show | 80 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(232): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(255): Show |
49 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0125others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.727+1139_727+1140i others(264): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(224): Show |
1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(233): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(255): Show |
1 | a0001c0001t0023g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(264): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(234): Show |
1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(243): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(256): Show |
1 | a0001c0001t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.727+1139_727+1140i others(265): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(204): Show |
1 | a0001c0001t0077g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(213): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(246): Show |
2 | a0002c0002t0059g0070a0002c0002t0070g0035 | 2 | HG01346.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(255): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(215): Show |
3 | a0001c0001t0001g0132a0001c0001t0004g0123a0001c0001t0136g0121 | 3 | HG03239.hp2 NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(224): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(283): Show |
2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(292): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(274): Show |
2 | a0001c0001t0023g0052a0001c0001t0060g0029 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(283): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(225): Show |
3 | a0002c0002t0066g0088a0002c0002t0120g0235a0002c0002t0121g0200 | 3 | HG00733.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(234): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(241): Show |
3 | a0001c0001t0135g0158a0002c0002t0006g0176a0002c0002t0019g0175 | 3 | HG01346.hp1 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(250): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(242): Show |
1 | a0004c0005t0100g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(251): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(232): Show |
1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(241): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(247): Show |
2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.727+1139_727+1140i others(256): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | AGGGGAGG others(227): Show |
1 | a0002c0002t0115g0199 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.727+1139_727+1140i others(236): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894561
|
A | G | 2 | a0001c0001t0025g0099a0001c0001t0088g0100 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.727+1140T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894561 | ||||||
chr18:69894564
|
G | GGAGGGGA others(197): Show |
1 | a0001c0001t0043g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.727+1136_727+1137i others(206): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894564 | ||||||
chr18:69894566
|
A | G | 1 | a0001c0001t0043g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.727+1135T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894566 | ||||||
chr18:69894578
|
T | C | 214 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.727+1123A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894578 | ||||||
chr18:69894585
|
G | A | 53 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.727+1116C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894585 | ||||||
chr18:69894586
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+1115C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894586 | ||||||
chr18:69894607
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+1094C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894607 | ||||||
chr18:69894650
|
G | A | 2 | a0002c0002t0007g0228a0002c0002t0020g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.727+1051C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894650 | ||||||
chr18:69894893
|
T | C | 1 | a0001c0001t0089g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.727+808A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894893 | ||||||
chr18:69894924
|
T | C | 1 | a0002c0002t0074g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.727+777A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69894924 | ||||||
chr18:69895091
|
C | T | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+610G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895091 | ||||||
chr18:69895120
|
A | G | 13 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.727+581T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895120 | ||||||
chr18:69895421
|
T | C | 78 | a0001c0001t0002g0124a0001c0001t0002g0216a0001c0001t0003g0086others(75): Show | 79 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.727+280A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895421 | ||||||
chr18:69895423
|
T | C | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727+278A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895423 | ||||||
chr18:69895441
|
G | C | 214 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.727+260C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 3/5 | chr18 | 69895441 | ||||||
chr18:69896073
|
A | C | 237 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.383-28T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896073 | ||||||
chr18:69896112
|
T | C | 227 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.383-67A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896112 | ||||||
chr18:69896180
|
A | C | 5 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(2): Show | 5 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-135T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896180 | ||||||
chr18:69896181
|
C | CT | 114 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.383-137dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896181 | ||||||
chr18:69896181
|
C | CTT | 92 | a0001c0001t0001g0207a0001c0001t0002g0139a0001c0001t0002g0154others(89): Show | 92 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.383-138_383-137dup others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896181 | ||||||
chr18:69896181
|
C | CTTTT | 12 | a0001c0001t0001g0132a0001c0001t0004g0113a0001c0001t0004g0116others(9): Show | 12 | HG00438.hp1 HG00609.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.383-140_383-137dup others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896181 | ||||||
chr18:69896297
|
T | C | 47 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.383-252A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896297 | ||||||
chr18:69896333
|
C | T | 1 | a0001c0001t0016g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.383-288G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896333 | ||||||
chr18:69896394
|
G | A | 1 | a0006c0008t0141g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.383-349C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896394 | ||||||
chr18:69896403
|
A | G | 1 | a0001c0001t0124g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.383-358T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896403 | ||||||
chr18:69896479
|
T | C | 8 | a0003c0003t0005g0045a0003c0003t0005g0078a0003c0003t0005g0081others(5): Show | 8 | HG01106.hp2 HG01243.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.383-434A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896479 | ||||||
chr18:69896493
|
T | G | 1 | a0001c0001t0134g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.383-448A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896493 | ||||||
chr18:69896510
|
G | GT | 16 | a0001c0001t0002g0164a0001c0001t0002g0225a0001c0001t0003g0086others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.383-466dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896510 | ||||||
chr18:69896736
|
T | C | 136 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.383-691A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896736 | ||||||
chr18:69896852
|
T | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-807A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896852 | ||||||
chr18:69896853
|
A | C | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-808T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896853 | ||||||
chr18:69896854
|
C | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-809G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896854 | ||||||
chr18:69896974
|
C | G | 1 | a0001c0001t0078g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.383-929G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69896974 | ||||||
chr18:69897077
|
T | C | 1 | a0001c0001t0004g0232 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.383-1032A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897077 | ||||||
chr18:69897134
|
T | C | 1 | a0002c0002t0059g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383-1089A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897134 | ||||||
chr18:69897315
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0003g0093 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.383-1270C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897315 | ||||||
chr18:69897627
|
TAGAG | T | 47 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.383-1586_383-1583d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897627 | ||||||
chr18:69897967
|
C | T | 3 | a0001c0001t0062g0018a0001c0001t0078g0064a0001c0001t0142g0243 | 3 | HG02723.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.383-1922G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897967 | ||||||
chr18:69897975
|
A | T | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1930T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897975 | ||||||
chr18:69897976
|
T | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1931A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897976 | ||||||
chr18:69897978
|
T | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1933A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897978 | ||||||
chr18:69897979
|
C | T | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.383-1934G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897979 | ||||||
chr18:69897980
|
G | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1935C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897980 | ||||||
chr18:69897982
|
C | A | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1937G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897982 | ||||||
chr18:69897983
|
T | G | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1938A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897983 | ||||||
chr18:69897984
|
C | T | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1939G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897984 | ||||||
chr18:69897985
|
T | G | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1940A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897985 | ||||||
chr18:69897987
|
A | T | 1 | a0002c0002t0103g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.383-1942T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69897987 | ||||||
chr18:69898207
|
T | C | 1 | a0004c0005t0100g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383-2162A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898207 | ||||||
chr18:69898227
|
C | T | 56 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(53): Show | 56 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.383-2182G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898227 | ||||||
chr18:69898233
|
T | C | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-2188A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898233 | ||||||
chr18:69898244
|
C | T | 2 | a0001c0001t0082g0013a0001c0001t0092g0057 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383-2199G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898244 | ||||||
chr18:69898325
|
T | C | 1 | a0001c0001t0137g0208 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.383-2280A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898325 | ||||||
chr18:69898343
|
G | A | 102 | a0001c0001t0001g0132a0001c0001t0001g0212a0001c0001t0002g0124others(99): Show | 103 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.383-2298C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898343 | ||||||
chr18:69898614
|
T | C | 146 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0157others(143): Show | 147 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.383-2569A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898614 | ||||||
chr18:69898662
|
T | C | 160 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0002g0124others(157): Show | 161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.383-2617A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898662 | ||||||
chr18:69898663
|
G | A | 2 | a0001c0001t0032g0025a0001c0001t0032g0068 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.383-2618C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898663 | ||||||
chr18:69898732
|
G | A | 128 | a0001c0001t0001g0203a0001c0001t0002g0124a0001c0001t0002g0139others(125): Show | 129 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.383-2687C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898732 | ||||||
chr18:69898866
|
C | T | 1 | a0002c0002t0096g0111 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.383-2821G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69898866 | ||||||
chr18:69899075
|
A | G | 18 | a0001c0001t0002g0154a0001c0001t0055g0009a0001c0001t0090g0054others(15): Show | 18 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.383-3030T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899075 | ||||||
chr18:69899246
|
G | A | 5 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(2): Show | 5 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-3201C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899246 | ||||||
chr18:69899263
|
C | T | 2 | a0002c0002t0014g0020a0002c0002t0015g0072 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.383-3218G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899263 | ||||||
chr18:69899318
|
G | A | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-3273C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899318 | ||||||
chr18:69899351
|
C | T | 134 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.383-3306G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899351 | ||||||
chr18:69899385
|
A | C | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-3340T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899385 | ||||||
chr18:69899412
|
A | G | 1 | a0001c0001t0077g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.383-3367T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899412 | ||||||
chr18:69899654
|
G | T | 3 | a0001c0001t0004g0123a0001c0001t0123g0194a0001c0001t0136g0121 | 3 | HG03239.hp2 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.383-3609C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899654 | ||||||
chr18:69899679
|
G | A | 2 | a0002c0002t0027g0027a0002c0002t0067g0028 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.383-3634C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899679 | ||||||
chr18:69899764
|
A | G | 12 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0002g0211others(9): Show | 12 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-3719T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899764 | ||||||
chr18:69899848
|
A | G | 6 | a0002c0002t0006g0176a0002c0002t0019g0175a0002c0002t0066g0088others(3): Show | 6 | HG00733.hp1 HG01175.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-3803T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899848 | ||||||
chr18:69899971
|
A | G | 3 | a0001c0001t0004g0123a0001c0001t0123g0194a0001c0001t0136g0121 | 3 | HG03239.hp2 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.383-3926T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69899971 | ||||||
chr18:69900284
|
C | T | 2 | a0002c0002t0028g0032a0002c0002t0028g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.383-4239G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900284 | ||||||
chr18:69900323
|
C | A | 26 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0023g0021others(23): Show | 26 | HG01346.hp2 HG02145.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.383-4278G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900323 | ||||||
chr18:69900343
|
A | C | 130 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.383-4298T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900343 | ||||||
chr18:69900345
|
T | TG | 130 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.383-4301dupC | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900345 | ||||||
chr18:69900384
|
A | G | 1 | a0001c0001t0024g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383-4339T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900384 | ||||||
chr18:69900395
|
T | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0167 | 2 | HG00099.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.383-4350A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900395 | ||||||
chr18:69900432
|
T | A | 1 | a0001c0001t0024g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-4387A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900432 | ||||||
chr18:69900454
|
C | T | 3 | a0001c0001t0004g0123a0001c0001t0123g0194a0001c0001t0136g0121 | 3 | HG03239.hp2 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.383-4409G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900454 | ||||||
chr18:69900470
|
C | T | 124 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.383-4425G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900470 | ||||||
chr18:69900492
|
C | T | 1 | a0002c0002t0069g0056 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-4447G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900492 | ||||||
chr18:69900507
|
C | T | 126 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.383-4462G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900507 | ||||||
chr18:69900528
|
C | T | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-4483G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900528 | ||||||
chr18:69900548
|
A | C | 2 | a0001c0001t0002g0154a0001c0001t0124g0169 | 2 | HG02074.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.383-4503T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900548 | ||||||
chr18:69900581
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.383-4536T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900581 | ||||||
chr18:69900589
|
G | A | 21 | a0001c0001t0055g0009a0001c0001t0090g0054a0001c0001t0135g0158others(18): Show | 21 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-4544C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900589 | ||||||
chr18:69900609
|
G | T | 2 | a0001c0001t0080g0103a0001c0001t0085g0102 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-4564C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900609 | ||||||
chr18:69900624
|
C | T | 1 | a0001c0001t0132g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.383-4579G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900624 | ||||||
chr18:69900632
|
T | C | 2 | a0001c0001t0080g0103a0001c0001t0085g0102 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-4587A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900632 | ||||||
chr18:69900646
|
G | A | 4 | a0001c0001t0002g0139a0001c0001t0002g0168a0001c0001t0133g0220others(1): Show | 4 | HG00733.hp2 HG01978.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-4601C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900646 | ||||||
chr18:69900657
|
G | A | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.383-4612C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900657 | ||||||
chr18:69900661
|
G | A | 118 | a0001c0001t0002g0124a0001c0001t0002g0154a0001c0001t0002g0195others(115): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.383-4616C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900661 | ||||||
chr18:69900664
|
G | A | 117 | a0001c0001t0002g0124a0001c0001t0002g0154a0001c0001t0002g0195others(114): Show | 118 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.383-4619C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900664 | ||||||
chr18:69900686
|
T | C | 135 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.383-4641A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900686 | ||||||
chr18:69900708
|
C | T | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-4663G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900708 | ||||||
chr18:69900738
|
C | CA | 11 | a0001c0001t0004g0123a0001c0001t0045g0244a0001c0001t0045g0245others(8): Show | 11 | HG01109.hp1 HG02922.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-4694dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900738 | ||||||
chr18:69900738
|
C | CAA | 17 | a0001c0001t0064g0096a0001c0001t0132g0174a0002c0002t0006g0219others(14): Show | 17 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.383-4695_383-4694d others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900738 | ||||||
chr18:69900738
|
C | CAAA | 70 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.383-4696_383-4694d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900738 | ||||||
chr18:69900738
|
C | CAAAA | 19 | a0001c0001t0001g0207a0001c0001t0002g0157a0001c0001t0002g0188others(16): Show | 19 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-4697_383-4694d others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900738 | ||||||
chr18:69900756
|
A | AT | 3 | a0001c0001t0060g0029a0002c0002t0028g0032a0002c0002t0028g0050 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.383-4712dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900756 | ||||||
chr18:69900756
|
A | T | 24 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0023g0021others(21): Show | 24 | HG01346.hp2 HG02145.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.383-4711T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900756 | ||||||
chr18:69900801
|
A | G | 2 | a0002c0002t0029g0058a0002c0002t0071g0015 | 2 | HG01109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.383-4756T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900801 | ||||||
chr18:69900909
|
T | C | 36 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0023g0052others(33): Show | 36 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.383-4864A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69900909 | ||||||
chr18:69901002
|
T | G | 1 | a0002c0002t0007g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.383-4957A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901002 | ||||||
chr18:69901013
|
A | G | 119 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.383-4968T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901013 | ||||||
chr18:69901081
|
G | T | 63 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.383-5036C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901081 | ||||||
chr18:69901152
|
GACA | G | 9 | a0001c0001t0139g0240a0002c0002t0008g0095a0002c0002t0013g0060others(6): Show | 9 | HG01255.hp2 HG02486.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.383-5110_383-5108d others(5): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901152 | ||||||
chr18:69901265
|
G | C | 85 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.383-5220C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901265 | ||||||
chr18:69901355
|
A | C | 4 | a0001c0001t0011g0122a0001c0001t0011g0192a0001c0001t0126g0209others(1): Show | 4 | HG00438.hp2 HG02040.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-5310T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901355 | ||||||
chr18:69901437
|
A | G | 5 | a0001c0001t0024g0067a0001c0001t0025g0099a0001c0001t0080g0103others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-5392T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901437 | ||||||
chr18:69901564
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.383-5519G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901564 | ||||||
chr18:69901572
|
A | G | 1 | a0001c0001t0060g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383-5527T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901572 | ||||||
chr18:69901600
|
C | G | 93 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0127others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.383-5555G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901600 | ||||||
chr18:69901607
|
A | G | 3 | a0001c0001t0023g0052a0001c0001t0143g0241a0002c0002t0074g0051 | 3 | HG02717.hp1 HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.383-5562T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901607 | ||||||
chr18:69901609
|
A | G | 2 | a0001c0001t0023g0052a0002c0002t0074g0051 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.383-5564T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901609 | ||||||
chr18:69901627
|
T | TC | 86 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0127others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.383-5583dupG | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901627 | ||||||
chr18:69901651
|
A | G | 99 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0195others(96): Show | 100 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.383-5606T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901651 | ||||||
chr18:69901676
|
A | C | 69 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0143others(66): Show | 69 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.383-5631T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901676 | ||||||
chr18:69901676
|
A | G | 35 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0032g0025others(32): Show | 36 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.383-5631T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901676 | ||||||
chr18:69901689
|
C | T | 2 | a0001c0001t0078g0064a0002c0002t0073g0063 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.383-5644G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901689 | ||||||
chr18:69901695
|
T | C | 3 | a0001c0001t0078g0064a0001c0001t0094g0135a0002c0002t0073g0063 | 3 | HG01243.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.383-5650A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901695 | ||||||
chr18:69901748
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0123g0194a0001c0001t0136g0121 | 3 | HG02738.hp2 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.383-5703T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901748 | ||||||
chr18:69901751
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0123g0194a0001c0001t0136g0121 | 3 | HG02738.hp2 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.383-5706A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901751 | ||||||
chr18:69901811
|
A | G | 139 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0125others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.383-5766T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901811 | ||||||
chr18:69901836
|
A | G | 6 | a0001c0001t0004g0116a0001c0001t0026g0066a0002c0002t0006g0219others(3): Show | 6 | HG00609.hp2 HG00735.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-5791T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901836 | ||||||
chr18:69901843
|
C | T | 216 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.383-5798G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901843 | ||||||
chr18:69901878
|
CA | C | 13 | a0001c0001t0045g0244a0001c0001t0139g0240a0001c0001t0142g0243others(10): Show | 13 | HG01255.hp2 HG02486.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.383-5834delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901878 | ||||||
chr18:69901878
|
CAAAAA | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0170a0001c0001t0001g0172others(8): Show | 11 | HG00621.hp2 HG02132.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-5838_383-5834d others(7): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69901878 | ||||||
chr18:69902274
|
C | G | 1 | a0001c0001t0026g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.383-6229G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902274 | ||||||
chr18:69902311
|
C | G | 164 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(161): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.383-6266G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902311 | ||||||
chr18:69902478
|
G | A | 1 | a0002c0002t0013g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383-6433C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902478 | ||||||
chr18:69902502
|
C | G | 2 | a0001c0001t0023g0052a0002c0002t0074g0051 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.383-6457G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902502 | ||||||
chr18:69902543
|
T | C | 1 | a0002c0002t0014g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.383-6498A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902543 | ||||||
chr18:69902682
|
G | C | 1 | a0002c0002t0013g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383-6637C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902682 | ||||||
chr18:69902715
|
C | G | 1 | a0001c0001t0094g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.383-6670G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902715 | ||||||
chr18:69902734
|
C | T | 1 | a0002c0002t0070g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.383-6689G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902734 | ||||||
chr18:69902796
|
C | A | 3 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383-6751G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902796 | ||||||
chr18:69902921
|
T | C | 2 | a0001c0001t0023g0052a0002c0002t0074g0051 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.383-6876A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902921 | ||||||
chr18:69902924
|
T | C | 20 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0023g0021others(17): Show | 20 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.383-6879A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69902924 | ||||||
chr18:69903132
|
G | A | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.383-7087C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903132 | ||||||
chr18:69903317
|
C | T | 1 | a0002c0002t0007g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.383-7272G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903317 | ||||||
chr18:69903600
|
G | A | 3 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383-7555C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903600 | ||||||
chr18:69903625
|
G | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02129.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.383-7580C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903625 | ||||||
chr18:69903699
|
T | C | 1 | a0001c0001t0078g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.383-7654A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903699 | ||||||
chr18:69903912
|
C | A | 1 | a0002c0002t0035g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.383-7867G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903912 | ||||||
chr18:69903921
|
C | T | 2 | a0001c0001t0060g0029a0002c0002t0008g0095 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.383-7876G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903921 | ||||||
chr18:69903977
|
T | C | 6 | a0001c0001t0064g0096a0001c0001t0077g0080a0002c0002t0028g0032others(3): Show | 6 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-7932A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69903977 | ||||||
chr18:69904194
|
G | T | 19 | a0001c0001t0011g0161a0001c0001t0012g0016a0001c0001t0012g0034others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.383-8149C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904194 | ||||||
chr18:69904327
|
T | C | 3 | a0001c0001t0142g0243a0001c0001t0143g0241a0002c0009t0140g0242 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.383-8282A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904327 | ||||||
chr18:69904366
|
C | A | 1 | a0001c0001t0002g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.383-8321G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904366 | ||||||
chr18:69904374
|
C | G | 221 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.383-8329G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904374 | ||||||
chr18:69904608
|
T | A | 1 | a0001c0001t0016g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.383-8563A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904608 | ||||||
chr18:69904611
|
T | G | 22 | a0001c0001t0004g0123a0001c0001t0012g0016a0001c0001t0012g0034others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.383-8566A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904611 | ||||||
chr18:69904895
|
C | T | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-8850G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904895 | ||||||
chr18:69904937
|
C | T | 1 | a0002c0002t0076g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.383-8892G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69904937 | ||||||
chr18:69905131
|
C | T | 1 | a0002c0002t0027g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.383-9086G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905131 | ||||||
chr18:69905163
|
G | A | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.383-9118C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905163 | ||||||
chr18:69905174
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383-9129C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905174 | ||||||
chr18:69905230
|
CATCAGCT others(107): Show |
C | 3 | a0002c0002t0027g0026a0002c0002t0027g0027a0002c0002t0067g0028 | 3 | HG01081.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.383-9299_383-9186d others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905230 | ||||||
chr18:69905236
|
C | A | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-9191G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905236 | ||||||
chr18:69905432
|
G | A | 1 | a0002c0002t0059g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383-9387C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905432 | ||||||
chr18:69905539
|
G | C | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.383-9494C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905539 | ||||||
chr18:69905596
|
C | A | 1 | a0001c0001t0124g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.383-9551G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905596 | ||||||
chr18:69905876
|
C | T | 2 | a0001c0001t0002g0164a0002c0002t0007g0145 | 2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.383-9831G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69905876 | ||||||
chr18:69906094
|
T | C | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-10049A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906094 | ||||||
chr18:69906112
|
A | G | 2 | a0001c0001t0044g0246a0001c0001t0044g0247 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.383-10067T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906112 | ||||||
chr18:69906238
|
C | G | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-10193G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906238 | ||||||
chr18:69906387
|
T | C | 5 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(2): Show | 5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-10342A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906387 | ||||||
chr18:69906419
|
A | C | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-10374T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906419 | ||||||
chr18:69906516
|
A | G | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-10471T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906516 | ||||||
chr18:69906521
|
G | A | 1 | a0001c0001t0025g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.383-10476C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906521 | ||||||
chr18:69906573
|
T | C | 253 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(250): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.383-10528A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906573 | ||||||
chr18:69906574
|
G | A | 222 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.383-10529C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906574 | ||||||
chr18:69906643
|
G | A | 2 | a0001c0001t0043g0159a0001c0001t0138g0239 | 2 | HG03540.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.383-10598C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906643 | ||||||
chr18:69906694
|
T | A | 1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383-10649A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906694 | ||||||
chr18:69906858
|
G | A | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.383-10813C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906858 | ||||||
chr18:69906955
|
C | A | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-10910G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906955 | ||||||
chr18:69906955
|
C | T | 8 | a0001c0001t0002g0225a0001c0001t0004g0123a0001c0001t0123g0194others(5): Show | 8 | HG01109.hp1 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.383-10910G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69906955 | ||||||
chr18:69907136
|
C | T | 1 | a0003c0003t0005g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.383-11091G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907136 | ||||||
chr18:69907155
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.383-11110G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907155 | ||||||
chr18:69907194
|
T | C | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-11149A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907194 | ||||||
chr18:69907305
|
G | A | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-11260C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907305 | ||||||
chr18:69907343
|
G | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-11298C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907343 | ||||||
chr18:69907391
|
A | G | 207 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.383-11346T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907391 | ||||||
chr18:69907455
|
A | G | 226 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.383-11410T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907455 | ||||||
chr18:69907817
|
T | C | 13 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(10): Show | 13 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.383-11772A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907817 | ||||||
chr18:69907926
|
A | G | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.383-11881T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69907926 | ||||||
chr18:69908040
|
C | T | 3 | a0003c0003t0005g0078a0003c0003t0005g0081a0003c0003t0056g0079 | 3 | HG01243.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.383-11995G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908040 | ||||||
chr18:69908101
|
C | T | 1 | a0002c0002t0006g0219 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.383-12056G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908101 | ||||||
chr18:69908133
|
G | A | 4 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-12088C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908133 | ||||||
chr18:69908230
|
TG | T | 4 | a0001c0001t0011g0192a0001c0001t0126g0209a0002c0002t0037g0206others(1): Show | 4 | HG02040.hp2 HG02135.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-12186delC | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908230 | ||||||
chr18:69908440
|
G | A | 1 | a0001c0001t0143g0241 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.383-12395C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908440 | ||||||
chr18:69908603
|
CTCTAATT others(11): Show |
C | 8 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0081g0047others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.383-12576_383-1255 others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908603 | ||||||
chr18:69908611
|
G | GTAGCC | 11 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0207others(8): Show | 11 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.383-12571_383-1256 others(9): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908611 | ||||||
chr18:69908657
|
C | CT | 31 | a0001c0001t0001g0178a0001c0001t0001g0190a0001c0001t0001g0203others(28): Show | 31 | HG00438.hp2 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.383-12613dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908657 | ||||||
chr18:69908738
|
T | C | 14 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0004g0113others(11): Show | 14 | HG00438.hp1 HG00609.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.383-12693A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908738 | ||||||
chr18:69908767
|
A | G | 8 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0081g0047others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.383-12722T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908767 | ||||||
chr18:69908838
|
A | C | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.383-12793T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908838 | ||||||
chr18:69908900
|
C | T | 1 | a0001c0001t0139g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.383-12855G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908900 | ||||||
chr18:69908987
|
T | C | 1 | a0002c0002t0030g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.383-12942A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69908987 | ||||||
chr18:69909370
|
T | C | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.383-13325A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69909370 | ||||||
chr18:69910117
|
C | T | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.383-14072G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910117 | ||||||
chr18:69910226
|
G | A | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-14181C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910226 | ||||||
chr18:69910343
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.383-14298T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910343 | ||||||
chr18:69910526
|
T | C | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.383-14481A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910526 | ||||||
chr18:69910543
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.383-14498G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910543 | ||||||
chr18:69910627
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-14582A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910627 | ||||||
chr18:69910693
|
T | C | 1 | a0001c0001t0125g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.383-14648A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910693 | ||||||
chr18:69910782
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-14737A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910782 | ||||||
chr18:69910835
|
G | C | 1 | a0001c0001t0023g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.383-14790C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910835 | ||||||
chr18:69910961
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-14916A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69910961 | ||||||
chr18:69911028
|
A | G | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-14983T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911028 | ||||||
chr18:69911167
|
T | A | 1 | a0002c0009t0140g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-15122A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911167 | ||||||
chr18:69911234
|
G | GCC | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15190_383-1518 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911234 | ||||||
chr18:69911235
|
G | T | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15190C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911235 | ||||||
chr18:69911236
|
A | T | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15191T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911236 | ||||||
chr18:69911237
|
A | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15192T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911237 | ||||||
chr18:69911238
|
C | T | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15193G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911238 | ||||||
chr18:69911239
|
A | G | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-15194T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911239 | ||||||
chr18:69911286
|
G | A | 4 | a0001c0001t0077g0080a0003c0003t0005g0078a0003c0003t0005g0081others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-15241C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911286 | ||||||
chr18:69911328
|
G | A | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-15283C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911328 | ||||||
chr18:69911398
|
C | G | 1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383-15353G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911398 | ||||||
chr18:69911433
|
T | A | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.383-15388A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911433 | ||||||
chr18:69911580
|
A | C | 206 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.383-15535T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911580 | ||||||
chr18:69911591
|
C | T | 1 | a0002c0002t0095g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.383-15546G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911591 | ||||||
chr18:69911695
|
T | C | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.383-15650A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911695 | ||||||
chr18:69911697
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-15652A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911697 | ||||||
chr18:69911706
|
T | C | 2 | a0002c0002t0068g0043a0003c0003t0005g0045 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.383-15661A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911706 | ||||||
chr18:69911843
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.383-15798A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911843 | ||||||
chr18:69911877
|
A | C | 1 | a0001c0001t0016g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.383-15832T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911877 | ||||||
chr18:69911997
|
A | G | 1 | a0001c0001t0084g0038 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.383-15952T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69911997 | ||||||
chr18:69912099
|
G | T | 1 | a0003c0003t0017g0221 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.383-16054C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69912099 | ||||||
chr18:69912231
|
T | C | 1 | a0002c0002t0113g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.383-16186A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69912231 | ||||||
chr18:69912300
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02129.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.383-16255G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69912300 | ||||||
chr18:69912619
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-16574A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69912619 | ||||||
chr18:69912883
|
T | TTC | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-16840_383-1683 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69912883 | ||||||
chr18:69913107
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-17062A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913107 | ||||||
chr18:69913175
|
C | G | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.383-17130G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913175 | ||||||
chr18:69913184
|
A | C | 203 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.383-17139T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913184 | ||||||
chr18:69913235
|
T | C | 1 | a0002c0002t0059g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383-17190A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913235 | ||||||
chr18:69913312
|
A | G | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-17267T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913312 | ||||||
chr18:69913334
|
G | A | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-17289C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913334 | ||||||
chr18:69913345
|
G | T | 4 | a0001c0001t0003g0085a0001c0001t0003g0089a0001c0001t0083g0087others(1): Show | 4 | HG00280.hp2 HG01981.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-17300C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913345 | ||||||
chr18:69913520
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-17475A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913520 | ||||||
chr18:69913557
|
A | T | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.383-17512T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913557 | ||||||
chr18:69913675
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-17630A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913675 | ||||||
chr18:69913773
|
T | C | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.383-17728A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913773 | ||||||
chr18:69913811
|
C | T | 4 | a0001c0001t0001g0207a0001c0001t0011g0192a0001c0001t0126g0209others(1): Show | 4 | HG02040.hp2 NA18956.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-17766G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913811 | ||||||
chr18:69913829
|
G | A | 1 | a0001c0001t0134g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.383-17784C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913829 | ||||||
chr18:69913960
|
T | C | 16 | a0001c0001t0001g0132a0001c0001t0002g0211a0001c0001t0003g0044others(13): Show | 16 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.383-17915A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69913960 | ||||||
chr18:69914062
|
A | C | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-18017T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914062 | ||||||
chr18:69914213
|
C | A | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.383-18168G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914213 | ||||||
chr18:69914275
|
T | C | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383-18230A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914275 | ||||||
chr18:69914352
|
A | G | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-18307T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914352 | ||||||
chr18:69914389
|
T | C | 1 | a0002c0002t0095g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.383-18344A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914389 | ||||||
chr18:69914414
|
G | A | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-18369C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914414 | ||||||
chr18:69914505
|
G | A | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-18460C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914505 | ||||||
chr18:69914801
|
G | T | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-18756C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914801 | ||||||
chr18:69914913
|
A | G | 1 | a0001c0001t0091g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.383-18868T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914913 | ||||||
chr18:69914981
|
G | T | 6 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0124g0169others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-18936C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69914981 | ||||||
chr18:69915056
|
G | A | 1 | a0002c0002t0019g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.383-19011C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915056 | ||||||
chr18:69915195
|
T | C | 4 | a0001c0001t0077g0080a0003c0003t0005g0078a0003c0003t0005g0081others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-19150A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915195 | ||||||
chr18:69915233
|
G | A | 1 | a0001c0001t0011g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383-19188C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915233 | ||||||
chr18:69915318
|
C | A | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.383-19273G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915318 | ||||||
chr18:69915544
|
T | C | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.383-19499A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915544 | ||||||
chr18:69915559
|
C | T | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-19514G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915559 | ||||||
chr18:69915714
|
C | T | 1 | a0002c0002t0097g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.383-19669G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915714 | ||||||
chr18:69915774
|
C | T | 1 | a0001c0001t0082g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383-19729G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915774 | ||||||
chr18:69915961
|
C | T | 1 | a0002c0002t0111g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.383-19916G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69915961 | ||||||
chr18:69916071
|
ATT | A | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.383-20028_383-2002 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69916071 | ||||||
chr18:69916195
|
G | T | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.383-20150C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69916195 | ||||||
chr18:69916336
|
C | A | 1 | a0002c0002t0051g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.383-20291G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69916336 | ||||||
chr18:69916697
|
T | C | 1 | a0002c0002t0006g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.383-20652A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69916697 | ||||||
chr18:69917116
|
T | C | 3 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383-21071A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917116 | ||||||
chr18:69917118
|
T | C | 2 | a0002c0002t0028g0032a0002c0002t0028g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.383-21073A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917118 | ||||||
chr18:69917121
|
A | T | 1 | a0002c0002t0114g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.383-21076T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917121 | ||||||
chr18:69917640
|
G | A | 24 | a0001c0001t0001g0120a0001c0001t0001g0170a0001c0001t0001g0172others(21): Show | 24 | HG00621.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.383-21595C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917640 | ||||||
chr18:69917728
|
G | A | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.383-21683C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917728 | ||||||
chr18:69917806
|
T | A | 1 | a0001c0001t0016g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.383-21761A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69917806 | ||||||
chr18:69918008
|
T | G | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-21963A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918008 | ||||||
chr18:69918164
|
C | T | 1 | a0001c0001t0048g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.383-22119G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918164 | ||||||
chr18:69918247
|
G | C | 2 | a0001c0001t0011g0161a0001c0001t0031g0042 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.383-22202C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918247 | ||||||
chr18:69918350
|
T | C | 226 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.383-22305A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918350 | ||||||
chr18:69918465
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.383-22420C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918465 | ||||||
chr18:69918656
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.383-22611G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918656 | ||||||
chr18:69918763
|
G | A | 5 | a0001c0001t0024g0073a0001c0001t0078g0064a0002c0002t0072g0061others(2): Show | 5 | HG02965.hp1 HG03225.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-22718C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918763 | ||||||
chr18:69918796
|
T | C | 1 | a0001c0001t0083g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.383-22751A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918796 | ||||||
chr18:69918881
|
T | A | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-22836A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918881 | ||||||
chr18:69918901
|
G | T | 2 | a0001c0001t0002g0139a0002c0004t0034g0136 | 2 | HG01071.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.383-22856C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918901 | ||||||
chr18:69918981
|
T | C | 200 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(197): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.383-22936A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69918981 | ||||||
chr18:69919344
|
T | C | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-23299A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919344 | ||||||
chr18:69919461
|
A | G | 1 | a0002c0002t0030g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383-23416T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919461 | ||||||
chr18:69919490
|
C | A | 1 | a0001c0001t0026g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.383-23445G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919490 | ||||||
chr18:69919633
|
T | C | 1 | a0001c0001t0021g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.383-23588A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919633 | ||||||
chr18:69919714
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-23669A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919714 | ||||||
chr18:69919820
|
G | A | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-23775C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919820 | ||||||
chr18:69919983
|
C | A | 1 | a0001c0001t0130g0109 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.383-23938G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69919983 | ||||||
chr18:69920085
|
G | A | 1 | a0002c0002t0009g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.383-24040C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920085 | ||||||
chr18:69920137
|
T | C | 1 | a0001c0001t0091g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.383-24092A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920137 | ||||||
chr18:69920178
|
T | G | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-24133A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920178 | ||||||
chr18:69920240
|
G | T | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.383-24195C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920240 | ||||||
chr18:69920389
|
T | C | 1 | a0001c0001t0092g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.383-24344A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920389 | ||||||
chr18:69920544
|
C | T | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.383-24499G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920544 | ||||||
chr18:69920545
|
A | G | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-24500T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920545 | ||||||
chr18:69920783
|
GAC | G | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-24740_383-2473 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920783 | ||||||
chr18:69920975
|
G | C | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-24930C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69920975 | ||||||
chr18:69921053
|
A | G | 1 | a0001c0001t0061g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.383-25008T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921053 | ||||||
chr18:69921128
|
G | A | 1 | a0002c0002t0035g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.383-25083C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921128 | ||||||
chr18:69921216
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-25171A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921216 | ||||||
chr18:69921305
|
C | T | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.383-25260G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921305 | ||||||
chr18:69921307
|
C | T | 1 | a0001c0001t0131g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.383-25262G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921307 | ||||||
chr18:69921369
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.383-25324G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921369 | ||||||
chr18:69921395
|
C | T | 226 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.382+25339G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921395 | ||||||
chr18:69921465
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+25269A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921465 | ||||||
chr18:69921471
|
T | A | 8 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0081g0047others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+25263A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921471 | ||||||
chr18:69921510
|
T | C | 10 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0081g0047others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.382+25224A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921510 | ||||||
chr18:69921632
|
G | A | 1 | a0002c0002t0006g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.382+25102C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921632 | ||||||
chr18:69921722
|
A | G | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.382+25012T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921722 | ||||||
chr18:69921806
|
C | T | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+24928G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921806 | ||||||
chr18:69921871
|
T | C | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+24863A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69921871 | ||||||
chr18:69922292
|
T | C | 31 | a0001c0001t0001g0178a0001c0001t0001g0190a0001c0001t0001g0203others(28): Show | 31 | HG00438.hp2 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+24442A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69922292 | ||||||
chr18:69922398
|
C | T | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+24336G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69922398 | ||||||
chr18:69922681
|
T | C | 23 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+24053A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69922681 | ||||||
chr18:69922730
|
G | A | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382+24004C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69922730 | ||||||
chr18:69923150
|
G | A | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+23584C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923150 | ||||||
chr18:69923161
|
A | G | 1 | a0002c0002t0030g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.382+23573T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923161 | ||||||
chr18:69923187
|
A | AAAGG | 8 | a0001c0001t0003g0012a0001c0001t0025g0099a0001c0001t0080g0103others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+23543_382+2354 others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923187 | ||||||
chr18:69923187
|
A | AAAGGAAG others(1): Show |
4 | a0001c0001t0061g0049a0001c0001t0063g0046a0002c0002t0028g0032others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+23539_382+2354 others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923187 | ||||||
chr18:69923396
|
C | T | 1 | a0002c0002t0013g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+23338G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923396 | ||||||
chr18:69923422
|
C | T | 223 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+23312G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923422 | ||||||
chr18:69923521
|
C | A | 1 | a0002c0002t0105g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.382+23213G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923521 | ||||||
chr18:69923549
|
T | C | 1 | a0002c0002t0015g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.382+23185A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923549 | ||||||
chr18:69923643
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.382+23091C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923643 | ||||||
chr18:69923675
|
C | T | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382+23059G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923675 | ||||||
chr18:69923680
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+23054C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923680 | ||||||
chr18:69923728
|
C | T | 1 | a0002c0002t0007g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.382+23006G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923728 | ||||||
chr18:69923749
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382+22985G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923749 | ||||||
chr18:69923770
|
C | T | 36 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0016g0084others(33): Show | 36 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.382+22964G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923770 | ||||||
chr18:69923836
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+22898G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923836 | ||||||
chr18:69923871
|
A | G | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+22863T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923871 | ||||||
chr18:69923879
|
A | G | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+22855T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923879 | ||||||
chr18:69923910
|
C | T | 1 | a0001c0001t0139g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.382+22824G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923910 | ||||||
chr18:69923919
|
A | G | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+22815T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923919 | ||||||
chr18:69923953
|
C | CA | 13 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+22780dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923953 | ||||||
chr18:69923998
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.382+22736G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69923998 | ||||||
chr18:69924240
|
T | C | 231 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.382+22494A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924240 | ||||||
chr18:69924242
|
C | T | 1 | a0001c0001t0043g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.382+22492G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924242 | ||||||
chr18:69924402
|
T | C | 227 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.382+22332A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924402 | ||||||
chr18:69924473
|
T | C | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+22261A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924473 | ||||||
chr18:69924550
|
CA | C | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+22183delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924550 | ||||||
chr18:69924564
|
C | A | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.382+22170G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924564 | ||||||
chr18:69924692
|
C | CA | 7 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(4): Show | 7 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+22041dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
C | CAAAAAA | 5 | a0001c0001t0003g0012a0001c0001t0079g0030a0001c0001t0094g0135others(2): Show | 5 | HG01106.hp2 HG01243.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+22036_382+2204 others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
C | CAAAAAAA | 151 | a0001c0001t0001g0112a0001c0001t0001g0120a0001c0001t0001g0125others(148): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.382+22035_382+2204 others(11): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
C | CAAAAAAA others(1): Show |
20 | a0001c0001t0001g0114a0001c0001t0002g0139a0001c0001t0002g0164others(17): Show | 20 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.382+22034_382+2204 others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0025g0099a0001c0001t0061g0049a0001c0001t0080g0103others(3): Show | 6 | HG02145.hp1 HG02148.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+22033_382+2204 others(13): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0085g0102a0002c0002t0013g0101 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.382+22032_382+2204 others(14): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924692
|
CA | C | 7 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083others(4): Show | 7 | HG00099.hp1 HG00639.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+22041delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924692 | ||||||
chr18:69924790
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0134g0187 | 2 | HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.382+21944T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924790 | ||||||
chr18:69924941
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0002g0168a0002c0002t0035g0234 | 3 | HG00099.hp2 HG02738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.382+21793C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69924941 | ||||||
chr18:69925005
|
A | G | 21 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+21729T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925005 | ||||||
chr18:69925333
|
A | G | 15 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(12): Show | 15 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+21401T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925333 | ||||||
chr18:69925582
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+21152T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925582 | ||||||
chr18:69925599
|
G | A | 1 | a0002c0002t0112g0119 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.382+21135C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925599 | ||||||
chr18:69925619
|
A | T | 1 | a0002c0002t0029g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.382+21115T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925619 | ||||||
chr18:69925803
|
C | T | 1 | a0001c0001t0041g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382+20931G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925803 | ||||||
chr18:69925914
|
G | A | 2 | a0001c0001t0058g0033a0001c0001t0142g0243 | 2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.382+20820C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69925914 | ||||||
chr18:69926011
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+20723G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926011 | ||||||
chr18:69926012
|
G | A | 1 | a0002c0002t0038g0180 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.382+20722C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926012 | ||||||
chr18:69926099
|
C | T | 1 | a0002c0002t0119g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.382+20635G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926099 | ||||||
chr18:69926216
|
C | T | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382+20518G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926216 | ||||||
chr18:69926319
|
T | C | 1 | a0001c0001t0124g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382+20415A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926319 | ||||||
chr18:69926343
|
T | C | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382+20391A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926343 | ||||||
chr18:69926568
|
C | T | 1 | a0001c0001t0032g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.382+20166G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926568 | ||||||
chr18:69926593
|
T | C | 1 | a0007c0007t0005g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.382+20141A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926593 | ||||||
chr18:69926638
|
T | C | 1 | a0001c0001t0139g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.382+20096A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926638 | ||||||
chr18:69926679
|
T | C | 23 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+20055A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926679 | ||||||
chr18:69926994
|
G | GAACT | 23 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+19736_382+1973 others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69926994 | ||||||
chr18:69927187
|
C | T | 1 | a0001c0001t0083g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382+19547G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927187 | ||||||
chr18:69927204
|
G | A | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.382+19530C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927204 | ||||||
chr18:69927283
|
C | T | 5 | a0001c0001t0077g0080a0001c0001t0138g0239a0003c0003t0005g0078others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+19451G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927283 | ||||||
chr18:69927299
|
T | C | 1 | a0002c0002t0020g0181 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.382+19435A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927299 | ||||||
chr18:69927363
|
T | TAC | 168 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(165): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.382+19369_382+1937 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927363 | ||||||
chr18:69927363
|
T | TACAC | 22 | a0001c0001t0001g0207a0001c0001t0003g0012a0001c0001t0011g0192others(19): Show | 22 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.382+19367_382+1937 others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927363 | ||||||
chr18:69927363
|
T | TACACAC | 16 | a0001c0001t0003g0036a0001c0001t0021g0248a0001c0001t0021g0249others(13): Show | 16 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.382+19365_382+1937 others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927363 | ||||||
chr18:69927363
|
TAC | T | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+19369_382+1937 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927363 | ||||||
chr18:69927363
|
TACACAC | T | 23 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+19365_382+1937 others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927363 | ||||||
chr18:69927379
|
C | T | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382+19355G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927379 | ||||||
chr18:69927393
|
C | G | 1 | a0001c0001t0130g0109 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.382+19341G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927393 | ||||||
chr18:69927397
|
C | A | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+19337G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927397 | ||||||
chr18:69927625
|
C | T | 223 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+19109G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927625 | ||||||
chr18:69927626
|
A | C | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.382+19108T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927626 | ||||||
chr18:69927847
|
A | C | 23 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+18887T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69927847 | ||||||
chr18:69928025
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+18709G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928025 | ||||||
chr18:69928148
|
C | A | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+18586G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928148 | ||||||
chr18:69928213
|
A | G | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+18521T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928213 | ||||||
chr18:69928367
|
G | A | 223 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+18367C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928367 | ||||||
chr18:69928402
|
G | A | 49 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0002g0124others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.382+18332C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928402 | ||||||
chr18:69928692
|
C | A | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+18042G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928692 | ||||||
chr18:69928694
|
A | G | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+18040T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928694 | ||||||
chr18:69928882
|
G | C | 1 | a0001c0001t0090g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382+17852C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69928882 | ||||||
chr18:69929117
|
T | C | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382+17617A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929117 | ||||||
chr18:69929303
|
A | G | 5 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(2): Show | 5 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+17431T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929303 | ||||||
chr18:69929438
|
G | T | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382+17296C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929438 | ||||||
chr18:69929842
|
C | A | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.382+16892G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929842 | ||||||
chr18:69929842
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0127g0197 | 3 | HG01168.hp2 HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.382+16892G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929842 | ||||||
chr18:69929850
|
C | A | 8 | a0001c0001t0078g0064a0002c0002t0013g0060a0002c0002t0014g0059others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+16884G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929850 | ||||||
chr18:69929859
|
T | C | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+16875A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929859 | ||||||
chr18:69929893
|
T | A | 1 | a0001c0001t0063g0046 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.382+16841A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69929893 | ||||||
chr18:69930027
|
G | A | 4 | a0001c0001t0061g0049a0001c0001t0063g0046a0002c0002t0028g0032others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+16707C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930027 | ||||||
chr18:69930097
|
C | T | 224 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.382+16637G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930097 | ||||||
chr18:69930160
|
A | G | 27 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0016g0084others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.382+16574T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930160 | ||||||
chr18:69930169
|
T | A | 2 | a0001c0001t0001g0183a0001c0001t0124g0169 | 2 | HG02074.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.382+16565A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930169 | ||||||
chr18:69930414
|
G | T | 1 | a0002c0002t0122g0133 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.382+16320C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930414 | ||||||
chr18:69930528
|
C | CA | 226 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.382+16205dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930528 | ||||||
chr18:69930563
|
C | T | 2 | a0001c0001t0061g0049a0001c0001t0063g0046 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.382+16171G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930563 | ||||||
chr18:69930575
|
G | T | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.382+16159C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930575 | ||||||
chr18:69930613
|
A | G | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+16121T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930613 | ||||||
chr18:69930691
|
T | C | 224 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.382+16043A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930691 | ||||||
chr18:69930943
|
C | T | 223 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+15791G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69930943 | ||||||
chr18:69931125
|
T | A | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+15609A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69931125 | ||||||
chr18:69931174
|
T | C | 38 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0016g0084others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.382+15560A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69931174 | ||||||
chr18:69931301
|
G | A | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+15433C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69931301 | ||||||
chr18:69931805
|
C | A | 1 | a0001c0001t0138g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.382+14929G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69931805 | ||||||
chr18:69931979
|
T | G | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+14755A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69931979 | ||||||
chr18:69932053
|
A | C | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.382+14681T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932053 | ||||||
chr18:69932148
|
C | T | 1 | a0001c0001t0134g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.382+14586G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932148 | ||||||
chr18:69932258
|
A | G | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382+14476T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932258 | ||||||
chr18:69932280
|
T | C | 219 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.382+14454A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932280 | ||||||
chr18:69932327
|
G | A | 1 | a0001c0001t0126g0209 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.382+14407C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932327 | ||||||
chr18:69932398
|
T | C | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.382+14336A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932398 | ||||||
chr18:69932472
|
C | T | 2 | a0002c0002t0116g0110a0002c0002t0117g0117 | 2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.382+14262G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932472 | ||||||
chr18:69932993
|
G | A | 1 | a0001c0001t0084g0038 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.382+13741C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69932993 | ||||||
chr18:69933075
|
G | A | 7 | a0001c0001t0025g0099a0001c0001t0058g0033a0001c0001t0080g0103others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+13659C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933075 | ||||||
chr18:69933090
|
A | C | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+13644T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933090 | ||||||
chr18:69933135
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+13599A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933135 | ||||||
chr18:69933147
|
T | C | 47 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0016g0084others(44): Show | 47 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+13587A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933147 | ||||||
chr18:69933191
|
G | A | 2 | a0001c0001t0011g0122a0005c0006t0036g0210 | 2 | HG00438.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.382+13543C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933191 | ||||||
chr18:69933274
|
G | C | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+13460C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933274 | ||||||
chr18:69933337
|
A | G | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+13397T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933337 | ||||||
chr18:69933429
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+13305G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933429 | ||||||
chr18:69933434
|
C | A | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+13300G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933434 | ||||||
chr18:69933591
|
T | C | 1 | a0001c0001t0130g0109 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.382+13143A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933591 | ||||||
chr18:69933755
|
C | T | 83 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0125others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.382+12979G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933755 | ||||||
chr18:69933789
|
C | T | 3 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.382+12945G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69933789 | ||||||
chr18:69934137
|
T | C | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+12597A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934137 | ||||||
chr18:69934219
|
T | C | 2 | a0001c0001t0054g0004a0002c0002t0053g0005 | 2 | HG01952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.382+12515A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934219 | ||||||
chr18:69934277
|
G | GATAC | 10 | a0001c0001t0001g0127a0001c0001t0002g0185a0001c0001t0003g0044others(7): Show | 11 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+12453_382+1245 others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934277 | ||||||
chr18:69934279
|
T | TACAC | 5 | a0001c0001t0016g0077a0001c0001t0061g0049a0001c0001t0063g0046others(2): Show | 5 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+12451_382+1245 others(8): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACACAC | 22 | a0001c0001t0016g0084a0001c0001t0024g0067a0001c0001t0024g0073others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.382+12449_382+1245 others(10): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACACACA others(1): Show |
6 | a0001c0001t0077g0080a0001c0001t0082g0013a0002c0002t0014g0065others(3): Show | 6 | HG01243.hp2 HG01255.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+12447_382+1245 others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACACACA others(5): Show |
2 | a0002c0002t0029g0058a0002c0002t0030g0053 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.382+12443_382+1245 others(16): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACATACA others(5): Show |
5 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0057g0017others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+12454_382+1245 others(16): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACATACA others(7): Show |
3 | a0001c0001t0022g0019a0001c0001t0023g0052a0002c0002t0074g0051 | 3 | HG02717.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.382+12454_382+1245 others(18): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACATACA others(9): Show |
7 | a0001c0001t0022g0023a0001c0001t0023g0021a0001c0001t0089g0014others(4): Show | 7 | HG02886.hp1 HG03225.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+12454_382+1245 others(20): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACATACA others(11): Show |
5 | a0001c0001t0032g0025a0001c0001t0060g0029a0002c0002t0027g0026others(2): Show | 5 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+12454_382+1245 others(22): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934279
|
T | TACATACA others(15): Show |
1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382+12454_382+1245 others(26): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934279 | ||||||
chr18:69934281
|
C | CAT | 144 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.382+12452_382+1245 others(6): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934281 | ||||||
chr18:69934283
|
C | T | 16 | a0001c0001t0001g0132a0001c0001t0003g0085a0001c0001t0003g0086others(13): Show | 16 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.382+12451G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934283 | ||||||
chr18:69934312
|
G | A | 21 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(18): Show | 21 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+12422C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934312 | ||||||
chr18:69934400
|
G | C | 153 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(150): Show | 154 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.382+12334C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934400 | ||||||
chr18:69934500
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0082g0013 | 2 | HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.382+12234C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934500 | ||||||
chr18:69934520
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0127g0197 | 3 | HG01168.hp2 HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.382+12214G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934520 | ||||||
chr18:69934582
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+12152A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934582 | ||||||
chr18:69934649
|
C | T | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+12085G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934649 | ||||||
chr18:69934663
|
CA | C | 6 | a0001c0001t0077g0080a0001c0001t0081g0047a0002c0002t0015g0048others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+12070delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934663 | ||||||
chr18:69934729
|
A | G | 31 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0021g0248others(28): Show | 31 | HG00099.hp1 HG00639.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+12005T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934729 | ||||||
chr18:69934745
|
T | C | 171 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.382+11989A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69934745 | ||||||
chr18:69935024
|
A | G | 223 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.382+11710T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935024 | ||||||
chr18:69935050
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.382+11684G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935050 | ||||||
chr18:69935160
|
T | G | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+11574A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935160 | ||||||
chr18:69935623
|
G | A | 1 | a0002c0002t0039g0186 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.382+11111C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935623 | ||||||
chr18:69935677
|
A | T | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+11057T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935677 | ||||||
chr18:69935685
|
T | G | 9 | a0001c0001t0024g0073a0001c0001t0078g0064a0002c0002t0013g0060others(6): Show | 9 | HG01255.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.382+11049A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935685 | ||||||
chr18:69935736
|
T | C | 5 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(2): Show | 5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+10998A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935736 | ||||||
chr18:69935749
|
C | G | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+10985G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935749 | ||||||
chr18:69935766
|
G | A | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+10968C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935766 | ||||||
chr18:69935909
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.382+10825G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69935909 | ||||||
chr18:69936003
|
C | T | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+10731G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936003 | ||||||
chr18:69936037
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382+10697C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936037 | ||||||
chr18:69936229
|
CT | C | 200 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.382+10504delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936229 | ||||||
chr18:69936380
|
T | A | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+10354A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936380 | ||||||
chr18:69936467
|
G | A | 3 | a0001c0001t0049g0010a0001c0001t0050g0008a0001c0001t0055g0009 | 3 | HG02451.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382+10267C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936467 | ||||||
chr18:69936744
|
G | A | 175 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(172): Show | 176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.382+9990C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936744 | ||||||
chr18:69936873
|
T | C | 3 | a0001c0001t0002g0211a0001c0001t0003g0044a0001c0001t0003g0093 | 3 | HG00642.hp2 HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.382+9861A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69936873 | ||||||
chr18:69937005
|
G | C | 12 | a0001c0001t0001g0212a0001c0001t0002g0213a0001c0001t0002g0214others(9): Show | 12 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+9729C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937005 | ||||||
chr18:69937115
|
T | C | 9 | a0001c0001t0025g0099a0001c0001t0058g0033a0001c0001t0080g0103others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.382+9619A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937115 | ||||||
chr18:69937305
|
A | T | 4 | a0001c0001t0077g0080a0003c0003t0005g0078a0003c0003t0005g0081others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+9429T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937305 | ||||||
chr18:69937392
|
A | G | 1 | a0001c0001t0089g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.382+9342T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937392 | ||||||
chr18:69937576
|
A | G | 172 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.382+9158T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937576 | ||||||
chr18:69937581
|
T | C | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+9153A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937581 | ||||||
chr18:69937708
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+9026G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937708 | ||||||
chr18:69937770
|
C | T | 1 | a0002c0002t0111g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.382+8964G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937770 | ||||||
chr18:69937799
|
C | G | 11 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0026g0097others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+8935G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937799 | ||||||
chr18:69937812
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382+8922A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937812 | ||||||
chr18:69937888
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0128g0189 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.382+8846A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937888 | ||||||
chr18:69937889
|
A | G | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382+8845T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69937889 | ||||||
chr18:69938009
|
G | C | 1 | a0003c0003t0017g0221 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.382+8725C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938009 | ||||||
chr18:69938150
|
T | G | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+8584A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938150 | ||||||
chr18:69938203
|
G | C | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+8531C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938203 | ||||||
chr18:69938416
|
T | A | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+8318A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938416 | ||||||
chr18:69938564
|
C | A | 2 | a0001c0001t0001g0190a0002c0002t0106g0222 | 2 | NA18966.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.382+8170G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938564 | ||||||
chr18:69938571
|
C | T | 210 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(207): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.382+8163G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938571 | ||||||
chr18:69938598
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.382+8136T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938598 | ||||||
chr18:69938617
|
C | T | 3 | a0001c0001t0142g0243a0001c0001t0143g0241a0002c0009t0140g0242 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.382+8117G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938617 | ||||||
chr18:69938700
|
C | T | 7 | a0001c0001t0025g0099a0001c0001t0058g0033a0001c0001t0080g0103others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+8034G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938700 | ||||||
chr18:69938782
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0061g0049a0001c0001t0063g0046others(3): Show | 6 | HG02300.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+7952G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938782 | ||||||
chr18:69938813
|
G | A | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+7921C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938813 | ||||||
chr18:69938851
|
A | G | 32 | a0001c0001t0003g0012a0001c0001t0012g0016a0001c0001t0012g0034others(29): Show | 32 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.382+7883T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69938851 | ||||||
chr18:69939069
|
G | C | 8 | a0001c0001t0002g0225a0001c0001t0004g0123a0001c0001t0123g0194others(5): Show | 8 | HG01168.hp1 HG01361.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+7665C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939069 | ||||||
chr18:69939149
|
A | G | 2 | a0001c0001t0123g0194a0001c0001t0136g0121 | 2 | NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.382+7585T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939149 | ||||||
chr18:69939224
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.382+7510A>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939224 | ||||||
chr18:69939280
|
C | T | 1 | a0002c0002t0110g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.382+7454G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939280 | ||||||
chr18:69939498
|
G | A | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+7236C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939498 | ||||||
chr18:69939603
|
G | A | 2 | a0001c0001t0003g0036a0002c0002t0070g0035 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382+7131C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939603 | ||||||
chr18:69939702
|
C | T | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+7032G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939702 | ||||||
chr18:69939793
|
T | C | 17 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.382+6941A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939793 | ||||||
chr18:69939894
|
A | G | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+6840T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69939894 | ||||||
chr18:69940056
|
T | C | 5 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(2): Show | 5 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+6678A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940056 | ||||||
chr18:69940414
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0082g0013 | 2 | HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.382+6320C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940414 | ||||||
chr18:69940529
|
T | G | 30 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0021g0248others(27): Show | 30 | HG00099.hp1 HG00639.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.382+6205A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940529 | ||||||
chr18:69940584
|
TG | T | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+6149delC | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940584 | ||||||
chr18:69940665
|
G | A | 1 | a0002c0002t0047g0002 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.382+6069C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940665 | ||||||
chr18:69940794
|
G | T | 1 | a0002c0002t0097g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.382+5940C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940794 | ||||||
chr18:69940931
|
G | A | 17 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0025g0099others(14): Show | 17 | HG00099.hp1 HG00639.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.382+5803C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69940931 | ||||||
chr18:69941094
|
A | C | 2 | a0001c0001t0041g0129a0002c0002t0113g0130 | 2 | HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.382+5640T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941094 | ||||||
chr18:69941587
|
T | C | 1 | a0002c0002t0095g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382+5147A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941587 | ||||||
chr18:69941606
|
A | G | 50 | a0001c0001t0003g0012a0001c0001t0012g0016a0001c0001t0012g0034others(47): Show | 50 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.382+5128T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941606 | ||||||
chr18:69941690
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.382+5044G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941690 | ||||||
chr18:69941911
|
A | G | 27 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0021g0248others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.382+4823T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941911 | ||||||
chr18:69941930
|
C | T | 226 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.382+4804G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941930 | ||||||
chr18:69941956
|
T | C | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.382+4778A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69941956 | ||||||
chr18:69942200
|
T | C | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+4534A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69942200 | ||||||
chr18:69942255
|
C | T | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.382+4479G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69942255 | ||||||
chr18:69942323
|
A | C | 1 | a0001c0001t0011g0192 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.382+4411T>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69942323 | ||||||
chr18:69943036
|
G | A | 2 | a0001c0001t0079g0030a0002c0002t0015g0031 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.382+3698C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943036 | ||||||
chr18:69943131
|
T | C | 254 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.382+3603A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943131 | ||||||
chr18:69943138
|
T | C | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+3596A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943138 | ||||||
chr18:69943362
|
T | C | 230 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.382+3372A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943362 | ||||||
chr18:69943461
|
T | C | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382+3273A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943461 | ||||||
chr18:69943493
|
C | T | 4 | a0001c0001t0026g0097a0001c0001t0064g0096a0001c0001t0081g0047others(1): Show | 4 | HG02145.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+3241G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943493 | ||||||
chr18:69943847
|
C | G | 5 | a0001c0001t0001g0125a0001c0001t0001g0127a0002c0002t0009g0001others(2): Show | 6 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+2887G>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943847 | ||||||
chr18:69943874
|
C | CA | 4 | a0001c0001t0061g0049a0001c0001t0063g0046a0002c0002t0028g0032others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+2859dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943874 | ||||||
chr18:69943971
|
G | T | 5 | a0001c0001t0042g0107a0001c0001t0042g0108a0001c0001t0129g0106others(2): Show | 5 | HG01069.hp1 HG01255.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+2763C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943971 | ||||||
chr18:69943973
|
C | CT | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.382+2760dupA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943973 | ||||||
chr18:69943973
|
CT | C | 59 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0001g0212others(56): Show | 59 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.382+2760delA | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943973 | ||||||
chr18:69943974
|
T | TGA | 8 | a0001c0001t0003g0012a0001c0001t0026g0097a0001c0001t0064g0096others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+2759_382+2760i others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943974 | ||||||
chr18:69943975
|
T | C | 8 | a0001c0001t0003g0012a0001c0001t0026g0097a0001c0001t0064g0096others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+2759A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943975 | ||||||
chr18:69943997
|
T | C | 2 | a0001c0001t0138g0239a0002c0002t0030g0075 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+2737A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69943997 | ||||||
chr18:69944161
|
G | A | 1 | a0002c0002t0030g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.382+2573C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944161 | ||||||
chr18:69944181
|
A | G | 4 | a0001c0001t0061g0049a0001c0001t0063g0046a0002c0002t0028g0032others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+2553T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944181 | ||||||
chr18:69944298
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.382+2436G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944298 | ||||||
chr18:69944307
|
G | A | 169 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(166): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.382+2427C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944307 | ||||||
chr18:69944450
|
G | T | 4 | a0001c0001t0003g0012a0001c0001t0026g0097a0001c0001t0064g0096others(1): Show | 4 | HG02145.hp2 HG02300.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+2284C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944450 | ||||||
chr18:69944462
|
T | C | 1 | a0002c0002t0104g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.382+2272A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944462 | ||||||
chr18:69944570
|
T | G | 1 | a0001c0001t0016g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.382+2164A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944570 | ||||||
chr18:69944676
|
T | C | 2 | a0002c0002t0007g0228a0002c0002t0020g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.382+2058A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944676 | ||||||
chr18:69944697
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+2037A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944697 | ||||||
chr18:69944934
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+1800C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69944934 | ||||||
chr18:69945020
|
G | C | 2 | a0001c0001t0081g0047a0002c0002t0015g0048 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382+1714C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945020 | ||||||
chr18:69945146
|
G | T | 9 | a0001c0001t0003g0012a0001c0001t0016g0084a0001c0001t0026g0097others(6): Show | 9 | HG00099.hp1 HG00639.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.382+1588C>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945146 | ||||||
chr18:69945291
|
T | G | 5 | a0001c0001t0058g0033a0001c0001t0061g0049a0001c0001t0063g0046others(2): Show | 5 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+1443A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945291 | ||||||
chr18:69945293
|
G | A | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+1441C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945293 | ||||||
chr18:69945362
|
A | G | 19 | a0001c0001t0012g0016a0001c0001t0012g0034a0001c0001t0022g0019others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.382+1372T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945362 | ||||||
chr18:69945619
|
C | T | 1 | a0001c0001t0058g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+1115G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945619 | ||||||
chr18:69945896
|
A | T | 6 | a0001c0001t0003g0012a0001c0001t0026g0097a0001c0001t0064g0096others(3): Show | 6 | HG02145.hp2 HG02300.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+838T>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69945896 | ||||||
chr18:69946045
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.382+689C>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946045 | ||||||
chr18:69946058
|
C | A | 12 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(9): Show | 12 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+676G>T | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946058 | ||||||
chr18:69946101
|
T | G | 3 | a0001c0001t0004g0230a0001c0001t0004g0231a0001c0001t0004g0232 | 3 | NA18956.hp1 NA18984.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.382+633A>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946101 | ||||||
chr18:69946180
|
CA | C | 11 | a0001c0001t0024g0067a0001c0001t0024g0073a0001c0001t0025g0069others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+553delT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946180
|
CAA | C | 41 | a0001c0001t0016g0084a0001c0001t0021g0248a0001c0001t0021g0249others(38): Show | 41 | HG01081.hp1 HG01175.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.382+552_382+553del others(2): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946180
|
CAAA | C | 153 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0132others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.382+551_382+553del others(3): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946180
|
CAAAA | C | 30 | a0001c0001t0001g0120a0001c0001t0003g0012a0001c0001t0004g0123others(27): Show | 30 | HG00438.hp2 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.382+550_382+553del others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946180
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0004g0116a0002c0002t0037g0115 | 2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.382+542_382+553del others(12): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946180
|
CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0004g0113others(9): Show | 12 | HG00438.hp1 HG01069.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.382+541_382+553del others(13): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946180 | ||||||
chr18:69946202
|
A | G | 3 | a0001c0001t0142g0243a0001c0001t0143g0241a0002c0009t0140g0242 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.382+532T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946202 | ||||||
chr18:69946246
|
AAAAG | A | 4 | a0001c0001t0077g0080a0003c0003t0005g0078a0003c0003t0005g0081others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+484_382+487del others(4): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946246 | ||||||
chr18:69946380
|
A | AATG | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+351_382+353dup others(3): Show |
CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946380 | ||||||
chr18:69946690
|
A | G | 225 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.382+44T>C | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946690 | ||||||
chr18:69946693
|
G | C | 3 | a0001c0001t0016g0084a0001c0001t0033g0082a0001c0001t0033g0083 | 3 | HG00099.hp1 HG00639.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.382+41C>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946693 | ||||||
chr18:69946708
|
T | TA | 15 | a0001c0001t0003g0012a0001c0001t0003g0085a0001c0001t0003g0086others(12): Show | 15 | HG00280.hp2 HG00597.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+25dupT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946708 | ||||||
chr18:69946708
|
T | TAA | 11 | a0001c0001t0021g0248a0001c0001t0021g0249a0001c0001t0021g0250others(8): Show | 11 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+24_382+25dupTT | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 2/5 | chr18 | 69946708 | ||||||
chr18:69947091
|
T | C | 1 | a0002c0002t0009g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.47-22A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/5 | chr18 | 69947091 | ||||||
chr18:69947216
|
T | C | 2 | a0001c0001t0026g0097a0001c0001t0064g0096 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.46+145A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/5 | chr18 | 69947216 | ||||||
chr18:69947298
|
C | T | 2 | a0001c0001t0003g0012a0001c0001t0082g0013 | 2 | HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+63G>A | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/5 | chr18 | 69947298 | ||||||
chr18:69947331
|
T | C | 6 | a0001c0001t0025g0099a0001c0001t0080g0103a0001c0001t0085g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+30A>G | CD226 | ENSG00000150637.9 | transcript | ENST00000582621.6 | protein_coding | 1/5 | chr18 | 69947331 |